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Characterization of the pig lower respiratory tract antibiotic resistome
Respiratory diseases and its treatments are highly concerned in both the pig industry and human health. However, the composition and distribution of antibiotic resistance genes (ARGs) in swine lower respiratory tract microbiome remain unknown. The relationships of ARGs with mobile genetic elements (...
Autores principales: | , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Nature Publishing Group UK
2023
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10423206/ https://www.ncbi.nlm.nih.gov/pubmed/37573429 http://dx.doi.org/10.1038/s41467-023-40587-1 |
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author | Zhou, Yunyan Li, Jingquan Huang, Fei Ai, Huashui Gao, Jun Chen, Congying Huang, Lusheng |
author_facet | Zhou, Yunyan Li, Jingquan Huang, Fei Ai, Huashui Gao, Jun Chen, Congying Huang, Lusheng |
author_sort | Zhou, Yunyan |
collection | PubMed |
description | Respiratory diseases and its treatments are highly concerned in both the pig industry and human health. However, the composition and distribution of antibiotic resistance genes (ARGs) in swine lower respiratory tract microbiome remain unknown. The relationships of ARGs with mobile genetic elements (MGEs) and lung health are unclear. Here, we characterize antibiotic resistomes of the swine lower respiratory tract microbiome containing 1228 open reading frames belonging to 372 ARGs using 745 metagenomes from 675 experimental pigs. Twelve ARGs conferring resistance to tetracycline are related to an MGE Tn916 family, and multiple types of ARGs are related to a transposase gene tnpA. Most of the linkage complexes between ARGs and MGEs (the Tn916 family and tnpA) are also observed in pig gut microbiomes and human lung microbiomes, suggesting the high risk of these MGEs mediating ARG transfer to both human and pig health. Gammaproteobacteria are the major ARG carriers, within which Escherichia coli harbored >50 ARGs and >10 MGEs. Although the microbial compositions structure the compositions of ARGs, we identify 73 ARGs whose relative abundances are significantly associated with the severity of lung lesions. Our results provide the first overview of ARG profiles in the swine lower respiratory tract microbiome. |
format | Online Article Text |
id | pubmed-10423206 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2023 |
publisher | Nature Publishing Group UK |
record_format | MEDLINE/PubMed |
spelling | pubmed-104232062023-08-14 Characterization of the pig lower respiratory tract antibiotic resistome Zhou, Yunyan Li, Jingquan Huang, Fei Ai, Huashui Gao, Jun Chen, Congying Huang, Lusheng Nat Commun Article Respiratory diseases and its treatments are highly concerned in both the pig industry and human health. However, the composition and distribution of antibiotic resistance genes (ARGs) in swine lower respiratory tract microbiome remain unknown. The relationships of ARGs with mobile genetic elements (MGEs) and lung health are unclear. Here, we characterize antibiotic resistomes of the swine lower respiratory tract microbiome containing 1228 open reading frames belonging to 372 ARGs using 745 metagenomes from 675 experimental pigs. Twelve ARGs conferring resistance to tetracycline are related to an MGE Tn916 family, and multiple types of ARGs are related to a transposase gene tnpA. Most of the linkage complexes between ARGs and MGEs (the Tn916 family and tnpA) are also observed in pig gut microbiomes and human lung microbiomes, suggesting the high risk of these MGEs mediating ARG transfer to both human and pig health. Gammaproteobacteria are the major ARG carriers, within which Escherichia coli harbored >50 ARGs and >10 MGEs. Although the microbial compositions structure the compositions of ARGs, we identify 73 ARGs whose relative abundances are significantly associated with the severity of lung lesions. Our results provide the first overview of ARG profiles in the swine lower respiratory tract microbiome. Nature Publishing Group UK 2023-08-12 /pmc/articles/PMC10423206/ /pubmed/37573429 http://dx.doi.org/10.1038/s41467-023-40587-1 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 | Article Zhou, Yunyan Li, Jingquan Huang, Fei Ai, Huashui Gao, Jun Chen, Congying Huang, Lusheng Characterization of the pig lower respiratory tract antibiotic resistome |
title | Characterization of the pig lower respiratory tract antibiotic resistome |
title_full | Characterization of the pig lower respiratory tract antibiotic resistome |
title_fullStr | Characterization of the pig lower respiratory tract antibiotic resistome |
title_full_unstemmed | Characterization of the pig lower respiratory tract antibiotic resistome |
title_short | Characterization of the pig lower respiratory tract antibiotic resistome |
title_sort | characterization of the pig lower respiratory tract antibiotic resistome |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10423206/ https://www.ncbi.nlm.nih.gov/pubmed/37573429 http://dx.doi.org/10.1038/s41467-023-40587-1 |
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