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Differential carbon utilization enables co-existence of recently speciated Campylobacteraceae in the cow rumen epithelial microbiome
The activities of different microbes in the cow rumen have been shown to modulate the host’s ability to utilize plant biomass, while the host–rumen interface has received little attention. As datasets collected worldwide have pointed to Campylobacteraceae as particularly abundant members of the rume...
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/PMC9894753/ https://www.ncbi.nlm.nih.gov/pubmed/36635570 http://dx.doi.org/10.1038/s41564-022-01300-y |
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author | Strachan, Cameron R. Yu, Xiaoqian A. Neubauer, Viktoria Mueller, Anna J. Wagner, Martin Zebeli, Qendrim Selberherr, Evelyne Polz, Martin F. |
author_facet | Strachan, Cameron R. Yu, Xiaoqian A. Neubauer, Viktoria Mueller, Anna J. Wagner, Martin Zebeli, Qendrim Selberherr, Evelyne Polz, Martin F. |
author_sort | Strachan, Cameron R. |
collection | PubMed |
description | The activities of different microbes in the cow rumen have been shown to modulate the host’s ability to utilize plant biomass, while the host–rumen interface has received little attention. As datasets collected worldwide have pointed to Campylobacteraceae as particularly abundant members of the rumen epithelial microbiome, we targeted this group in a subset of seven cows with meta- and isolate genome analysis. We show that the dominant Campylobacteraceae lineage has recently speciated into two populations that were structured by genome-wide selective sweeps followed by population-specific gene import and recombination. These processes led to differences in gene expression and enzyme domain composition that correspond to the ability to utilize acetate, the main carbon source for the host, at the cost of inhibition by propionate. This trade-off in competitive ability further manifests itself in differential dynamics of the two populations in vivo. By exploring population-level adaptations that otherwise remain cryptic in culture-independent analyses, our results highlight how recent evolutionary dynamics can shape key functional roles in the rumen microbiome. |
format | Online Article Text |
id | pubmed-9894753 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2023 |
publisher | Nature Publishing Group UK |
record_format | MEDLINE/PubMed |
spelling | pubmed-98947532023-02-04 Differential carbon utilization enables co-existence of recently speciated Campylobacteraceae in the cow rumen epithelial microbiome Strachan, Cameron R. Yu, Xiaoqian A. Neubauer, Viktoria Mueller, Anna J. Wagner, Martin Zebeli, Qendrim Selberherr, Evelyne Polz, Martin F. Nat Microbiol Article The activities of different microbes in the cow rumen have been shown to modulate the host’s ability to utilize plant biomass, while the host–rumen interface has received little attention. As datasets collected worldwide have pointed to Campylobacteraceae as particularly abundant members of the rumen epithelial microbiome, we targeted this group in a subset of seven cows with meta- and isolate genome analysis. We show that the dominant Campylobacteraceae lineage has recently speciated into two populations that were structured by genome-wide selective sweeps followed by population-specific gene import and recombination. These processes led to differences in gene expression and enzyme domain composition that correspond to the ability to utilize acetate, the main carbon source for the host, at the cost of inhibition by propionate. This trade-off in competitive ability further manifests itself in differential dynamics of the two populations in vivo. By exploring population-level adaptations that otherwise remain cryptic in culture-independent analyses, our results highlight how recent evolutionary dynamics can shape key functional roles in the rumen microbiome. Nature Publishing Group UK 2023-01-12 2023 /pmc/articles/PMC9894753/ /pubmed/36635570 http://dx.doi.org/10.1038/s41564-022-01300-y 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 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 Strachan, Cameron R. Yu, Xiaoqian A. Neubauer, Viktoria Mueller, Anna J. Wagner, Martin Zebeli, Qendrim Selberherr, Evelyne Polz, Martin F. Differential carbon utilization enables co-existence of recently speciated Campylobacteraceae in the cow rumen epithelial microbiome |
title | Differential carbon utilization enables co-existence of recently speciated Campylobacteraceae in the cow rumen epithelial microbiome |
title_full | Differential carbon utilization enables co-existence of recently speciated Campylobacteraceae in the cow rumen epithelial microbiome |
title_fullStr | Differential carbon utilization enables co-existence of recently speciated Campylobacteraceae in the cow rumen epithelial microbiome |
title_full_unstemmed | Differential carbon utilization enables co-existence of recently speciated Campylobacteraceae in the cow rumen epithelial microbiome |
title_short | Differential carbon utilization enables co-existence of recently speciated Campylobacteraceae in the cow rumen epithelial microbiome |
title_sort | differential carbon utilization enables co-existence of recently speciated campylobacteraceae in the cow rumen epithelial microbiome |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9894753/ https://www.ncbi.nlm.nih.gov/pubmed/36635570 http://dx.doi.org/10.1038/s41564-022-01300-y |
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