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An exploration of the gut and environmental resistome in a community in northern Vietnam in relation to antibiotic use

BACKGROUND: Antibiotic resistance is a major global public health threat. Antibiotic use can directly impact the antibiotic resistant genes (ARGs) profile of the human intestinal microbiome and consequently the environment through shedding. METHODS: We determined the resistome of human feces, animal...

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Autores principales: Bich, Vu Thi Ngoc, Thanh, Le Viet, Thai, Pham Duy, Van Phuong, Tran Thi, Oomen, Melissa, Driessen, Christel, Beuken, Erik, Hoang, Tran Huy, van Doorn, H. Rogier, Penders, John, Wertheim, Heiman F. L.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2019
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6883630/
https://www.ncbi.nlm.nih.gov/pubmed/31798840
http://dx.doi.org/10.1186/s13756-019-0645-9
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author Bich, Vu Thi Ngoc
Thanh, Le Viet
Thai, Pham Duy
Van Phuong, Tran Thi
Oomen, Melissa
Driessen, Christel
Beuken, Erik
Hoang, Tran Huy
van Doorn, H. Rogier
Penders, John
Wertheim, Heiman F. L.
author_facet Bich, Vu Thi Ngoc
Thanh, Le Viet
Thai, Pham Duy
Van Phuong, Tran Thi
Oomen, Melissa
Driessen, Christel
Beuken, Erik
Hoang, Tran Huy
van Doorn, H. Rogier
Penders, John
Wertheim, Heiman F. L.
author_sort Bich, Vu Thi Ngoc
collection PubMed
description BACKGROUND: Antibiotic resistance is a major global public health threat. Antibiotic use can directly impact the antibiotic resistant genes (ARGs) profile of the human intestinal microbiome and consequently the environment through shedding. METHODS: We determined the resistome of human feces, animal stools, human food and environmental (rain, well, and irrigative water) samples (n = 304) in 40 households within a community cohort and related the data to antibiotic consumption. Metagenomic DNA was isolated and qPCR was used to determine presence of mobile colistin resistance (mcr) genes, genes encoding extended-spectrum β-lactamases (ESBL), carbapenemases and quinolone resistance genes. RESULTS: Nearly 40 % (39.5%, 120/304) of samples contained ESBL genes (most frequent were CTX-M-9 (23.7% [72/304]), CTX-M-1 (18.8% [57/304]). Quinolone resistance genes (qnrS) were detected in all human and 91% (41/45) of animal stool samples. Mcr-1 and mcr-3 were predominantly detected in human feces at 88% (82/93) and 55% (51/93) and animal feces at 93% (42/45) and 51% (23/45), respectively. Mcr-2, mrc-4 and mcr-5 were not detected in human feces, and only sporadically (< 6%) in other samples. Carbapenemase-encoding genes were most common in water (15% [14/91]) and cooked food (13% [10/75]) samples, while their prevalence in human and animal stools was lower at 4% in both human (4/93) and animal (2/45) samples. We did not find an association between recent antibiotic consumption and ARGs in human stools. Principal component analysis showed that the resistome differs between ecosystems with a strong separation of ARGs profiles of human and animal stools on the one hand versus cooked food and water samples on the other. CONCLUSIONS: Our study indicated that ARGs were abundant in human and animal stools in a rural Vietnamese community, including ARGs targeting last resort antibiotics. The resistomes of animal and human stools were similar as opposed to the resistomes from water and food sources. No association between antibiotic use and ARG profiles was found in a setting of high background rates of AMR.
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spelling pubmed-68836302019-12-03 An exploration of the gut and environmental resistome in a community in northern Vietnam in relation to antibiotic use Bich, Vu Thi Ngoc Thanh, Le Viet Thai, Pham Duy Van Phuong, Tran Thi Oomen, Melissa Driessen, Christel Beuken, Erik Hoang, Tran Huy van Doorn, H. Rogier Penders, John Wertheim, Heiman F. L. Antimicrob Resist Infect Control Research BACKGROUND: Antibiotic resistance is a major global public health threat. Antibiotic use can directly impact the antibiotic resistant genes (ARGs) profile of the human intestinal microbiome and consequently the environment through shedding. METHODS: We determined the resistome of human feces, animal stools, human food and environmental (rain, well, and irrigative water) samples (n = 304) in 40 households within a community cohort and related the data to antibiotic consumption. Metagenomic DNA was isolated and qPCR was used to determine presence of mobile colistin resistance (mcr) genes, genes encoding extended-spectrum β-lactamases (ESBL), carbapenemases and quinolone resistance genes. RESULTS: Nearly 40 % (39.5%, 120/304) of samples contained ESBL genes (most frequent were CTX-M-9 (23.7% [72/304]), CTX-M-1 (18.8% [57/304]). Quinolone resistance genes (qnrS) were detected in all human and 91% (41/45) of animal stool samples. Mcr-1 and mcr-3 were predominantly detected in human feces at 88% (82/93) and 55% (51/93) and animal feces at 93% (42/45) and 51% (23/45), respectively. Mcr-2, mrc-4 and mcr-5 were not detected in human feces, and only sporadically (< 6%) in other samples. Carbapenemase-encoding genes were most common in water (15% [14/91]) and cooked food (13% [10/75]) samples, while their prevalence in human and animal stools was lower at 4% in both human (4/93) and animal (2/45) samples. We did not find an association between recent antibiotic consumption and ARGs in human stools. Principal component analysis showed that the resistome differs between ecosystems with a strong separation of ARGs profiles of human and animal stools on the one hand versus cooked food and water samples on the other. CONCLUSIONS: Our study indicated that ARGs were abundant in human and animal stools in a rural Vietnamese community, including ARGs targeting last resort antibiotics. The resistomes of animal and human stools were similar as opposed to the resistomes from water and food sources. No association between antibiotic use and ARG profiles was found in a setting of high background rates of AMR. BioMed Central 2019-11-28 /pmc/articles/PMC6883630/ /pubmed/31798840 http://dx.doi.org/10.1186/s13756-019-0645-9 Text en © The Author(s). 2019 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
Bich, Vu Thi Ngoc
Thanh, Le Viet
Thai, Pham Duy
Van Phuong, Tran Thi
Oomen, Melissa
Driessen, Christel
Beuken, Erik
Hoang, Tran Huy
van Doorn, H. Rogier
Penders, John
Wertheim, Heiman F. L.
An exploration of the gut and environmental resistome in a community in northern Vietnam in relation to antibiotic use
title An exploration of the gut and environmental resistome in a community in northern Vietnam in relation to antibiotic use
title_full An exploration of the gut and environmental resistome in a community in northern Vietnam in relation to antibiotic use
title_fullStr An exploration of the gut and environmental resistome in a community in northern Vietnam in relation to antibiotic use
title_full_unstemmed An exploration of the gut and environmental resistome in a community in northern Vietnam in relation to antibiotic use
title_short An exploration of the gut and environmental resistome in a community in northern Vietnam in relation to antibiotic use
title_sort exploration of the gut and environmental resistome in a community in northern vietnam in relation to antibiotic use
topic Research
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6883630/
https://www.ncbi.nlm.nih.gov/pubmed/31798840
http://dx.doi.org/10.1186/s13756-019-0645-9
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