Cargando…
Longitudinal metagenomic study reveals the dynamics of fecal antibiotic resistome in pigs throughout the lifetime
BACKGROUND: The dissemination of antibiotic resistance genes (ARGs) poses a substantial threat to environmental safety and human health. Herein, we present a longitudinal paired study across the swine lifetime from birth to market, coupled with metagenomic sequencing to explore the dynamics of ARGs...
Autores principales: | , , , , , , , , |
---|---|
Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
BioMed Central
2023
|
Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10634126/ https://www.ncbi.nlm.nih.gov/pubmed/37941060 http://dx.doi.org/10.1186/s42523-023-00279-z |
_version_ | 1785132765180592128 |
---|---|
author | Ma, Lingyan Song, Yuanyuan Lyu, Wentao Chen, Qu Xiao, Xingning Jin, Yuanxiang Yang, Hua Wang, Wen Xiao, Yingping |
author_facet | Ma, Lingyan Song, Yuanyuan Lyu, Wentao Chen, Qu Xiao, Xingning Jin, Yuanxiang Yang, Hua Wang, Wen Xiao, Yingping |
author_sort | Ma, Lingyan |
collection | PubMed |
description | BACKGROUND: The dissemination of antibiotic resistance genes (ARGs) poses a substantial threat to environmental safety and human health. Herein, we present a longitudinal paired study across the swine lifetime from birth to market, coupled with metagenomic sequencing to explore the dynamics of ARGs and their health risk in the swine fecal microbiome. RESULTS: We systematically characterized the composition and distribution of ARGs among the different growth stages. In total, 829 ARG subtypes belonging to 21 different ARG types were detected, in which tetracycline, aminoglycoside, and MLS were the most abundant types. Indeed, 134 core ARG subtypes were shared in all stages and displayed a growth stage-associated pattern. Furthermore, the correlation between ARGs, gut microbiota and mobile genetic elements (MGEs) revealed Escherichia coli represented the main carrier of ARGs. We also found that in most cases, the dominant ARGs could be transmitted to progeny piglets, suggesting the potential ARGs generation transmission. Finally, the evaluation of the antibiotic resistance threats provides us some early warning of those high health risk ARGs. CONCLUSIONS: Collectively, this relatively more comprehensive study provides a primary overview of ARG profile in swine microbiome across the lifetime and highlights the health risk and the intergenerational spread of ARGs in pig farm. GRAPHICAL ABSTRACT: [Image: see text] SUPPLEMENTARY INFORMATION: The online version contains supplementary material available at 10.1186/s42523-023-00279-z. |
format | Online Article Text |
id | pubmed-10634126 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2023 |
publisher | BioMed Central |
record_format | MEDLINE/PubMed |
spelling | pubmed-106341262023-11-10 Longitudinal metagenomic study reveals the dynamics of fecal antibiotic resistome in pigs throughout the lifetime Ma, Lingyan Song, Yuanyuan Lyu, Wentao Chen, Qu Xiao, Xingning Jin, Yuanxiang Yang, Hua Wang, Wen Xiao, Yingping Anim Microbiome Research BACKGROUND: The dissemination of antibiotic resistance genes (ARGs) poses a substantial threat to environmental safety and human health. Herein, we present a longitudinal paired study across the swine lifetime from birth to market, coupled with metagenomic sequencing to explore the dynamics of ARGs and their health risk in the swine fecal microbiome. RESULTS: We systematically characterized the composition and distribution of ARGs among the different growth stages. In total, 829 ARG subtypes belonging to 21 different ARG types were detected, in which tetracycline, aminoglycoside, and MLS were the most abundant types. Indeed, 134 core ARG subtypes were shared in all stages and displayed a growth stage-associated pattern. Furthermore, the correlation between ARGs, gut microbiota and mobile genetic elements (MGEs) revealed Escherichia coli represented the main carrier of ARGs. We also found that in most cases, the dominant ARGs could be transmitted to progeny piglets, suggesting the potential ARGs generation transmission. Finally, the evaluation of the antibiotic resistance threats provides us some early warning of those high health risk ARGs. CONCLUSIONS: Collectively, this relatively more comprehensive study provides a primary overview of ARG profile in swine microbiome across the lifetime and highlights the health risk and the intergenerational spread of ARGs in pig farm. GRAPHICAL ABSTRACT: [Image: see text] SUPPLEMENTARY INFORMATION: The online version contains supplementary material available at 10.1186/s42523-023-00279-z. BioMed Central 2023-11-08 /pmc/articles/PMC10634126/ /pubmed/37941060 http://dx.doi.org/10.1186/s42523-023-00279-z Text en © The Author(s) 2023 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 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/) . |
spellingShingle | Research Ma, Lingyan Song, Yuanyuan Lyu, Wentao Chen, Qu Xiao, Xingning Jin, Yuanxiang Yang, Hua Wang, Wen Xiao, Yingping Longitudinal metagenomic study reveals the dynamics of fecal antibiotic resistome in pigs throughout the lifetime |
title | Longitudinal metagenomic study reveals the dynamics of fecal antibiotic resistome in pigs throughout the lifetime |
title_full | Longitudinal metagenomic study reveals the dynamics of fecal antibiotic resistome in pigs throughout the lifetime |
title_fullStr | Longitudinal metagenomic study reveals the dynamics of fecal antibiotic resistome in pigs throughout the lifetime |
title_full_unstemmed | Longitudinal metagenomic study reveals the dynamics of fecal antibiotic resistome in pigs throughout the lifetime |
title_short | Longitudinal metagenomic study reveals the dynamics of fecal antibiotic resistome in pigs throughout the lifetime |
title_sort | longitudinal metagenomic study reveals the dynamics of fecal antibiotic resistome in pigs throughout the lifetime |
topic | Research |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10634126/ https://www.ncbi.nlm.nih.gov/pubmed/37941060 http://dx.doi.org/10.1186/s42523-023-00279-z |
work_keys_str_mv | AT malingyan longitudinalmetagenomicstudyrevealsthedynamicsoffecalantibioticresistomeinpigsthroughoutthelifetime AT songyuanyuan longitudinalmetagenomicstudyrevealsthedynamicsoffecalantibioticresistomeinpigsthroughoutthelifetime AT lyuwentao longitudinalmetagenomicstudyrevealsthedynamicsoffecalantibioticresistomeinpigsthroughoutthelifetime AT chenqu longitudinalmetagenomicstudyrevealsthedynamicsoffecalantibioticresistomeinpigsthroughoutthelifetime AT xiaoxingning longitudinalmetagenomicstudyrevealsthedynamicsoffecalantibioticresistomeinpigsthroughoutthelifetime AT jinyuanxiang longitudinalmetagenomicstudyrevealsthedynamicsoffecalantibioticresistomeinpigsthroughoutthelifetime AT yanghua longitudinalmetagenomicstudyrevealsthedynamicsoffecalantibioticresistomeinpigsthroughoutthelifetime AT wangwen longitudinalmetagenomicstudyrevealsthedynamicsoffecalantibioticresistomeinpigsthroughoutthelifetime AT xiaoyingping longitudinalmetagenomicstudyrevealsthedynamicsoffecalantibioticresistomeinpigsthroughoutthelifetime |