Cargando…

Dissecting microbial communities and resistomes for interconnected humans, soil, and livestock

A debate is currently ongoing as to whether intensive livestock farms may constitute reservoirs of clinically relevant antimicrobial resistance (AMR), thus posing a threat to surrounding communities. Here, combining shotgun metagenome sequencing, machine learning (ML), and culture-based methods, we...

Descripción completa

Detalles Bibliográficos
Autores principales: Maciel-Guerra, Alexandre, Baker, Michelle, Hu, Yue, Wang, Wei, Zhang, Xibin, Rong, Jia, Zhang, Yimin, Zhang, Jing, Kaler, Jasmeet, Renney, David, Loose, Matthew, Emes, Richard D., Liu, Longhai, Chen, Junshi, Peng, Zixin, Li, Fengqin, Dottorini, Tania
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Nature Publishing Group UK 2022
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9751072/
https://www.ncbi.nlm.nih.gov/pubmed/36151458
http://dx.doi.org/10.1038/s41396-022-01315-7
_version_ 1784850394522845184
author Maciel-Guerra, Alexandre
Baker, Michelle
Hu, Yue
Wang, Wei
Zhang, Xibin
Rong, Jia
Zhang, Yimin
Zhang, Jing
Kaler, Jasmeet
Renney, David
Loose, Matthew
Emes, Richard D.
Liu, Longhai
Chen, Junshi
Peng, Zixin
Li, Fengqin
Dottorini, Tania
author_facet Maciel-Guerra, Alexandre
Baker, Michelle
Hu, Yue
Wang, Wei
Zhang, Xibin
Rong, Jia
Zhang, Yimin
Zhang, Jing
Kaler, Jasmeet
Renney, David
Loose, Matthew
Emes, Richard D.
Liu, Longhai
Chen, Junshi
Peng, Zixin
Li, Fengqin
Dottorini, Tania
author_sort Maciel-Guerra, Alexandre
collection PubMed
description A debate is currently ongoing as to whether intensive livestock farms may constitute reservoirs of clinically relevant antimicrobial resistance (AMR), thus posing a threat to surrounding communities. Here, combining shotgun metagenome sequencing, machine learning (ML), and culture-based methods, we focused on a poultry farm and connected slaughterhouse in China, investigating the gut microbiome of livestock, workers and their households, and microbial communities in carcasses and soil. For both the microbiome and resistomes in this study, differences are observed across environments and hosts. However, at a finer scale, several similar clinically relevant antimicrobial resistance genes (ARGs) and similar associated mobile genetic elements were found in both human and broiler chicken samples. Next, we focused on Escherichia coli, an important indicator for the surveillance of AMR on the farm. Strains of E. coli were found intermixed between humans and chickens. We observed that several ARGs present in the chicken faecal resistome showed correlation to resistance/susceptibility profiles of E. coli isolates cultured from the same samples. Finally, by using environmental sensing these ARGs were found to be correlated to variations in environmental temperature and humidity. Our results show the importance of adopting a multi-domain and multi-scale approach when studying microbial communities and AMR in complex, interconnected environments.
format Online
Article
Text
id pubmed-9751072
institution National Center for Biotechnology Information
language English
publishDate 2022
publisher Nature Publishing Group UK
record_format MEDLINE/PubMed
spelling pubmed-97510722022-12-16 Dissecting microbial communities and resistomes for interconnected humans, soil, and livestock Maciel-Guerra, Alexandre Baker, Michelle Hu, Yue Wang, Wei Zhang, Xibin Rong, Jia Zhang, Yimin Zhang, Jing Kaler, Jasmeet Renney, David Loose, Matthew Emes, Richard D. Liu, Longhai Chen, Junshi Peng, Zixin Li, Fengqin Dottorini, Tania ISME J Article A debate is currently ongoing as to whether intensive livestock farms may constitute reservoirs of clinically relevant antimicrobial resistance (AMR), thus posing a threat to surrounding communities. Here, combining shotgun metagenome sequencing, machine learning (ML), and culture-based methods, we focused on a poultry farm and connected slaughterhouse in China, investigating the gut microbiome of livestock, workers and their households, and microbial communities in carcasses and soil. For both the microbiome and resistomes in this study, differences are observed across environments and hosts. However, at a finer scale, several similar clinically relevant antimicrobial resistance genes (ARGs) and similar associated mobile genetic elements were found in both human and broiler chicken samples. Next, we focused on Escherichia coli, an important indicator for the surveillance of AMR on the farm. Strains of E. coli were found intermixed between humans and chickens. We observed that several ARGs present in the chicken faecal resistome showed correlation to resistance/susceptibility profiles of E. coli isolates cultured from the same samples. Finally, by using environmental sensing these ARGs were found to be correlated to variations in environmental temperature and humidity. Our results show the importance of adopting a multi-domain and multi-scale approach when studying microbial communities and AMR in complex, interconnected environments. Nature Publishing Group UK 2022-09-23 2023-01 /pmc/articles/PMC9751072/ /pubmed/36151458 http://dx.doi.org/10.1038/s41396-022-01315-7 Text en © The Author(s) 2022 https://creativecommons.org/licenses/by/4.0/Open Access This 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 license, and indicate if changes were made. The images or other third party material in this article are included in the article’s Creative Commons license, unless indicated otherwise in a credit line to the material. If material is not included in the article’s Creative Commons license 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 license, visit http://creativecommons.org/licenses/by/4.0/ (https://creativecommons.org/licenses/by/4.0/) .
spellingShingle Article
Maciel-Guerra, Alexandre
Baker, Michelle
Hu, Yue
Wang, Wei
Zhang, Xibin
Rong, Jia
Zhang, Yimin
Zhang, Jing
Kaler, Jasmeet
Renney, David
Loose, Matthew
Emes, Richard D.
Liu, Longhai
Chen, Junshi
Peng, Zixin
Li, Fengqin
Dottorini, Tania
Dissecting microbial communities and resistomes for interconnected humans, soil, and livestock
title Dissecting microbial communities and resistomes for interconnected humans, soil, and livestock
title_full Dissecting microbial communities and resistomes for interconnected humans, soil, and livestock
title_fullStr Dissecting microbial communities and resistomes for interconnected humans, soil, and livestock
title_full_unstemmed Dissecting microbial communities and resistomes for interconnected humans, soil, and livestock
title_short Dissecting microbial communities and resistomes for interconnected humans, soil, and livestock
title_sort dissecting microbial communities and resistomes for interconnected humans, soil, and livestock
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9751072/
https://www.ncbi.nlm.nih.gov/pubmed/36151458
http://dx.doi.org/10.1038/s41396-022-01315-7
work_keys_str_mv AT macielguerraalexandre dissectingmicrobialcommunitiesandresistomesforinterconnectedhumanssoilandlivestock
AT bakermichelle dissectingmicrobialcommunitiesandresistomesforinterconnectedhumanssoilandlivestock
AT huyue dissectingmicrobialcommunitiesandresistomesforinterconnectedhumanssoilandlivestock
AT wangwei dissectingmicrobialcommunitiesandresistomesforinterconnectedhumanssoilandlivestock
AT zhangxibin dissectingmicrobialcommunitiesandresistomesforinterconnectedhumanssoilandlivestock
AT rongjia dissectingmicrobialcommunitiesandresistomesforinterconnectedhumanssoilandlivestock
AT zhangyimin dissectingmicrobialcommunitiesandresistomesforinterconnectedhumanssoilandlivestock
AT zhangjing dissectingmicrobialcommunitiesandresistomesforinterconnectedhumanssoilandlivestock
AT kalerjasmeet dissectingmicrobialcommunitiesandresistomesforinterconnectedhumanssoilandlivestock
AT renneydavid dissectingmicrobialcommunitiesandresistomesforinterconnectedhumanssoilandlivestock
AT loosematthew dissectingmicrobialcommunitiesandresistomesforinterconnectedhumanssoilandlivestock
AT emesrichardd dissectingmicrobialcommunitiesandresistomesforinterconnectedhumanssoilandlivestock
AT liulonghai dissectingmicrobialcommunitiesandresistomesforinterconnectedhumanssoilandlivestock
AT chenjunshi dissectingmicrobialcommunitiesandresistomesforinterconnectedhumanssoilandlivestock
AT pengzixin dissectingmicrobialcommunitiesandresistomesforinterconnectedhumanssoilandlivestock
AT lifengqin dissectingmicrobialcommunitiesandresistomesforinterconnectedhumanssoilandlivestock
AT dottorinitania dissectingmicrobialcommunitiesandresistomesforinterconnectedhumanssoilandlivestock