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Mobile resistome of human gut and pathogen drives anthropogenic bloom of antibiotic resistance

BACKGROUND: The impact of human activities on the environmental resistome has been documented in many studies, but there remains the controversial question of whether the increased antibiotic resistance observed in anthropogenically impacted environments is just a result of contamination by resistan...

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Autores principales: Lee, Kihyun, Kim, Dae-Wi, Lee, Do-Hoon, Kim, Yong-Seok, Bu, Ji-Hye, Cha, Ju-Hee, Thawng, Cung Nawl, Hwang, Eun-Mi, Seong, Hoon Je, Sul, Woo Jun, Wellington, Elizabeth M. H., Quince, Christopher, Cha, Chang-Jun
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2020
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6947943/
https://www.ncbi.nlm.nih.gov/pubmed/31910889
http://dx.doi.org/10.1186/s40168-019-0774-7
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author Lee, Kihyun
Kim, Dae-Wi
Lee, Do-Hoon
Kim, Yong-Seok
Bu, Ji-Hye
Cha, Ju-Hee
Thawng, Cung Nawl
Hwang, Eun-Mi
Seong, Hoon Je
Sul, Woo Jun
Wellington, Elizabeth M. H.
Quince, Christopher
Cha, Chang-Jun
author_facet Lee, Kihyun
Kim, Dae-Wi
Lee, Do-Hoon
Kim, Yong-Seok
Bu, Ji-Hye
Cha, Ju-Hee
Thawng, Cung Nawl
Hwang, Eun-Mi
Seong, Hoon Je
Sul, Woo Jun
Wellington, Elizabeth M. H.
Quince, Christopher
Cha, Chang-Jun
author_sort Lee, Kihyun
collection PubMed
description BACKGROUND: The impact of human activities on the environmental resistome has been documented in many studies, but there remains the controversial question of whether the increased antibiotic resistance observed in anthropogenically impacted environments is just a result of contamination by resistant fecal microbes or is mediated by indigenous environmental organisms. Here, to determine exactly how anthropogenic influences shape the environmental resistome, we resolved the microbiome, resistome, and mobilome of the planktonic microbial communities along a single river, the Han, which spans a gradient of human activities. RESULTS: The bloom of antibiotic resistance genes (ARGs) was evident in the downstream regions and distinct successional dynamics of the river resistome occurred across the spatial continuum. We identified a number of widespread ARG sequences shared between the river, human gut, and pathogenic bacteria. These human-related ARGs were largely associated with mobile genetic elements rather than particular gut taxa and mainly responsible for anthropogenically driven bloom of the downstream river resistome. Furthermore, both sequence- and phenotype-based analyses revealed environmental relatives of clinically important proteobacteria as major carriers of these ARGs. CONCLUSIONS: Our results demonstrate a more nuanced view of the impact of anthropogenic activities on the river resistome: fecal contamination is present and allows the transmission of ARGs to the environmental resistome, but these mobile genes rather than resistant fecal bacteria proliferate in environmental relatives of their original hosts.
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spelling pubmed-69479432020-01-09 Mobile resistome of human gut and pathogen drives anthropogenic bloom of antibiotic resistance Lee, Kihyun Kim, Dae-Wi Lee, Do-Hoon Kim, Yong-Seok Bu, Ji-Hye Cha, Ju-Hee Thawng, Cung Nawl Hwang, Eun-Mi Seong, Hoon Je Sul, Woo Jun Wellington, Elizabeth M. H. Quince, Christopher Cha, Chang-Jun Microbiome Research BACKGROUND: The impact of human activities on the environmental resistome has been documented in many studies, but there remains the controversial question of whether the increased antibiotic resistance observed in anthropogenically impacted environments is just a result of contamination by resistant fecal microbes or is mediated by indigenous environmental organisms. Here, to determine exactly how anthropogenic influences shape the environmental resistome, we resolved the microbiome, resistome, and mobilome of the planktonic microbial communities along a single river, the Han, which spans a gradient of human activities. RESULTS: The bloom of antibiotic resistance genes (ARGs) was evident in the downstream regions and distinct successional dynamics of the river resistome occurred across the spatial continuum. We identified a number of widespread ARG sequences shared between the river, human gut, and pathogenic bacteria. These human-related ARGs were largely associated with mobile genetic elements rather than particular gut taxa and mainly responsible for anthropogenically driven bloom of the downstream river resistome. Furthermore, both sequence- and phenotype-based analyses revealed environmental relatives of clinically important proteobacteria as major carriers of these ARGs. CONCLUSIONS: Our results demonstrate a more nuanced view of the impact of anthropogenic activities on the river resistome: fecal contamination is present and allows the transmission of ARGs to the environmental resistome, but these mobile genes rather than resistant fecal bacteria proliferate in environmental relatives of their original hosts. BioMed Central 2020-01-07 /pmc/articles/PMC6947943/ /pubmed/31910889 http://dx.doi.org/10.1186/s40168-019-0774-7 Text en © The Author(s). 2020 Open AccessThis article is distributed under the terms of the Creative Commons Attribution 4.0 International License (http://creativecommons.org/licenses/by/4.0/), which permits unrestricted use, distribution, and reproduction in any medium, provided you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons license, and indicate if changes were made. The Creative Commons Public Domain Dedication waiver (http://creativecommons.org/publicdomain/zero/1.0/) applies to the data made available in this article, unless otherwise stated.
spellingShingle Research
Lee, Kihyun
Kim, Dae-Wi
Lee, Do-Hoon
Kim, Yong-Seok
Bu, Ji-Hye
Cha, Ju-Hee
Thawng, Cung Nawl
Hwang, Eun-Mi
Seong, Hoon Je
Sul, Woo Jun
Wellington, Elizabeth M. H.
Quince, Christopher
Cha, Chang-Jun
Mobile resistome of human gut and pathogen drives anthropogenic bloom of antibiotic resistance
title Mobile resistome of human gut and pathogen drives anthropogenic bloom of antibiotic resistance
title_full Mobile resistome of human gut and pathogen drives anthropogenic bloom of antibiotic resistance
title_fullStr Mobile resistome of human gut and pathogen drives anthropogenic bloom of antibiotic resistance
title_full_unstemmed Mobile resistome of human gut and pathogen drives anthropogenic bloom of antibiotic resistance
title_short Mobile resistome of human gut and pathogen drives anthropogenic bloom of antibiotic resistance
title_sort mobile resistome of human gut and pathogen drives anthropogenic bloom of antibiotic resistance
topic Research
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6947943/
https://www.ncbi.nlm.nih.gov/pubmed/31910889
http://dx.doi.org/10.1186/s40168-019-0774-7
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