Epidemiology of Shigella infections and diarrhea in the first two years of life using culture-independent diagnostics in 8 low-resource settings

Elizabeth T Rogawski McQuade, Fariha Shaheen, Furqan Kabir, Arjumand Rizvi, James A Platts-Mills, Fatima Aziz, Adil Kalam, Shahida Qureshi, Sarah Elwood, Jie Liu, Aldo A M Lima, Gagandeep Kang, Pascal Bessong, Amidou Samie, Rashidul Haque, Estomih R Mduma, Margaret N Kosek, Sanjaya Shrestha, Jose Paulo Leite, Ladaporn Bodhidatta, Nicola Page, Ireen Kiwelu, Sadia Shakoor, Ali Turab, Sajid Bashir Soofi, Tahmeed Ahmed, Eric R Houpt, Zulfiqar Bhutta, Najeeha Talat Iqbal, Elizabeth T Rogawski McQuade, Fariha Shaheen, Furqan Kabir, Arjumand Rizvi, James A Platts-Mills, Fatima Aziz, Adil Kalam, Shahida Qureshi, Sarah Elwood, Jie Liu, Aldo A M Lima, Gagandeep Kang, Pascal Bessong, Amidou Samie, Rashidul Haque, Estomih R Mduma, Margaret N Kosek, Sanjaya Shrestha, Jose Paulo Leite, Ladaporn Bodhidatta, Nicola Page, Ireen Kiwelu, Sadia Shakoor, Ali Turab, Sajid Bashir Soofi, Tahmeed Ahmed, Eric R Houpt, Zulfiqar Bhutta, Najeeha Talat Iqbal

Abstract

Culture-independent diagnostics have revealed a larger burden of Shigella among children in low-resource settings than previously recognized. We further characterized the epidemiology of Shigella in the first two years of life in a multisite birth cohort. We tested 41,405 diarrheal and monthly non-diarrheal stools from 1,715 children for Shigella by quantitative PCR. To assess risk factors, clinical factors related to age and culture positivity, and associations with inflammatory biomarkers, we used log-binomial regression with generalized estimating equations. The prevalence of Shigella varied from 4.9%-17.8% in non-diarrheal stools across sites, and the incidence of Shigella-attributable diarrhea was 31.8 cases (95% CI: 29.6, 34.2) per 100 child-years. The sensitivity of culture compared to qPCR was 6.6% and increased to 27.8% in Shigella-attributable dysentery. Shigella diarrhea episodes were more likely to be severe and less likely to be culture positive in younger children. Older age (RR: 1.75, 95% CI: 1.70, 1.81 per 6-month increase in age), unimproved sanitation (RR: 1.15, 95% CI: 1.03, 1.29), low maternal education (<10 years, RR: 1.14, 95% CI: 1.03, 1.26), initiating complementary foods before 3 months (RR: 1.10, 95% CI: 1.01, 1.20), and malnutrition (RR: 0.91, 95% CI: 0.88, 0.95 per unit increase in weight-for-age z-score) were risk factors for Shigella. There was a linear dose-response between Shigella quantity and myeloperoxidase concentrations. The burden of Shigella varied widely across sites, but uniformly increased through the second year of life and was associated with intestinal inflammation. Culture missed most clinically relevant cases of severe diarrhea and dysentery.

Conflict of interest statement

The authors have declared that no competing interests exist.

Figures

Fig 1
Fig 1
Cumulative incidence of Shigella infection (A) and Shigella-attributable diarrhea episodes (B) among 1715 children in the MAL-ED cohort.
Fig 2. Seasonality of Shigella detections in…
Fig 2. Seasonality of Shigella detections in non-diarrheal stools by site.
Top plots: weekly incidence (bars) and modeled incidence (solid dark lines); bottom plots: historical monthly averages for rainfall (bars) and temperature (dotted lines) at each sites.

References

    1. Khalil IA, Troeger C, Blacker BF, Rao PC, Brown A, Atherly DE, et al. Morbidity and mortality due to shigella and enterotoxigenic Escherichia coli diarrhoea: the Global Burden of Disease Study 1990–2016. Lancet Infect Dis. 2018. 10.1016/S1473-3099(18)30475-4
    1. Kotloff KL, Riddle MS, Platts-Mills JA, Pavlinac P, Zaidi AKM. Shigellosis. The Lancet. 2018;391: 801–812. 10.1016/S0140-6736(17)33296-8
    1. Williams PCM, Berkley JA. Guidelines for the treatment of dysentery (shigellosis): a systematic review of the evidence. Paediatr Int Child Health. 2018;38: S50–S65. 10.1080/20469047.2017.1409454
    1. Liu J, Platts-Mills JA, Juma J, Kabir F, Nkeze J, Okoi C, et al. Use of quantitative molecular diagnostic methods to identify causes of diarrhoea in children: a reanalysis of the GEMS case-control study. Lancet. 2016;388: 1291–1301. 10.1016/S0140-6736(16)31529-X
    1. Platts-Mills JA, Liu J, Rogawski ET, Kabir F, Lertsethtakarn P, Siguas M, et al. Use of quantitative molecular diagnostic methods to assess the aetiology, burden, and clinical characteristics of diarrhoea in children in low-resource settings: a reanalysis of the MAL-ED cohort study. Lancet Glob Health. 2018;6: e1309–e1318. 10.1016/S2214-109X(18)30349-8
    1. Rogawski ET, Liu J, Platts-Mills JA, Kabir F, Lertsethtakarn P, Siguas M, et al. Use of quantitative molecular diagnostic methods to investigate the effect of enteropathogen infections on linear growth in children in low-resource settings: longitudinal analysis of results from the MAL-ED cohort study. Lancet Glob Health. 2018;6: e1319–e1328. 10.1016/S2214-109X(18)30351-6
    1. Tickell KD, Brander RL, Atlas HE, Pernica JM, Walson JL, Pavlinac PB. Identification and management of Shigella infection in children with diarrhoea: a systematic review and meta-analysis. Lancet Glob Health. 2017;5: e1235–e1248. 10.1016/S2214-109X(17)30392-3
    1. Black RE, Brown KH, Becker S. Effects of diarrhea associated with specific enteropathogens on the growth of children in rural Bangladesh. Pediatrics. 1984;73: 799–805.
    1. Lee G, Paredes Olortegui M, Peñataro Yori P, Black RE, Caulfield L, Banda Chavez C, et al. Effects of Shigella-, Campylobacter- and ETEC-associated Diarrhea on Childhood Growth. Pediatr Infect Dis J. 2014;33: 1004–1009. 10.1097/INF.0000000000000351
    1. Mani S, Wierzba T, Walker RI. Status of vaccine research and development for Shigella. Vaccine. 2016;34: 2887–2894. 10.1016/j.vaccine.2016.02.075
    1. MAL-ED Network Investigators. The MAL-ED study: a multinational and multidisciplinary approach to understand the relationship between enteric pathogens, malnutrition, gut physiology, physical growth, cognitive development, and immune responses in infants and children up to 2 years of age in resource-poor environments. Clin Infect Dis. 2014;59 Suppl 4: S193–206. 10.1093/cid/ciu653
    1. Lee GO, Richard SA, Kang G, Houpt ER, Seidman JC, Pendergast LL, et al. A Comparison of Diarrheal Severity Scores in the MAL-ED Multisite Community Based Cohort Study. J Pediatr Gastroenterol Nutr. 2016. 10.1097/MPG.0000000000001286
    1. Lee G, Yori PP, Olortegui MP, Caulfield LE, Sack DA, Fischer-Walker C, et al. An instrument for the assessment of diarrhoeal severity based on a longitudinal community-based study. BMJ Open. 2014;4: e004816 10.1136/bmjopen-2014-004816
    1. World Health Organization. WHO Child Growth Standards: Length/height-for-age, weight-for-age, weight-for-length, weight-for-height and body mass index-for-age, Methods and development. 2006. Available:
    1. Psaki SR, Seidman JC, Miller M, Gottlieb M, Bhutta ZA, Ahmed T, et al. Measuring socioeconomic status in multicountry studies: results from the eight-country MAL-ED study. Population Health Metrics. 2014;12: 8 10.1186/1478-7954-12-8
    1. Liu J, Kabir F, Manneh J, Lertsethtakarn P, Begum S, Gratz J, et al. Development and assessment of molecular diagnostic tests for 15 enteropathogens causing childhood diarrhoea: a multicentre study. Lancet Infect Dis. 2014;14: 716–724. 10.1016/S1473-3099(14)70808-4
    1. Liu J, Gratz J, Amour C, Nshama R, Walongo T, Maro A, et al. Optimization of Quantitative PCR Methods for Enteropathogen Detection. PLoS ONE. 2016;11: e0158199 10.1371/journal.pone.0158199
    1. Houpt E, Gratz J, Kosek M, Zaidi AKM, Qureshi S, Kang G, et al. Microbiologic Methods Utilized in the MAL-ED Cohort Study. Clin Infect Dis. 2014;59: S225–S232. 10.1093/cid/ciu413
    1. McCormick BJJ, Lee GO, Seidman JC, Haque R, Mondal D, Quetz J, et al. Dynamics and Trends in Fecal Biomarkers of Gut Function in Children from 1–24 Months in the MAL-ED Study. Am J Trop Med Hyg. 2017;96: 465–472. 10.4269/ajtmh.16-0496
    1. Kosek M, Guerrant RL, Kang G, Bhutta Z, Yori PP, Gratz J, et al. Assessment of Environmental Enteropathy in the MAL-ED Cohort Study: Theoretical and Analytic Framework. Clin Infect Dis. 2014;59: S239–S247. 10.1093/cid/ciu457
    1. Kosek MN, Lee GO, Guerrant RL, Haque R, Kang G, Ahmed T, et al. Age and Sex Normalization of Intestinal Permeability Measures for the Improved Assessment of Enteropathy in Infancy and Early Childhood: Results From the MAL-ED Study. J Pediatr Gastroenterol Nutr. 2017;65: 31–39. 10.1097/MPG.0000000000001610
    1. Data sources—. [cited 3 Oct 2019]. Available:
    1. Quinn E, Najjar Z, Huhtinen E, Jegasothy E, Gupta L. Culture-positive shigellosis cases are epidemiologically different to culture-negative/PCR-positive cases. Aust N Z J Public Health. 2019;43: 41–45. 10.1111/1753-6405.12844
    1. Kosek M, Yori PP, Pan WK, Olortegui MP, Gilman RH, Perez J, et al. Epidemiology of highly endemic multiply antibiotic-resistant shigellosis in children in the Peruvian Amazon. Pediatrics. 2008;122: e541–549. 10.1542/peds.2008-0458
    1. Vubil D, Acácio S, Quintò L, Ballesté-Delpierre C, Nhampossa T, Kotloff K, et al. Clinical features, risk factors, and impact of antibiotic treatment of diarrhea caused by Shigella in children less than 5 years in Manhiça District, rural Mozambique. Infect Drug Resist. 2018;11: 2095–2106. 10.2147/IDR.S177579
    1. Abu-Elyazeed RR, Wierzba TF, Frenck RW, Putnam SD, Rao MR, Savarino SJ, et al. Epidemiology of Shigella-associated diarrhea in rural Egyptian children. Am J Trop Med Hyg. 2004;71: 367–372.
    1. Black RE, Brown KH, Becker S, Alim ARMA, Huq I. Longitudinal Studies of Infectious Diseases and Physical Growth of Children in Rural Bangladesh Ii. Incidence of Diarrhea and Association with Known Pathogens. Am J Epidemiol. 1982;115: 315–324. 10.1093/oxfordjournals.aje.a113308
    1. Rogawski McQuade ET, Clark S, Bayo E, Scharf RJ, DeBoer MD, Patil CL, et al. Seasonal Food Insecurity in Haydom, Tanzania, Is Associated with Low Birthweight and Acute Malnutrition: Results from the MAL-ED Study. Am J Trop Med Hyg. 2019;100: 681–687. 10.4269/ajtmh.18-0547
    1. Farag TH, Faruque AS, Wu Y, Das SK, Hossain A, Ahmed S, et al. Housefly Population Density Correlates with Shigellosis among Children in Mirzapur, Bangladesh: A Time Series Analysis. PLOS Neglected Tropical Diseases. 2013;7: e2280 10.1371/journal.pntd.0002280
    1. Arndt MB, Richardson BA, Ahmed T, Mahfuz M, Haque R, John-Stewart GC, et al. Fecal Markers of Environmental Enteropathy and Subsequent Growth in Bangladeshi Children. Am J Trop Med Hyg. 2016;95: 694–701. 10.4269/ajtmh.16-0098
    1. Colston JM, Peñataro Yori P, Colantuoni E, Moulton LH, Ambikapathi R, Lee G, et al. A methodologic framework for modeling and assessing biomarkers of environmental enteropathy as predictors of growth in infants: an example from a Peruvian birth cohort. Am J Clin Nutr. 2017;106: 245–255. 10.3945/ajcn.116.151886
    1. Iqbal NT, Sadiq K, Syed S, Akhund T, Umrani F, Ahmed S, et al. Promising Biomarkers of Environmental Enteric Dysfunction: A Prospective Cohort study in Pakistani Children. Sci Rep. 2018;8: 2966 10.1038/s41598-018-21319-8
    1. Liu J, Almeida M, Kabir F, Shakoor S, Qureshi S, Zaidi A, et al. Direct Detection of Shigella in Stool Specimens by Use of a Metagenomic Approach. J Clin Microbiol. 2018;56 10.1128/JCM.01374-17
    1. Levine MM, Nasrin D, Acácio S, Bassat Q, Powell H, Tennant SM, et al. Diarrhoeal disease and subsequent risk of death in infants and children residing in low-income and middle-income countries: analysis of the GEMS case-control study and 12-month GEMS-1A follow-on study. Lancet Glob Health. 2020;8: e204–e214. 10.1016/S2214-109X(19)30541-8

Source: PubMed

3
Subskrybuj