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Divergent functional isoforms drive niche specialisation for nutrient acquisition and use in rumen microbiome

Many microbes in complex competitive environments share genes for acquiring and utilising nutrients, questioning whether niche specialisation exists and if so, how it is maintained. We investigated the genomic signatures of niche specialisation in the rumen microbiome, a highly competitive, anaerobi...

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Autores principales: Rubino, Francesco, Carberry, Ciara, M Waters, Sinéad, Kenny, David, McCabe, Matthew S, Creevey, Christopher J
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Nature Publishing Group 2017
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5364355/
https://www.ncbi.nlm.nih.gov/pubmed/28085156
http://dx.doi.org/10.1038/ismej.2016.172
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author Rubino, Francesco
Carberry, Ciara
M Waters, Sinéad
Kenny, David
McCabe, Matthew S
Creevey, Christopher J
author_facet Rubino, Francesco
Carberry, Ciara
M Waters, Sinéad
Kenny, David
McCabe, Matthew S
Creevey, Christopher J
author_sort Rubino, Francesco
collection PubMed
description Many microbes in complex competitive environments share genes for acquiring and utilising nutrients, questioning whether niche specialisation exists and if so, how it is maintained. We investigated the genomic signatures of niche specialisation in the rumen microbiome, a highly competitive, anaerobic environment, with limited nutrient availability determined by the biomass consumed by the host. We generated individual metagenomic libraries from 14 cows fed an ad libitum diet of grass silage and calculated functional isoform diversity for each microbial gene identified. The animal replicates were used to calculate confidence intervals to test for differences in diversity of functional isoforms between microbes that may drive niche specialisation. We identified 153 genes with significant differences in functional isoform diversity between the two most abundant bacterial genera in the rumen (Prevotella and Clostridium). We found Prevotella possesses a more diverse range of isoforms capable of degrading hemicellulose, whereas Clostridium for cellulose. Furthermore, significant differences were observed in key metabolic processes indicating that isoform diversity plays an important role in maintaining their niche specialisation. The methods presented represent a novel approach for untangling complex interactions between microorganisms in natural environments and have resulted in an expanded catalogue of gene targets central to rumen cellulosic biomass degradation.
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spelling pubmed-53643552017-05-15 Divergent functional isoforms drive niche specialisation for nutrient acquisition and use in rumen microbiome Rubino, Francesco Carberry, Ciara M Waters, Sinéad Kenny, David McCabe, Matthew S Creevey, Christopher J ISME J Original Article Many microbes in complex competitive environments share genes for acquiring and utilising nutrients, questioning whether niche specialisation exists and if so, how it is maintained. We investigated the genomic signatures of niche specialisation in the rumen microbiome, a highly competitive, anaerobic environment, with limited nutrient availability determined by the biomass consumed by the host. We generated individual metagenomic libraries from 14 cows fed an ad libitum diet of grass silage and calculated functional isoform diversity for each microbial gene identified. The animal replicates were used to calculate confidence intervals to test for differences in diversity of functional isoforms between microbes that may drive niche specialisation. We identified 153 genes with significant differences in functional isoform diversity between the two most abundant bacterial genera in the rumen (Prevotella and Clostridium). We found Prevotella possesses a more diverse range of isoforms capable of degrading hemicellulose, whereas Clostridium for cellulose. Furthermore, significant differences were observed in key metabolic processes indicating that isoform diversity plays an important role in maintaining their niche specialisation. The methods presented represent a novel approach for untangling complex interactions between microorganisms in natural environments and have resulted in an expanded catalogue of gene targets central to rumen cellulosic biomass degradation. Nature Publishing Group 2017-04 2017-01-13 /pmc/articles/PMC5364355/ /pubmed/28085156 http://dx.doi.org/10.1038/ismej.2016.172 Text en Copyright © 2017 International Society for Microbial Ecology http://creativecommons.org/licenses/by/4.0/ This work is licensed under a Creative Commons Attribution 4.0 International License. The images or other third party material in this article are included in the article’s Creative Commons license, unless indicated otherwise in the credit line; if the material is not included under the Creative Commons license, users will need to obtain permission from the license holder to reproduce the material. To view a copy of this license, visit http://creativecommons.org/licenses/by/4.0/
spellingShingle Original Article
Rubino, Francesco
Carberry, Ciara
M Waters, Sinéad
Kenny, David
McCabe, Matthew S
Creevey, Christopher J
Divergent functional isoforms drive niche specialisation for nutrient acquisition and use in rumen microbiome
title Divergent functional isoforms drive niche specialisation for nutrient acquisition and use in rumen microbiome
title_full Divergent functional isoforms drive niche specialisation for nutrient acquisition and use in rumen microbiome
title_fullStr Divergent functional isoforms drive niche specialisation for nutrient acquisition and use in rumen microbiome
title_full_unstemmed Divergent functional isoforms drive niche specialisation for nutrient acquisition and use in rumen microbiome
title_short Divergent functional isoforms drive niche specialisation for nutrient acquisition and use in rumen microbiome
title_sort divergent functional isoforms drive niche specialisation for nutrient acquisition and use in rumen microbiome
topic Original Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5364355/
https://www.ncbi.nlm.nih.gov/pubmed/28085156
http://dx.doi.org/10.1038/ismej.2016.172
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