Cargando…

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...

Descripción completa

Detalles Bibliográficos
Autores principales: Strachan, Cameron R., Yu, Xiaoqian A., Neubauer, Viktoria, Mueller, Anna J., Wagner, Martin, Zebeli, Qendrim, Selberherr, Evelyne, Polz, Martin F.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Nature Publishing Group UK 2023
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
_version_ 1784881804695568384
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
work_keys_str_mv AT strachancameronr differentialcarbonutilizationenablescoexistenceofrecentlyspeciatedcampylobacteraceaeinthecowrumenepithelialmicrobiome
AT yuxiaoqiana differentialcarbonutilizationenablescoexistenceofrecentlyspeciatedcampylobacteraceaeinthecowrumenepithelialmicrobiome
AT neubauerviktoria differentialcarbonutilizationenablescoexistenceofrecentlyspeciatedcampylobacteraceaeinthecowrumenepithelialmicrobiome
AT muellerannaj differentialcarbonutilizationenablescoexistenceofrecentlyspeciatedcampylobacteraceaeinthecowrumenepithelialmicrobiome
AT wagnermartin differentialcarbonutilizationenablescoexistenceofrecentlyspeciatedcampylobacteraceaeinthecowrumenepithelialmicrobiome
AT zebeliqendrim differentialcarbonutilizationenablescoexistenceofrecentlyspeciatedcampylobacteraceaeinthecowrumenepithelialmicrobiome
AT selberherrevelyne differentialcarbonutilizationenablescoexistenceofrecentlyspeciatedcampylobacteraceaeinthecowrumenepithelialmicrobiome
AT polzmartinf differentialcarbonutilizationenablescoexistenceofrecentlyspeciatedcampylobacteraceaeinthecowrumenepithelialmicrobiome