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Review

Efficacy and Mechanism of Traditional Medicinal Plants and Bioactive Compounds against Clinically Important Pathogens

by
Suresh Mickymaray
Department of Biology, College of Science, Al-Zulfi-, Majmaah University, Majmaah 11952, Saudi Arabia
Submission received: 4 November 2019 / Revised: 27 November 2019 / Accepted: 28 November 2019 / Published: 9 December 2019
(This article belongs to the Special Issue Natural Compounds as Antimicrobial Agents)

Abstract

:
Traditional medicinal plants have been cultivated to treat various human illnesses and avert numerous infectious diseases. They display an extensive range of beneficial pharmacological and health effects for humans. These plants generally synthesize a diverse range of bioactive compounds which have been established to be potent antimicrobial agents against a wide range of pathogenic organisms. Various research studies have demonstrated the antimicrobial activity of traditional plants scientifically or experimentally measured with reports on pathogenic microorganisms resistant to antimicrobials. The antimicrobial activity of medicinal plants or their bioactive compounds arising from several functional activities may be capable of inhibiting virulence factors as well as targeting microbial cells. Some bioactive compounds derived from traditional plants manifest the ability to reverse antibiotic resistance and improve synergetic action with current antibiotic agents. Therefore, the advancement of bioactive-based pharmacological agents can be an auspicious method for treating antibiotic-resistant infections. This review considers the functional and molecular roles of medicinal plants and their bioactive compounds, focusing typically on their antimicrobial activities against clinically important pathogens.

1. Introduction

The incidence of microbial infectious diseases and their hitches consistently elevates, mostly due to microbial drug resistance to presently offered antimicrobial agents [1]. These multidrug-resistant microbes cause various infections globally and are connected with greater levels of morbidity and mortality [2]. These augmentations of antibiotic resistance and higher recurrence rates of such common infections have a great impact on our society [3,4,5]. Several investigations associated with antimicrobial resistance predict that the mortality toll owing to antimicrobial resistance may exceed 10 million by 2050, theoretically leading to greater mortality in the context of other infectious diseases and malignancies [6]. It is well known that infections are generally difficult to treat due to the development of biofilm in the host, which aids the proliferation of microbes as well as the aggressiveness of the infections [7]. Studies have also well-established that the physical structures of biofilm establishing organisms confer natural resistance to hostile environments, including antimicrobial agents [8]. Therefore, it is an urgent requirement to generate novel antimicrobial drugs which can inhibit the development of, or abolish the complete biofilms, and hence increase the vulnerability of microbes to antimicrobials. The requisite for new antimicrobials which could meritoriously fight against antimicrobial resistant clinical pathogens is extremely augmented.
Plant-derived antimicrobials have been established to be one of the most auspicious sources considered as safe due to their natural origin when compared with synthetic compounds [9,10]. There is an accumulating interest in the practice of either crude extract of medicinal plants, as well as the screening plant-derived compounds as an alternative therapy for microbial infections [11]. Plants generally produce a diverse range of bioactive compounds which have been widely used in clinical practice [12]. Remarkably, a significant number of marketed drugs are obtained from nature or result in natural products through either chemical transformations or de novo synthesis [13]. Plant-derived compounds are a group of secondary metabolites that are used to treat chronic as well as infectious diseases. These traditional medicinal plants or active compounds remain included as part of the habitual treatment of various maladies [9]. These compounds could have other target sites than conventional antimicrobials as well as diverse mechanisms of action against pathogenic microbes. An electronic search was performed using PubMed, Science Direct, and Google Scholar using the keywords “medicinal plants” AND “bioactive compounds” AND “antimicrobial activities” AND “antibiotic resistance” in “Title/Abstract/Keywords” without date restriction in order to identify all published studies (in vitro, in vivo, clinical and case-control) that have investigated the connection between medicinal plants and their antimicrobial effects. Antimicrobial mechanisms were gathered and for review.

2. Traditional Medicinal Plants

The species of the plant kingdom are estimated to number about 500,000 and only a minor portion of them have been investigated for antimicrobial activity [9,14]. Traditional medicinal plants can be cultivated by humans over centuries without existing systematic standards and analysis due to their safety and efficacy. Hence, bioactive compounds derived from these medicinal plants apparently have more potential to succeed in toxicology screening when compared with the de novo synthesis of chemicals. The cumulative attention on traditional ethnomedicine may lead to the revealing of innovative therapeutic agents since traditional medicinal plant contains potential antimicrobial components that are beneficial for the development of pharmaceutical agents for the therapy of ailments. Nowadays, studies are progressively turning their consideration to traditional medicine and advancing better drugs to treat diabetes, cancer, and microbial infections [15,16]. A large number of studies have been piloted using medicinal plant extracts and their active principles on bacteria, fungi, algae, and viruses in different localities of the world [9,10]. Various families of traditional medicinal plants have been scientifically tested for their antimicrobial activities and are presented in Table 1. The extracts of plant organs, namely the root, stem, rhizome, bulb, leaf, bark, flower, fruit, and seed, may encompass distinctive phytochemicals with antimicrobial activities [17]. It is well-known that sole plant species of traditional medicine are habitually used to heal a great number of infections or diseases [18]. The plant extracts with an antiquity of folk use should be confirmed using contemporary methods for activities against human pathogens with the intention of identifying potential novel therapeutic drugs.

Phytocomponent Fractions and Antimicrobial Methods

Fresh or dried plant extracts were prepared using aqueous and different organic solvents in traditional extraction techniques (maceration, percolation, Soxhlet extraction). During the extraction method, the solvents penetrate into the plant material and dissolve active compounds with a related polarity [62]. At the completion of the technique, solvents have been vaporized, resulting in the formation of a concentrated mixture that yields the active compounds [63]. A successful extraction is mainly reliant on the nature of the solvent utilized during the extraction. The most regularly established extracts are aqueous extract followed by organic solvents, which include using methanol, ethanol, hexane, isopropanol, ethyl acetate, benzene, acetone, chloroform, and dichloromethane [64].
Two popular types of antibacterial susceptibility test, namely diffusion and dilution methods, are generally performed to determine the antibacterial efficacy of the plant materials. The method of diffusion is a screening test to classify bacteria that aid susceptibility or resistance to the tested plant material based on the size or diameter of the inhibition zone [62]. On the other hand, the activity of plant materials is determined as minimum inhibitory concentration (MIC) in the dilution method. In the MIC method, the lowest concentration is capable of inhibiting bacterial growth. Redox indicators and turbidity are most often measured for the analysis of results in broth dilution methods. The turbidity can be calculated colorimetrically while changing the indicator color represents the inhibition of bacterial growth [62]. The screening of traditional plant extracts has been of great attention to researchers investigating novel bioactive compounds effective in the treatment of microbial infections. Plant extracts exhibit: (a) direct antimicrobial activity presenting effects on metabolism and development of microbes and (b) indirect activity as antibiotic resistance adapting substances which, joint with antibiotics, upsurge their efficiency. Numerous studies have considered the antimicrobial screening of traditional plant extracts. The studies of medicinal plants from diverse topographical areas include: Armenia [65], Iran [66], Mexico [67], Saudi Arabia [68], Libya [26], Ethiopia [64], India [63], Poland [69], Cameroon [70], Nigeria [71], and other Middle Eastern countries [72]. Based on the available information, the traditional plant extracts showed antimicrobial activity against a huge number of pathogenic bacteria, fungi, viruses, algae, protozoan, and Trypanosoma [26,63,64,66].

3. Bioactive Compounds (Bioactive Phytocomponents)

Traditional medicinal plants possess various chemical substances that support certain physiological and biochemical activities in the human body and they are known as phytochemicals or phytocomponents. These chemicals are non-nutritive substances used to heal various infectious diseases, as well as provide disease preventive properties [9,10]. With advances in phytochemical practices, numerous active principles have been isolated from medicinal plants and presented as a valuable drug in contemporary systems of medicine. Mostly, the pharmacological activity of medicinal plants resides in their secondary metabolites, which are relatively smaller in quantity in contrast to the primary molecules such as carbohydrates, proteins, and lipids. Plant secondary metabolites are commonly accountable for their antimicrobial properties [62]. These metabolites offer clues to manufacture new structural types of antimicrobial and antifungal chemicals that are comparatively safe to humans [62]. The classes of secondary metabolites that have greater antimicrobial properties are flavonoids (flavones, flavonols, flavanols, isoflavones, anthocyanidins), phenolic acids (hydroxybenzoic, hydroxycinnamic acids), stilbenes, lignans, quinones, tannins, coumarins (simple coumarins, furanocoumarins, pyranocoumarins), terpenoids (sesquiterpene lactones, diterpenes, triterpenes, polyterpenes), alkaloids, glycosides, saponins, lectins, steroids, and polypeptides [6,16,56,62,73,74,75,76,77,78,79,80,81,82,83]. These compounds have copious mechanisms that underlie antimicrobial activity, e.g., disturbing microbial membranes, weakening cellular metabolism, control biofilm formation, inhibiting bacterial capsule production, attenuating bacterial virulence by controlling quorum-sensing, and reducing microbial toxin production [3,4,5,6,73,74,75,76,77,78,79,80,81,82,83,84,85]. Various bioactive compounds have been scientifically tested for their antimicrobial activities and are presented in Table 2.

4. Mechanism of Actions of Antibacterial Bioactive Compounds

As proven by in vitro experiments, medicinal plants produce a boundless quantity of secondary metabolites that have great antimicrobial activity [9,10,18]. These plant-produced low molecular weight antibiotics are classified according to two types, namely phytoanticipins, which are involved in microbial inhibitory actions, and phytoalexins, which are generally anti-oxidative and synthesized de novo by plants in response to microbial infection [16,74]. Plant antimicrobial secondary metabolites are generally categorized into three broad classes, namely phenolic compounds, terpenes, and alkaloids. Numerous studies have shown that the antimicrobial activity of the plant extracts and their active compounds have the following potential: to promote cell wall disruption and lysis, induce reactive oxygen species production, inhibit biofilm formation, inhibit cell wall construction, inhibit microbial DNA replication, inhibit energy synthesis, and inhibit bacterial toxins to the host [75,85,105,106,107,108,109]. In addition, these compounds may prevent antibacterial resistance as well as synergetics to antibiotics, which can ultimately kill pathogenic organisms (Figure 1).

4.1. Promote Cell Wall Disruption and Lysis

Phenolic compounds are a family of aromatic rings consisting of a hydroxyl functional group (-OH) which is alleged to absolute toxicity to microorganisms, although increased reactions of hydroxylation result in microbial cell lysis [110]. Quinones also have aromatic rings with two ketone molecules, which enables the production of an irreversible complex with nucleophilic amino acids, resulting in greater antimicrobial properties. These potential aromatic compounds are usually targeted to microbial cell surface adhesins, membrane-bound polypeptides, enzymes, and eventually lysis of the microbes [111]. Flavonoids are hydroxylated phenolic substances which are also able to complex with bacterial cell walls and disrupt microbial membranes [75,105]. Highly active flavonoids, quercetin (1), rutin (2), naringenin (3), sophoraflavanone (4), tiliroside (5) and 2, 4, 6-trihydroxy-30-methyl chalcone (6) (Figure 2) decreased lipid bilayer thickness and fluidity levels and increased membrane permeability, supporting the leaking of intracellular protein and ions in S. aureus and S. mutans [112,113]. These compounds contribute to the synergistic effect with ampicillin and tetracycline [114]. The other active flavonoids, acacetin (7), apigenin (8), morin (9), and rhamnetin (10) (Figure 2) cause weakening of the bacterial cell wall by disarrangement and disorientation of the lipid bilayer and ultimately persuade vesicle leakage [115,116,117]. The synthetic flavonoid lipophilic 3-arylidene (11) was found to be very active against S. aureus, S. epidermidis, and E. faecalis due to a bacterial cell clump that influences the integrity of the cell wall as a result of biofilm disruption [118]. Tannins are classes of another polymeric phenolic substance, characterized as astringency, which is capable to deactivate microbial adhesins, enzymes, and membrane transporter systems [105,119]. Coumarins (12) are benzo-α-pyrones known to stimulate macrophages, which could have an adverse effect on infections [7,120]. Terpenes are organic compounds containing isoprene subunits, which involve microbial membrane disruption [121,122]. Thymol (13), eugenol (14), Cinnamaldehyde (15), carvone (16), and carvacrol (17) (Figure 2) disintegrate the external membrane of various Gram-negative bacteria, releasing LPS and increasing the permeability [123,124,125].

4.2. Inhibition of Biofilm Formation

The key features of bacteria developing biofilms are generally 100–1000 times more resistant to antimicrobial drugs while related to their usual planktonic forms [64]. Interestingly, numerous researchers have described how flavonoids cause the aggregation of multicellular composites of bacteria and inhibit bacterial growth after aggregation, which indicates that flavonoids are potent antibiofilm compounds. The bioactive flavonoids such as galangin (18), isovitexin (19), EGCG (20) and 3-O-octanoyl-epicatechin (21), as well as 5, 7, and 40-trihydroxyflavanol (22) induce pseudo multicellular aggregation of S. aureus and S. mutans [106,107,108,109]. Quorum sensing involves cell signaling molecules called autoinducers present in E. coli, Vibrio cholerae, and S. typhi, which is a notable regulatory factor for biofilm formation [126]. Interestingly, apigenin (8), kaempferol (23), quercetin (1), and naringenin (3) are effective antagonists of cell–cell signaling [126,127] that have been revealed to inhibit enteroaggregative biofilm formation in E. coli and P. aeruginosa in a concentration-dependent manner [128,129]. Moreover, chrysin (24), phloretin (25), naringenin (3), kaempferol (23), epicatechin gallate (26), proanthocyanidins (27), and EGCG (20) (Figure 2) inhibited N-acyl homoserine lactones-mediated QS [130,131,132]. Hydrophilic flavonoids such as 6-aminoflavone (28), 6-hydroxyflavone (29), apigenin (8), chrysin (24), daidzein (30), genistein (31), auronol (32), and phloretin (25) (Figure 2) have inhibitory effects on E. coli biofilm formation [133,134]. In addition, Phloretin (25) inhibited fimbriae formation in E. coli by reducing the expression of the curli genes (csgA, csgB) and toxin genes (hemolysin E, Shiga toxin 2) [6], eventually inhibiting the formation of biofilm. Hence, phloretin (25) is well known as an antibiotic resistant compound. Pinostrobin (33), EGCG (20) and prenylated flavonoids enhanced membrane permeability in E. faecalis, S. aureus, E. coli, and P. aeruginosa, Porphyromonas gingivalis, which is consistent with its effect on efflux-pump inhibitors and anti-biofilm formation [34,135,136].

4.3. Inhibition of Cell Wall Construction

The bacterial cell wall is accountable for osmoregulation, respiration, the transport mechanism, and biosynthesis of lipids. For the execution of these functions, membrane integrity is very important, and its disruption can directly or indirectly cause metabolic dysfunction eventually leads to bacterial death. Catechins (34) attract lipid bilayers of the membrane which involves the following mechanisms [137]. Catechins form hydrogen bonds, which attract polar head groups of lipids at the membrane edge. Epicatechin (35) and epigallocatechin gallate (26) alter phospholipids, which can alter structural changes in the cell membrane. Moreover, these catechins promote the inactivation or inhibition of intracellular and extracellular enzyme synthesis [137]. Generally, the inhibition of enzymes in fatty acid biosynthesis is an excellent target for antimicrobial agents for blocking bacterial growth, especially the key enzyme fatty acid synthase II (FAS-II) inhibitor is significant as an antimicrobial drug. Quercetin (1), apigenin (8), and sakuranetin (36) have been demonstrated to inhibit 3-hydroxyacyl-ACP dehydrase from Helicobacter pylori [138] and eriodictyol (37). Further, naringenin (3) and taxifolin (38) (Figure 2) inhibit 3-ketoacyl- ACP synthase from E. faecalis [139]. Flavonoids such as Epigallocatechin gallate (EGCG) (20), 5, 6, 7, 40, 50- pentahydroxyflavone (39), and 5-hydroxy-40, 7-dimethoxyflavone (40) inhibit the malonyl CoA-acyl carrier protein transacylase that regulates bacterial FAS-II [140,141]. EGCG (20) inhibits 3-ketoacyl-ACP reductase and enoyl-ACP reductase and prevents fatty acid biosynthesis [142]. Quercetin (1), kaempferol (23), 4, 20, 40-trihydroxychalcone (41), fisetin (42), morin (9), myricetin (43), baicalein (44), luteolin (45), EGCG (20), butein (46), and isoliquirtigenin (47) (Figure 2) inhibit various enzymes involved in fatty acid synthesis, including, FAS-II, enoyl-ACP-reductase, β-ketoacyl-ACP reductase, and β-hydroxy acyl-ACP dehydratases in Mycobacterium sp. [143]. Baicalein (44), EGCG (20), galangin (18), kaempferide (48), DL-cycloserine (49), quercetin (1), apigenin (8), and kaempferide-3-O-glucoside (50) (Figure 2) inhibit the synthesis of peptidoglycan, which is an essential component of the bacterial cell wall, resulting in cell wall damage [144,145,146].

4.4. Inhibition of Prokaryotic DNA Replication

Alkaloids are nitrogenous compounds characterized by their alkaline nature, which aids the inhibition of cell respiration, intercalates with DNA, and inhibits various enzymes involved in replication, transcription, and translation [147]. Plant-based bioactive compounds such as quercetin (1), nobiletin (51), myricetin (43), tangeritin (52,) genistein (31), apigenin (8), chrysin (24), kaempferol (23), and 3, 6, 7, 30, 40-pentahydroxyflavone (39) have been recognized as noteworthy DNA gyrase inhibitors, which are essential for DNA replication in prokaryotes including V. harveyi, B. subtilis, M. smegmatis, M. tuberculosis, and E. coli [146,148,149,150,151]. These bioactive compounds binding to the β subunit of gyrase and the corresponding blockage of the ATP binding pocket eventually contribute to the antimicrobial activity. Bioactive compounds have mediated the dysfunction of DNA gyrase functions in a dose-dependent manner that leads to the impairment of cell division and/or completion of chromosome replication, resulting in the inhibition of bacterial growth [149]. Luteolin (45), morin (9), and myricetin (43) have been demonstrated to inhibit the helicases of E. coli [152]. Helicases consititute another significant replicative enzyme responsible for separating and/or rearranging DNA double-strands [153]. Furthermore, myricetin (43) and baicalein (44) have been proposed as potent inhibitors of numerous DNA and RNA polymerases, as well as viral reverse transcriptase, resulting in the inhibition of bacterial growth [154]. EGCG (20), myricetin (43), and robinetin (53) have been demonstrated as inhibitors of dihydrofolate reductase in Streptomonas maltophilia, P.vulgaris, S. aureus, M. tuberculosis, and E. coli [43,155,156]. Dihydrofolate reductase is key enzyme for the synthesis of the purine and pyrimidine rings of nucleic acid, resulting in reduced DNA, RNA, and protein synthesis [156].

4.5. Inhibition of Energy Production

Energy production or ATP synthesis is the supreme vital requirement for the existence and development of bacteria as these chemicals are the main source of living systems. The treatment of flavonoids such as isobavachalcone (54) and 6-prenylapigenin (55) with S. aureus cause membrane depolarization, resulting in bacterial cell wall lysis [101]. Similarly, licochalcones (56) inhibited oxygen consumption in M. luteus, interruping the electron transport system eventually killing the bacteria [6]. It has been described that flavonoids such as baicalein (44), morin (9), silibinin (57), quercetin (1), isoquercetin (58), quercitrin (59), and silymarin (60) can constrain the F1FO ATPase system of E. coli and result in the obstruction of ATP synthesis [157,158,159]. Additionally, EGCG (20), 40, 50, 5-trihydroxy-6, 7-dimethoxy-flavone (61), and proanthocyanidins (27) have also inhibited S. mutans, P. aeruginosa and S. aureus through the enzymatic activity of F1FO ATPase respectively [100,104,141].

4.6. Inhibition of Bacterial Toxins

It is noteworthy that catechins and other flavonoids can cause bacterial cell wall destruction, resulting in an inability to discharge toxins [160,161]. Catechins (34), pinocembrin, kaempferol, EGCG (20), gallocatechin gallate (26), kaempferol-3-O-rutinoside (62), genistein (31), quercetin glycoside (63), and proanthocyanidins (27) (Figure 2) are suggested to neutralize bacterial toxic factors initiating from V. cholerae, E. coli, S. aureus, V. vulnificus, B. anthracis, N. gonorrhoeae, and C. botulinum [162,163,164,165]. Bacterial hyaluronidases are enzymes formed by both Gram-positive and Gram-negative bacteria and directly interact with host tissues, causing the permeability of connective tissues and reducing the viscosity of body fluids due to hyaluronidase-mediated degradation [166]. Flavonoids such as myricetin (43) and quercetin (1) have been identified as hyaluronic acid lyase inhibitors in Streptococcus equisimilis and Streptococcus agalactiae [167].

4.7. Mechanism of Resistance to Antibacterial Agents

Pathogenic bacteria generally receive the resistance to various antibiotics through diverse mechanisms. Such mechanisms include: (a) bacteria can share the resistance genes through transformation, transduction, and conjugation; (b) bacteria produce various enzymes to deactivate the antibiotics through the process of phosphorylation, adenylation, or acetylation; (c) damage or alteration of the drug compound; (c) prevent the interaction of the drug with the target; (d) efflux of the antibiotic from the cell [168,169,170]. Emodin (1, 2, 8-trihydroxy-6-methylanthraquinone) (64) is an anthraquinone derivative which prevents the transformation of resistance genes in S. aureus [171]. Baicalein is a potent inhibitor of the expression of the SOS genes, RecA, LexA, and SACOL1400 that prevent rifampin-resistant mutation in S. aureus [172]. Phenolic compounds such as Carnosic (65) and rosmarinic acids (66) inactivate cmeB, cmeF, and cmeR genes in Campylobacter jejuni [173].

4.8. Antimicrobial Action with Generation of Reactive Oxygen Species

Reactive oxygen species (ROS) can be formed by the partial reduction of molecular oxygen that targets the exertion of antimicrobial activity, which aids host defense against various disease-causing pathogens. The suggested method of antimicrobial activity of catechins (34) involves augmentation of the production of oxidative stress (ROS and RNS), which can alter membrane permeability and cause as cell wall damage [174]. In addition, catechins damage liposomes as they contain a high amount of negatively charged lipids and are susceptible to damage [175]. An earlier study indicated that catechins support the leaking of potassium and disturbs the membrane transport system in a methicillin-resistant S. aureus strain [85]. This team has further demonstrated that acylated 3-O-octanoyl-epicatechin (21) is a lipophilic compound that produces more outcomes in antibacterial activity.

5. Conclusions

Since time immemorial, traditional medicinal plants have been cultivated by diverse populations to treat a great number of infectious diseases. Various investigations on the pharmacognostics and kinetics of medicinal plants have shown that crude extracts and plant-derived bioactive compounds may enhance the effects of traditional antimicrobials, which may be cost-effective, have fewer side effects, and improve the quality of treatment. Numerous studies have shown that the antimicrobial activity of plant extracts and their active compounds have the following potential: promote cell wall disruption and lysis, induce reactive oxygen species production, inhibit biofilm formation, inhibit cell wall construction, inhibit microbial DNA replication, inhibit energy synthesis, and inhibit bacterial toxins to the host. In addition, these compounds may prevent antibacterial resistance as well as synergetics to antibiotics, which can ultimately kill pathogenic organisms. Based on these comprehensive antimicrobial mechanisms, the cultivation of traditional plant extracts and bioactive compounds offers a promising treatment for disease-causing infectious microbial pathogens. Hence, this mechanism constitutes an encouraging ally in the development of pharmacological agents required to combat the growing number of microbial strains that have become resistant to extant antibiotics in clinical practice.

Author Contributions

S.M. as sole author conceived, designed, written, revised and improved the review.

Funding

The author would like to thank the Deanship of Scientific Research, Majmaah University, Kingdom of Saudi Arabia for academic support under the project no: R-1441-41.

Conflicts of Interest

The authors declare no conflict of interest.

Abbreviations

A. bohemicusAcinetobacter bohemicus
A. flavusAspergillus flavus
A. fumigatusAspergillus fumigatus
A. nigerAspergillus niger
A. solaniAlternaria solani
B. agriBrevibacillus agri
B. brevisBrevibacillus brevis
B. cereusBacillus cereus
B. megateriumBacillus megaterium
B. pumilusBacillus pumilus
B. subtilisBacillus subtilis
C. albicansCandida albicans
C. DipthieriaeCorynebacterium Dipthieriae
C. dubliniensisCandida dubliniensis
C. glabrataCandida glabrata
C. graminicolaColletotrichum graminicola
C. jejuniCampylobacter jejuni
C. kruseiCandida krusei
C. lunatCandida lunat
C. lunatusCochliobolus lunatus
C. macrocarpumCladosporium macrocarpum
C. neoformansCryptococcus neoformans
C. parapsilosisCandida parapsilosis
C. sphaerospermumCladosporium sphaerospermum
C. tropicalisCandida tropicalis
C. maydisCercospora zeae-maydis
D. turcicaDrechslera turcica
E. aerogenesEnterobacter aerogenes
E. cloacaeEnterobacter cloacae
E. coliEscherichia coli
E. faecalisEnterococcus faecalis
E. ficariaeEntyloma ficariae
E. floccosumEpidermophyton floccosum
F. nucleatumFusobacterium nucleatum
F. oxysporumFusarium oxysporum
F. verticillioidesFusarium verticillioides
H. carbonumHelminthosporium carbonum
H. pyloriHelicobacter pylori
K. aerogenesKlebsiella aerogenes
K. kristinaeKocuria kristinae
K. pneumoniaKlebsiella pneumonia
L. acidophilusLactobacillus acidophilus
L. caseiLactobacillus casei
L. innocuaListeria innocua
L. monocytogenesListeria monocytogenes
L. sporogenesLactobacillus sporogenes
M. canisMicrosporum canis
M. luteusMicrococcus luteus
M. morganiiMorganella morganii
M. ruberMonascus ruber
M. smegmatisMycobacterium smegmatis
M. tuberculosisMycobacterium tuberculosis
M. verticillataMortierella verticillata
P. acnesPropionibacterium acnes
P. aeruginosaPseudomonas aeruginosa
P. brasiliensisParacoccidioides brasiliensis
P. fluorescensPseudomonas fluorescens
P. gingivalisPorphrymonas gingivalis
P. herbarumPleospora herbarum
P. innundatusProtomyces innundatus
P. intermediaPrevotella intermedia
P. lilacinumPurpureocillium lilacinum
P. mirabilisProteus mirabilis
P. sojaePhytophthora sojae
P. vulgarisProteus vulgaris
R. rubrumRhodospirillum rubrum
R. solanacearumRalstonia solanacearum
R. solaniRhizoctonia solani
R. stoloniferaRhizopus stolonifera
S. agalactiaeStreptococcus agalactiae
S. anginosusStreptococcus anginosus
S. aureusStaphylococcus aureus
S. auricularisStaphylococcus auricularis
S. boydiiShigella boydii
S. dysenteriaeshigella dysenteriae
S. epidermidisStaphylococcus epidermidis
S. fecalisStreptococcus fecalis
S. flexneriShigella flexneri
S. gordoniiStreptococcus gordonii
S. haemolyticusStaphylococcus haemolyticus
S. heidelbergSalmonella heidelberg
S. hominisStaphylococcus hominis
S. japonicasSchizosaccharomyces japonicas
S. kneipiiSpizellomyces kneipii
S. luteaSarcina lutea
S. marcescensSerratia marcescens
S. mutansStreptococcus mutans
S. para typhiSalmonella para typhi
S. pneumoniaeStreptococcus pneumoniae
S. pseudodichotomusSpizellomyces pseudodichotomus
S. pyogenesStreptococcus pyogenes
S. sanguisStreptococcus sanguis
S. saprophyticusStaphylococcus saprophyticus
S. shigaShigella shiga
S. typhiSalmonella typhi
T. deformansTaphrina deformans
T. mentagraphytesTrichophyton mentagraphytes
T. rubrumTrichophyton rubrum
T. tonsuransTrichophyton tonsurans
T. uransTrichophytontonsurans
V. choleraeVibrio cholerae
V. fischeriVibrio fischeri
X. axonopodis Pv. malvacearumXanthomonas axonopodis pv. Malvacearum
X. vesicatoriaXanthomonas vesicatoria
Y. enterocoliticaYersinia enterocolitica

References

  1. Mozirandi, W.; Tagwireyi, D.; Mukanganyama, S. Evaluation of antimicrobial activity of chondrillasterol isolated from Vernonia adoensis (Asteraceae). BMC Complement. Altern. Med. 2019, 19. [Google Scholar] [CrossRef] [PubMed] [Green Version]
  2. Mickymaray, S. One-step synthesis of silver nanoparticles using Saudi Arabian desert seasonal plant Sisymbrium irio and antibacterial activity against multidrug-resistant bacterial strains. Biomolecules 2019, 9, 662. [Google Scholar] [CrossRef] [PubMed] [Green Version]
  3. Kannaiyan, M.; Manuel, V.N.; Raja, V.; Thambidurai, P.; Mickymaray, S.; Nooruddin, T. Antimicrobial activity of the ethanolic and aqueous extracts of Salacia chinensis Linn. against human pathogens. Asian Pac. J. Trop. Dis. 2012, 2, S416–S420. [Google Scholar] [CrossRef]
  4. Kannaiyan, M.; Meseret Abebe, G.; Kanimozhi, C.; Thambidurai, P.; Ashokapuram Selvam, S.; Vinodhini, R.; Suresh, M. Prevalence of extended-spectrum beta-lactamase producing enterobacteriaceae members isolated from clinically suspected patients. Asian J. Pharm. Clin. Res. 2018, 11, 364. [Google Scholar] [CrossRef]
  5. Vijayakumar, R.; Aboody, M.; AlFonaisan, M.; Turaiki, W.; Mickymaray, S.; Mariappan, P.; Alsagaby, S.; Sandle, T. Determination of Minimum inhibitory concentrations of Common Biocides to Multidrug-Resistant Gram-negative bacteria. Appl. Med. Res. 2016, 2, 56. [Google Scholar] [CrossRef]
  6. Mickymaray, S.; Alturaiki, W. Antifungal efficacy of marine macroalgae against fungal isolates from bronchial asthmatic cases. Molecules 2018, 23, 3032. [Google Scholar] [CrossRef] [Green Version]
  7. Fotso, G.W.; Mogue Kamdem, L.; Dube, M.; Fobofou, S.A.; Ndjie Ebene, A.; Arnold, N.; Tchaleu Ngadjui, B. Antimicrobial secondary metabolites from the stem barks and leaves of Monotes kerstingii Gilg (Dipterocarpaceae). Fitoterapia 2019, 137, 104239. [Google Scholar] [CrossRef]
  8. Houlihan, A.J.; Conlin, P.; Chee-Sanford, J.C. Water-soluble exudates from seeds of Kochia scoparia exhibit antifungal activity against Colletotrichum graminicola. PLoS ONE 2019, 14, e0218104. [Google Scholar] [CrossRef]
  9. Mickymaray, S.; Al Aboody, M.S.; Rath, P.K.; Annamalai, P.; Nooruddin, T. Screening and antibacterial efficacy of selected Indian medicinal plants. Asian Pac. J. Trop. Biomed. 2016, 6, 185–191. [Google Scholar] [CrossRef] [Green Version]
  10. Casciaro, B.; Calcaterra, A.; Cappiello, F.; Mori, M.; Loffredo, M.R.; Ghirga, F.; Mangoni, M.L.; Botta, B.; Quaglio, D. Nigritanine as a New Potential Antimicrobial Alkaloid for the Treatment of Staphylococcus aureus-Induced Infections. Toxins 2019, 11, 511. [Google Scholar] [CrossRef] [Green Version]
  11. Phan, A.D.T.; Netzel, G.; Chhim, P.; Netzel, M.E.; Sultanbawa, Y. Phytochemical Characteristics and Antimicrobial Activity of Australian Grown Garlic (Allium Sativum L.) Cultivars. Foods 2019, 8, 358. [Google Scholar] [CrossRef] [Green Version]
  12. Toiu, A.; Vlase, L.; Vodnar, D.C.; Gheldiu, A.-M.; Oniga, I. Solidago graminifolia L. Salisb. (Asteraceae) as a Valuable Source of Bioactive Polyphenols: HPLC Profile, In Vitro Antioxidant and Antimicrobial Potential. Molecules 2019, 24, 2666. [Google Scholar] [CrossRef] [Green Version]
  13. Değirmenci, H.; Erkurt, H. Relationship between volatile components, antimicrobial and antioxidant properties of the essential oil, hydrosol and extracts of Citrus aurantium L. flowers. J. Infect. Public Health 2019. [Google Scholar] [CrossRef]
  14. Gómez-Rivera, A.; González-Cortazar, M.; Herrera-Ruíz, M.; Zamilpa, A.; Rodríguez-López, V. Sessein and isosessein with anti-inflammatory, antibacterial and antioxidant activity isolated from Salvia sessei Benth. J. Ethnopharmacol. 2018, 217, 212–219. [Google Scholar] [CrossRef] [PubMed]
  15. Sukalingam, K.; Ganesan, K.; Ponnusamy, K. Evaluation of antidiabetic activity of polyherbal formulations on type 2 diabetic patients: A single blinded randomized study. Int. J. Integ. Medl. Sci. 2015, 2. [Google Scholar] [CrossRef]
  16. Sukalingam, K.; Ganesan, K.; Xu, B. Trianthema portulacastrum L. (giant pigweed): Phytochemistry and pharmacological properties. Phytochem. Rev. 2017, 16, 461–478. [Google Scholar] [CrossRef]
  17. Karalija, E.; Parić, A.; Dahija, S.; Bešta-Gajević, R.; Ćavar Zeljković, S. Phenolic compounds and bioactive properties of Verbascum glabratum subsp. bosnense (K. Malý) Murb., an endemic plant species. Nat. Prod. Res. 2018. [Google Scholar] [CrossRef]
  18. Dewapriya, P.; Khalil, Z.G.; Prasad, P.; Salim, A.A.; Cruz-Morales, P.; Marcellin, E.; Capon, R.J. Talaropeptides A-D: Structure and Biosynthesis of Extensively N-methylated Linear Peptides From an Australian Marine Tunicate-Derived Talaromyces sp. Front. Chem. 2018, 6. [Google Scholar] [CrossRef]
  19. Nath, D.; Banerjee, P.; Shaw, M.; Mukhopadhyay, M.K. Bottle Gourd (Lagenaria Siceraria). In Fruit and Vegetable Phytochemicals: Chemistry and Human Health, 2nd ed.; John Wiley & Sons, Ltd: Hoboken, NJ, USA, 2018; Volume II, pp. 909–920. [Google Scholar] [CrossRef]
  20. Prasannabalaji, N.; Muralitharan, G.; Sivanandan, R.N.; Kumaran, S.; Pugazhvendan, S.R. Antibacterial activities of some Indian traditional plant extracts. Asian Pac. J. Trop. Dis. 2012, 2, S291–S295. [Google Scholar] [CrossRef]
  21. Mabona, U.; Viljoen, A.; Shikanga, E.; Marston, A.; Van Vuuren, S. Antimicrobial activity of southern African medicinal plants with dermatological relevance: From an ethnopharmacological screening approach, to combination studies and the isolation of a bioactive compound. J. Ethnopharmacol. 2013, 148, 45–55. [Google Scholar] [CrossRef]
  22. Benevides Bahiense, J.; Marques, F.M.; Figueira, M.M.; Vargas, T.S.; Kondratyuk, T.P.; Endringer, D.C.; Scherer, R.; Fronza, M. Potential anti-inflammatory, antioxidant and antimicrobial activities ofSambucus australis. Pharm. Biol. 2017, 55, 991–997. [Google Scholar] [CrossRef] [PubMed] [Green Version]
  23. Akhalwaya, S.; van Vuuren, S.; Patel, M. An in vitro investigation of indigenous South African medicinal plants used to treat oral infections. J. Ethnopharmacol. 2018, 210, 359–371. [Google Scholar] [CrossRef] [PubMed]
  24. Lim, S.S.; Selvaraj, A.; Ng, Z.Y.; Palanisamy, M.; Mickmaray, S.; Cheong, P.C.H.; Lim, R.L.H. Isolation of actinomycetes with antibacterial activity against multi-drug resistant bacteria. Malays. J. Microbiol. 2018. [Google Scholar] [CrossRef]
  25. Ke, Y.; Al Aboody, M.S.; Alturaiki, W.; Alsagaby, S.A.; Alfaiz, F.A.; Veeraraghavan, V.P.; Mickymaray, S. Photosynthesized gold nanoparticles from Catharanthus roseus induces caspase-mediated apoptosis in cervical cancer cells (HeLa). Artif. Cells Nanomed. Biotechnol. 2019, 47, 1938–1946. [Google Scholar] [CrossRef] [Green Version]
  26. Muhaisen, H.M.H.; Ab–Mous, M.M.; Ddeeb, F.A.; Rtemi, A.A.; Taba, O.M.; Parveen, M. Antimicrobial agents from selected medicinal plants in Libya. Chin. J. Integr. Med. 2015, 22, 177–184. [Google Scholar] [CrossRef]
  27. Mubarack, H.; Doss, A.; Vijayasanthi, M.; Venkataswamy, R. Antimicrobial drug susceptibility of Staphylococcus aureus from subclinical bovine mastitis in Coimbatore, Tamilnadu, South India. Vet. World 2012, 5, 352. [Google Scholar] [CrossRef]
  28. Okwu, M.U.; Olley, M.; Akpoka, A.O.; Izevbuwa, O.E. Methicillin-resistant Staphylococcus aureus (MRSA) and anti-MRSA activities of extracts of some medicinal plants: A brief review. AIMS Microbiol. 2019, 5, 117–137. [Google Scholar] [CrossRef]
  29. Obeidat, M.; Shatnawi, M.; Al-alawi, M.; Al-Zu‘bi, E.; Al-Dmoor, H.; Al-Qudah, M.; El-Qudah, J.; Otri, I. Antimicrobial Activity of Crude Extracts of Some Plant Leaves. Res. J. Microbiol. 2012, 7, 59–67. [Google Scholar] [CrossRef] [Green Version]
  30. Aristolochia indica Linn. In SpringerReference; Springer: Berlin, Germany, 2016.
  31. Vinodhini, R.; Moorthy, K.; Suresh, M. Incidence and virulence traits of Candida dubliniensis isolated from clinically suspected patients. Asian J. Pharm. Clin. Res. 2016, 9, 77. [Google Scholar] [CrossRef] [Green Version]
  32. Zuo, G.-Y.; Zhang, X.-J.; Yang, C.-X.; Han, J.; Wang, G.-C.; Bian, Z.-Q. Evaluation of Traditional Chinese Medicinal Plants for Anti-MRSA Activity with Reference to the Treatment Record of Infectious Diseases. Molecules 2012, 17, 2955–2967. [Google Scholar] [CrossRef] [Green Version]
  33. Singh, A.; Bajpai, V.; Kumar, S.; Kumar, B.; Srivastava, M.; Arya, K.R.; Sharma, K.R. Distribution and Discrimination Study of Bioactive Compounds from Berberis species using HPLC-ESI-QTOF-MS/MS with Principle Component Analysis. Nat. Prod. Commun. 2016, 11, 1807–1812. [Google Scholar] [CrossRef] [PubMed]
  34. Kariu, T.; Nakao, R.; Ikeda, T.; Nakashima, K.; Potempa, J.; Imamura, T. Inhibition of gingipains andPorphyromonas gingivalisgrowth and biofilm formation by prenyl flavonoids. J. Periodontal Res. 2016, 52, 89–96. [Google Scholar] [CrossRef] [PubMed] [Green Version]
  35. Spathodea campanulata Beauv. In SpringerReference; Springer: Berlin, Germany, 2016.
  36. dos Santos, E.; Pereira, M.; da Silva, C.; Souza-Neta, L.; Geris, R.; Martins, D.; Santana, A.; Barbosa, L.; Silva, H.; Freitas, G.; et al. Antibacterial Activity of the Alkaloid-Enriched Extract from Prosopis juliflora Pods and Its Influence on in Vitro Ruminal Digestion. Int. J. Mol. Sci. 2013, 14, 8496–8516. [Google Scholar] [CrossRef]
  37. Kumar, G.; Maheswaran, R.; Sharmila Banu, G. Antihyperlipideamic effect of Solanum trilobatum L. leaves extract on streptozotocin induced diabetic rats. Asian J. Biomed. Pharm. Sci. 2013, 3, 51–57. [Google Scholar]
  38. Semalty, M.; Semalty, A.; Badola, A.; Joshi, G.; Rawat, M.S.M. Semecarpus anacardium Linn.: A review. Pharm. Rev. 2010, 4, 88. [Google Scholar] [CrossRef] [Green Version]
  39. Rawat, S.; Jugran, A.K.; Bahukhandi, A.; Bahuguna, A.; Bhatt, I.D.; Rawal, R.S.; Dhar, U. Anti-oxidant and anti-microbial properties of some ethno-therapeutically important medicinal plants of Indian Himalayan Region. 3 Biotech. 2016, 6, 154. [Google Scholar] [CrossRef] [Green Version]
  40. Gujjeti, R.P.; Namthabad, S.; Mamidala, E. HIV-1 reverse transcriptase inhibitory activity of Aerva lanata plant extracts. BMC Infect. Dis. 2014, 14. [Google Scholar] [CrossRef] [Green Version]
  41. Mohotti, S.; Rajendran, S.; Muhammad, T.; Strömstedt, A.A.; Adhikari, A.; Burman, R.; de Silva, E.D.; Göransson, U.; Hettiarachchi, C.M.; Gunasekera, S. Screening for bioactive secondary metabolites in Sri Lankan medicinal plants by microfractionation and targeted isolation of antimicrobial flavonoids from Derris scandens. J. Ethnopharmacol. 2020, 246, 112158. [Google Scholar] [CrossRef]
  42. Ghasemi, P.; Jahanbazi, P.; Enteshari, S.; Malekpoor, F.; Hamedi, B. Antimicrobial activity of some Iranian medicinal plants. Arch. Biol. Sci. 2010, 62, 633–641. [Google Scholar] [CrossRef]
  43. Mickymaray, S.; Al Aboody, M.S. In Vitro Antioxidant and Bactericidal Efficacy of 15 Common Spices: Novel Therapeutics for Urinary Tract Infections? Medicina 2019, 55, 289. [Google Scholar] [CrossRef] [Green Version]
  44. Banothu, V.; Neelagiri, C.; Adepally, U.; Lingam, J.; Bommareddy, K. Phytochemical screening and evaluation of in vitro antioxidant and antimicrobial activities of the indigenous medicinal plant Albizia odoratissima. Pharm. Biol. 2017, 55, 1155–1161. [Google Scholar] [CrossRef] [PubMed] [Green Version]
  45. Sahu, M.C.; Padhy, R.N. In vitro antibacterial potency of Butea monosperma Lam. against 12 clinically isolated multidrug resistant bacteria. Asian Pac. J. Trop. Dis. 2013, 3, 217–226. [Google Scholar] [CrossRef]
  46. Wikaningtyas, P.; Sukandar, E.Y. The antibacterial activity of selected plants towards resistant bacteria isolated from clinical specimens. Asian Pac. J. Trop. Biomed. 2016, 6, 16–19. [Google Scholar] [CrossRef]
  47. Mwinga, J.L.; Asong, J.A.; Amoo, S.O.; Nkadimeng, S.M.; McGaw, L.J.; Aremu, A.O.; Otang-Mbeng, W. In vitro antimicrobial effects of Hypoxis hemerocallidea against six pathogens with dermatological relevance and its phytochemical characterization and cytotoxicity evaluation. J. Ethnopharmacol. 2019, 242, 112048. [Google Scholar] [CrossRef]
  48. Armas, J.; Quiroz, J.; Roman, R.; Sanchez, J.; Pacheco, M.; Valdivia, L.; Rivera, E.; Asmat, R.; Anampa, A. Antibacterial Activities of Essential Oils from Three Medicinal Plants in Combination with EDTA against Methicillin-resistant Staphylococcus aureus. Br. Microbiol. Res. J. 2016, 17, 1–10. [Google Scholar] [CrossRef]
  49. Ferhat, M.; Erol, E.; Beladjila, K.A.; Çetintaş, Y.; Duru, M.E.; Öztürk, M.; Kabouche, A.; Kabouche, Z. Antioxidant, anticholinesterase and antibacterial activities of Stachys guyoniana and Mentha aquatica. Pharm. Biol. 2016, 55, 324–329. [Google Scholar] [CrossRef] [Green Version]
  50. Guan, C.P.; Luo, H.X.; Fang, H.E.; Zhou, X.Z. Global Transcriptome Changes of Biofilm-Forming Staphylococcus epidermidis Responding to Total Alkaloids of Sophorea alopecuroides. Pol. J. Microbiol. 2018, 67, 223–226. [Google Scholar] [CrossRef] [Green Version]
  51. Zhou, J.-X.; Braun, M.; Wetterauer, P.; Wetterauer, B.; Wink, M. Antioxidant, Cytotoxic, and Antimicrobial Activities of Glycyrrhiza glabra L., Paeonia lactiflora Pall., and Eriobotrya japonica (Thunb.) Lindl. Extracts. Medicines 2019, 6, 43. [Google Scholar] [CrossRef] [Green Version]
  52. Arefin, M.K.; Rahman, M.M.; Uddin, M.Z.; Hassan, M.A. Angiosperm flora of Satchari National Park, Habiganj, Bangladesh. Bangladesh J. Plant. Taxon. 1970, 18, 117–140. [Google Scholar] [CrossRef] [Green Version]
  53. Koona, S.; Budida, S. Antibacterial Potential of the Extracts of the Leaves of Azadirachta indica Linn. Not. Sci. Biol. 2011, 3, 65–69. [Google Scholar] [CrossRef] [Green Version]
  54. Durairaj, B.; Dorai, A. Antiplatelet activity of white and pink Nelumbo nucifera Gaertn flowers. Braz. J. Pharm. Sci. 2010, 46, 579–583. [Google Scholar] [CrossRef]
  55. Bhattacharjee, I.; Chatterjee, S.K.; Chandra, G. Isolation and identification of antibacterial components in seed extracts of Argemone mexicana L. (Papaveraceae). Asian Pac. J. Trop. Med. 2010, 3, 547–551. [Google Scholar] [CrossRef] [Green Version]
  56. Jayachandran, M.; Zhang, T.; Ganesan, K.; Xu, B.; Chung, S.S.M. Isoquercetin ameliorates hyperglycemia and regulates key enzymes of glucose metabolism via insulin signaling pathway in streptozotocin-induced diabetic rats. Eur. J. Pharmcol. 2018, 829, 112–120. [Google Scholar] [CrossRef] [PubMed]
  57. Chatterjee, S.K.; Bhattacharjee, I.; Chandra, G. Isolation and identification of bioactive antibacterial components in leaf extracts of Vangueria spinosa (Rubiaceae). Asian Pac. J. Trop. Med. 2011, 4, 35–40. [Google Scholar] [CrossRef] [Green Version]
  58. Gaziano, R.; Campione, E.; Iacovelli, F.; Marino, D.; Pica, F.; Di Francesco, P.; Aquaro, S.; Menichini, F.; Falconi, M.; Bianchi, L. Antifungal activity of Cardiospermum halicacabum L. (Sapindaceae) against Trichophyton rubrum occurs through molecular interaction with fungal Hsp90. Drug Des. Dev. 2018, 12, 2185–2193. [Google Scholar] [CrossRef] [PubMed] [Green Version]
  59. Nefzi, A.; Ben Abdallah, R.A. Antifungal activity of aqueous and organic extracts from Withania somnifera L. against Fusarium oxysporum f. sp. Radicis lycopersici. J. Microb. Biochem. Technol. 2016, 8. [Google Scholar] [CrossRef]
  60. Chahal, S.S.; Matthews, H.R.; Bradbury, E.M. Acetylation of histone H4 and its role in chromatin structure and function. Nature 1980, 287, 76–79. [Google Scholar] [CrossRef]
  61. Venkataswamy, R.; Doss, A.; Sukumar, M.; Mubarack, H.M. Preliminary phytochemical screening and antimicrobial studies of Lantana indica roxb. Ind. J. Pharm. Sci. 2010, 72, 229. [Google Scholar] [CrossRef] [Green Version]
  62. Pandian, M.R.; Banu, G.S.; Kumar, G. A study of the antimicrobial activity of Alangium salviifolium. Indian J. Pharm. 2006, 38, 203. [Google Scholar] [CrossRef]
  63. Arulmozhi, P.; Vijayakumar, S.; Kumar, T. Phytochemical analysis and antimicrobial activity of some medicinal plants against selected pathogenic microorganisms. Microb. Pathog. 2018, 123, 219–226. [Google Scholar] [CrossRef]
  64. Kahaliw, W.; Aseffa, A.; Abebe, M.; Teferi, M.; Engidawork, E. Evaluation of the antimycobacterial activity of crude extracts and solvent fractions of selected Ethiopian medicinal plants. BMC Complement. Altern. Med. 2017, 17. [Google Scholar] [CrossRef] [PubMed] [Green Version]
  65. Ginovyan, M.; Petrosyan, M.; Trchounian, A. Antimicrobial activity of some plant materials used in Armenian traditional medicine. BMC Complement. Altern. Med. 2017, 17. [Google Scholar] [CrossRef] [PubMed] [Green Version]
  66. Asgarpanah, J.; Hashemi, S.J.; Hashemi, E.; Askari, K. In vitro antifungal activity of some traditional Persian medicinal plants on pathogenic fungi. Chin. J. Integ. Med. 2015, 23, 433–437. [Google Scholar] [CrossRef] [PubMed]
  67. Sharma, A.; Flores-Vallejo, R.D.C.; Cardoso-Taketa, A.; Villarreal, M.L. Antibacterial activities of medicinal plants used in Mexican traditional medicine. J. Ethnopharmacol. 2017, 208, 264–329. [Google Scholar] [CrossRef] [PubMed]
  68. Shahat, A.A.; Mahmoud, E.A.; Al-Mishari, A.A.; Alsaid, M.S. Antimicrobial activities of some Saudi Arabian herbal plants. Afr. J. Trad. Complement. Altern. Med. 2017, 14, 161–165. [Google Scholar] [CrossRef] [PubMed] [Green Version]
  69. Cioch, M.; Satora, P.; Skotniczny, M.; Semik-Szczurak, D.; Tarko, T. Characterisation of Antimicrobial Properties of Extracts of Selected Medicinal Plants. Pol. J. Microbiol. 2017, 66, 463–472. [Google Scholar] [CrossRef] [Green Version]
  70. Voukeng, I.K.; Beng, V.P.; Kuete, V. Antibacterial activity of six medicinal Cameroonian plants against Gram-positive and Gram-negative multidrug resistant phenotypes. BMC Complement. Altern. Med. 2016, 16. [Google Scholar] [CrossRef] [Green Version]
  71. Anyanwu, M.U.; Okoye, R.C. Antimicrobial activity of Nigerian medicinal plants. J. Intercult Ethnopharmacol. 2017, 6, 240–259. [Google Scholar] [CrossRef]
  72. Othman, L.; Sleiman, A.; Abdel-Massih, R.M. Antimicrobial Activity of Polyphenols and Alkaloids in Middle Eastern Plants. Front. Microbiol. 2019, 10, 911. [Google Scholar] [CrossRef]
  73. Ganesan, K.; Xu, B. Telomerase Inhibitors from Natural Products and Their Anticancer Potential. Int. J. Mol. Sci. 2017, 19, 13. [Google Scholar] [CrossRef] [Green Version]
  74. Sukalingam, K.; Ganesan, K.; Xu, B. Protective Effect of Aqueous Extract from the Leaves of Justicia tranquebariesis against Thioacetamide-Induced Oxidative Stress and Hepatic Fibrosis in Rats. Antioxidants 2018, 7, 78. [Google Scholar] [CrossRef] [PubMed] [Green Version]
  75. Ganesan, K.; Xu, B. Polyphenol-Rich Lentils and Their Health Promoting Effects. Int. J.Mol. Sci. 2017, 18, 2390. [Google Scholar] [CrossRef] [PubMed] [Green Version]
  76. Ganesan, K.; Xu, B. Molecular targets of vitexin and isovitexin in cancer therapy: A critical review. Ann. N. Y. Acad. Sci. 2017, 1401, 102–113. [Google Scholar] [CrossRef] [PubMed]
  77. Ganesan, K.; Gani, S.B.; Ganesan Murugesan, A. Influence of Helicteres isora L. bark extracts on glycemic control and renoprotective activity in streptozotocin-induced diabetic rats. Int. J. Pharm. Sci. Nanotechnol. 2008, 1, 275–280. [Google Scholar]
  78. Kumar, G.; Murugesan, A.G. Hypolipidaemic activity of Helicteres isora L. bark extracts in streptozotocin induced diabetic rats. J. Ethnopharmacol. 2008, 116, 161–166. [Google Scholar] [CrossRef]
  79. Kumar, G.; Banu, G.S.; Murugesan, A.G.; Pandian, M.R. Hypoglycaemic effect of Helicteres isora bark extract in rats. J. Ethnopharmacol. 2006, 107, 304–307. [Google Scholar] [CrossRef]
  80. Kumar, G.; Sharmila Banu, G.; Murugesan, A.G.; Rajasekara Pandian, M. Effect ofHelicteres isora. Bark Extracts on Brain Antioxidant Status and Lipid Peroxidation in Streptozotocin Diabetic Rats. Pharm. Biol. 2007, 45, 753–759. [Google Scholar] [CrossRef]
  81. Kumar, G.; Sharmila Banu, G.; Ganesan Murugesan, A. Effect of Helicteres isora bark extracts on heart antioxidant status and lipid peroxidation in streptozotocin diabetic rats. J. Appl. Biomed. 2008, 6, 89–95. [Google Scholar] [CrossRef] [Green Version]
  82. Ganesan, K.; Xu, B. Anti-Obesity Effects of Medicinal and Edible Mushrooms. Molecules 2018, 23, 2880. [Google Scholar] [CrossRef] [Green Version]
  83. Ganesan, K.; Gani, S.B.; Ganesan Murugesan, A. Antidiabetic activity of Helicteres isora L. bark extracts on streptozotocin-induced diabetic rats. Int. J. Pharm. Sci. Nanotechnol. 2009, 1, 379–382. [Google Scholar]
  84. Ganesan, K.; Chung, S.K.; Vanamala, J.; Xu, B. Causal Relationship between Diet-Induced Gut Microbiota Changes and Diabetes: A Novel Strategy to Transplant Faecalibacterium prausnitzii in Preventing Diabetes. Int. J. Mol. Sci. 2018, 19, 3720. [Google Scholar] [CrossRef] [Green Version]
  85. Górniak, I.; Bartoszewski, R.; Króliczewski, J. Comprehensive review of antimicrobial activities of plant flavonoids. Phytochem. Rev. 2019, 18, 241–272. [Google Scholar] [CrossRef] [Green Version]
  86. Madikizela, B.; Aderogba, M.A.; Van Staden, J. Isolation and characterization of antimicrobial constituents of Searsia chirindensis L. (Anacardiaceae) leaf extracts. J. Ethnopharmacol. 2013, 150, 609–613. [Google Scholar] [CrossRef] [PubMed]
  87. Alolga, R.N.; Chávez León, M.A.S.C.; Osei-Adjei, G.; Onoja, V. GC-MS-based metabolomics, antibacterial and anti-inflammatory investigations to characterize the quality of essential oil obtained from dried Xylopia aethiopica fruits from Ghana and Nigeria. J. Pharm. Pharmacol. 2019, 71, 1544–1552. [Google Scholar] [CrossRef] [PubMed]
  88. Vieira, M.L.A.; Johann, S.; Hughes, F.M.; Rosa, C.A.; Rosa, L.H. The diversity and antimicrobial activity of endophytic fungi associated with medicinal plant Baccharis trimera (Asteraceae) from the Brazilian savannah. Can. J. Microbiol. 2014, 60, 847–856. [Google Scholar] [CrossRef] [PubMed]
  89. Lourenção Brighenti, F.; Salvador, M.J.; Vidal Lacerda Gontijo, A.; Botazzo Delbem, A.C.; Botazzo Delbem, Á.C.; Soares, C.P.; Carvalho de Oliveira, M.A.; Miorelli Girondi, C.; Koga-Ito, C.Y. Plant extracts: Initial screening, identification of bioactive compounds and effect against Candida albicansbiofilms. Fut. Microbiol. 2017, 12, 15–27. [Google Scholar] [CrossRef] [PubMed]
  90. Abu-Darwish, M.S.; Cabral, C.; Gonçalves, M.J.; Cavaleiro, C.; Cruz, M.T.; Efferth, T.; Salgueiro, L. Artemisia herba-alba essential oil from Buseirah (South Jordan): Chemical characterization and assessment of safe antifungal and anti-inflammatory doses. J. Ethnopharmacol. 2015, 174, 153–160. [Google Scholar] [CrossRef]
  91. Gazoni, V.F.; Balogun, S.O.; Arunachalam, K.; Oliveira, D.M.; Filho, V.C.; Lima, S.R.; Colodel, E.M.; Soares, I.M.; Ascêncio, S.D.; Martins, D.T.d.O. Assessment of toxicity and differential antimicrobial activity of methanol extract of rhizome of Simaba ferruginea A. St.-Hil. and its isolate canthin-6-one. J. Ethnopharmacol. 2018, 223, 122–134. [Google Scholar] [CrossRef]
  92. Perianayagam, J.B.; Sharma, S.K.; Pillai, K.K.; Pandurangan, A.; Kesavan, D. Evaluation of antimicrobial activity of ethanol extract and compounds isolated from Trichodesma indicum (Linn.) R. Br. root. J. Ethnopharmacol. 2012, 142, 283–286. [Google Scholar] [CrossRef]
  93. Dandashire, B.; Magashi, A.; Abdulkadir, B.; Abbas, M.; Goni, M.; Yakubu, A. Toxicological studies and bioactivity-guided identification of antimicrobially active compounds from crude aqueous stem bark extract of Boswellia dalzielii. J. Advan. Vet. Anim. Res. 2019, 6, 183. [Google Scholar] [CrossRef]
  94. Olmedo-Juárez, A.; Briones-Robles, T.I.; Zaragoza-Bastida, A.; Zamilpa, A.; Ojeda-Ramírez, D.; Mendoza de Gives, P.; Olivares-Pérez, J.; Rivero-Perez, N. Antibacterial activity of compounds isolated from Caesalpinia coriaria (Jacq) Willd against important bacteria in public health. Microb. Pathog. 2019, 136, 103660. [Google Scholar] [CrossRef] [PubMed]
  95. Madikizela, B.; Aderogba, M.A.; Finnie, J.F.; Van Staden, J. Isolation and characterization of antimicrobial compounds from Terminalia phanerophlebia Engl. & Diels leaf extracts. J. Ethnopharmacol. 2014, 156, 228–234. [Google Scholar] [CrossRef] [PubMed]
  96. Teodoro, G.R.; Brighenti, F.L.; Delbem, A.C.B.; Delbem, Á.C.B.; Khouri, S.; Gontijo, A.V.L.; Pascoal, A.C.R.F.; Salvador, M.J.; Koga-Ito, C.Y. Antifungal activity of extracts and isolated compounds fromBuchenavia tomentosaonCandida albicansand non-albicans. Fut. Microbiol. 2015, 10, 917–927. [Google Scholar] [CrossRef] [PubMed]
  97. Pramila, D.M. Phytochemical analysis and antimicrobial potential of methanolic leaf extract of peppermint (Mentha piperita: Lamiaceae). J. Med. Plants Res. 2012, 6. [Google Scholar] [CrossRef]
  98. Rezzoug, M.; Bakchiche, B.; Gherib, A.; Roberta, A.; FlaminiGuido; Kilinçarslan, Ö.; Mammadov, R.; Bardaweel, S.K. Chemical composition and bioactivity of essential oils and Ethanolic extracts of Ocimum basilicum L. and Thymus algeriensis Boiss. & Reut. from the Algerian Saharan Atlas. BMC Complement. Altern. Med. 2019, 19. [Google Scholar] [CrossRef]
  99. Mustaffa, F.; Indurkar, J.; Ismail, S.; Shah, M.; Mansor, S.M. An Antimicrobial Compound Isolated from Cinnamomum Iners Leaves with Activity against Methicillin-Resistant Staphylococcus Aureus. Molecules 2011, 16, 3037–3047. [Google Scholar] [CrossRef]
  100. Xu, X.; Zhou, X.D.; Wu, C.D. The Tea Catechin Epigallocatechin Gallate Suppresses Cariogenic Virulence Factors ofStreptococcus mutans. Antimicrob. Agents Chemother. 2010, 55, 1229–1236. [Google Scholar] [CrossRef] [Green Version]
  101. Kuete, V.; Ango, P.Y.; Fotso, G.W.; Kapche, G.D.W.F.; Dzoyem, J.P.; Wouking, A.G.; Ngadjui, B.T.; Abegaz, B.M. Antimicrobial activities of the methanol extract and compounds from Artocarpus communis (Moraceae). BMC Complement. Altern. Med. 2011, 11. [Google Scholar] [CrossRef] [Green Version]
  102. Bouzabata, A.; Bazzali, O.; Cabral, C.; Gonçalves, M.J.; Cruz, M.T.; Bighelli, A.; Cavaleiro, C.; Casanova, J.; Salgueiro, L.; Tomi, F. New compounds, chemical composition, antifungal activity and cytotoxicity of the essential oil from Myrtus nivellei Batt. & Trab., an endemic species of Central Sahara. J. Ethnopharmacol. 2013, 149, 613–620. [Google Scholar] [CrossRef]
  103. González-Alamilla, E.N.; Gonzalez-Cortazar, M.; Valladares-Carranza, B.; Rivas-Jacobo, M.A.; Herrera-Corredor, C.A.; Ojeda-Ramírez, D.; Zaragoza-Bastida, A.; Rivero-Perez, N. Chemical Constituents of Salix babylonica L. and Their Antibacterial Activity Against Gram-Positive and Gram-Negative Animal Bacteria. Molecules 2019, 24, 2992. [Google Scholar] [CrossRef] [Green Version]
  104. Xu, X.; Zhou, X.D.; Wu, C.D. Tea catechin epigallocatechin gallate inhibits Streptococcus mutans biofilm formation by suppressing gtf genes. Arch. Oral Biol. 2012, 57, 678–683. [Google Scholar] [CrossRef] [PubMed]
  105. Ganesan, K.; Xu, B. Polyphenol-Rich Dry Common Beans (Phaseolus vulgaris L.) and Their Health Benefits. Int. J. Mol. Sci. 2017, 18, 2331. [Google Scholar] [CrossRef] [PubMed] [Green Version]
  106. Stapleton, P. Anti-Staphylococcus aureus activity and oxacillin resistance modulating capacity of 3-O-acyl-catechins. Int. J. Antimicrob. Agents 2004, 24, 374–380. [Google Scholar] [CrossRef] [PubMed]
  107. Cushnie, T.P.T.; Hamilton, V.E.S.; Chapman, D.G.; Taylor, P.W.; Lamb, A.J. Aggregation of Staphylococcus aureus following treatment with the antibacterial flavonol galangin. J. Appl. Microbiol. 2007, 103, 1562–1567. [Google Scholar] [CrossRef] [Green Version]
  108. El-Adawi, H. Inhibitory effect of grape seed extract (GSE) on cariogenic bacteria. J. Med. Plants Res. 2012, 6. [Google Scholar] [CrossRef]
  109. Awolola, G.V.; Koorbanally, N.A.; Chenia, H.; Shode, F.O.; Baijnath, H. Antibacterial and Anti-Biofilm Activity of Flavonoids and Triterpenes Isolated from The Extracts of Ficus Sansibarica Warb. Subsp. Sansibarica (Moraceae) Extracts. Afr. J. Trad. Complement. Altern. Med. 2014, 11, 124. [Google Scholar] [CrossRef] [Green Version]
  110. Ganesan, K.; Xu, B. A critical review on phytochemical profile and health promoting effects of mung bean (Vigna radiata ). Food Sci. Hum. Wellness 2018, 7, 11–33. [Google Scholar] [CrossRef]
  111. Ganesan, K.; Xu, B. A Critical Review on Polyphenols and Health Benefits of Black Soybeans. Nutrients 2017, 9, 455. [Google Scholar] [CrossRef] [Green Version]
  112. Tsuchiya, H.; Iinuma, M. Reduction of membrane fluidity by antibacterial sophoraflavanone G isolated from Sophora exigua. Phytomedicine 2000, 7, 161–165. [Google Scholar] [CrossRef]
  113. Sanver, D.; Murray, B.S.; Sadeghpour, A.; Rappolt, M.; Nelson, A.L. Experimental Modeling of Flavonoid–Biomembrane Interactions. Langmuir 2016, 32, 13234–13243. [Google Scholar] [CrossRef]
  114. Stepanović, S.; Antić, N.; Dakić, I.; Švabić-Vlahović, M. In vitro antimicrobial activity of propolis and synergism between propolis and antimicrobial drugs. Microbiol. Res. 2003, 158, 353–357. [Google Scholar] [CrossRef] [PubMed]
  115. Ollila, F.; Halling, K.; Vuorela, P.; Vuorela, H.; Slotte, J.P. Characterization of Flavonoid–Biomembrane Interactions. Arch. Biochem. Biophys. 2002, 399, 103–108. [Google Scholar] [CrossRef] [PubMed]
  116. Mishra, A.K.; Mishra, A.; Kehri, H.K.; Sharma, B.; Pandey, A.K. Inhibitory activity of Indian spice plant Cinnamomum zeylanicum extracts against Alternaria solani and Curvularia lunata, the pathogenic dematiaceous moulds. Ann. Clin. Microbiol. Antimicrob. 2009, 8, 9. [Google Scholar] [CrossRef] [PubMed] [Green Version]
  117. Matijašević, D.; Pantić, M.; Rašković, B.; Pavlović, V.; Duvnjak, D.; Sknepnek, A.; Nikšić, M. The Antibacterial Activity of Coriolus versicolor Methanol Extract and Its Effect on Ultrastructural Changes of Staphylococcus aureus and Salmonella Enteritidis. Front. Microbiol. 2016, 7. [Google Scholar] [CrossRef] [PubMed]
  118. Budzynska, A.; Rozalski, M.; Karolczak, W.; Wieckowska-Szakiel, M.; Sadowska, B.; Rozalska, B. Synthetic 3-Arylidenefl avanones as Inhibitors of the Initial Stages of Biofilm Formation by Staphylococcus aureus and Enterococcus faecalis. Z. Für Naturforschung C 2011, 66, 0104. [Google Scholar] [CrossRef] [Green Version]
  119. Ganesan, K.; Jayachandran, M.; Xu, B. A critical review on hepatoprotective effects of bioactive food components. Crit. Rev. Food Sci. Nutr. 2017, 58, 1165–1229. [Google Scholar] [CrossRef] [PubMed]
  120. Srikrishna, D.; Godugu, C.; Dubey, P.K. A Review on Pharmacological Properties of Coumarins. Mini-Rev. Med. Chem. 2018, 18. [Google Scholar] [CrossRef]
  121. Guimarães, A.C.; Meireles, L.M.; Lemos, M.F.; Guimarães, M.C.C.; Endringer, D.C.; Fronza, M.; Scherer, R. Antibacterial Activity of Terpenes and Terpenoids Present in Essential Oils. Molecules 2019, 24, 2471. [Google Scholar] [CrossRef] [Green Version]
  122. Moghrovyan, A.; Sahakyan, N.; Babayan, A.; Chichoyan, N.; Petrosyan, M.; Trchounian, A. Essential Oil and Ethanol Extract of Oregano (Origanum vulgare L.) from Armenian Flora as a Natural Source of Terpenes, Flavonoids and other Phytochemicals with Antiradical, Antioxidant, Metal Chelating, Tyrosinase Inhibitory and Antibacterial Activity. Curr. Pharm. Des. 2019, 25, 1809–1816. [Google Scholar] [CrossRef]
  123. Lambert, R.J.W.; Skandamis, P.N.; Coote, P.J.; Nychas, G.J.E. A study of the minimum inhibitory concentration and mode of action of oregano essential oil, thymol and carvacrol. J. Appl. Microbiol. 2001, 91, 453–462. [Google Scholar] [CrossRef] [Green Version]
  124. Ultee, A.; Bennik, M.H.J.; Moezelaar, R. The Phenolic Hydroxyl Group of Carvacrol Is Essential for Action against the Food-Borne Pathogen Bacillus cereus. Appl. Environ. Microbiol. 2002, 68, 1561–1568. [Google Scholar] [CrossRef] [Green Version]
  125. Silva, N.C.C.; Fernandes Júnior, A. Biological properties of medicinal plants: A review of their antimicrobial activity. J. Venom. Anim. Toxins Trop. Dis. 2010, 16, 402–413. [Google Scholar] [CrossRef]
  126. Vikram, A.; Jayaprakasha, G.K.; Jesudhasan, P.R.; Pillai, S.D.; Patil, B.S. Suppression of bacterial cell-cell signalling, biofilm formation and type III secretion system by citrus flavonoids. J. Appl. Microbiol. 2010. [Google Scholar] [CrossRef] [PubMed]
  127. Prasad, V.G.N.V.; krishna, B.V.; Swamy, P.L.; Rao, T.S.; Rao, G.S. Antibacterial synergy between quercetin and polyphenolic acids against bacterial pathogens of fish. Asian Pac. J. Trop. Dis. 2014, 4, S326–S329. [Google Scholar] [CrossRef]
  128. Thiago, J.D.S.B.; Andréa, F.F.; Ana, C.D.P.R.I.; Norma, A. Cytotoxic, antibacterial and antibiofilm activities of aqueous extracts of leaves and flavonoids occurring in Kalanchoe pinnata (Lam.) Pers. J. Med. Plants Res. 2016, 10, 763–770. [Google Scholar] [CrossRef] [Green Version]
  129. Ouyang, J.; Sun, F.; Feng, W.; Sun, Y.; Qiu, X.; Xiong, L.; Liu, Y.; Chen, Y. Quercetin is an effective inhibitor of quorum sensing, biofilm formation and virulence factors inPseudomonas aeruginosa. J. Appl. Microbiol. 2016, 120, 966–974. [Google Scholar] [CrossRef] [Green Version]
  130. Ulrey, R.K.; Barksdale, S.M.; Zhou, W.; van Hoek, M.L. Cranberry proanthocyanidins have anti-biofilm properties against Pseudomonas aeruginosa. BMC Complement. Altern. Med. 2014, 14. [Google Scholar] [CrossRef] [Green Version]
  131. Paczkowski, J.E.; Mukherjee, S.; McCready, A.R.; Cong, J.-P.; Aquino, C.J.; Kim, H.; Henke, B.R.; Smith, C.D.; Bassler, B.L. Flavonoids SuppressPseudomonas aeruginosaVirulence through Allosteric Inhibition of Quorum-sensing Receptors. J. Biol. Chem. 2017, 292, 4064–4076. [Google Scholar] [CrossRef] [Green Version]
  132. Roy, R.; Tiwari, M.; Donelli, G.; Tiwari, V. Strategies for combating bacterial biofilms: A focus on anti-biofilm agents and their mechanisms of action. Virulence 2017, 9, 522–554. [Google Scholar] [CrossRef]
  133. Oteiza, P.I.; Erlejman, A.G.; Verstraeten, S.V.; Keen, C.L.; Fraga, C.G. Flavonoid-membrane Interactions: A Protective Role of Flavonoids at the Membrane Surface? Clin. Dev. Immunol. 2005, 12, 19–25. [Google Scholar] [CrossRef] [Green Version]
  134. Vasconcelos, M.A.; Arruda, F.V.S.; de Alencar, D.B.; Saker-Sampaio, S.; Albuquerque, M.R.J.R.; dos Santos, H.S.; Bandeira, P.N.; Pessoa, O.D.L.; Cavada, B.S.; Henriques, M.; et al. Antibacterial and Antioxidant Activities of Derriobtusone A Isolated from Lonchocarpus obtusus. Biomed. Res. Int. 2014, 2014, 1–9. [Google Scholar] [CrossRef] [Green Version]
  135. Christena, L.R.; Subramaniam, S.; Vidhyalakshmi, M.; Mahadevan, V.; Sivasubramanian, A.; Nagarajan, S. Dual role of pinostrobin-a flavonoid nutraceutical as an efflux pump inhibitor and antibiofilm agent to mitigate food borne pathogens. RSC Adv. 2015, 5, 61881–61887. [Google Scholar] [CrossRef]
  136. Lee, P.; Tan, K.S. Effects of Epigallocatechin gallate against Enterococcus faecalis biofilm and virulence. Arch. Oral Biol. 2015, 60, 393–399. [Google Scholar] [CrossRef] [PubMed]
  137. Reygaert, W.C. The antimicrobial possibilities of green tea. Front. Microbiol. 2014, 5. [Google Scholar] [CrossRef] [PubMed]
  138. Zhang, L.; Kong, Y.; Wu, D.; Zhang, H.; Wu, J.; Chen, J.; Ding, J.; Hu, L.; Jiang, H.; Shen, X. Three flavonoids targeting the β-hydroxyacyl-acyl carrier protein dehydratase from Helicobacter pylori: Crystal structure characterization with enzymatic inhibition assay. Protein Sci. 2008, 17, 1971–1978. [Google Scholar] [CrossRef] [Green Version]
  139. Jeong, K.-W.; Lee, J.-Y.; Kang, D.-I.; Lee, J.-U.; Shin, S.Y.; Kim, Y. Screening of Flavonoids as Candidate Antibiotics againstEnterococcus faecalis. J. Nat. Prod. 2009, 72, 719–724. [Google Scholar] [CrossRef]
  140. Zhang, Y.-M.; Rock, C.O. Evaluation of Epigallocatechin Gallate and Related Plant Polyphenols as Inhibitors of the FabG and FabI Reductases of Bacterial Type II Fatty-acid Synthase. J. Biol. Chem. 2004, 279, 30994–31001. [Google Scholar] [CrossRef] [Green Version]
  141. Elmasri, W.A.; Zhu, R.; Peng, W.; Al-Hariri, M.; Kobeissy, F.; Tran, P.; Hamood, A.N.; Hegazy, M.F.; Paré, P.W.; Mechref, Y. Multitargeted Flavonoid Inhibition of the Pathogenic Bacterium Staphylococcus aureus: A Proteomic Characterization. J. Proteome Res. 2017, 16, 2579–2586. [Google Scholar] [CrossRef]
  142. Zhang, F.; Luo, S.-Y.; Ye, Y.-B.; Zhao, W.-H.; Sun, X.-G.; Wang, Z.-Q.; Li, R.; Sun, Y.-H.; Tian, W.-X.; Zhang, Y.-X. The antibacterial efficacy of an aceraceous plant [Shantung maple (Acer truncatum Bunge)] may be related to inhibition of bacterial β-oxoacyl-acyl carrier protein reductase (FabG). Biotechnol. Appl. Biochem. 2008, 51, 73. [Google Scholar] [CrossRef]
  143. Brown, A.K.; Papaemmanouil, A.; Bhowruth, V.; Bhatt, A.; Dover, L.G.; Besra, G.S. Flavonoid inhibitors as novel antimycobacterial agents targeting Rv0636, a putative dehydratase enzyme involved in Mycobacterium tuberculosis fatty acid synthase II. Microbiology 2007, 153, 3314–3322. [Google Scholar] [CrossRef] [Green Version]
  144. Fujita, M.; Shiota, S.; Kuroda, T.; Hatano, T.; Yoshida, T.; Mizushima, T.; Tsuchiya, T. Remarkable Synergies between Baicalein and Tetracycline, and Baicalein and β-Lactams against Methicillin-ResistantStaphylococcus aureus. Microbiol. Immunol. 2005, 49, 391–396. [Google Scholar] [CrossRef] [PubMed]
  145. Eumkeb, G.; Siriwong, S.; Phitaktim, S.; Rojtinnakorn, N.; Sakdarat, S. Synergistic activity and mode of action of flavonoids isolated from smaller galangal and amoxicillin combinations against amoxicillin-resistant Escherichia coli. J. Appl. Microbiol. 2011, 112, 55–64. [Google Scholar] [CrossRef] [PubMed]
  146. Vijayakumar, R.; Sandle, T.; Al-Aboody, M.S.; AlFonaisan, M.K.; Alturaiki, W.; Mickymaray, S.; Premanathan, M.; Alsagaby, S.A. Distribution of biocide resistant genes and biocides susceptibility in multidrug-resistant Klebsiella pneumoniae, Pseudomonas aeruginosa and Acinetobacter baumannii - A first report from the Kingdom of Saudi Arabia. J. Infect. Public Health 2018, 11, 812–816. [Google Scholar] [CrossRef] [PubMed]
  147. Zielińska, S.; Wójciak-Kosior, M.; Dziągwa-Becker, M.; Gleńsk, M.; Sowa, I.; Fijałkowski, K.; Rurańska-Smutnicka, D.; Matkowski, A.; Junka, A. The Activity of Isoquinoline Alkaloids and Extracts from Chelidonium majus against Pathogenic Bacteria and Candida sp. Toxins 2019, 11, 406. [Google Scholar] [CrossRef] [Green Version]
  148. Plaper, A.; Golob, M.; Hafner, I.; Oblak, M.; Šolmajer, T.; Jerala, R. Characterization of quercetin binding site on DNA gyrase. Biochem. Biophy. Res. Comm. 2003, 306, 530–536. [Google Scholar] [CrossRef]
  149. Verdrengh, M.; Collins, L.V.; Bergin, P.; Tarkowski, A. Phytoestrogen genistein as an anti-staphylococcal agent. Microb. Infect. 2004, 6, 86–92. [Google Scholar] [CrossRef]
  150. Ulanowska, K.; Tkaczyk, A.; Konopa, G.; Węgrzyn, G. Differential antibacterial activity of genistein arising from global inhibition of DNA, RNA and protein synthesis in some bacterial strains. Arch. Microbiol. 2005, 184, 271–278. [Google Scholar] [CrossRef]
  151. Wu, D.; Kong, Y.; Han, C.; Chen, J.; Hu, L.; Jiang, H.; Shen, X. d-Alanine:d-alanine ligase as a new target for the flavonoids quercetin and apigenin. Int. J. Antimicrob. Agents 2008, 32, 421–426. [Google Scholar] [CrossRef]
  152. Xu, H. Flavones inhibit the hexameric replicative helicase RepA. Nucleic Acids Res. 2001, 29, 5058–5066. [Google Scholar] [CrossRef] [Green Version]
  153. Shadrick, W.R.; Ndjomou, J.; Kolli, R.; Mukherjee, S.; Hanson, A.M.; Frick, D.N. Discovering New Medicines Targeting Helicases. J. Biomol. Screen. 2013, 18, 761–781. [Google Scholar] [CrossRef] [Green Version]
  154. Bhosle, A.; Chandra, N. Structural analysis of dihydrofolate reductases enables rationalization of antifolate binding affinities and suggests repurposing possibilities. FEBS J. 2016, 283, 1139–1167. [Google Scholar] [CrossRef] [PubMed] [Green Version]
  155. Navarro-Martinez, M.D.; Navarro-Peran, E.; Cabezas-Herrera, J.; Ruiz-Gomez, J.; Garcia-Canovas, F.; Rodriguez-Lopez, J.N. Antifolate Activity of Epigallocatechin Gallate against Stenotrophomonas maltophilia. Antimicrob. Agents Chemother. 2005, 49, 2914–2920. [Google Scholar] [CrossRef] [PubMed] [Green Version]
  156. Raju, A.; Degani, M.S.; Khambete, M.P.; Ray, M.K.; Rajan, M.G.R. Antifolate Activity of Plant Polyphenols againstMycobacterium tuberculosis. Phytother. Res. 2015, 29, 1646–1651. [Google Scholar] [CrossRef] [PubMed]
  157. Walker, E.H.; Pacold, M.E.; Perisic, O.; Stephens, L.; Hawkins, P.T.; Wymann, M.P.; Williams, R.L. Structure determinants of phosphoinositide 3-kinase inhibition by wortmannin, LY294002, quercetin, myricetin and staurosporine. Mol. Cell 2000, 6, 909–919. [Google Scholar] [CrossRef]
  158. Gledhill, J.R.; Montgomery, M.G.; Leslie, A.G.W.; Walker, J.E. Mechanism of inhibition of bovine F1-ATPase by resveratrol and related polyphenols. Proc. Natl. Acad. Sci. USA 2007, 104, 13632–13637. [Google Scholar] [CrossRef] [Green Version]
  159. Chinnam, N.; Dadi, P.K.; Sabri, S.A.; Ahmad, M.; Kabir, M.A.; Ahmad, Z. Dietary bioflavonoids inhibit Escherichia coli ATP synthase in a differential manner. Int. J. Biol. Macromol. 2010, 46, 478–486. [Google Scholar] [CrossRef] [Green Version]
  160. Shah, S.; Stapleton, P.D.; Taylor, P.W. The polyphenol (−)-epicatechin gallate disrupts the secretion of virulence-related proteins by Staphylococcus aureus. Lett. Appl. Microbiol. 2007, 46, 181–185. [Google Scholar] [CrossRef] [Green Version]
  161. Lee, J.-H.; Regmi, S.C.; Kim, J.-A.; Cho, M.H.; Yun, H.; Lee, C.-S.; Lee, J. Apple Flavonoid Phloretin Inhibits Escherichia coli O157:H7 Biofilm Formation and Ameliorates Colon Inflammation in Rats. Infect. Immun. 2011, 79, 4819–4827. [Google Scholar] [CrossRef] [Green Version]
  162. Choi, O.; Yahiro, K.; Morinaga, N.; Miyazaki, M.; Noda, M. Inhibitory effects of various plant polyphenols on the toxicity of Staphylococcal α-toxin. Microb. Pathog. 2007, 42, 215–224. [Google Scholar] [CrossRef]
  163. Ruddock, P.S.; Charland, M.; Ramirez, S.; López, A.; Neil Towers, G.H.; Arnason, J.T.; Liao, M.; Dillon, J.-A.R. Antimicrobial Activity of Flavonoids From Piper lanceaefolium and Other Colombian Medicinal Plants Against Antibiotic Susceptible and Resistant Strains of Neisseria gonorrhoeae. Sex. Transm. Dis. 2011, 38, 82–88. [Google Scholar] [CrossRef]
  164. Rasul, A.; Millimouno, F.M.; Ali Eltayb, W.; Ali, M.; Li, J.; Li, X. Pinocembrin: A Novel Natural Compound with Versatile Pharmacological and Biological Activities. Biomed Res. Int. 2013, 2013, 1–9. [Google Scholar] [CrossRef]
  165. Ahmed, S.I.; Hayat, M.Q.; Tahir, M.; Mansoor, Q.; Ismail, M.; Keck, K.; Bates, R.B. Pharmacologically active flavonoids from the anticancer, antioxidant and antimicrobial extracts of Cassia angustifolia Vahl. Bmc Complement. Altern. Med. 2016, 16. [Google Scholar] [CrossRef] [Green Version]
  166. Girish, K.S.; Kemparaju, K. The magic glue hyaluronan and its eraser hyaluronidase: A biological overview. Life Sci. 2007, 80, 1921–1943. [Google Scholar] [CrossRef]
  167. Hertel, W.; Peschel, G.; Ozegowski, J.-H.; Müller, P.-J. Inhibitory Effects of Triterpenes and Flavonoids on the Enzymatic Activity of Hyaluronic Acid-Splitting Enzymes. Arch. Pharm. 2006, 339, 313–318. [Google Scholar] [CrossRef]
  168. Bush, K.; Fisher, J.F. Epidemiological Expansion, Structural Studies, and Clinical Challenges of New β-Lactamases from Gram-Negative Bacteria. Annu. Rev. Microbiol. 2011, 65, 455–478. [Google Scholar] [CrossRef]
  169. Bush, K. The ABCD’s of β-lactamase nomenclature. J. Infect. Chemother. 2013, 19, 549–559. [Google Scholar] [CrossRef]
  170. Munita, J.M.; Arias, C.A. Mechanisms of Antibiotic Resistance. In Virulence Mechanisms of Bacterial Pathogens, 5th ed.; American Society of Microbiology: Washington, DC, USA, 2016; pp. 481–511. [Google Scholar] [CrossRef] [Green Version]
  171. Yan, X.; Gu, S.; Shi, Y.; Cui, X.; Wen, S.; Ge, J. The effect of emodin on Staphylococcus aureus strains in planktonic form and biofilm formation in vitro. Arch. Microbiol. 2017, 199, 1267–1275. [Google Scholar] [CrossRef]
  172. Peng, Q.; Zhou, S.; Yao, F.; Hou, B.; Huang, Y.; Hua, D.; Zheng, Y.; Qian, Y. Baicalein Suppresses the SOS Response System of Staphylococcus Aureus Induced by Ciprofloxacin. Cell. Physiol. Biochem. 2011, 28, 1045–1050. [Google Scholar] [CrossRef]
  173. Klančnik, A.; Možina, S.S.; Zhang, Q. Anti-Campylobacter Activities and Resistance Mechanisms of Natural Phenolic Compounds in Campylobacter. PLoS ONE 2012, 7, e51800. [Google Scholar] [CrossRef] [Green Version]
  174. Fathima, A.; Rao, J.R. Selective toxicity of Catechin—A natural flavonoid towards bacteria. Appl. Microbiol. Biotechnol. 2016, 100, 6395–6402. [Google Scholar] [CrossRef]
  175. Cushnie, T.P.T.; Taylor, P.W.; Nagaoka, Y.; Uesato, S.; Hara, Y.; Lamb, A.J. Investigation of the antibacterial activity of 3-O-octanoyl-(-)-epicatechin. J. Appl. Microbiol. 2008, 105, 1461–1469. [Google Scholar] [CrossRef]
Figure 1. Mechanisms of antimicrobial activity of bioactive compounds.
Figure 1. Mechanisms of antimicrobial activity of bioactive compounds.
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Figure 2. Chemical structures of antibacterial bioactive compounds.
Figure 2. Chemical structures of antibacterial bioactive compounds.
Antibiotics 08 00257 g002aAntibiotics 08 00257 g002bAntibiotics 08 00257 g002cAntibiotics 08 00257 g002d
Table 1. Antimicrobial screening performed on various medicinal plants.
Table 1. Antimicrobial screening performed on various medicinal plants.
Botanical Name FamilyPlant UsedExtracts MIC *Gram PositiveGram NegativeFungi References
Barleria prionitis L.AcanthaceaeLeavesPet. Ether 3.33–33.3 mg/mLB. subtilis, M. luteus, B. cereus, S. mutans, S. aureus, L. sporogenesS. typhi, V. Cholera, M. luteus, Citrobacter-[19]
Chloroform5–50 mg/mLB. subtilis, L. sporogenesS. typhi, V. cholerae, Citrobacter, Providencia-
Methanol10–100 mg/mLB. subtilis, L. sporogenesV. cholerae, S. typhi,-
Ethanol 50–600 μg/mL-S. typhi-
BarkAcetone25, 50, 100 mg/mLBacillus spp., S. mutans, S. aureus,Pseudomonas spp.,S. cerevisiae, C. albicans
Ethanol 25, 50, 100 mg/mL
Methanol 25, 50, 100 mg/mL
Adhatoda vasica L.AcanthaceaeLeavesAqueous4% v/vM. tuberculosis,E. coli, S. typhi-[20]
Methanol 625 µg/mLS. aureusE. coli, S. typhi-
Pellaea calomelanos L.AdiantaceaeLeaves, Rhizomes Aqueous, 250 μg/mLS. aureus, methicillin- resistant S. aureus, gentamycin– methicillin-resistant S. aureus, S. epidermidis, B. agri, P. acnesP. aeruginosaT. mentagrophytes, M. canis[21]
Dichloromethane/Methanol750–12,000 μg/mL
Sambucus australis Cham. & Schltdl.AdoxaceaeLeaves and BarkHexane50 μg/mLS. aureus, S. agalactiaeE. coli, S. typhimurium and K. pneumoniaeC. albicans[22]
Ethanol
Carpobrotus edulis L N.E.Br.AizoaceaeLeavesAqueous100 μg/mLS. mutans, S. sanguis, L. acidophilus L. caseiP. gingivalis F. nucleatumC. albicans C. glabrataC. krusei[23]
Dichloromethane/Methanol750–12,000 μg/mL
Achyranthes aspera L.AmaranthaceaeRoot, Leaves, Stem Ethanol1 mg/mLS. aureus, B. subtilis,E. coli, P. vulgaris, K. pneumoniae-[16]
Alternanthera Sessile L.AmaranthaceaeLeavesEthanol75 μg/mLS. pyogenesS. typhi-[24,25]
Amaranthus caudatus L.AmaranthaceaeLeaves Ethyl Acetate162.2–665 mg/mLS. aureus, Bacillus spp.E. coli, S. typhi, P. mirabilis-[26]
Chloroform1.25 mg/mL
Methanol3–5 mg/mL
Amaranthus hybridus L.AmaranthaceaeLeavesEthyl Acetate200–755 mg/mL-E. coli, S. typhi, k. pneumoniae, P. aeruginosa-[26]
Chloroform1.25 mg/mL
Methanol3–5 mg/mL
Amaranthus spinosus L.AmaranthaceaeLeavesEthyl Acetate129 mg/mL-S. typhi-[26]
Chloroform1.25 mg/mL
Methanol3–5 mg/mL
Boophane disticha L.f.AmaryllidaceaeLeaves Aqueous, 20–100 mg/mLS. aureus, methicillin- resistant S. aureus, gentamycin– methicillin-resistant S. aureus, S. epidermidis, B. agri, P. acnesP. aeruginosaT. mentagrophytes, M. canis[21]
Dichloromethane/Methanol750–12,000 μg/mL
Scadoxus puniceus (L.) Friis &Nordal.AmaryllidaceaeRhizomes, RootsAqueous50 μg/mLS. aureus, methicillin- resistant S. aureus, gentamycin– methicillin-resistant S. aureus, S. epidermidis, B. agri, P. acnesP. aeruginosaT. mentagrophytes, M. canis[21]
Dichloromethane/Methanol750–12,000 μg/mL
Harpephyllum caffrum Bernh. exKraussAnacardiaceaeBark, LeavesAqueous125–500 μg/mLS. aureus, methicillin- resistant S. aureus, gentamycin– methicillin-resistant S. aureus, S. epidermidis, B. agri, P. acnesP. aeruginosaT. mentagrophytes, M. canis[21]
Dichloromethane/Methanol 750–12,000 μg/mL
Lannea discolor Engl.AnacardiaceaeLeavesAqueous 50–200 μg/mLS. aureus, methicillin- resistant S. aureus, gentamycin– methicillin-resistant S. aureus, S. epidermidis, B. agri, P. acnesP. aeruginosaT. mentagrophytes, M. canis[21]
Dichloromethane/Methanol 750–12,000 μg/mL
Polyalthia cerascides L.AnnonaceaeStem BarkDichloromethane100 μg/mLC. Dipthieriae--[27]
Berula erecta Huds., CovilleApiaceaeRhizome, Leaves, Stem Aqueous 2–16 μg/mLS. mutans, S. sanguis, L. acidophilus L. caseiP. gingivalis F. nucleatumC. albicans C. glabrata C. krusei[23]
Dichloromethane/Methanol 750–12,000 μg/mL
Acokanthera oppositifolia L. Codd.ApocynaceaeLeaves, StemAqueous25–200 μg/mLS. mutans, S. sanguis, L. acidophilus L. caseiP. gingivalis F. nucleatumC. albicans C. glabrata C. krusei[23]
Dichloromethane/Methanol750–12,000 μg/mL
Plumeria ruba L.ApocynaceaeLeavesAqueous50–200 μg/mLS. epidermidisE. coli-[16]
Dichloromethane/Methanol100 μg/mL
Acokanthera oppositifolia (Laim.) Codd.,ApocynaceaeLeavesAqueous10–50 μg/mLS. aureus, methicillin- resistant S. aureus, gentamycin– methicillin-resistant S. aureus, S. epidermidis, B. agri, P. acnesP. aeruginosaT. mentagrophytes, M. canis[21]
Dichloromethane/Methanol750–12,000 μg/mL
Rauvolfia caffra Sond. ApocynaceaeLeaves Aqueous25, 50 μg/mLS. aureus, methicillin- resistant S. aureus, gentamycin– methicillin-resistant S. aureus, S. epidermidis, B. agri, P. acnesP. aeruginosaT. mentagrophytes, M. canis[21]
Dichloromethane/Methanol 750–12,000 μg/mL
Calotropis gigantea L.ApocynaceaeLatex Ethanol1–8 mg/mL--C. albicans, T. mentagrophytes, T. rubrum[16]
Plumeria alba L.ApocynaceaeRoot Methanol 10–40 μg/mL-E. coli [16]
Ilex mitis Radlk. AquifoliaceaeBark, LeavesAqueous 1–8 mg/mLS. aureus, methicillin- resistant S. aureus, gentamycin– methicillin-resistant S. aureus, S. epidermidis, B. agri, P. acnesP. aeruginosaT. mentagrophytes, M. canis[21]
Dichloromethane/Methanol 750–12,000 μg/mL
Anchomanes difformis Engl.AraceaeRootsMethanol20–100 mg/mLmethicillin-resistant S. aureus--[28]
Zantedeschia aethiopica SprengAraceaeLeavesAqueous 50 μg/mLS. aureus, methicillin- resistant S. aureus, gentamycin– methicillin-resistant S. aureus, S. epidermidis, B. agri, P. acnesP. aeruginosaT. mentagrophytes, M. canis[21]
Dichloromethane/Methanol 15–150 μg/mL
Arum dioscoridis L.AraceaeLeaves Aqueous 125–500 μg/mLS. aureus, S. pneumoniaeE. coli, S. typhi, P. aeruginosa-[29]
Aristolochia Indica L.AristolochiaceaeLeaves Ethanol 1–8 mg/mL--A. niger A. flavus A. fumigatus[3,4,30,31]
Vernonia blumeoides Hook. f.AsteraceaeAerial PartEthanol100 μg/mLmethicillin-resistant S. aureus--[28]
Artemisia afra Jacq. ex Willd.AsteraceaeLeaves, StemAqueous 2–16 μg/mLS. mutans, S. sanguis, L. acidophilus L. caseiP. gingivalis F. nucleatumC. albicans C. glabrata C. krusei[23]
Dichloromethane/Methanol 750–12,000 μg/mL
Tarchonanthus camphoratus L.AsteraceaeLeaves Aqueous 25–200 μg/mLS. mutans, S. sanguis, L. acidophilus L. caseiP. gingivalis F. nucleatumC. albicans C. glabrata C. krusei[23]
Dichloromethane/Methanol 750–12,000 μg/mL
Helichrysum paronychioides L.AsteraceaeWhole PlantPet ether50–200 μg/mLB. cereusS. flexneriC. glabrata, C. krusei, T. rubrum and T. tonsurans[2]
Methanol 50–200 μg/mL
Senecio longiflorus L.AsteraceaeStem and LeavesPet ether125–625 μg/mLB. cereusS. flexneriC. glabrata, C. krusei, T. rubrum and T. tonsurans[2]
Methanol 50–200 μg/mL
Dahlia pinnata L.AsteraceaeLeavesChloroform 2–16 μg/mLE. aerogenes, P. aeruginosa[16]
Athrixia phylicoides DC.AsteraceaeLeavesAqueous25–200 μg/mLS. aureus, methicillin- resistant S. aureus, gentamycin– methicillin-resistant S. aureus, S. epidermidis, B. agri, P. acnesP. aeruginosaT. mentagrophytes, M. canis[21]
Dichloromethane/Methanol 750–12,000 μg/ml
Dicoma anomala Sond.AsteraceaeTuberAqueous50–200 μg/mLS. aureus, methicillin- resistant S. aureus, gentamycin– methicillin-resistant S. aureus, S. epidermidis, B. agri, P. acnesP. aeruginosaT. mentagrophytes, M. canis[21]
Dichloromethane/Methanol 750–12,000 μg/mL
Vernonia natalensis Sch. Bip. exWalp.AsteraceaeLeaves, RootsAqueous10–50 μg/mLS. aureus, methicillin- resistant S. aureus, gentamycin– methicillin-resistant S. aureus, S. epidermidis, B. agri, P. acnesP. aeruginosaT. mentagrophytes, M. canis[21]
Dichloromethane/Methanol750–12,000 μg/mL
Achillea millefolium L.AsteraceaeLeavesEthanol100 μg/mLS. aureusP. aeruginosa S. typhi, E. coliC. albicans[29]
Blumea balsamifer (Linn.) D.C.AsteraceaeWhole PlantEthanol250 μg/mLmethicillin-resistant S. aureus--[32]
Impatiens balsamina L.BalsaminaceaeLeafEthanol50–200 μg/ml methicillin-resistant S. aureus--[28]
Berberis chitria L.BerberidaceaeRootsEthanol, 5.5–6.5 mg/mLS. aureusE. coli-[33]
Methanol 2.5–3.5 mg/mL
Alnus nepalensis D. Don.BetulaceaeTBLEthanol50–200 μg/mLMethicillin-resistant S. aureus--[32]
Tecoma capensis Lindl.BignoniaceaeLeaves, StemAqueous, 10–50 μg/mLS. mutans, S. sanguis, L. acidophilus L. caseiP. gingivalis F. nucleatumC. albicans C. glabrata C. krusei[23]
Dichloromethane/Methanol 2.5 mg/mL
Spathodea campanulata L.BignoniaceaeLeaves Ethanol 221–254 μg/mLB. subtilis, S. aureus,E. coli, K. pneumonia, P. vulgaris, S. typhi, Pseudomonas spp., V. cholerae -[6,34,35]
Flowers 156–173 μg/mL
Kigelia africana (Lam.) Benth. BignoniaceaeFruit Aqueous 2–16 μg/mLS. aureus, methicillin- resistant S. aureus, gentamycin– methicillin-resistant S. aureus, S. epidermidis, B. agri, P. acnesP. aeruginosaT. mentagrophytes, M. canis[21]
Dichloromethane/Methanol 750–12,000 μg/mL
Opuntia ficus-indica Mill.CactaceaeLeaves Aqueous25–200 μg/mLS. aureus, methicillin- resistant S. aureus, gentamycin– methicillin-resistant S. aureus, S. epidermidis, B. agri, P. acnesP. aeruginosaT. mentagrophytes, M. canis[21]
Dichloromethane 750–12,000 μg/mL
Methanol
Senna italic L.CaesalpiniaceaeLeavesAcetone2.5 mg/mLB. cereus, B. pumilus, B. subtilis, S. aureus, E. faecalis,--[36]
Cassia fistula L.CaesalpiniaceaeSeeds Aqueous780–6250 μg /mLS. aureus--[6]
Ethanol2–16 μg/mL
Warburgia salutaris (G. Bertol.) Chiov.CanellaceaeBark, TwigsAqueous5.0–10 mg/mLS. mutans, S. sanguis, L. acidophilus L. caseiP. gingivalis F. nucleatumC. albicans C. glabrata
C. krusei
[23]
50–200 μg/mLS. aureus, methicillin- resistant S. aureus, gentamycin– methicillin-resistant S. aureus, S. epidermidis, B. agri, P. acnesP. aeruginosaT. mentagrophytes, M. canis[21]
Dichloromethane, Methanol750–12,000 μg/mL
Cadaba fruticosa L.CapparaceaeLeaves Acetone100–200 μg/mLS. pyogens, S. aureus, B. subtilisS. typhi, P. vulgaris, K. pneumoniae, P. aeruginosa, E. coli-[37]
Aqueous 4–16 μg/mL
Benzene 4–16 μg/mL
Butanol 4–16 μg/mL
Chloroform 4–16 μg/mL
Ethanol 4–16 μg/mL
Boscia senegalensis Del.CapparidaceaeRootsMethanol10–20 μg/mLmethicillin-resistant S. aureus--[28]
Celastrus orbiculatus Thunb.CelastraceaeVaneEthanol1–2 mg/mLmethicillin-resistant S. aureus--[32]
Euonymus fortunei (Turcz.); Hand. Mazz.CelastraceaeLeaves Ethanol10–40 μg/mLmethicillin-resistant S. aureus--[32]
Chenopodium ambrosioides Bert. ex Steud. ChenopodiaceaeLeaves Aqueous2–16 μg/mLS. aureus, methicillin- resistant S. aureus, gentamycin– methicillin-resistant S. aureus, S. epidermidis, B. agri, P. acnesP. aeruginosaT. mentagrophytes, M. canis[21]
Dichloromethane/Methanol750–12,000 μg/mL
Garcinia mangostana L.ClusiaceaeFruit ShellEthanol25–200 μg/mLmethicillin-resistant S. aureus--[28]
Garcinia morella Desr.ClusiaceaeWhole PlantEthanol100–400 μg/mLmethicillin-resistant S. aureus--[32]
Terminalia paniculata L.CombretaceaeStem BarkEthyl Acetate3.25, 3.5 mg/mLS. aureus, B. subtilis--[38]
Methanol 5–20 μg/mL
Terminalia sericea Burch. ex DC.CombretaceaeRoots Aqueous100–300 μg/mLS. aureus, methicillin- resistant S. aureus, gentamycin– methicillin-resistant S. aureus, S. epidermidis, B. agri, P. acnesP. aeruginosaT. mentagrophytes, M. canis[21]
Dichloromethane/Methanol 750–12,000 μg/mL
Eupatorium odoratum L.CompositaeLeaves Benzene300–600 μg/mLB. cereus, S. aureusE. coli, K. pneumoniae, V. choleraeC. albicans[39]
Aqueous 300–600 μg/mL
Acetone300–600 μg/mL
Acmella paniculata L.CompositaeWhole PlantChloroform15 μg/mL-E. aerogenes-[40]
Pet. ether 5–15 μg/mL
Methanol 5–15 μg/mL
Cotyledon orbiculata L.CrassulaceaeLeavesAqueous 5–30 μg/mLS. mutans, S. sanguis, L. acidophilus L. caseiP. gingivalis F. nucleatumC. albicans C. glabrata
C. krusei
[23]
Dichloromethane 750–12,000 μg/mL
Methanol
Cotyledono rbiculata Forssk.CrassulaceaeLeaves Aqueous 25–200 μg/mLS. aureus, methicillin- resistant S. aureus, gentamycin– methicillin-resistant S. aureus, S. epidermidis, B. agri, P. acnesP. aeruginosaT. mentagrophytes, M. canis[21]
Dichloromethane/Methanol 750–12,000 μg/mL
Mormodica basalmina L.CucurbitaceaeWhole PlantMethanol500 μg/mLmethicillin-resistant S. aureus--[28]
Coccinia grandis L.CucurbitaceaeLeavesAqueous 500 μg/mLB. cereus, S. aureus--[41]
Dichloromethane/Methanol 2 mg/mL
Luffa acyntangula L.CucurbitaceaeLeavesAqueous 5 mg/mLB. cereus, S. aureus--[41]
Dichloromethane 2 mg/mL
Methanol
Mukia maderspatana L.CucurbitaceaeLeavesAqueous 5 mg/mLB. cereus, S. aureus--[41]
Dichloromethane/Methanol 1 mg/mL
Trichosanthes cucumerina L.CucurbitaceaeLeavesAqueous 5 mg/mLB. cereus, S. aureus--[41]
Dichloromethane/Methanol 1 mg/mL
Momordica balsami- na L.CucurbitaceaeLeaves, RootsAcetone 500 μg/mLB. cereus, B. pumilus, B. subtilis, S. aureus, E. faecalisE. coli, E. cloaceae, K. pneumoniae, P. aeruginosa, S. marcescens-[42]
Carex prainii C.B. ClarkeCyperaceaeWhole PlantEthanol15–45 μg/mLmethicillin-resistant S. aureus--[32]
Dioscorea dregeana T. Durand & Schinz.DioscoreaceaeTuber Aqueous 5–30 μg/mLS. aureus, methicillin- resistant S. aureus, gentamycin– methicillin-resistant S. aureus, S. epidermidis, B. agri, P. acnesP. aeruginosaT. mentagrophytes, M. canis[21]
Dichloromethane/Methanol 750–12,000 μg/mL
Sansevieria hyacinthoides L.DracaenaceaeLeaves, rhizomeAqueous, 1–4 mg/mLS. mutans, S. sanguis, L. acidophilus L. caseiP. gingivalis F. nucleatumC. albicans C. glabrataC. krusei[23]
Dichloromethane/Methanol 750–12,000 μg/mL
Diospyros mespiliformis Hochst. exA. DC.EbenaceaeLeaves Aqueous15–45 μg/mLS. aureus, methicillin- resistant S. aureus, gentamycin– methicillin-resistant S. aureus, S. epidermidis, B. agri, P. acnesP. aeruginosaT. mentagrophytes, M. canis[21]
Dichloromethane/Methanol 750–12,000 μg/mL
Phyllanthus amarus Schum. Thonn.EuphorbiaceaeWhole PlantMethanol650–600 μg/mL methicillin-resistant S. aureus--[28]
Croton gratissimus Burch.EuphorbiaceaeLeaves, Stem, Aqueous 5 mg/mLS. mutans, S. sanguis, L. acidophilus L. caseiP. gingivalis F. nucleatumC. albicans C. glabrataC. krusei[23]
Dichloromethane/Methanol 750–12,000 μg/mL
Spirostachys africana Sond.EuphorbiaceaeLeaves, BarkAqueous 490 μg/mLS. mutans, S. sanguis, L. acidophilus L. caseiP. gingivalis F. nucleatumC. albicans C. glabrataC. krusei[23]
Dichloromethane/Methanol 750–12,000 μg/mL
Acalypha indica L.EuphorbiaceaeLeaves Aqueous 4% v/v M. tuberculosis--[43]
Bridelia micrantha Baill.EuphorbiaceaeBark, LeavesAqueous 5 mg/mLS. aureus, methicillin- resistant S. aureus, gentamycin– methicillin-resistant S. aureus, S. epidermidis, B. agri, P. acnesP. aeruginosaT. mentagrophytes, M. canis[21]
Dichloromethane/Methanol 750–12,000 μg/mL
Emblica officinalis L.EuphorbiaceaeLeaves Benzene350–600 μg/mL B. cereus, S. aureusE. coli, K. pneumoniae, V. choleraeC. albicans[39]
Aqueous 300–600 μg/mL
Acetone300–600 μg/mL
Hevea brasiliensis L.EuphorbiaceaeLeaves Benzene350–600 μg/mLB. cereus, S. aureusE. coli, K. pneumoniae, V. choleraeC. albicans[39]
Aqueous 300–600 μg/mL
Acetone300–600 μg/mL
Mallotus yunnanensis Pax et. Hoffm.EuphorbiaceaeTender Branches & Leaves Ethanol8–256 μg/mLmethicillin-resistant S. aureus--[32]
Acacia albida Del.FabaceaeStem BarkMethanol50 μg/mL methicillin-resistant S. aureus--[28]
Acacia catechu (L. f.) WilldFabaceaeWoodEthanol100 μg/mL methicillin-resistant S. aureus--[28]
Peltophorum ptercarpum (DC.)FabaceaeBarkEthanol4% v/v methicillin-resistant S. aureus--[28]
Acacia erioloba Edgew.FabaceaeBark and LeavesAqueous 1.56–3.12 mg/mLS. aureus, methicillin– resistant S. aureus, gentamycin– methicillin-resistant S. aureus, S. epidermidis, B. agri, P. acnesP. aeruginosaT. mentagrophytes, M. canis[21]
Dichloromethane/Methanol 750–12,000 μg/mL
Dichrostachys cinerea L. FabaceaeStem Aqueous 129 mg/mLS. mutans, S. sanguis, L. acidophilus L. caseiP. gingivalis F. nucleatumC. albicans C. glabrata
C. krusei
[23]
Dichloromethane/Methanol 750–12,000 μg/mL
Albizia odoratissima (L.f.) BenthFabaceaeLeaves Hexane7.5–15 mg/mLS. aureusK. pneumoniae, E. coli, P. aeruginosa, P. vulgaris-[44]
Chloroform 859–6875 μg/mL
Ethyl Acetate136–546 μg/mL
Methanol136–546 μg/mL
Prosopis juliflora L.FabaceaePodChloroform250 μg/mLM. luteus, S. aureus, S. mutans--[36]
Bauhinia macranthera Benth. Ex Hemsl.FabaceaeLeaves Aqueous, 1.56–3.12 mg/mL S. aureus, methicillin- resistant S. aureus, gentamycin– methicillin-resistant S. aureus, S. epidermidis, B. agri, P. acnesP. aeruginosaT. mentagrophytes, M. canis[21]
Dichloromethane/Methanol 750–12,000 μg/mL
Erythrina lysistemon Hutch. FabaceaeLeaves Aqueous4 mg/mLS. aureus, methicillin- resistant S. aureus, gentamycin– methicillin-resistant S. aureus, S. epidermidis, B. agri, P. acnes, S. mutans, S. sanguis, L. acidophilus L. caseiP. aeruginosa, P. gingivalis F. nucleatumT. mentagrophytes, M. canis, C. albicans C. glabrata
C. krusei
[21]
Dichloromethane/Methanol 750–12,000 μg/mL
Elephantorrhiza elephantina (Burch.) Skeels FabaceaeLeaves, roots and rhizomes Aqueous1–4 mg/mLS. aureus, methicillin- resistant S. aureus, gentamycin– methicillin-resistant S. aureus, S. epidermidis, B. agri, P. acnes, B. cereusP. aeruginosa, S. flexneriT. mentagrophytes, M. canis, C. glabrata, C. krusei, T. rubrum and T. tonsurans[21]
Dichloromethane/Methanol750–12,000 μg/mL
Albizia lebbeck L.FabaceaeLeaves Benzene, Aqueous and Acetone350–600 μg/mLB. cereus, S. aureusE. coli, K. pneumoniae, V. choleraC. albicans[39]
Adenanthera pavonina L.FabaceaeLeaves Aqueous 5 mg/mLB. cereus, S. aureus--[41]
Dichloromethane/Methanol60 μg mg/mL
Alysicarpus vaginalis L.FabaceaeLeaves Aqueous 5 mg/mLB. cereus, S. aureus--[41]
Dichloromethane/Methanol2 mg/mL
Bauhinia acuminate L.FabaceaeLeaves Aqueous 5 mg/mLB. cereus, S. aureus--[41]
Dichloromethane/Methanol50 μg mg/mL
Bauhinia purpurea L.FabaceaeLeaves Aqueous 5 mg/mLB. cereus, S. aureus--[41]
Dichloromethane/Methanol1 mg/mL
Bauhinia racemose L.FabaceaeLeaves, Stem Bark Aqueous 500 μg/mLB. cereus, S. aureus--[41]
Dichloromethane/Methanol500 μg/mL
Cassia alata L.FabaceaeLeaves Aqueous 250 μg/mLB. cereus, S. aureus--[41]
Dichloromethane/Methanol500 μg/mL
Cassia auriculata L.FabaceaeLeaves Aqueous 1 mg/mLB. cereus, S. aureus--[41]
Dichloromethane/Methanol4 mg/mL
Cassia fistula L.FabaceaeRoot Bark, Stem Bark Aqueous 1–5 mg/mL B. cereus, S. aureus--[41]
Dichloromethane/Methanol500–1000 μg/mL
Cassia tora L.FabaceaeLeaves, Root Bark, Stem BarkAqueous 250–4000 μg/mLB. cereus, S. aureus--[41]
Dichloromethane/Methanol 1000–4000 μg/mL
Crotalaria retusa L.FabaceaeLeavesAqueous 4 mg/mLB. cereus, S. aureus--[41]
Dichloromethane/Methanol60 μg/mL
Crotalaria verrucosa L.FabaceaeLeavesAqueous 1 mg/mLB. cereus, S. aureus--[41]
Dichloromethane/Methanol1 mg/mL
Derris Scandens L.FabaceaeLeavesAqueous 100 μg/mLB. cereus, S. aureus--[41]
Dichloromethane/Methanol4 mg/mL
Desmodiumtriflorum (L.) DC. var. majus Wight & Arn.FabaceaeStem BarkAqueous 1 mg/mLB. cereus, S. aureus--[41]
Dichloromethane/Methanol25 μg/mL
Erythuria variegate L.FabaceaeLeaves, Stem BarkAqueous 1–5 mg/mL B. cereus, S. aureus--[41]
Dichloromethane/Methanol250–1000 μg/mL
Indigofera tinctoria L.FabaceaeLeavesAqueous 500 μg/mLB. cereus, S. aureus--[41]
Dichloromethane/Methanol4 mg/mL
Mimosa pudica L.FabaceaeStem BarkAqueous 1–2 mg/mLB. cereus, S. aureus--[41]
Dichloromethane/Methanol250–5000 μg/mL
Myroxylon balsamum L.FabaceaeLeavesAqueous 1 mg/mLB. cereus, S. aureus--[41]
Dichloromethane/Methanol500 μg/mL
Pterocarpus marsupium Roxb.FabaceaeLeavesAqueous 4 mg/mLB. cereus, S. aureus--[41]
Dichloromethane/Methanol250 μg/mL
Pterocarpus santalinus L.FabaceaeLeavesAqueous 2 mg/mLB. cereus, S. aureus--[41]
Dichloromethane/Methanol4 mg/mL
Saraca asoca (Roxb.) WilldFabaceaeLeavesAqueous 120 μg/mLB. cereus, S. aureus--[41]
Dichloromethane/Methanol5 mg/mL
Sesbania grandiflora (L.) PoiretFabaceaeStem Bark, Root Bark, LeavesAqueous, 2 mg/mLB. cereus, S. aureus--[41]
Dichloromethane/Methanol100 μg/mL
Tamarindus indica L.FabaceaeLeaves Aqueous250–500 μg/mLB. cereus, S. aureus--[41]
Dichloromethane/Methanol60–100 μg/mL
Tephrosia purpurea L. Pers.Fabaceae LeavesAqueous5 mg/mLB. cereus, S. aureus--[41]
Dichloromethane/Methanol5 mg/mL
Butea monosperma L.FabaceaeLeaves Aqueous4 mg/mLB. cereus, S. aureus, methicillin-resistant S. aureus--[41,45]
Dichloromethane/Methanol2 mg/mL
Ethanol 100–200 μg/mL
Senna alataFabaceaeLeafEthanol100 μg/mL methicillin-resistant S. aureus--[46]
Quercus infectoria OlivierFagaceaeNutgallsEthanol100–200 μg/mL methicillin-resistant S. aureus--[16]
Cyclobalanopsis austroglauca Y.T. ChangFagaceaeTBLEthanol8–256 μg/mLmethicillin-resistant S. aureus--[32]
Scaevola spinescens L.GoodeniaceaeAerial partsEthyl Acetate, Methanol500 μg/mLS. pyogenes, S. aureus--[38]
Gunnera perpensa L. GunneraceaeLeaves, RhizomeAqueous, 4 mg/mLS. aureus, methicillin- resistant S. aureus, gentamycin– methicillin-resistant S. aureus, S. epidermidis, B. agri, P. acnesP. aeruginosaT. mentagrophytes, M. canis[21]
Dichloromethane/Methanol750–12,000 μg/mL
Eucomis punctate L’Her.HyacinthaceaeLeavesAqueous, 500 μg/mLS. mutans, S. sanguis, L. acidophilus L. caseiP. gingivalis F. nucleatumC. albicans C. glabrata
C. krusei
[23]
Dichloromethane/Methanol750–12,000 μg/mL
Drimia sanguinea L.HyacinthaceaeBulbPet ether18.75, 37.5, 300, 600, 1200 μg/mL B. cereusS. flexneriC. glabrata, C. krusei, T. rubrum and T. tonsurans[2]
Hypoxis hemerocallidea L.HypoxidaceaeLeaves Pet ether195–12,500 μg/mLB. cereusS. flexneriT. rubrum, T.urans, C. glabrata C. krusei[47]
Methanol390–3125 μg/mL
Curculigo orchioides Gaertn.HypoxidaceaeWhole PlantEthanol8–256 μg/mLmethicillin-resistant S. aureus--[32]
Illicium simonsii Maxim.IlliciaceaeTBLEthanol8–256 μg/mLmethicillin-resistant S. aureus--[32]
Aristea ecklonii Baker.IridaceaeLeaves and RootsAqueous129 mg/mLS. aureus, methicillin- resistant S. aureus, gentamycin– methicillin-resistant S. aureus, S. epidermidis, B. agri, P. acnesP. aeruginosaT. mentagrophytes, M. canis[21]
Dichloromethane/Methanol750–12,000 μg/mL
Tetradenia riparia Hochst.LamiaceaeLeaves, StemAqueous200–755 mg/mLS. mutans, S. sanguis, L. acidophilus L. caseiP. gingivalis F. nucleatumC. albicans C. glabrata
C. krusei
[23]
Dichloromethane/Methanol750–12,000 μg/mL
Thymus vulgaris L.LamiaceaeLeavesEssential Oil50 μg/mL methicillin-resistant S. aureus--[48]
Mentha aquatica L.LamiaceaeAerial PartsMethanol1.56–3.12 mg/mLS. aureusE. coli, P. aeruginosa, S. heidelberg, K. pneumoniae, E. aerogenes, M. morganii-[49]
Chloroform 128 μg/mL
Acetone 32–128 μg/mL
Stachys guyoniana Noë ex. Batt.LamiaceaeLeaves n-Butanol4 mg/mLS. aureusE. coli, P. aeruginosa, S. heidelberg, K. pneumoniae, E. aerogenes, M. morganii-[49]
Ethyl Acetate 128 μg/mL
Chloroform32–128 μg/mL
Ocimum basilicum L.LamiaceaeStem, leavesEthanol 1–4 mg/mLS. aureus--[38]
Ocimum gratissimum L.LamiaceaeLeaves Methanol 780–6250 μg/mLS. aureusS. typhi, E. coli, S. paratyphi-[38]
Ocimum sanctum L.LamiaceaeWhole PlantMethanol360 μg/mLS. aureus, S. saprophyticusS. typhi, E. coli, S. paratyphi-[6]
Mentha longifolia Huds.LamiaceaeLeavesAqueous150, 300, 600 μg/mLS. aureus, methicillin- resistant S. aureus, gentamycin– methicillin-resistant S. aureus, S. epidermidis, B. agri, P. acnesP. aeruginosaT. mentagrophytes, M. canis[21]
Dichloromethane/Methanol750–12,000 μg/mL
Melissa officinalis L.LamiaceaeLeaves Ethanol 49 μg/mL-K. pneumoniae-[42]
Ocimum americanum L.LamiaceaeLeaves Acetone 2.5 mg/mLB. cereus, B. pumilus, B. subtilis, S. aureus, E. faecalis--[16]
Machilus salicina Hance.LauraceaeTender Branches & LeavesEthanol500 μg/mLmethicillin-resistant S. aureus--[32]
Meliosma squamulata Hance.LauraceaeTBLEthanol1–4 mg/mLmethicillin-resistant S. aureus--[32]
Sophora alopecuroidesLeguminosaeAerial Parts, SeedsEthanol 129 mg/mLB. subtilis, S. aureus, B. subtilisP. aeruginosa-[50]
Acacia karroo Hayne.LeguminosaeLeaves, StemAqueous, 200–755 mg/mL S. mutans, S. sanguis, L. acidophilus L. caseiP. gingivalis F. nucleatumC. albicans C. glabrata
C. krusei
[23]
Dichloromethane/Methanol750–12,000 μg/mL
Acacia polyacantha Willd.LeguminosaeLeaves, StemAqueous50 μg/mL S. mutans, S. sanguis, L. acidophilus L. caseiP. gingivalis F. nucleatumC. albicans C. glabrata
C. krusei
[23]
Dichloromethane/Methanol750–12,000 μg/mL
Dalbergia obovate E. Mey.LeguminosaeLeaves, stemAqueous1.56–3.12 mg/mLS. mutans, S. sanguis, L. acidophilus L. caseiP. gingivalis F. nucleatumC. albicans C. glabrata
C. krusei
[23]
Dichloromethane/Methanol750–12,000 μg/mL
Sophora jaubertiiLeguminosaeAerial Parts, SeedsEthanol 4 mg/mLB. subtilis, P. aeruginosa, S. aureus--[38]
Glycyrrhiza glabra L.Leguminosae Leaves Methanol 1–4 mg/mLK. kristinae, M. luteus, S. auricularis, B. megateriumA. bohemicus, E. coli-[51]
Allium cepa L.LiliaceaeBulb Aqueous 780–6250 μg/mLM. tuberculosis--[43]
Allium sativum L.LiliaceaeBulb Aqueous 4% v/v M. tuberculosis--[43]
Allium vera L.LiliaceaeGel Aqueous 4% v/v M. tuberculosis--[43]
Lobelia nicotianaefolia L.LobeliaceaeRoot Chloroform129 mg/mLS. aureusP. aeruginosa-[39]
Acetone 6 mg/mL
Ethanol 6 mg/mL
Woodfordia fruticose L.LythraceaeFlower Aqueous 200–755 mg/mL S. aureus, B. cereusS. typhi, E. coli, S. dysenteriae. V. cholerae-[37]
Dichloromethane/Methanol100 mg/mL
Manglietia hongheensis Y.m Shui et. W.H. Chen.MagnoliaceaeTBLEthanol50 μg/mL methicillin-resistant S. aureus--[32]
Malva parviflora L. MalvaceaeLeaves Aqueous 500 μg/mLS. aureus, methicillin- resistant S. aureus, gentamycin– methicillin-resistant S. aureus, S. epidermidis, B. agri, P. acnesP. aeruginosaT. mentagrophytes, M. canis[21]
Dichloromethane/Methanol750–12,000 μg/mL
Sida rhombifolia L.MalvaceaeStemChloroform162.2–665 mg/mL S. lutea, B. subtilis,E. coli, Shigella shiga-[38]
Walsura robusta L.MeliaceaeWoodEthanol250 μg/mLmethicillin-resistant S. aureus--[28]
Swietenia mahagoniMeliaceaeSeedEthanol500 μg/mLmethicillin-resistant S. aureus--[52]
Azadirachta indicaMeliaceaeLeavesStem MethanolAqueous1.56–3.12 mg/mLM. luteusS. aureus, S. pyogenesP. vulgarisE. coli, P. aeruginosa--[53]
Ekebergia capensis Sparrm. MeliaceaeBark, Leaves Aqueous 1.59–25 mg/mL S. aureus, methicillin- resistant S. aureus, gentamycin– methicillin-resistant S. aureus, S. epidermidis, B. agri, P. acnesP. aeruginosaT. mentagrophytes, M. canis[21]
Dichloromethane/Methanol750–12,000 μg/mL
Trichilia emetica VahlMeliaceaeLeavesAqueous 50–600 μg/mLS. aureus, methicillin- resistant S. aureus, gentamycin– methicillin-resistant S. aureus, S. epidermidis, B. agri, P. acnesP. aeruginosaT. mentagrophytes, M. canis[21]
Dichloromethane/Methanol 750–12,000 μg/mL
Melia azedarach L.MeliaceaeLeaves Methanol 3.33–33.3 mg/mLB. cereus, S. aureusE. coli, P. aeruginosaA. niger, A. flavus, F. oxysporum, R. stolonifer[16]
Ethanol 500 μg/mL
Pet.ether1.56–3.12 mg/mL
Aqueous 10–30 mg/mL
Melianthus comosus Vahl. MelianthaceaeLeaves Aqueous50 mg/mLS. aureus, methicillin- resistant S. aureus, gentamycin– methicillin-resistant S. aureus, S. epidermidis, B. agri, P. acnes, methicillin-resistant S. aureusP. aeruginosaT. mentagrophytes, M. canis[28]
Dichloromethane/Methanol4–64 mg/mL
Melianthus major L.MelianthaceaeLeavesEthanol10–100 mg/mLmethicillin-resistant S. aureus--[28]
Melianthus major L.MelianthaceaeLeaves Aqueous5–50 mg/mLS. aureus, methicillin- resistant S. aureus, gentamycin– methicillin-resistant S. aureus, S. epidermidis, B. agri, P. acnesP. aeruginosaT. mentagrophytes, M. canis[21]
Dichloromethane/Methanol750–12,000 μg/mL
Cissampelos torulosa E. Mey. Ex Harv.MenispermaceaeLeaves, StemAqueous25, 50, 100 mg/mLS. mutans, S. sanguis, L. acidophilus L. caseiP. gingivalis F. nucleatumC. albicans C. glabrata
C. krusei
[23]
Dichloromethane/Methanol750–12,000 μg/mL
Tinospora crispa L.MenispermaceaeStemEthanol10 mg/mLmethicillin-resistant S. aureus--[21]
Cissampelos capensis Thunb.MenispermaceaeLeaves Aqueous3.33–33.3 mg/mL S. aureus, methicillin- resistant S. aureus, gentamycin– methicillin-resistant S. aureus, S. epidermidis, B. agri, P. acnesP. aeruginosaT. mentagrophytes, M. canis[21]
Dichloromethane/Methanol750–12,000 μg/mL
Ficus natalensis Hochst. MoraceaeLeaves Aqueous 250 mg/mLS. aureus, methicillin- resistant S. aureus, gentamycin– methicillin-resistant S. aureus, S. epidermidis, B. agri, P. acnesP. aeruginosaT. mentagrophytes, M. canis[21]
Dichloromethane/Methanol750–12,000 μg/mL
Ficus sur Forssk.MoraceaeBark, LeavesAqueous, 10–100 mg/mL S. aureus, methicillin- resistant S. aureus, gentamycin– methicillin-resistant S. aureus, S. epidermidis, B. agri, P. acnesP. aeruginosaT. mentagrophytes, M. canis[21]
Dichloromethane/Methanol750–12,000 μg/mL
Moringa oleifera Lam.MoringacceaeLeafEthanol5–50 mg/mL methicillin-resistant S. aureus--[28]
Myrothamnus flabellifolia Welw.,MyrothamnaceaeLeavesAqueous156–625 μg/mLS. mutans, S. sanguis, L. acidophilus L. caseiP. gingivalis F. nucleatumC. albicans C. glabrata
C. krusei
[23]
Dichloromethane/Methanol750–12,000 μg/mL
Embelia ruminate (E. Mey.exA.Dc.) Mez MyrsinaceaeleavesAqueous350–600 μg/mLS. aureus, methicillin- resistant S. aureus, gentamycin– methicillin-resistant S. aureus, S. epidermidis, B. agri, P. acnesP. aeruginosaT. mentagrophytes, M. canis[21]
Dichloromethane/Methanol750–12,000 μg/mL
Embelia burm f.MyrsinaceaeLeavesEthanol500 μg/mLmethicillin-resistant S. aureus--[32]
Callistemon rigidus R.Br.MyrtaceaeLeafMethanol800 mg/disc methicillin-resistant S. aureus--[28]
Psidium guajava L.MyrtaceaeLeafEthanol600, 1200 μg/mL methicillin-resistant S. aureus--[28]
Heteropyxis natalenesis Harv.MyrtaceaeLeaves, StemAqueous, 5 mg/mLS. mutans, S. sanguis, L. acidophilus L. caseiP. gingivalis F. nucleatumC. albicans C. glabrata
C. krusei
[23]
Dichloromethane/Methanol750–12,000 μg/mL
Eucalyptus camaldulensis Dehnh. MyrtaceaeBarkAqueous9.375, 18.75, 37.5, 75, 150, 300, 600 μg/mLS. aureus, methicillin- resistant S. aureus, gentamycin– methicillin-resistant S. aureus, S. epidermidis, B. agri, P. acnesP. aeruginosaT. mentagrophytes, M. canis[21]
Dichloromethane/Methanol750–12,000 μg/mL
Eucalyptus degluptaMyrtaceaeLeaves Benzene37.5, 75, 150, 300, 600 μg/mL B. cereus, S. aureusE. coli, K. pneumoniae, V. choleraeC. albicans[39]
Aqueous4–8 mg/mL
Acetone6 mg/mL
Myrtus communis L.MyrtaceaeLeaves Ethanol 12.5–50 mg/mL B. cereus, L. monocytogenesE. coliC. albicans[42]
Nelumbo nucifera L.NelumbonaceaeFlower Ethanol 8–32 mg/mL B. subtilis, S. aureus,E. coli, K. pneumonia, P. aeruginosa-[54]
Nymphaea lotus L.NymphaeaceaeLeafEthanol500 μg/mLmethicillin-resistant S. aureus--[21]
Oxalis corniculata L.OxalidaceaeLeaves Aqueous5 mg/mLB. cereus, S. aureusE. coli, K. pneumoniae, V. choleraC. albicans[39]
Benzene 37.5, 75, 150, 300, 600 μg/mL
Acetone6 mg/mL
Paeonia lactiflora Pall.PaeoniaceaeLeaves Ethanol 22.4–52.3 μg/mL K. kristinae, M. luteus, S. auricularis, B. megateriumA. bohemicus, E. coli-[51]
Argemone mexicanaPapaveraceaeStem Chloroform 32.4–55.8 μg/mLS. aureusE. coli, P. aeruginosa, k. pneumoniae-[55]
Passiflora Mexicana L.PassifloraceaeAerial PartsEthanol 33.7–58.3 μg/mL S. aureus--[21]
Cleistanthus collinusPhyllanthaceaeLeaves Benzene100 mg/mLB. cereus, S. aureusE. coli, K. pneumoniae, V. choleraeC. albicans[39]
Aqueous 4–8 mg/mL
Acetone 5 mg/mL
Piper nigrum L.PiperaceaeBark, Seeds Ethanol500 μg/mLS. aureus, B. cereus, S. fecalisP. aeruginosa, E. coli, S. typhi-[38]
Acetone 6 mg/mL
Dichloromethane/Methanol12.5–50 μg/mL
Pittosporum viridiflorum Sims.PittosporaceaeLeaves Aqueous600 μg/mLS. aureus, methicillin- resistant S. aureus, gentamycin– methicillin-resistant S. aureus, S. epidermidis, B. agri, P. acnesP. aeruginosaT. mentagrophytes, M. canis[21]
Dichloromethane/Methanol750–12,000 μg/mL
Spinifex littoreusPoaceaeGrassAcetone2.5 mg/mL--Dermatophytes[27]
Polygonum molle D. Don.PolygonaceaeWhole PlantEthanol25–50 μg/mL Methicillin-resistant S. aureus--[32]
Eichhornia crassipes L.PontederiaceaeLeaves, Shoot Ethanol500–4000 μg/mLM. luteusR. rubrumM. ruber, A. fumigates[56]
Chloroform 32.4–55.8 μg/mL
Aqueous2.5–15 μg/mL
Punica granatum L.PunicaceaeFruit ShellEthanol70 mg/mLMethicillin-resistant S. aureus--[28]
Clematis brachiate Thunb.RanunculaceaeFlower, Leaves, Stem, RootAqueous, 1 mg/mLS. mutans, S. sanguis, L. acidophilus L. caseiP. gingivalis F. nucleatumC. albicans C. glabrata
C. krusei
[23]
Dichloromethane/Methanol750–12,000 μg/mL
Ziziphus mucronata Willd.RhamnaceaeBark, LeabesAqueous2.5 mg/mLS. aureus, methicillin- resistant S. aureus, gentamycin– methicillin-resistant S. aureus, S. epidermidis, B. agri, P. acnes, S. mutans, S. sanguis, L. acidophilus L. caseiP. aeruginosa, P. gingivalis F. nucleatumT. mentagrophytes, M. canis, C. albicans C. glabrata C. krusei[21]
Dichloromethane/Methanol750–12,000 μg/mL
Eriobotrya japonica (Thunb.) Lindl.RosaceaeLeaves Ethanol 2–16 μg/mLK. kristinae, M. luteus, S. auricularis, B. megateriumA. bohemicus, E. coli-[51]
Pavetta crassipes K. Schum.RubiaceaeLeafMethanol12.5–50 mg/mL methicillin-resistant S. aureus--[28]
Uncaria gambir (Hunter) Roxb.RubiaceaeLeaf, StemEthanol8–32 mg/mLmethicillin-resistant S. aureus--[28]
Vangueria spinose L.RubiaceaeLeavesEthyl Acetate500 μg/mLS. aureusE. coli, K. pneumoniae, P. aeruginosa-[57]
Pentanisia prunelloides Walp. RubiaceaeRoot BarkAqueous 5 mg/mL S. aureus, methicillin- resistant S. aureus, gentamycin– methicillin-resistant S. aureus, S. epidermidis, B. agri, P. acnesP. aeruginosaT. mentagrophytes, M. canis[21]
Dichloromethane/Methanol750–12,000 μg/mL
Rothmannia capensis Thunb.RubiaceaeLeaves Aqueous22.4–52.3 μg/mLS. aureus, methicillin- resistant S. aureus, gentamycin– methicillin-resistant S. aureus, S. epidermidis, B. agri, P. acnesP. aeruginosaT. mentagrophytes, M. canis[21]
Dichloromethane/Methanol750–12,000 μg/mL
Geophila repens L.RubiaceaeLeaves, Stem BarkAqueous1 mg/mLB. cereus, S. aureus--[41]
Dichloromethane/methanol250 μg/mL
Guettarda speciose L.RubiaceaeLeavesAqueous 2 mg/mL B. cereus, S. aureus--[41]
Dichloromethane/Methanol 2 mg/mL
Haldina cordifolia L.RubiaceaeLeavesAqueous1 mg/mLB. cereus, S. aureus--[41]
Dichloromethane/Methanol500 μg/mL
Hedyotis auricularia L.RubiaceaeLeavesAqueous300 μg/mLB. cereus, S. aureus--[41]
Dichloromethane/Methanol250 μg/mL
Knoxia zeylanica L.RubiaceaeLeaves, StemAqueous250 μg/mLB. cereus, S. aureus--[41]
Dichloromethane/Methanol1 mg/mL
Mitragyna parvifolia L.RubiaceaeLeavesAqueous300 μg/mLB. cereus, S. aureus--[41]
Dichloromethane/Methanol 1 mg/mL
Morinda umbellate L.RubiaceaeLeaves, Stem BarkAqueous100 μg/mLB. cereus, S. aureus--[41]
Dichloromethane/Methanol250 μg/mL
Nauclea orientalis L.RubiaceaeLeavesAqueous500 μg/mL B. cereus, S. aureus--[41]
Dichloromethane/Methanol500 μg/mL
Oldenlandia biflora L.RubiaceaeLeaves Aqueous2 mg/mL B. cereus, S. aureus--[41]
Dichloromethane/Methanol5 mg/mL
Oldenlandia herbacea L.RubiaceaeStem, Root Aqueous5mg/mLB. cereus, S. aureus--[41]
Dichloromethane/Methanol 60 μg/mL
Ophiorrhiza mungos L.RubiaceaeLeavesAqueous2 mg/mLB. cereus, S. aureus--[41]
Dichloromethane/Methanol 500 μg/mL
Paederia foetida L.RubiaceaeLeaves, StemAqueous300 μg/mLB. cereus, S. aureus--[41]
Dichloromethane/Methanol 60 μg/mL
Pavetta lanceolate Eckl.RubiaceaeLeavesAqueous 1 mg/mL B. cereus, S. aureus--[41]
Dichloromethane/Methanol 250 μg/mL
Spermacoce hispida L.RubiaceaeLeaves, StemAqueous300 μg/mL B. cereus, S. aureus--[41]
Dichloromethane/Methanol 120 μg/mL
Wendlandia bicuspidate Wight & Arn.RubiaceaeLeavesAqueous60 μg/mL B. cereus, S. aureus--[41]
Dichloromethane/Methanol 5 mg/mL
Chassalia kollyRubiaceaeWhole PlantMthanol5 mg/mL S. aureusE. coli, P. aeruginosa, S. typhi, P. aeruginosa-[16]
Randia dumetorum L.RubiaceaeFruitsMethanol 9.375, 18.75, 37.5, 75, 150, 300, 600 μg/mL S. aureus, S. epidermidis, B. subtilisE. coli, S. typhi-[23]
Mitragyna speciosa L.RubiaceaeLeaves Methanol 37.5, 75, 150, 300, 600 μg/mL S. typhi [42]
Clausena anisate (Willd) Hook. f. ex.RutaceaeLeaves, Stem, TwigsAqueous12.5–50 mg/mL S. mutans, S. sanguis, L. acidophilus L. caseiP. gingivalis F. nucleatumC. albicans C. glabrata C. krusei[23]
Dichloromethane/Methanol750–12,000 μg/mL
Zanthoxylum capense Harv.RutaceaeStem Aqueous8–32 mg/mL S. mutans, S. sanguis, L. acidophilus L. caseiP. gingivalis F. nucleatumC. albicans C. glabrata C. krusei[23]
Dichloromethane/Methanol750–12,000 μg/mL
Aegle marmelos L.RutaceaeLeaves and FruitsMethanol 500 μg/mlS.aureus, B. cereusE. coli, S. typhi, P. aeruginosa, S. boydii, K. aerogenes, P.vulgaris, [20]
Evodia daneillii (Benn) Hemsl.RutaceaeTender Branches & LeavesEthanol3.33–33.3 mg/mLMethicillin-resistant S. aureus--[32]
Skimmia arborescens Anders.RutaceaeTBLEthanol250 mg/mLMethicillin-resistant S. aureus--[32]
Salvadora australisSalvadoraceaeLeavesAcetone10–100 mg/mL B. cereus, B. pumilus, B. subtilis, S. aureus, E. faecalis--[18]
Viscum capense L.f.SantalaceaeLeavesAqueous 5–50 mg/mL S. aureus, methicillin- resistant S. aureus, gentamycin– methicillin-resistant S. aureus, S. epidermidis, B. agri, P. acnesP. aeruginosaT. mentagrophytes, M. canis[21]
Dichloromethane/Methanol 750–12,000 μg/mL
Dodonaea angustifolia (L.f.) BenthSapindaceaeLeavesEthanol156–625 μg/mLmethicillin-resistant S. aureus--[28]
Dodonaea viscosa Jacq. SapindaceaeLeaves, StemAqueous 350–600 μg/mLS. mutans, S. sanguis, L. acidophilus L. caseiP. gingivalis F. nucleatumC. albicans C. glabrata
C. krusei
[23]
Dichloromethane/Methanol 750–12,000 μg/mL
Cardiospermum halicacabum L.SapindaceaeLeaves n-Butanol500 μg/mL S. aureus, S. agalactiaeE. coli, S. typhimurium and K. pneumoniaeT. rubrum, C. albicans[58]
Ethyl acetate 60 μg/mL
Chloroform40 μg/mL
Dodonaea angustifolia L. f.SapindaceaeLeaves Aqueous 800 mg/disc S. aureus, methicillin- resistant S. aureus, gentamycin– methicillin-resistant S. aureus, S. epidermidis, B. agri, P. acnesP. aeruginosaT. mentagrophytes, M. canis[21]
Dichloromethane/Methanol 750–12,000 μg/mL
Englerophytum magalismontanum Sonder.SapotaceaeLeaves, StemAqueous 600, 1200 μg/mL S. mutans, S. sanguis, L. acidophilus L. caseiP. gingivalis F. nucleatumC. albicans C. glabrataC. krusei[23]
Dichloromethane/Methanol 750–12,000 μg/mL
Schisandra viridis A.c. Smith.SchisandraceaeVaneEthanol5 mg/mLMethicillin-resistant S. aureus--[32]
Halleria lucida L.ScrophulariaceaeLeaves Stem Aqueous 1–8 mg/mLS. aureus, methicillin- resistant S. aureus, gentamycin– methicillin-resistant S. aureus, S. epidermidis, B. agri, P. acnesP. aeruginosaT. mentagrophytes, M. canis[21]
Dichloromethane/Methanol 750–12,000 μg/mL
Brandisia hancei Hook.f.ScrophulariaceaeWhole PlantEthanol3.33–33.3 mg/mLMethicillin-resistant S. aureus--[32]
Selaginella tamariscina (Seauv.) Spring.SelaginellaceaeWhole PlantEthanol250 mg/mLMethicillin-resistant S. aureus--[32]
Datura stramonium L. SolanaceaeLeaves, Stem, FruitAqueous 10–100 mg/mL S. mutans, S. sanguis, L. acidophilus L. caseiP. gingivalis F. nucleatumC. albicans C. glabrata
C. krusei
[23]
Dichloromethane/Methanol 750–12,000 μg/mL
Solanum incanum LSolanaceaeLeaves Aqueous5–50 mg/mL S. aureus, methicillin- resistant S. aureus, gentamycin– methicillin-resistant S. aureus, S. epidermidis, B. agri, P. acnesP. aeruginosaT. mentagrophytes, M. canis[21]
Dichloromethane/Methanol 750–12,000 μg/mL
Solanum trilobatum L.SolanaceaeLeaves Acetone156–625 μg/mLS. pyogens, S. aureus, B. subtilisS. typhi, P. vulgaris, K. pneumoniae, P. aeruginosa, E. coli-[37]
Aqueous 250 mg/mL
Benzene 10–100 mg/mL
Butanol 5–50 mg/mL
Chloroform 60 μg/mL
Ethanol 5 mg/mL
Datura metel L.SolanaceaeLeavesAqueous350–600 μg/mLB. cereus, S. aureus--[41]
Dichloromethane/Methanol 1 mg/mL
Solanum macrocarpon L.SolanaceaeLeaves, StemAqueous500 μg/mLB. cereus, S. aureus--[41]
Dichloromethane/Methanol60 μg/mL
Solanum melongena L.SolanaceaeLeaves, Root StemAqueous800 mg/disc B. cereus, S. aureus--[41]
Dichloromethane/Methanol100 μg/mL
Solanum nigrum L.SolanaceaeLeaves, StemAqueous600, 1200 μg/mL B. cereus, S. aureus--[41]
Dichloromethane/Methanol1 mg/mL
Solanum torvum Sw.SolanaceaeLeaves Aqueous 3.33–33.3 mg/mL B. cereus, S. aureus--[41]
Dichloromethane/Methanol 60 μg/mL
Solanum virginianum L.SolanaceaeLeaves, Stem, RootAqueous 250 mg/mLB. cereus, S. aureus--[41]
Dichloromethane/Methanol 4 mg/mL
Withania somnifera (L.) DunalSolanaceaeRoots & LeavesAqueous 10–100 mg/mL B. cereus, S. aureus, methicillin-resistant S. aureus--[41,59]
Dichloromethane/Methanol 1 mg/mL
Cola acuminate L.SterculiaceaeStem Acetone5–50 mg/mL S. aureus-C. albicans[16]
Methanol 100 μg/mL
Schima sinensis (Hemsl. et. Wils) Airy-shaw.TheaceaeTblEthanol156–625 μg/mLmethicillin-resistant S. aureus--[32]
Coriandrum sativumUmbelliferaeSeeds Aqueous 350–600 μg/mLS. aureusK. pneumoniae, P. aeruginosa,A. niger, P. lilacinum[27]
Clerodendrum inerme LVerbenaceaeLeaves Methanol 500 μg/mLS. aureus-A. niger[60]
Lantana rugosa Thunb.VerbenaceaeLeavesAqueous 800 mg/disc S. aureus, methicillin- resistant S. aureus, gentamycin– methicillin-resistant S. aureus, S. epidermidis, B. agri, P. acnesP. aeruginosaT. mentagrophytes, M. canis[21]
Dichloromethane/Methanol750–12,000 μg/mL
Lantana camara L.VerbenaceaeLeaves, FlowerChloroform600, 1200 μg/mL S. aureus, B. cereusE. coli, S. typhi, P. aeruginosa, K. aerogenes, P. vulgaris, S. Boydii, K. pneumoniae, V. choleraeA. fumigatus, A. flavus, A. niger, C. albicans[39]
Acetone 5 mg/mL
Methanol 1–8 mg/mL
Aqueous 1–2 mg/mL
Lantana indica L.VerbenaceaeLeaves Methanol 3.33–33.3 mg/mL B. subtilis, S. aureus, S. pyogenes,E. coli, P. vulgaris, K. pneumoniaeC.albicans,[61]
Aqueous 4 mg/mL
Cyphostemma lanigerum Harv.VitaceaeLeaves, StemAqueous 250 mg/mLS. mutans, S. sanguis, L. acidophilus L. caseiP. gingivalis F. nucleatumC. albicans C. glabrata
C. krusei
[23]
Dichloromethane/Methanol750–12,000 μg/mL
Cyphostemma setosum
Roxb.
VitaceaeLeaves, Stem, FruitAqueous 10–100 mg/mL S. mutans, S. sanguis, L. acidophilus L. caseiP. gingivalis F. nucleatumC. albicans C. glabrata C. krusei[23]
Dichloromethane/Methanol 750–12,000 μg/mL
Aloe arborescens Mill.XanthorrhoeaceaeLeaves Aqueous 5–50 mg/mL S. aureus, methicillin- resistant S. aureus, gentamycin– methicillin-resistant S. aureus, S. epidermidis, B. agri, P. acnesP. aeruginosaT. mentagrophytes, M. canis[21]
Dichloromethane/Methanol750–12,000 μg/mL
Siphonochilus aethiopicus Schweinf.,ZingiberaceaeLeaves, Stem, RootAqueous 156–625 μg/mLS. mutans, S. sanguis, L. acidophilus L. caseiP. gingivalis F. nucleatumC. albicans C. glabrata C. krusei[23]
Dichloromethane/Methanol 750–12,000 μg/mL
Curcuma xanthorrhizaZingiberaceaeRhizomeEthanol350–600 μg/mLmethicillin-resistant S. aureus--[46]
Kaempferia pandurata Roxb.ZingiberaceaeRhizomeEthanol500 μg/mLmethicillin-resistant S. aureus--[46]
Peganum harmala L.ZygophyllaceaeSeeds Ethanol 800 mg/disc S. aureusE. coli-[21]
* MIC (minimum inhibitory concentration) is the lowest drug concentration at which a given antimicrobial extract inhibits the visible growth of a tested organism. MIC absolute value: the given absolute value of drug concentration inhibits the growth of all tested organisms/ MIC ranges: the given range of drug concentrations (minimum to maximum) inhibit the growth of the individual to all tested organisms.
Table 2. Antimicrobial activities of bioactive compounds.
Table 2. Antimicrobial activities of bioactive compounds.
Botanical NameFamilyExtractsBioactive CompoundsMIC *Organism InhibitedReferences
Allium sativum L.AlliaceaeMethanolCyanidin-3-(6’-malonyl)-glucoside, vanillic acid caffeic acid, p-coumaric acid, ferulic acid, sinapic acid, L-alliin, alliin isomer and methiin-B. cereus, L. monocytogenes S. aureus, P. aeruginosa, E. coli[11]
Searsia chirindensis (Baker f.) MoffettAnacardiaceaeEthanolMethyl gallate30–130 μg/mL C. jejuni, E. coli, S. flexneri, S. aureus[86]
myricetin-3-O-arabinopyranoside 60–250 μg/mL
myricetrin-3-O-rhamnoside60–250 μg/mL
kaempferol-3-O-rhamnoside 130–250 μg/mL
quercetin-3-O-arabinofuranoside250 μg/mL
Dichloromethane/Methanol 250–6250 μg/mL
n-butanol 130–3125 μg/mL
Ethyl Acetate 60–780 μg/mL
Crude 60–780 μg/mL
Xylopia aethiopica (Dunal) A. Rich.AnnonaceaeAqueous 1R-a-Pinene, β-Pinene, 2-Carene, Cyclohexene,5-methyl-3-(1-methylethenyl)-trans-(-)- Bicyclo [3.1.0] hexane,6-isopropylidene-1-methyl-, Eucalyptol, Ethyl 2-(5-methyl-5-vinyltetrahydrofuran-2-yl) propan-2-yl carbonate, Isogeraniol, ɑ-Campholenal, L-trans-Pinocarveol, Pinocarvone, Myrtenal, (-)-Spathulenol1–256 μg/mLS. aureus, B. licheniformis, E. coli, K. pneumoniae[87]
Polyalthia cerasoidesAnnonaceaeHexaneN-(4-hydroxy-β-phenethyl-4-hydroxy cinnamide64–128 μg/mLC. diphtheria, B. subtilis, B. cereus, M. lutens[88]
Dichloromethane32–256 μg/mL
Unonopsis lindmanii R. E. FriesAnonaceaeHexane Gallic acid, kaempferol, ellagic acid, epicatechin, vitexin, corilagin25–250 μg/mLC.albicans[89]
Allagoptera leucocalyx (Drude) Kuntze,ArecaceaeHexaneGallic acid, kaempferol, ellagic acid, epicatechin, vitexin, corilagin162.2–665 mg/mL C.albicans[89]
Bactris glaucescens DrudeArecaceaeHexaneGallic acid, kaempferol, ellagic acid, epicatechin, vitexin, corilagin200–755 mg/mLC.albicans[89]
Scheelea phalerata MartArecaceaeHexaneGallic acid, kaempferol, ellagic acid, epicatechin, vitexin, corilagin129 mg/mL C.albicans[89]
Artemisia herba-alba AssoAsteraceaeAqueous 1,8-cineole, β-thujone, α-thujone, camphor640–2500 μg/mL T. rubrum and E. floccosum[90]
Vernonia adoensis Sch. Bip. ex Walp.AsteraceaeAcetone Chondrillasterol50 μg/mLS. aureus, K. pneumonia, P. aeruginosa[1]
Matricaria chamomillaAsteraceaeEthanol Phenolic acid1.56–3.12 mg/mLS. typhimurium[19]
Solidago graminifolia L. Salisb.AsteraceaeEthanol di-C-glycosylflavones (schaftoside, isoschaftoside), caftaric acid, gentisic acid, chlorogenic acid, p-coumaric acid, ferulic acid, hyperoside, rutin, quercitrin, quercetin, Luteolin, kaempferol, gallic acid, protocatechuic acid, vanillic acid, syringic acid, rosmarinic acid40–3120 μg/mLS. aureus, C. albicans, C. parapsilosis.[12]
Methanol 90–3120 μg/mL
Aqueous 190–6250 μg/mL
Baccharis trimeraAsteraceaeCrude Polyphenols, flavonoids, alkaloids, and terpenes7.8–500 μg/mLE. coli, S. aureus, P. aeruginosa, C. albicans, C. tropicalis, C. parapsilosis, Epicoccum sp., C. sphaerospermum, C. neoformans, P. brasiliensis, C. gatti, Pestalotiopsis sp., C. lunatus, Nigrospora sp.[88]
Tecoma stansBignoniaceaeAqueous Phenolic compounds50–600 μg/mLS. aureus[91]
Bixa orellana L.BixaceaeAqueousBixin, catechin, chlorogenic acid, chrysin, butein, hypolaetin, licochalcone A, and xanthohumol.16–32 μg/mL B. cereus, S. aureus[9]
Trichodesma indicumBoraginaceaeEthanol Lanast-5-en-3β-D- glucopyranosyl-21(24)-oilde 2.4–19.2 μg/mL S. aureus[92]
Boswellia dalzielii Hutch.BurseraceaeCrude Oleic acid, squalene and n-hexadecanoic acid-S. pyogenes, S. aureus, E. coli, E. faecalis, K. pneumonia, P. aeruginosa, P. mirabilis, S. typhi, and C. albicans[93]
Caesalpinia coriaria (Jacq) WilldCaesalpiniaceaeAqueousMethyl gallate and gallic acid1.56–25 mg/mLS. typhi, E. coli, P. aeruginosa, L. monocytogenes, S. aureus.[94]
Ethanol 390–6250 μg/mL
Senna aculeate (Bth.) Irw et BarnCeasalpinioideaeHexane Gallic acid, kaempferol, ellagic acid, epicatechin, vitexin, corilagin25, 50, 100 mg/mLC.albicans[89]
Kochia scopariaChenopodiaceaeCrude Polyphenols, flavonoids, alkaloids, and terpenes3.125 mg/mLC. graminicola, T. deformans, A. flavus, H. carbonum, C. zeaemaydis, C. macrocarpum, P. innundatus, S. japonicas, E. ficariae, P. herbarum, M. verticillata, Rhisoclosmatium sp., S. pseudodichotomus, S. kneipii, R. solani, P. sojae.[8]
Buchenavia tomentosa (Mart) Eichler CombretaceaeHexane Gallic acid, Kaempferol, Ellagic acid, epicatechin, Vitexin, Corilagin10 mg/mLC.albicans[89]
Terminalia phanerophlebia Engl. & DielsCombretaceaeCrude Methyl gallate (methyl-3,4,5-trihydroxybenzoate) and a phenylpropanoid glucoside, 1,6-di-O-coumaroyl glucopyranoside125 μg/mLM. aurum, M. tuberculosis, S. aureus, K. pneumoniae[95]
Dichloromethane16–250 μg/mL
Hexane 31–250 μg/mL
Ethyl Acetate8–125 μg/mL
n-butanol31–250 μg/mL
Buchenavia tomentosa L.CombretaceaeCrude Gallic acid, quinic acid, kaempferol, (-) epicatechin, ellagic acid, buchenavianine, eschweilenol b, eschweilenol c, vitexin, corilagin, 1α,23β-dihydroxy-12-oleanen-29-oicacid-23β-o-α-l-4-acetylramnopiranoside and punicalin200–12500 μg/mLCandida albicans, Candida tropicalis, Candida parapsilosis, Candida glabrata, Candida krusei and Candida dubliniensis.[96]
Diadema setosum f. depressa Dollfus & Roman.DiadematidaeAcetone Polyunsaturated fatty acids (PUFAs) and β-carotene500–4000 μg/mLS. typhi, S. typhimurium, S. flexneri, P. aeruginosa, A. hydrophila, Acinetobacter sp, C. freundii and K. pneumonia, B. subtilis, S. epidermidis S. aureus[1]
Monotes kerstingii GilgDipterocarpaceaeCrude Stilbene-coumarin derivative, coumarin-carbinol and fatty glycoside1–8 mg/mLB. subtilis, Septoria tritici Desm[7]
Croton doctoris S MooreEuphorbiaceaeHexane Gallic acid, kaempferol, ellagic acid, epicatechin, vitexin, corilagin500 μg/mLC.albicans[89]
Jatropha weddelliana BaillonEuphorbiaceaeHexane Gallic acid, kaempferol, ellagic acid, epicatechin, vitexin, corilagin4–32 μg/mLC.albicans[89]
Cassia alataFabaceaeEthanol 4-butylamine, cannabinoid, dronabinol, methyl-6-hydroxy1.25, 1.5 mg/mLS. aureus, E. coli, P. aeruginosa, C. albicans[28]
Dalbergia scandens Roxb., Corom.FabaceaeEthanol Dalpanitin, vicenin-2 and 3, rutin780–6250 mg/mLB. cereus, S. aureus, E. coli, P. aeruginosa, C. albicans[41]
Acacia niloticaFabaceaeCrude Alkaloids 600–1200 μg/mLS. aureus[27]
Salvia sessei BenthLamiaceaeHexane Sessein, isosessein12.5–100 μg/mLS. haemolyticus, S. hominis, E. faecalis, S. epidermis, S. pyogenes, S.aureus[14]
Dichloromethane 100 μg/mL
Methanol 12.5–100 μg/mL
Mentha piperitaLamiaceaeMethanol 1,1-diphenyl-2-picrylhydazyl-hydrate1–4 mg/mLS. aureus, E. coli, C. albicans[97]
Ocimum basilicum L.LamiaceaeEthanol Gallic acid, 3,4-dihydroxy benzoic acid, 4-hydroxy benzoic acid, 2,5 dihydroxybenzoic acid, chlorogenic acid, vanillic acid, Epicatechin, caffeic acid, p-coumaric acid, ferulic acid, rutin, ellagic acid, naringin, quercetin, cinnamic acid, α-pinene, camphene, sabinene, β-pinene, myrcene, 3-octanol, α-terpinene, p-cymene, limonene, 1,8-cineole, (Z)-β-ocimene, (E)-β-ocimene, γ-terpinene, cis-sabinene hydrate, terpinolene, linalool, nonanal, pentylisovalerate, 1-octen-3-yl acetate, cis-p-menth-2-en-1-ol, 3-octyl acetate, α-campholenal, camphor, trans-verbenol, δ-terpineol, 4-terpineol, α-terpineol, cis-dihydrocarvone, trans-carveol, (Z)-3-hexenyl isovalerate, pulegone, neral, carvone, linalyl acetate, bornyl acetate, dihydroedulan IA, isodihydrocarvyl acetate, α-terpinyl acetate, cis-carvyl acetate, neryl acetate, geranyl acetate, β-elemene, (Z)-jasmone, β-caryophyllene, β-copaene, aromadendrene, α-humulene, (E)-β-farnesene, cis-muurola-4(14), 5-diene germacrene D, bicyclogermacrene, germacrene A, δ-cadinene, (E)-α-bisabolene, (E)-nerolidol, Spathulenol, caryophyllene oxide, viridiflorol, 1, 10-di-epi-cubenol, T-cadinol, T-muurolol, monoterpene hydrocarbons, oxygenated monoterpenes, sesquiterpene hydrocarbons, oxygenated sesquiterpenes, apocarotenes
non-terpene derivatives
16–256 μg/mLS. epidermidis S. aureus, B. subtilis, E. coli, P. aeruginosa, K. pneumoniae, C. glabrata, C. albicans[98]
Thymus algeriensis Boiss. & ReutLamiaceaeEthanol Gallic acid, 3,4-dihydroxy benzoic acid, 4-hydroxy benzoic acid, 2,5 dihydroxybenzoic acid, chlorogenic acid, vanillic acid, epicatechin, caffeic acid, p-coumaric acid, ferulic acid, rutin, ellagic acid, naringin, quercetin, cinnamic acid, α-pinene, camphene, sabinene, β-pinene, myrcene, 3-octanol, α-terpinene, p-cymene, limonene, 1,8-cineole, (Z)-β-ocimene, (E)-β-ocimene, γ-terpinene, cis-sabinene hydrate, terpinolene, linalool, nonanal, pentylisovalerate, 1-octen-3-yl acetate, cis-p-menth-2-en-1-ol, 3-octyl acetate, α-campholenal, camphor, trans-verbenol, δ-terpineol, 4-terpineol, α-terpineol, cis-dihydrocarvone, trans-carveol, (Z)-3-hexenyl isovalerate, pulegone, neral, carvone, linalyl acetate, bornyl acetate, dihydroedulan IA, isodihydrocarvyl acetate, α-terpinyl acetate, cis-carvyl acetate, neryl acetate, geranyl acetate, β-elemene, (Z)-jasmone, β-caryophyllene, β-copaene, aromadendrene, α-humulene, (E)-β-farnesene, cis-muurola-4(14), 5-diene germacrene D, bicyclogermacrene, germacrene A, δ-cadinene, (E)-α-bisabolene, (E)-nerolidol, spathulenol, caryophyllene oxide, viridiflorol, 1, 10-di-epi-cubenol, T-cadinol, T-muurolol, monoterpene hydrocarbons, oxygenated monoterpenes, sesquiterpene hydrocarbons, oxygenated sesquiterpenes, apocarotenes
non-terpene derivatives
32–512 μg/mLS. epidermidis S. aureus, B. subtilis, E. coli, P. aeruginosa, K. pneumoniae, C. glabrata, C. albicans[98]
Cinnamomun inermeLauraceaeEthyl Acetate5-(1,5-dimethyl-2-4-hexenyl)- methyl phenol) 100–800 μg/mLS. aureus, E. coli[99]
Hexane 8000 μg/mL
Acetone 8000 μg/mL
n-butanol 100–800 μg/mL
Allium sativamLiliaceaeCrude Allicin49 μg/mLC. albicans[100]
Strychnos nigritana Baker LoganiaceaeCrude Nigritanine, Speciociliatine, Mytragine Paynantheine Rhyncophylline128–256 μg/mLS. aureus[10]
Mascagnia benthamiana (Gries) WR AndersonMalpighiaceaeHexane Gallic acid, kaempferol, ellagic acid, epicatechin, vitexin, corilagin17.84 mg/mLC.albicans[89]
Mouriri elliptica MartMemecylaceaeHexane Gallic acid, kaempferol, ellagic acid, epicatechin, vitexin, corilagin100 μg/mLC.albicans[89]
Artocarpus communisMoraceaeCrude Atonin E, 2-(3,5-dihydroxy)-(Z)-4-(3 methyl but-1-etnyl 4–512 μg/mLP. aeruginosa, S.typhi, S.aureus, K.pneumoniae[101]
Myrtus nivellei Batt. & Trab.MyrtaceaeCrude 1,8-cineole, limonene, isoamylcyclopentane, di-nor-sesquiterpenoids5 mg/mLC. neoformans[102]
Myrtus communis LMyrtaceaeCrude α-pinene, 1,8-cineole, linalool, and linalyl acetate156–625 μg/mLE. floccosum, M. canis, T. rubrum[102]
Piper nigrumPiperaceaeAqueous Piperine500–1000 μg/mLE. coli, M. luteus[91]
Citrus aurantium L.RutaceaeEthanol Polyphenols, flavonoids, alkaloids, and terpenes1562–6250 μg/mLAmoxycillin resistant B. cereus[13]
Salix babylonica L.SalicaceaeHydroalcoholic Luteolin, luteolin 7-O-glucoside 1.56–100 mg/mLE. coli, S. aureus and L. monocytogenes[103]
Verbascum glabratum subsp. bosnense (K. Malý) MurbScrophulariaceaeEthanol quercitrin and rosmarinic acid, 4-hydroxybenzoic acid, salicylic acid, morin, and apigenin600, 1200 μg/mLE. coli, S. aureus, Candida albicans[17]
Simaba ferruginea A. St.-HilSimaroubaceaeMethanol Canthin-6-one, indole β-carboxylic12.5–200 μg/mLS. flexneri, S. aureus and S. aureus[91]
Camellia sinensisTheaceaeAqueous Catechin7.81–31.25 μg/mL S. mutans[104]
Talaromyces sp.TrichocomaceaeAqueousTalaropeptide A and B5 mg/mLB. subtilis[18]
Hybanthus enneasperm
us
ViolaceaeCrude Flavonoids, Tannins37.5, 75, 150, 300, 600 μg/mLP. vulgaris, V. cholera[100]
* MIC (minimum inhibitory concentration) is the lowest drug concentration at which a given antimicrobial extract inhibits the visible growth of a tested organism. MIC absolute value: the given absolute value of drug concentration inhibits the growth of all tested organisms/MIC ranges: the given range of drug concentrations (minimum to maximum) inhibit the growth of the individual to all tested organisms.

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Mickymaray, S. Efficacy and Mechanism of Traditional Medicinal Plants and Bioactive Compounds against Clinically Important Pathogens. Antibiotics 2019, 8, 257. https://0-doi-org.brum.beds.ac.uk/10.3390/antibiotics8040257

AMA Style

Mickymaray S. Efficacy and Mechanism of Traditional Medicinal Plants and Bioactive Compounds against Clinically Important Pathogens. Antibiotics. 2019; 8(4):257. https://0-doi-org.brum.beds.ac.uk/10.3390/antibiotics8040257

Chicago/Turabian Style

Mickymaray, Suresh. 2019. "Efficacy and Mechanism of Traditional Medicinal Plants and Bioactive Compounds against Clinically Important Pathogens" Antibiotics 8, no. 4: 257. https://0-doi-org.brum.beds.ac.uk/10.3390/antibiotics8040257

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