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Expressions of resistome is linked to the key functions and stability of active rumen microbiome
BACKGROUND: The resistome describes the array of antibiotic resistant genes (ARGs) present within a microbial community. Recent research has documented the resistome in the rumen of ruminants and revealed that the type and abundance of ARGs could be affected by diet and/or antibiotic treatment. Howe...
Autores principales: | , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
BioMed Central
2022
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9167530/ https://www.ncbi.nlm.nih.gov/pubmed/35659381 http://dx.doi.org/10.1186/s42523-022-00189-6 |
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author | Ma, Tao Zaheer, Rahat McAllister, Tim A. Guo, Wei Li, Fuyong Tu, Yan Diao, Qiyu Guan, Le Luo |
author_facet | Ma, Tao Zaheer, Rahat McAllister, Tim A. Guo, Wei Li, Fuyong Tu, Yan Diao, Qiyu Guan, Le Luo |
author_sort | Ma, Tao |
collection | PubMed |
description | BACKGROUND: The resistome describes the array of antibiotic resistant genes (ARGs) present within a microbial community. Recent research has documented the resistome in the rumen of ruminants and revealed that the type and abundance of ARGs could be affected by diet and/or antibiotic treatment. However, most of these studies only assessed ARGs using metagenomics, and expression of the resistome and its biological function within the microbiome remains largely unexplored. RESULTS: We characterized the pools of ARGs (resistome) and their activities in the rumen of 48 beef cattle belonging to three breeds (Angus, Charolais, Kinsella composite hybrid), using shotgun metagenomics and metatranscriptomics. Sixty (including 20 plasmid-associated) ARGs were expressed which accounted for about 30% of the total number of ARGs (187) identified in metagenomic datasets, with tetW and mefA exhibiting the highest level of expression. In addition, the bacterial hosts of 17 expressed ARGs were identified. The active resistome was less diverse in Kinsella composite hybrid than Angus, however, expression of ARGs did not differ among breeds. Although not associated with feed efficiency, the total abundance of expressed ARGs was positively correlated with metabolic pathways and ‘attenuation values’ (a measurement of stability) of the active rumen microbiome, suggesting that ARGs expression influences the stability and functionality of the rumen microbiome. Moreover, Ruminococcus spp., Prevotella ruminicola, Muribaculaceae spp. and Collinsella aerofaciens were all identified as hosts of expressed ARGs, possibly promoting the dominance of these carbohydrate degraders within the rumen microbiome. CONCLUSIONS: Findings from this study provide new insight into the active rumen resistome in vivo, which may inform strategies to limit the spread of ubiquitously found ARGs from the rumen to the broader environment without negatively impacting the key functional outcomes of the rumen microbiome. SUPPLEMENTARY INFORMATION: The online version contains supplementary material available at 10.1186/s42523-022-00189-6. |
format | Online Article Text |
id | pubmed-9167530 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2022 |
publisher | BioMed Central |
record_format | MEDLINE/PubMed |
spelling | pubmed-91675302022-06-06 Expressions of resistome is linked to the key functions and stability of active rumen microbiome Ma, Tao Zaheer, Rahat McAllister, Tim A. Guo, Wei Li, Fuyong Tu, Yan Diao, Qiyu Guan, Le Luo Anim Microbiome Research Article BACKGROUND: The resistome describes the array of antibiotic resistant genes (ARGs) present within a microbial community. Recent research has documented the resistome in the rumen of ruminants and revealed that the type and abundance of ARGs could be affected by diet and/or antibiotic treatment. However, most of these studies only assessed ARGs using metagenomics, and expression of the resistome and its biological function within the microbiome remains largely unexplored. RESULTS: We characterized the pools of ARGs (resistome) and their activities in the rumen of 48 beef cattle belonging to three breeds (Angus, Charolais, Kinsella composite hybrid), using shotgun metagenomics and metatranscriptomics. Sixty (including 20 plasmid-associated) ARGs were expressed which accounted for about 30% of the total number of ARGs (187) identified in metagenomic datasets, with tetW and mefA exhibiting the highest level of expression. In addition, the bacterial hosts of 17 expressed ARGs were identified. The active resistome was less diverse in Kinsella composite hybrid than Angus, however, expression of ARGs did not differ among breeds. Although not associated with feed efficiency, the total abundance of expressed ARGs was positively correlated with metabolic pathways and ‘attenuation values’ (a measurement of stability) of the active rumen microbiome, suggesting that ARGs expression influences the stability and functionality of the rumen microbiome. Moreover, Ruminococcus spp., Prevotella ruminicola, Muribaculaceae spp. and Collinsella aerofaciens were all identified as hosts of expressed ARGs, possibly promoting the dominance of these carbohydrate degraders within the rumen microbiome. CONCLUSIONS: Findings from this study provide new insight into the active rumen resistome in vivo, which may inform strategies to limit the spread of ubiquitously found ARGs from the rumen to the broader environment without negatively impacting the key functional outcomes of the rumen microbiome. SUPPLEMENTARY INFORMATION: The online version contains supplementary material available at 10.1186/s42523-022-00189-6. BioMed Central 2022-06-04 /pmc/articles/PMC9167530/ /pubmed/35659381 http://dx.doi.org/10.1186/s42523-022-00189-6 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/) . |
spellingShingle | Research Article Ma, Tao Zaheer, Rahat McAllister, Tim A. Guo, Wei Li, Fuyong Tu, Yan Diao, Qiyu Guan, Le Luo Expressions of resistome is linked to the key functions and stability of active rumen microbiome |
title | Expressions of resistome is linked to the key functions and stability of active rumen microbiome |
title_full | Expressions of resistome is linked to the key functions and stability of active rumen microbiome |
title_fullStr | Expressions of resistome is linked to the key functions and stability of active rumen microbiome |
title_full_unstemmed | Expressions of resistome is linked to the key functions and stability of active rumen microbiome |
title_short | Expressions of resistome is linked to the key functions and stability of active rumen microbiome |
title_sort | expressions of resistome is linked to the key functions and stability of active rumen microbiome |
topic | Research Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9167530/ https://www.ncbi.nlm.nih.gov/pubmed/35659381 http://dx.doi.org/10.1186/s42523-022-00189-6 |
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