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Genomic epidemiology of Escherichia coli: antimicrobial resistance through a One Health lens in sympatric humans, livestock and peri-domestic wildlife in Nairobi, Kenya

BACKGROUND: Livestock systems have been proposed as a reservoir for antimicrobial-resistant (AMR) bacteria and AMR genetic determinants that may infect or colonise humans, yet quantitative evidence regarding their epidemiological role remains lacking. Here, we used a combination of genomics, epidemi...

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Autores principales: Muloi, Dishon M., Hassell, James M., Wee, Bryan A., Ward, Melissa J., Bettridge, Judy M., Kivali, Velma, Kiyong’a, Alice, Ndinda, Christine, Gitahi, Nduhiu, Ouko, Tom, Imboma, Titus, Akoko, James, Murungi, Maurice K., Njoroge, Samuel M., Muinde, Patrick, Alumasa, Lorren, Kaitho, Titus, Amanya, Fredrick, Ogendo, Allan, van Bunnik, Bram A. D., Kiiru, John, Robinson, Timothy P., Kang’ethe, Erastus K., Kariuki, Samuel, Pedersen, Amy B., Fèvre, Eric M., Woolhouse, Mark E. J.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2022
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9730568/
https://www.ncbi.nlm.nih.gov/pubmed/36482440
http://dx.doi.org/10.1186/s12916-022-02677-7
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author Muloi, Dishon M.
Hassell, James M.
Wee, Bryan A.
Ward, Melissa J.
Bettridge, Judy M.
Kivali, Velma
Kiyong’a, Alice
Ndinda, Christine
Gitahi, Nduhiu
Ouko, Tom
Imboma, Titus
Akoko, James
Murungi, Maurice K.
Njoroge, Samuel M.
Muinde, Patrick
Alumasa, Lorren
Kaitho, Titus
Amanya, Fredrick
Ogendo, Allan
van Bunnik, Bram A. D.
Kiiru, John
Robinson, Timothy P.
Kang’ethe, Erastus K.
Kariuki, Samuel
Pedersen, Amy B.
Fèvre, Eric M.
Woolhouse, Mark E. J.
author_facet Muloi, Dishon M.
Hassell, James M.
Wee, Bryan A.
Ward, Melissa J.
Bettridge, Judy M.
Kivali, Velma
Kiyong’a, Alice
Ndinda, Christine
Gitahi, Nduhiu
Ouko, Tom
Imboma, Titus
Akoko, James
Murungi, Maurice K.
Njoroge, Samuel M.
Muinde, Patrick
Alumasa, Lorren
Kaitho, Titus
Amanya, Fredrick
Ogendo, Allan
van Bunnik, Bram A. D.
Kiiru, John
Robinson, Timothy P.
Kang’ethe, Erastus K.
Kariuki, Samuel
Pedersen, Amy B.
Fèvre, Eric M.
Woolhouse, Mark E. J.
author_sort Muloi, Dishon M.
collection PubMed
description BACKGROUND: Livestock systems have been proposed as a reservoir for antimicrobial-resistant (AMR) bacteria and AMR genetic determinants that may infect or colonise humans, yet quantitative evidence regarding their epidemiological role remains lacking. Here, we used a combination of genomics, epidemiology and ecology to investigate patterns of AMR gene carriage in Escherichia coli, regarded as a sentinel organism. METHODS: We conducted a structured epidemiological survey of 99 households across Nairobi, Kenya, and whole genome sequenced E. coli isolates from 311 human, 606 livestock and 399 wildlife faecal samples. We used statistical models to investigate the prevalence of AMR carriage and characterise AMR gene diversity and structure of AMR genes in different host populations across the city. We also investigated household-level risk factors for the exchange of AMR genes between sympatric humans and livestock. RESULTS: We detected 56 unique acquired genes along with 13 point mutations present in variable proportions in human and animal isolates, known to confer resistance to nine antibiotic classes. We find that AMR gene community composition is not associated with host species, but AMR genes were frequently co-located, potentially enabling the acquisition and dispersal of multi-drug resistance in a single step. We find that whilst keeping livestock had no influence on human AMR gene carriage, the potential for AMR transmission across human-livestock interfaces is greatest when manure is poorly disposed of and in larger households. CONCLUSIONS: Findings of widespread carriage of AMR bacteria in human and animal populations, including in long-distance wildlife species, in community settings highlight the value of evidence-based surveillance to address antimicrobial resistance on a global scale. Our genomic analysis provided an in-depth understanding of AMR determinants at the interfaces of One Health sectors that will inform AMR prevention and control. SUPPLEMENTARY INFORMATION: The online version contains supplementary material available at 10.1186/s12916-022-02677-7.
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spelling pubmed-97305682022-12-09 Genomic epidemiology of Escherichia coli: antimicrobial resistance through a One Health lens in sympatric humans, livestock and peri-domestic wildlife in Nairobi, Kenya Muloi, Dishon M. Hassell, James M. Wee, Bryan A. Ward, Melissa J. Bettridge, Judy M. Kivali, Velma Kiyong’a, Alice Ndinda, Christine Gitahi, Nduhiu Ouko, Tom Imboma, Titus Akoko, James Murungi, Maurice K. Njoroge, Samuel M. Muinde, Patrick Alumasa, Lorren Kaitho, Titus Amanya, Fredrick Ogendo, Allan van Bunnik, Bram A. D. Kiiru, John Robinson, Timothy P. Kang’ethe, Erastus K. Kariuki, Samuel Pedersen, Amy B. Fèvre, Eric M. Woolhouse, Mark E. J. BMC Med Research Article BACKGROUND: Livestock systems have been proposed as a reservoir for antimicrobial-resistant (AMR) bacteria and AMR genetic determinants that may infect or colonise humans, yet quantitative evidence regarding their epidemiological role remains lacking. Here, we used a combination of genomics, epidemiology and ecology to investigate patterns of AMR gene carriage in Escherichia coli, regarded as a sentinel organism. METHODS: We conducted a structured epidemiological survey of 99 households across Nairobi, Kenya, and whole genome sequenced E. coli isolates from 311 human, 606 livestock and 399 wildlife faecal samples. We used statistical models to investigate the prevalence of AMR carriage and characterise AMR gene diversity and structure of AMR genes in different host populations across the city. We also investigated household-level risk factors for the exchange of AMR genes between sympatric humans and livestock. RESULTS: We detected 56 unique acquired genes along with 13 point mutations present in variable proportions in human and animal isolates, known to confer resistance to nine antibiotic classes. We find that AMR gene community composition is not associated with host species, but AMR genes were frequently co-located, potentially enabling the acquisition and dispersal of multi-drug resistance in a single step. We find that whilst keeping livestock had no influence on human AMR gene carriage, the potential for AMR transmission across human-livestock interfaces is greatest when manure is poorly disposed of and in larger households. CONCLUSIONS: Findings of widespread carriage of AMR bacteria in human and animal populations, including in long-distance wildlife species, in community settings highlight the value of evidence-based surveillance to address antimicrobial resistance on a global scale. Our genomic analysis provided an in-depth understanding of AMR determinants at the interfaces of One Health sectors that will inform AMR prevention and control. SUPPLEMENTARY INFORMATION: The online version contains supplementary material available at 10.1186/s12916-022-02677-7. BioMed Central 2022-12-08 /pmc/articles/PMC9730568/ /pubmed/36482440 http://dx.doi.org/10.1186/s12916-022-02677-7 Text en © The Author(s) 2022 https://creativecommons.org/licenses/by/4.0/Open AccessThis article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons licence, and indicate if changes were made. The images or other third party material in this article are included in the article's Creative Commons licence, unless indicated otherwise in a credit line to the material. If material is not included in the article's Creative Commons licence and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this licence, visit http://creativecommons.org/licenses/by/4.0/ (https://creativecommons.org/licenses/by/4.0/) . The Creative Commons Public Domain Dedication waiver (http://creativecommons.org/publicdomain/zero/1.0/ (https://creativecommons.org/publicdomain/zero/1.0/) ) applies to the data made available in this article, unless otherwise stated in a credit line to the data.
spellingShingle Research Article
Muloi, Dishon M.
Hassell, James M.
Wee, Bryan A.
Ward, Melissa J.
Bettridge, Judy M.
Kivali, Velma
Kiyong’a, Alice
Ndinda, Christine
Gitahi, Nduhiu
Ouko, Tom
Imboma, Titus
Akoko, James
Murungi, Maurice K.
Njoroge, Samuel M.
Muinde, Patrick
Alumasa, Lorren
Kaitho, Titus
Amanya, Fredrick
Ogendo, Allan
van Bunnik, Bram A. D.
Kiiru, John
Robinson, Timothy P.
Kang’ethe, Erastus K.
Kariuki, Samuel
Pedersen, Amy B.
Fèvre, Eric M.
Woolhouse, Mark E. J.
Genomic epidemiology of Escherichia coli: antimicrobial resistance through a One Health lens in sympatric humans, livestock and peri-domestic wildlife in Nairobi, Kenya
title Genomic epidemiology of Escherichia coli: antimicrobial resistance through a One Health lens in sympatric humans, livestock and peri-domestic wildlife in Nairobi, Kenya
title_full Genomic epidemiology of Escherichia coli: antimicrobial resistance through a One Health lens in sympatric humans, livestock and peri-domestic wildlife in Nairobi, Kenya
title_fullStr Genomic epidemiology of Escherichia coli: antimicrobial resistance through a One Health lens in sympatric humans, livestock and peri-domestic wildlife in Nairobi, Kenya
title_full_unstemmed Genomic epidemiology of Escherichia coli: antimicrobial resistance through a One Health lens in sympatric humans, livestock and peri-domestic wildlife in Nairobi, Kenya
title_short Genomic epidemiology of Escherichia coli: antimicrobial resistance through a One Health lens in sympatric humans, livestock and peri-domestic wildlife in Nairobi, Kenya
title_sort genomic epidemiology of escherichia coli: antimicrobial resistance through a one health lens in sympatric humans, livestock and peri-domestic wildlife in nairobi, kenya
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9730568/
https://www.ncbi.nlm.nih.gov/pubmed/36482440
http://dx.doi.org/10.1186/s12916-022-02677-7
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