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Extensive metagenomic analysis of the porcine gut resistome to identify indicators reflecting antimicrobial resistance

BACKGROUND: Antimicrobial resistance (AMR) has been regarded as a major threat to global health. Pigs are considered an important source of antimicrobial resistance genes (ARGs). However, there is still a lack of large-scale quantitative data on the distribution of ARGs in the pig production industr...

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Autores principales: Zhou, Yunyan, Fu, Hao, Yang, Hui, Wu, Jinyuan, Chen, Zhe, Jiang, Hui, Liu, Min, Liu, Qin, Huang, Lusheng, Gao, Jun, Chen, Congying
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2022
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8895625/
https://www.ncbi.nlm.nih.gov/pubmed/35246246
http://dx.doi.org/10.1186/s40168-022-01241-y
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author Zhou, Yunyan
Fu, Hao
Yang, Hui
Wu, Jinyuan
Chen, Zhe
Jiang, Hui
Liu, Min
Liu, Qin
Huang, Lusheng
Gao, Jun
Chen, Congying
author_facet Zhou, Yunyan
Fu, Hao
Yang, Hui
Wu, Jinyuan
Chen, Zhe
Jiang, Hui
Liu, Min
Liu, Qin
Huang, Lusheng
Gao, Jun
Chen, Congying
author_sort Zhou, Yunyan
collection PubMed
description BACKGROUND: Antimicrobial resistance (AMR) has been regarded as a major threat to global health. Pigs are considered an important source of antimicrobial resistance genes (ARGs). However, there is still a lack of large-scale quantitative data on the distribution of ARGs in the pig production industry. The bacterial species integrated ARGs in the gut microbiome have not been clarified. RESULTS: In the present study, we used deep metagenomic sequencing data of 451 samples from 425 pigs including wild boars, Tibetan pigs, and commercial or cross-bred experimental pigs under different rearing modes, to comprehensively survey the diversity and distribution of ARGs and detect the bacteria integrated in these ARGs. We identified a total of 1295 open reading frames (ORFs) recognized as antimicrobial resistance protein-coding genes. The ORFs were clustered into 349 unique types of ARGs, and these could be further classified into 69 drug resistance classes. Tetracycline resistance was most enriched in pig feces. Pigs raised on commercial farms had a significantly higher AMR level than pigs under semi-free ranging conditions or wild boars. We tracked the changes in the composition of ARGs at different growth stages and gut locations. There were 30 drug resistance classes showing significantly different abundances in pigs between 25 and 240 days of age. The richness of ARGs and 41 drug resistance classes were significantly different between cecum lumen and feces in pigs from commercial farms, but not in wild boars. We identified 24 bacterial species that existed in almost all tested samples (core bacteria) and were integrated 128 ARGs in their genomes. However, only nine ARGs of these 128 ARGs were core ARGs, suggesting that most of the ARGs in these bacterial species might be acquired rather than constitutive. We selected three subsets of ARGs as indicators for evaluating the pollution level of ARGs in samples with high accuracy (r = 0.73~0.89). CONCLUSIONS: This study provides a primary overview of ARG profiles in various farms under different rearing modes, and the data serve as a reference for optimizing the use of antimicrobials and evaluating the risk of pollution by ARGs in pig farms. SUPPLEMENTARY INFORMATION: The online version contains supplementary material available at 10.1186/s40168-022-01241-y.
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spelling pubmed-88956252022-03-10 Extensive metagenomic analysis of the porcine gut resistome to identify indicators reflecting antimicrobial resistance Zhou, Yunyan Fu, Hao Yang, Hui Wu, Jinyuan Chen, Zhe Jiang, Hui Liu, Min Liu, Qin Huang, Lusheng Gao, Jun Chen, Congying Microbiome Research BACKGROUND: Antimicrobial resistance (AMR) has been regarded as a major threat to global health. Pigs are considered an important source of antimicrobial resistance genes (ARGs). However, there is still a lack of large-scale quantitative data on the distribution of ARGs in the pig production industry. The bacterial species integrated ARGs in the gut microbiome have not been clarified. RESULTS: In the present study, we used deep metagenomic sequencing data of 451 samples from 425 pigs including wild boars, Tibetan pigs, and commercial or cross-bred experimental pigs under different rearing modes, to comprehensively survey the diversity and distribution of ARGs and detect the bacteria integrated in these ARGs. We identified a total of 1295 open reading frames (ORFs) recognized as antimicrobial resistance protein-coding genes. The ORFs were clustered into 349 unique types of ARGs, and these could be further classified into 69 drug resistance classes. Tetracycline resistance was most enriched in pig feces. Pigs raised on commercial farms had a significantly higher AMR level than pigs under semi-free ranging conditions or wild boars. We tracked the changes in the composition of ARGs at different growth stages and gut locations. There were 30 drug resistance classes showing significantly different abundances in pigs between 25 and 240 days of age. The richness of ARGs and 41 drug resistance classes were significantly different between cecum lumen and feces in pigs from commercial farms, but not in wild boars. We identified 24 bacterial species that existed in almost all tested samples (core bacteria) and were integrated 128 ARGs in their genomes. However, only nine ARGs of these 128 ARGs were core ARGs, suggesting that most of the ARGs in these bacterial species might be acquired rather than constitutive. We selected three subsets of ARGs as indicators for evaluating the pollution level of ARGs in samples with high accuracy (r = 0.73~0.89). CONCLUSIONS: This study provides a primary overview of ARG profiles in various farms under different rearing modes, and the data serve as a reference for optimizing the use of antimicrobials and evaluating the risk of pollution by ARGs in pig farms. SUPPLEMENTARY INFORMATION: The online version contains supplementary material available at 10.1186/s40168-022-01241-y. BioMed Central 2022-03-04 /pmc/articles/PMC8895625/ /pubmed/35246246 http://dx.doi.org/10.1186/s40168-022-01241-y Text en © The Author(s) 2022 https://creativecommons.org/licenses/by/4.0/Open AccessThis 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/) . The Creative Commons Public Domain Dedication waiver (http://creativecommons.org/publicdomain/zero/1.0/ (https://creativecommons.org/publicdomain/zero/1.0/) ) applies to the data made available in this article, unless otherwise stated in a credit line to the data.
spellingShingle Research
Zhou, Yunyan
Fu, Hao
Yang, Hui
Wu, Jinyuan
Chen, Zhe
Jiang, Hui
Liu, Min
Liu, Qin
Huang, Lusheng
Gao, Jun
Chen, Congying
Extensive metagenomic analysis of the porcine gut resistome to identify indicators reflecting antimicrobial resistance
title Extensive metagenomic analysis of the porcine gut resistome to identify indicators reflecting antimicrobial resistance
title_full Extensive metagenomic analysis of the porcine gut resistome to identify indicators reflecting antimicrobial resistance
title_fullStr Extensive metagenomic analysis of the porcine gut resistome to identify indicators reflecting antimicrobial resistance
title_full_unstemmed Extensive metagenomic analysis of the porcine gut resistome to identify indicators reflecting antimicrobial resistance
title_short Extensive metagenomic analysis of the porcine gut resistome to identify indicators reflecting antimicrobial resistance
title_sort extensive metagenomic analysis of the porcine gut resistome to identify indicators reflecting antimicrobial resistance
topic Research
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8895625/
https://www.ncbi.nlm.nih.gov/pubmed/35246246
http://dx.doi.org/10.1186/s40168-022-01241-y
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