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Shigella in Africa: New Insights From the Vaccine Impact on Diarrhea in Africa (VIDA) Study

BACKGROUND: We evaluated the burden of Shigella spp from children aged 0–59 months with medically attended moderate-to-severe diarrhea and matched controls at sites in Mali, The Gambia, and Kenya participating in the Vaccine Impact on Diarrhea in Africa (VIDA) study from 2015 to 2018. METHODS: Shige...

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Autores principales: Kasumba, Irene N, Badji, Henry, Powell, Helen, Hossain, M Jahangir, Omore, Richard, Sow, Samba O, Verani, Jennifer R, Platts-Mills, James A, Widdowson, Marc-Alain, Zaman, Syed M A, Jones, Jennifer, Sen, Sunil, Permala-Booth, Jasnehta, Nasrin, Shamima, Roose, Anna, Nasrin, Dilruba, Ochieng, John Benjamin, Juma, Jane, Doh, Sanogo, Jones, Joquina Chiquita M, Antonio, Martin, Awuor, Alex O, Sugerman, Ciara E, Watson, Nora, Focht, Christopher, Liu, Jie, Houpt, Eric, Kotloff, Karen L, Tennant, Sharon M
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Oxford University Press 2023
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10116563/
https://www.ncbi.nlm.nih.gov/pubmed/37074444
http://dx.doi.org/10.1093/cid/ciac969
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author Kasumba, Irene N
Badji, Henry
Powell, Helen
Hossain, M Jahangir
Omore, Richard
Sow, Samba O
Verani, Jennifer R
Platts-Mills, James A
Widdowson, Marc-Alain
Zaman, Syed M A
Jones, Jennifer
Sen, Sunil
Permala-Booth, Jasnehta
Nasrin, Shamima
Roose, Anna
Nasrin, Dilruba
Ochieng, John Benjamin
Juma, Jane
Doh, Sanogo
Jones, Joquina Chiquita M
Antonio, Martin
Awuor, Alex O
Sugerman, Ciara E
Watson, Nora
Focht, Christopher
Liu, Jie
Houpt, Eric
Kotloff, Karen L
Tennant, Sharon M
author_facet Kasumba, Irene N
Badji, Henry
Powell, Helen
Hossain, M Jahangir
Omore, Richard
Sow, Samba O
Verani, Jennifer R
Platts-Mills, James A
Widdowson, Marc-Alain
Zaman, Syed M A
Jones, Jennifer
Sen, Sunil
Permala-Booth, Jasnehta
Nasrin, Shamima
Roose, Anna
Nasrin, Dilruba
Ochieng, John Benjamin
Juma, Jane
Doh, Sanogo
Jones, Joquina Chiquita M
Antonio, Martin
Awuor, Alex O
Sugerman, Ciara E
Watson, Nora
Focht, Christopher
Liu, Jie
Houpt, Eric
Kotloff, Karen L
Tennant, Sharon M
author_sort Kasumba, Irene N
collection PubMed
description BACKGROUND: We evaluated the burden of Shigella spp from children aged 0–59 months with medically attended moderate-to-severe diarrhea and matched controls at sites in Mali, The Gambia, and Kenya participating in the Vaccine Impact on Diarrhea in Africa (VIDA) study from 2015 to 2018. METHODS: Shigella spp were identified using coprocultures and serotyping in addition to quantitative polymerase chain reaction (qPCR). Episode-specific attributable fractions (AFe) for Shigella were calculated using Shigella DNA quantity; cases with AFe ≥0.5 were considered to have shigellosis. RESULTS: The prevalence of Shigella was determined to be 359 of 4840 (7.4%) cases and 83 of 6213 (1.3%) controls by culture, and 1641 of 4836 (33.9%) cases and 1084 of 4846 (22.4%) controls by qPCR (cycle threshold <35); shigellosis was higher in The Gambia (30.8%) than in Mali (9.3%) and Kenya (18.7%). Bloody diarrhea attributed to Shigella was more common in 24- to 59-month-old children (50.1%) than 0- to 11-month-old infants (39.5%). The Shigella flexneri serogroup predominated among cases (67.6% of isolates), followed by Shigella sonnei (18.2%), Shigella boydii (11.8%), and Shigella dysenteriae (2.3%). The most frequent S. flexneri serotypes were 2a (40.6%), 1b (18.8%), 6 (17.5%), 3a (9.0%), and 4a (5.1%). Drug-specific resistance among 353 (98.3%) Shigella cases with AMR data was as follows: trimethoprim-sulfamethoxazole (94.9%), ampicillin (48.4%), nalidixic acid (1.7%), ceftriaxone (0.3%), azithromycin (0.3%), and ciprofloxacin (0.0%). CONCLUSIONS: A high prevalence of shigellosis continues in sub-Saharan Africa. Strains are highly resistant to commonly used antibiotics while remaining susceptible to ciprofloxacin, ceftriaxone, and azithromycin.
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spelling pubmed-101165632023-04-21 Shigella in Africa: New Insights From the Vaccine Impact on Diarrhea in Africa (VIDA) Study Kasumba, Irene N Badji, Henry Powell, Helen Hossain, M Jahangir Omore, Richard Sow, Samba O Verani, Jennifer R Platts-Mills, James A Widdowson, Marc-Alain Zaman, Syed M A Jones, Jennifer Sen, Sunil Permala-Booth, Jasnehta Nasrin, Shamima Roose, Anna Nasrin, Dilruba Ochieng, John Benjamin Juma, Jane Doh, Sanogo Jones, Joquina Chiquita M Antonio, Martin Awuor, Alex O Sugerman, Ciara E Watson, Nora Focht, Christopher Liu, Jie Houpt, Eric Kotloff, Karen L Tennant, Sharon M Clin Infect Dis VIDA Supplement BACKGROUND: We evaluated the burden of Shigella spp from children aged 0–59 months with medically attended moderate-to-severe diarrhea and matched controls at sites in Mali, The Gambia, and Kenya participating in the Vaccine Impact on Diarrhea in Africa (VIDA) study from 2015 to 2018. METHODS: Shigella spp were identified using coprocultures and serotyping in addition to quantitative polymerase chain reaction (qPCR). Episode-specific attributable fractions (AFe) for Shigella were calculated using Shigella DNA quantity; cases with AFe ≥0.5 were considered to have shigellosis. RESULTS: The prevalence of Shigella was determined to be 359 of 4840 (7.4%) cases and 83 of 6213 (1.3%) controls by culture, and 1641 of 4836 (33.9%) cases and 1084 of 4846 (22.4%) controls by qPCR (cycle threshold <35); shigellosis was higher in The Gambia (30.8%) than in Mali (9.3%) and Kenya (18.7%). Bloody diarrhea attributed to Shigella was more common in 24- to 59-month-old children (50.1%) than 0- to 11-month-old infants (39.5%). The Shigella flexneri serogroup predominated among cases (67.6% of isolates), followed by Shigella sonnei (18.2%), Shigella boydii (11.8%), and Shigella dysenteriae (2.3%). The most frequent S. flexneri serotypes were 2a (40.6%), 1b (18.8%), 6 (17.5%), 3a (9.0%), and 4a (5.1%). Drug-specific resistance among 353 (98.3%) Shigella cases with AMR data was as follows: trimethoprim-sulfamethoxazole (94.9%), ampicillin (48.4%), nalidixic acid (1.7%), ceftriaxone (0.3%), azithromycin (0.3%), and ciprofloxacin (0.0%). CONCLUSIONS: A high prevalence of shigellosis continues in sub-Saharan Africa. Strains are highly resistant to commonly used antibiotics while remaining susceptible to ciprofloxacin, ceftriaxone, and azithromycin. Oxford University Press 2023-04-19 /pmc/articles/PMC10116563/ /pubmed/37074444 http://dx.doi.org/10.1093/cid/ciac969 Text en © The Author(s) 2023. Published by Oxford University Press on behalf of Infectious Diseases Society of America. https://creativecommons.org/licenses/by/4.0/This is an Open Access article distributed under the terms of the Creative Commons Attribution License (https://creativecommons.org/licenses/by/4.0/), which permits unrestricted reuse, distribution, and reproduction in any medium, provided the original work is properly cited.
spellingShingle VIDA Supplement
Kasumba, Irene N
Badji, Henry
Powell, Helen
Hossain, M Jahangir
Omore, Richard
Sow, Samba O
Verani, Jennifer R
Platts-Mills, James A
Widdowson, Marc-Alain
Zaman, Syed M A
Jones, Jennifer
Sen, Sunil
Permala-Booth, Jasnehta
Nasrin, Shamima
Roose, Anna
Nasrin, Dilruba
Ochieng, John Benjamin
Juma, Jane
Doh, Sanogo
Jones, Joquina Chiquita M
Antonio, Martin
Awuor, Alex O
Sugerman, Ciara E
Watson, Nora
Focht, Christopher
Liu, Jie
Houpt, Eric
Kotloff, Karen L
Tennant, Sharon M
Shigella in Africa: New Insights From the Vaccine Impact on Diarrhea in Africa (VIDA) Study
title Shigella in Africa: New Insights From the Vaccine Impact on Diarrhea in Africa (VIDA) Study
title_full Shigella in Africa: New Insights From the Vaccine Impact on Diarrhea in Africa (VIDA) Study
title_fullStr Shigella in Africa: New Insights From the Vaccine Impact on Diarrhea in Africa (VIDA) Study
title_full_unstemmed Shigella in Africa: New Insights From the Vaccine Impact on Diarrhea in Africa (VIDA) Study
title_short Shigella in Africa: New Insights From the Vaccine Impact on Diarrhea in Africa (VIDA) Study
title_sort shigella in africa: new insights from the vaccine impact on diarrhea in africa (vida) study
topic VIDA Supplement
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10116563/
https://www.ncbi.nlm.nih.gov/pubmed/37074444
http://dx.doi.org/10.1093/cid/ciac969
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