Population genomics of Escherichia coli in livestock-keeping households across a rapidly developing urban landscape
-
Published:2022-03-14
Issue:4
Volume:7
Page:581-589
-
ISSN:2058-5276
-
Container-title:Nature Microbiology
-
language:en
-
Short-container-title:Nat Microbiol
Author:
Muloi Dishon M.ORCID, Wee Bryan A.ORCID, McClean Deirdre M. H.ORCID, Ward Melissa J., Pankhurst Louise, Phan Hang, Ivens Alasdair C., Kivali Velma, Kiyong’a Alice, Ndinda Christine, Gitahi NduhiuORCID, Ouko Tom, Hassell James M., Imboma Titus, Akoko James, Murungi Maurice K.ORCID, Njoroge Samuel M.ORCID, Muinde Patrick, Nakamura YukikoORCID, Alumasa Lorren, Furmaga Erin, Kaitho Titus, Öhgren Elin M., Amanya Fredrick, Ogendo Allan, Wilson Daniel J., Bettridge Judy M.ORCID, Kiiru John, Kyobutungi Catherine, Tacoli Cecila, Kang’ethe Erastus K., Davila Julio D., Kariuki SamuelORCID, Robinson Timothy P., Rushton Jonathan, Woolhouse Mark E. J.ORCID, Fèvre Eric M.ORCID
Abstract
AbstractQuantitative evidence for the risk of zoonoses and the spread of antimicrobial resistance remains lacking. Here, as part of the UrbanZoo project, we sampled Escherichia coli from humans, livestock and peri-domestic wildlife in 99 households across Nairobi, Kenya, to investigate its distribution among host species in this rapidly developing urban landscape. We performed whole-genome sequencing of 1,338 E. coli isolates and found that the diversity and sharing patterns of E. coli were heavily structured by household and strongly shaped by host type. We also found evidence for inter-household and inter-host sharing and, importantly, between humans and animals, although this occurs much less frequently. Resistome similarity was differently distributed across host and household, consistent with being driven by shared exposure to antimicrobials. Our results indicate that a large, epidemiologically structured sampling framework combined with WGS is needed to uncover strain-sharing events among different host populations in complex environments and the major contributing pathways that could ultimately drive the emergence of zoonoses and the spread of antimicrobial resistance.
Funder
RCUK | Medical Research Council Wellcome Trust CGIAR Agriculture for Nutrition and Health Program
Publisher
Springer Science and Business Media LLC
Subject
Cell Biology,Microbiology (medical),Genetics,Applied Microbiology and Biotechnology,Immunology,Microbiology
Reference65 articles.
1. Karesh, W. B. et al. Ecology of zoonoses: natural and unnatural histories. Lancet 380, 1936–1945 (2012). 2. Wolfe, N. D., Dunavan, C. P. & Diamond, J. Origins of major human infectious diseases. Nature 447, 279–283 (2007). 3. Allen, T. et al. Global hotspots and correlates of emerging zoonotic diseases. Nat. Commun. 8, 1124 (2017). 4. Zhang, F. et al. Global discovery of human-infective RNA viruses: a modelling analysis. PLoS Pathog. https://doi.org/10.1371/journal.ppat.1009079 (2020). 5. Gottdenker, N. L., Streicker, D. G., Faust, C. L. & Carroll, C. R. Anthropogenic land use change and infectious diseases: a review of the evidence. EcoHealth 11, 619–632 (2014).
Cited by
45 articles.
订阅此论文施引文献
订阅此论文施引文献,注册后可以免费订阅5篇论文的施引文献,订阅后可以查看论文全部施引文献
|
|