Figures
Abstract
Background
Shigellosis continues to be a public health challenge for developing countries, including Bangladesh. The aim of the study is to demonstrate recent changes in Shigella sero-groups and their geographical diversity.
Methods
Data were extracted from data archive of four diarrheal disease surveillance systems. A 2% sub sample from urban Dhaka Hospital (2008–2011; n = 10,650), and 10% from urban Mirpur Treatment Centre (2009–2011; n = 3,585), were enrolled systematically; whereas, all patients coming from the Health and Demographic Surveillance System area in rural Matlab (2008–2011; n = 6,399) and rural Mirzapur (2010–2011; n = 2,812) were included irrespective of age, sex, and disease severity. A fresh stool specimen was collected for identification of Shigella spp. Of them, 315 (3%) were positive for Shigella in Dhaka, 490 (8%) from Matlab, 109 (3%) from Mirpur and 369 (13%) from Mirzapur and considered as analyzable sample size.
Results
Among all Shigella isolates regardless of age, significant decreases in percentage of S. flexneri over time was observed in Mirpur (55→29%; p value of χ2-for trend = 0.019) and Mirzapur (59→47%; p = 0.025). A non-significant decrease was also seen in Dhaka (58→48%), while in Matlab there was a non-significant increase (73→81%). Similar patterns were observed among under-5 children at all sites. Emergence of S. sonnei was found in Dhaka (8→25%; p<0.001) and Mirpur (10→33%; p = 0.015), whereas it decreased in Mirzapur (32→23%; p = 0.056). The emergence of S. boydii was seen in all ages in Mirzapur [(3→28%; p<0.001); (3→27%; p<0.001)]. On the other hand, we saw non-significant percent reductions in S. boydii in Dhaka [overall (25→16%); under-5 (16→9%)]. Decreasing rates of Shigella dysenteriae were observed in Matlab, Mirpur and Mirzapur; whereas, in Dhaka it remained unchanged.
Citation: Das SK, Ahmed S, Ferdous F, Farzana FD, Chisti MJ, Leung DT, et al. (2013) Changing Emergence of Shigella Sero-Groups in Bangladesh: Observation from Four Different Diarrheal Disease Hospitals. PLoS ONE 8(4): e62029. https://doi.org/10.1371/journal.pone.0062029
Editor: Dongsheng Zhou, Beijing Institute of Microbiology and Epidemiology, China
Received: December 12, 2012; Accepted: March 16, 2013; Published: April 29, 2013
Copyright: © 2013 Das et al. This is an open-access article distributed under the terms of the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are credited.
Funding: The research protocol was funded by Swedish International Development Cooperation Agency (Sida), grant number MD-0020 and GR-00599. icddr,b acknowledges with gratitude the commitment of Sida to its research efforts. Hospital surveillance was funded by icddr,b and the Government of the People’s Republic of Bangladesh through IHP-HNPRP. icddr,b acknowledges with gratitude the commitment of the Government of the People’s Republic of Bangladesh to the Centre’s research efforts. icddr,b also gratefully acknowledges the following donors who provide unrestricted support to the Centre’s research efforts: Australian Agency for International Development (AusAID), Government of the People’s Republic of Bangladesh, Canadian International Development Agency (CIDA), Embassy of the Kingdom of the Netherlands (EKN), Swedish International Development Cooperation Agency (Sida), Swiss Agency for Development and Cooperation (SDC), and Department for International Development, UK (DFID). The funders had no role in study design, data collection and analysis, decision to publish, or preparation of the manuscript.
Competing interests: The authors have declared that no competing interests exist.
Introduction
Shigellosis, a food-borne illness caused by the genus Shigella, is usually transmitted through person-to-person contact [1]. It is one of the most common causes of childhood dysentery and an important infectious cause of morbidity and mortality in children under 5 years of age. Annually, approximately 90 million cases occur with at least 100,000 deaths, mostly (60%) among children under five years of age in developing countries [2]. S. flexneri, S. sonnei, S. boydii and S. dysenteriae, the four species or sero-groups, based on biochemical properties and group-specific O antigens in the outer membrane of the cell wall, are responsible for the disease [3]. The disease is characterized by a short period of watery diarrhea with intestinal cramps and general malaise, soon followed by emission of bloody, mucoid, often mucopurulent stools [2]. A population-based prospective multi-country study in Asia aiming to get a better understanding of the current disease burden, clinical manifestations, and microbiology of shigellosis revealed that Shigella appears to be more universal in Asian impoverished populations than previously estimated and antibiotic-resistant strains of different species and serotypes have emerged [4].
Like other Shigella prevalent countries, Bangladesh is considered an endemic zone of shigellosis. A recent study of isolation patterns of different sero-groups of Shigella in a large diarrheal disease hospital in Dhaka showed a decreased proportion of shigellosis from 8–12% in the 1980s to 3% in 2008 [5]. This study also documented the interquartile range of isolation rate of the sero-groups over the period as S. flexneri 46–63%, S. dysenteriae 0–25%, S. boydii 10–21% and Shigella sonnei 4–9% [5]. However, there is a paucity of data on the rate of change of specific sero-groups. Furthermore, data is lacking regarding the isolation of Shigella in rural versus urban settings. Knowledge on the changing patterns of isolation of Shigella sero-groups and their geographical diversity have potential public health implications [6]. Thus, our aim was to demonstrate the changing pattern of Shigella sero-groups and their geographical diversity in four different diarrheal disease treatment facilities in Bangladesh.
Materials and Methods
Study sites
Dhaka Hospital – Dhaka.
The Dhaka Hospital of International Centre for Diarrheal Disease Research, Bangladesh (icddr,b) offers free treatment to at least 140,000 people a year. A diarrheal disease surveillance system (DDSS) was established in 1979. The urban DDSS currently collects information on the clinical, epidemiological and demographic characteristics, feeding practices (particularly of infants and young children), and use of drug and fluid therapy at home of every 50th patient, irrespective of age, sex, disease severity or socioeconomic status by administering structured questionnaire. The generated data provides valuable information to hospital clinicians in their decision-making processes and enables the detection of emerging pathogens and early identification of outbreaks and their locations as well as antimicrobial susceptibility pattern (Figure 1).
Matlab Hospital-Matlab.
ICDDR,B maintains one of the richest, most comprehensive and longest running, longitudinal data resources in the developing world, producing regular accurate demographic and health data for rural Matlab, Bangladesh. With over 40 years of continuous demographic information on a population of over 200,000 people, Matlab is our major rural field site, and a major public health resource for the world. The site is a model for public health strategies around the world. The Health and Demographic Surveillance System at Matlab covers a population of about 225,000, providing data necessary to plan, conduct, and evaluate various types of public-health intervention research. Since 1963, icddr,b has been maintaining a treatment facility in rural Matlab (located about 55 km from Dhaka) for treating diarrhea patients. It provides free treatment to 12,000–15,000 diarrhea patients annually reporting from Health and Demographic Surveillance System area and other adjoining sub-districts (Figure 1).
Mirpur treatment Centre-Mirpur.
The Mirpur area is in the north-west of the Dhaka, the capital city. This 60-bed urban hospital at Mirpur began it’s operations in April, 2009. More than 12,000 patients annually receive care in this facility. Every 10th patient presenting to the facility is included into the surveillance system (Figure 1).
Kumudini Hospital – Mirzapur.
Mirzapur sub-district covers 374 km2 in Tangail district (Figure 1), and is located about 60 km north-west of Dhaka. It has a total of 58,300 households and a population of 238,463, according to a 2007 census. Almost all households have access to a tube well as a source of drinking water; around half have hygienic sanitary toilets, and 60% have electricity. Agriculture is the main occupation for men, while women work mainly in the home. Kumudini Hospital is located in the middle of the Demographic Surveillance System (DSS) area, is a philanthropic institution established in 1938 in Mirzapur (under Tangail District) providing health services to the surrounding poor rural population. Since 1982, a separate diarrhea treatment unit was started that serves nearly 1,500 diarrhea patients each year for treatment (Figure 1).
Sample Framing
A 2% sub sample from Dhaka Hospital and 10% from Mirpur Treatment Centre were enrolled systematically; whereas, all patients coming from the Health and Demographic Surveillance System area in Matlab and Mirzapur were included irrespective of age, sex, and disease severity. We extracted data from the data archive of the different diarrheal disease surveillance system as follows: Dhaka Hospital (2008–2011; n = 10,650), Matlab (2008–2011; n = 6,399), Mirpur (2009–2011; n = 3,585), and Mirzapur (2010–2011; n = 2,812) (Table 1).
Specimen Collection and Laboratory Procedure
A single fresh whole stool specimen (at least 3 ml/grams) were collected. Maintaining cool temperature (+4 to +8 degree Celsius), all specimens from Dhaka, Mirpur and Mirzapur were submitted to the central laboratory in Dhaka within 6 hours of collection in Carry - Blair media. Stool samples from Matlab were processed in the Matlab Microbiology Laboratory. Shigella spp. [7] were isolated using standard methods.
Data Management and Analysis
Statistical Package for Social Sciences (SPSS) Windows (Version 15.2; Chicago, IL) was used for data entry and subsequent analysis. Descriptive analysis was employed and categorical variables were expressed in proportion. Chi-square for trend was performed to determine the changing trend of Shigella sero-groups over the study period provided that the observation period was of three or more years. However, for less than three years (Mirzapur) Chi-square test was equated to determine any statistical difference with a probability value of <0.05.
Ethical Statement
The Diarrhoeal Disease Surveillance System (DDSS) of icddr,b is a routine ongoing activity of the Dhaka Hospital, Matlab Hospital and Mirpur Treatment Centre which has been approved by the Research Review Committee (RRC) and Ethical Review Committee (ERC) of icddr,b. At the time of enrollment, verbal consent was taken from the caregivers or guardians on behalf of the patients. The information was stored in the hospital database and used for conducting researches. The DDSS of icddr,b is a scheduled activity on the hospital patients, and used to be performed after taking verbal consent from the parents or guardians of the patients following the hospital policy. Parents or guardians were assured about the non-disclosure of information collected from them, and were also informed about the use of data for analysis and using the results for improving patient care activities as well as publication without disclosing the name or identity of their children. ERC was satisfied with the voluntary participation, maintenance of the rights of the participants and confidential handling of personal information by the hospital physicians and has approved this consent procedure. However, the surveillance activities in Mirzapur Kumudini Hospital has also been approved by the RRC and ERC of icddr,b. Both informed written consent as well as accent has been taken from the study population. Thus, verbal consent is taken from patients enrolled in Dhaka, Matlab and Mirpur surveillance system and for Mirzapur, written consent from adults or guardians and assent from 11–17 years old children has been taken.
Results
Overall isolation of Shigella was higher in rural Mirzapur compared to other sites. However, a higher rate was also observed in rural Matlab in contrast to the two urban sites (Table 1). Among children under 5 years, such observation remained similar between sites over the period.
Distinct socio-demographic diversity among individuals infected with Shigella was observed across the sites. In urban Dhaka and Mirpur, Shigella was more often detected among males compared to that of rural Matlab and Mirzapur. Maternal literacy rate was also higher in urban sites. Considering poor socio-economic status, lesser proportion of individuals with shigellosis belonged to Mirpur compared to others sites. Proportion of individuals having access to sanitary toilets and used antimicrobials before hospital visit was low in rural Matlab. On the other hand, urban individuals with shigellosis often presented with watery stool and some or severe dehydration compared to rural sites. However, rural residents had often abdominal pain and fever. Duration of diarrhea, vomiting and nutritional status (underweight, stunting and wasting) were found identical across the sites (Table 2).
In Dhaka, of all Shigella isolates, the proportion of –S. flexneri in 2008 was 58% which gradually decreased to 48% in 2011 (Figure 2). The proportion of S. flexneri among total Shigella isolated in <5 years old children also decreased (Figure 3). Similarly, in the Mirpur Treatment Centre, there was a decreasing trend of S. flexneri in all age groups as well as among under-5 children in 2009–11 (Figure 2, 3). Decreasing trend in proportion of S. flexneri was also observed in Mirzapur during 2010 and 2011 (Figure 2). Among the under-5 years old children, similar change in proportion was found in Dhaka and Mirzapur (Figure 3). On the other hand, in Matlab, the distribution of S. flexneri was similar over the 4-year period (Figure 2) which remained the highest isolate among all the Shigella spp. Among the under 5 children, the scenario was similar (Figure 3).
In contrast to S. flexneri, proportion of S. sonnei among all Shigella isolates increased steadily - in all age groups in the Dhaka Hospital and Mirpur Treatment Centre (Figure 2). In line with this, among the under-5 children the proportion also increased substantially (Figure 3). In Matlab, the isolation rate of S. sonnei remained static in all age groups (Figure 2); although in under-5 children, the proportion increased two folds (Figure 3). In Mirzapur, the prevalence of S. sonnei declined somewhat in all age groups as well as in under-5 children (Figure 2, 3).
The proportion of S. boydii was higher in 2008 that decreased over years in 2011 in both Dhaka Hospital and in Matlab (Figure 2). A similar trend was noted in the under-5 children (Figure 3). However, the proportion of S. boydii among all Shigella isolates in Mirpur and Mirzapur (Figures 2, 3) was the opposite with dramatic increase in the isolation rates, especially in the under 5 children. Proportion of S. dysenteriae remained the same over the 4-year period in Dhaka, Matlab and Mirzapur (Figure 2, 3). Interestingly, in the Mirpur Treatment Center there was no isolation of S. dysenteriae in the year 2011 among children less than 5 years of age (Figure 3).
Discussion
The observation of increasing rates of infectious diarrhea caused by S. sonnei and S. boydii and decreasing rates of S. flexneri in four different diarrheal disease facilities has important public health implications. S. sonnei is one of the primary causes of dysentery in developed countries, and is now replacing S. flexneri as the leading cause of the illness in many developing countries or countries in transition [4] [8], [9], [10]. It has been hypothesized that these changes may be due to varying host characteristics such as reduction of overall malnutrition that in turn leads to improved immune response. It may also be due to genetic mutation of the non-virulent microbes becoming pathogenic [11]. Moreover, changing meteorological indicators, such as rising temperatures, decreased rainfall, increased sea level and temperature [10]; irrational use and increased minimum inhibitory concentration (MIC) level to common antimicrobials [12], [13] and disappearance of epidemic strains such as S. dysenteriae type 1, resulting in resurgence of non-epidemic strains as hyperendemic strains, may also have contributed [5], [14].
Shigella spp. are dynamic and able to survive in a range of ecological niches under diverse environmental conditions. Recent phylogenetic analysis showed that the current S. sonnei population descends from a common ancestor that existed about 500 years ago and that diversified into several distinct lineages with unique characteristics which mainly occurred in Europe [8]. Such mutations may also play a role in our context, and deserves further study. Shigellosis due to S. sonnei is reported to occur at low rates among people living in developing countries. Plesiomonas shigelloides is a gram-negative bacteria often found in surface water that shares antigens with S. sonnei, and until recently P. shigelloides has been a frequently isolated enteric pathogen from <2 years old Bangladeshi children in the diarrhea hospital [15], [16]. It is well accepted that exposure to P shigelloides, through contaminated drinking water, may immunize people to S. sonnei in these developing countries [17]. Increased and sustained access to safe drinking water, one of the major components of Millennium Development Goals to control and prevent food and water borne diseases, is a major step that is taken into account by the policy makers of transitional countries. With economic development and accompanying water quality improvements, susceptibility to S. sonnei in a population may increase [8], [17]. Bangladesh is a country in transition and the national GDP per capita of Bangladesh increased from US$ 356 to 674 from 2008 to 2010 [18]. This gross economic improvement might have impacted positively on the overall behavioral change in general population with more and more of the population using bottled water in urban areas and having access to piped water in comparison to rural areas. The changing trend in the serotype distribution of Shigella spp. may reflect this phenomenon. In the rural community such as Matlab, the distribution of the different species of Shigella was different than that in urban areas (Dhaka, Mirpur) suggesting differences in life style, access to different types of water and food, and local environmental conditions.
The heterogeneous distribution of Shigella serotypes in urban and rural Bangladesh suggests that multivalent vaccines will be needed to prevent shigellosis in these settings. Currently, there are no licensed vaccines available for the prevention of shigellosis, especially given the wide range of Shigella serotypes as well as undifferentiated strains that differ from the known available strains [19]. Therefore, the findings of the study underscore the need for a multivalent Shigella vaccine for the prevalent species and serotypes.
All together, further investigations on factors such as host and environmental characteristics, and climate change need to be prioritized to address the phenomenon. Meanwhile, surveillance systems play a critical role in monitoring the changes of the sero-groups and serotypes of Shigella. Furthermore, such systems may identify factors to predict outbreaks of disease as well as changes in antimicrobial susceptibility patterns.
Limitations
Hospital based data may not adequately represent the sick population at large in the community. However, our strengths were that we followed an unbiased systematic sampling irrespective of age, sex, nutrition status, disease severity or socioeconomic context, observed isolation patterns in different geographical locations, and used a large and longitudinal data set for this analysis. Moreover, despite variations over the study period in different sites, some differences however were not statistically significant possibly due to lack of power with small sample size.
Acknowledgments
We would like to express our sincere thanks to clinical, epidemiological and laboratory personnel for their invaluable support and contribution in patient enrollment, data collection and laboratory activities.
Author Contributions
Conceived and designed the experiments: SKD ASGF MJC. Performed the experiments: ASGF RR. Analyzed the data: MAM SA FF FDF. Contributed reagents/materials/analysis tools: KAT DTL. Wrote the paper: SKD MJC PKB MAS.
References
- 1.
Clemens J, Kotloff K, Kay B (1999) Generic protocol to estimate the burden of Shigella diarrhoea and dysenteric mortalit.World Health Organization: Department of Vaccines and Biologicals. Geneva: World Health Organization.
- 2.
WHO (2009) Initiative for Vaccine Research. Diarrhoeal Diseases (Updated February 2009): Shigellosis. Geneva: World Health Organization.
- 3.
Hale TL, Keusch GT (1996) Shigella. Medical Microbiology. Galveston (TX): University of Texas Medical Branch at Galveston: Baron S, editor.
- 4. von Seidlein L, Kim DR, Ali M, Lee H, Wang X, et al. (2006) A multicentre study of Shigella diarrhoea in six Asian countries: disease burden, clinical manifestations, and microbiology. PLoS Med 3: e353.
- 5. Khatun F, Faruque AS, Koeck JL, Olliaro P, Millet P, et al. (2011) Changing species distribution and antimicrobial susceptibility pattern of Shigella over a 29-year period (1980–2008). Epidemiol Infect 139: 446–452.
- 6. Vinh H, Nhu NT, Nga TV, Duy PT, Campbell JI, et al. (2009) A changing picture of shigellosis in southern Vietnam: shifting species dominance, antimicrobial susceptibility and clinical presentation. BMC Infect Dis 9: 204.
- 7.
World Health Organization (1987) Programme for control of diarrheal disease. In Manual for laboratory investigation of acute enteric infections. Geneva, Switzerland: World Health Organization. 9–20 p.
- 8. Holt KE, Baker S, Weill FX, Holmes EC, Kitchen A, et al. (2012) Shigella sonnei genome sequencing and phylogenetic analysis indicate recent global dissemination from Europe. Nat Genet 44: 1056–1059.
- 9. Chompook P, Samosornsuk S, von Seidlein L, Jitsanguansuk S, Sirima N, et al. (2005) Estimating the burden of shigellosis in Thailand: 36-month population-based surveillance study. Bull World Health Organ 83: 739–746.
- 10. Kelly-Hope LA, Alonso WJ, Thiem VD, Anh DD, Canh do G, et al. (2007) Geographical distribution and risk factors associated with enteric diseases in Vietnam. Am J Trop Med Hyg 76: 706–712.
- 11. Greenhill C (2012) Infectious disease: Genome sequencing reveals how Shigella sonnei spread around the world. Nat Rev Gastroenterol Hepatol 9: 487.
- 12.
Christopher PR, David KV, John SM, Sankarapandian V (2010) Antibiotic therapy for Shigella dysentery. Cochrane Database Syst Rev: CD006784.
- 13. Vinh H, Anh VT, Anh ND, Campbell JI, Hoang NV, et al. (2011) A multi-center randomized trial to assess the efficacy of gatifloxacin versus ciprofloxacin for the treatment of shigellosis in Vietnamese children. PLoS Negl Trop Dis 5: e1264.
- 14. Feil EJ (2012) The emergence and spread of dysentery. Nat Genet 44: 964–965.
- 15. Khan AM, Faruque AS, Hossain MS, Sattar S, Fuchs GJ, et al. (2004) Plesiomonas shigelloides-associated diarrhoea in Bangladeshi children: a hospital-based surveillance study. J Trop Pediatr 50: 354–356.
- 16. Khan AM, Hossain MS, Khan AI, Chisti MJ, Chowdhury F, et al. (2009) Bacterial enteropathogens of neonates admitted to an urban diarrhoeal hospital in Bangladesh. J Trop Pediatr 55: 122–124.
- 17. Sack DA, Hoque AT, Huq A, Etheridge M (1994) Is protection against shigellosis induced by natural infection with Plesiomonas shigelloides? Lancet 343: 1413–1415.
- 18.
Index Mundi website. Available: http://www.indexmundi.com/facts/indicators/NY.GDP.PCAP.PP.CD. Accessed 2012 Dec 5.
- 19. Kaminski RW, Oaks EV (2009) Inactivated and subunit vaccines to prevent shigellosis. Expert Rev Vaccines 8: 1693–1704.