Cargando…

The predictive power of phylogeny on growth rates in soil bacterial communities

Predicting ecosystem function is critical to assess and mitigate the impacts of climate change. Quantitative predictions of microbially mediated ecosystem processes are typically uninformed by microbial biodiversity. Yet new tools allow the measurement of taxon-specific traits within natural microbi...

Descripción completa

Detalles Bibliográficos
Autores principales: Walkup, Jeth, Dang, Chansotheary, Mau, Rebecca L., Hayer, Michaela, Schwartz, Egbert, Stone, Bram W., Hofmockel, Kirsten S., Koch, Benjamin J., Purcell, Alicia M., Pett-Ridge, Jennifer, Wang, Chao, Hungate, Bruce A., Morrissey, Ember M.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Nature Publishing Group UK 2023
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10349831/
https://www.ncbi.nlm.nih.gov/pubmed/37454187
http://dx.doi.org/10.1038/s43705-023-00281-1
_version_ 1785074009148227584
author Walkup, Jeth
Dang, Chansotheary
Mau, Rebecca L.
Hayer, Michaela
Schwartz, Egbert
Stone, Bram W.
Hofmockel, Kirsten S.
Koch, Benjamin J.
Purcell, Alicia M.
Pett-Ridge, Jennifer
Wang, Chao
Hungate, Bruce A.
Morrissey, Ember M.
author_facet Walkup, Jeth
Dang, Chansotheary
Mau, Rebecca L.
Hayer, Michaela
Schwartz, Egbert
Stone, Bram W.
Hofmockel, Kirsten S.
Koch, Benjamin J.
Purcell, Alicia M.
Pett-Ridge, Jennifer
Wang, Chao
Hungate, Bruce A.
Morrissey, Ember M.
author_sort Walkup, Jeth
collection PubMed
description Predicting ecosystem function is critical to assess and mitigate the impacts of climate change. Quantitative predictions of microbially mediated ecosystem processes are typically uninformed by microbial biodiversity. Yet new tools allow the measurement of taxon-specific traits within natural microbial communities. There is mounting evidence of a phylogenetic signal in these traits, which may support prediction and microbiome management frameworks. We investigated phylogeny-based trait prediction using bacterial growth rates from soil communities in Arctic, boreal, temperate, and tropical ecosystems. Here we show that phylogeny predicts growth rates of soil bacteria, explaining an average of 31%, and up to 58%, of the variation within ecosystems. Despite limited overlap in community composition across these ecosystems, shared nodes in the phylogeny enabled ancestral trait reconstruction and cross-ecosystem predictions. Phylogenetic relationships could explain up to 38% (averaging 14%) of the variation in growth rates across the highly disparate ecosystems studied. Our results suggest that shared evolutionary history contributes to similarity in the relative growth rates of related bacteria in the wild, allowing phylogeny-based predictions to explain a substantial amount of the variation in taxon-specific functional traits, within and across ecosystems.
format Online
Article
Text
id pubmed-10349831
institution National Center for Biotechnology Information
language English
publishDate 2023
publisher Nature Publishing Group UK
record_format MEDLINE/PubMed
spelling pubmed-103498312023-07-17 The predictive power of phylogeny on growth rates in soil bacterial communities Walkup, Jeth Dang, Chansotheary Mau, Rebecca L. Hayer, Michaela Schwartz, Egbert Stone, Bram W. Hofmockel, Kirsten S. Koch, Benjamin J. Purcell, Alicia M. Pett-Ridge, Jennifer Wang, Chao Hungate, Bruce A. Morrissey, Ember M. ISME Commun Article Predicting ecosystem function is critical to assess and mitigate the impacts of climate change. Quantitative predictions of microbially mediated ecosystem processes are typically uninformed by microbial biodiversity. Yet new tools allow the measurement of taxon-specific traits within natural microbial communities. There is mounting evidence of a phylogenetic signal in these traits, which may support prediction and microbiome management frameworks. We investigated phylogeny-based trait prediction using bacterial growth rates from soil communities in Arctic, boreal, temperate, and tropical ecosystems. Here we show that phylogeny predicts growth rates of soil bacteria, explaining an average of 31%, and up to 58%, of the variation within ecosystems. Despite limited overlap in community composition across these ecosystems, shared nodes in the phylogeny enabled ancestral trait reconstruction and cross-ecosystem predictions. Phylogenetic relationships could explain up to 38% (averaging 14%) of the variation in growth rates across the highly disparate ecosystems studied. Our results suggest that shared evolutionary history contributes to similarity in the relative growth rates of related bacteria in the wild, allowing phylogeny-based predictions to explain a substantial amount of the variation in taxon-specific functional traits, within and across ecosystems. Nature Publishing Group UK 2023-07-15 /pmc/articles/PMC10349831/ /pubmed/37454187 http://dx.doi.org/10.1038/s43705-023-00281-1 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 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
Walkup, Jeth
Dang, Chansotheary
Mau, Rebecca L.
Hayer, Michaela
Schwartz, Egbert
Stone, Bram W.
Hofmockel, Kirsten S.
Koch, Benjamin J.
Purcell, Alicia M.
Pett-Ridge, Jennifer
Wang, Chao
Hungate, Bruce A.
Morrissey, Ember M.
The predictive power of phylogeny on growth rates in soil bacterial communities
title The predictive power of phylogeny on growth rates in soil bacterial communities
title_full The predictive power of phylogeny on growth rates in soil bacterial communities
title_fullStr The predictive power of phylogeny on growth rates in soil bacterial communities
title_full_unstemmed The predictive power of phylogeny on growth rates in soil bacterial communities
title_short The predictive power of phylogeny on growth rates in soil bacterial communities
title_sort predictive power of phylogeny on growth rates in soil bacterial communities
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10349831/
https://www.ncbi.nlm.nih.gov/pubmed/37454187
http://dx.doi.org/10.1038/s43705-023-00281-1
work_keys_str_mv AT walkupjeth thepredictivepowerofphylogenyongrowthratesinsoilbacterialcommunities
AT dangchansotheary thepredictivepowerofphylogenyongrowthratesinsoilbacterialcommunities
AT maurebeccal thepredictivepowerofphylogenyongrowthratesinsoilbacterialcommunities
AT hayermichaela thepredictivepowerofphylogenyongrowthratesinsoilbacterialcommunities
AT schwartzegbert thepredictivepowerofphylogenyongrowthratesinsoilbacterialcommunities
AT stonebramw thepredictivepowerofphylogenyongrowthratesinsoilbacterialcommunities
AT hofmockelkirstens thepredictivepowerofphylogenyongrowthratesinsoilbacterialcommunities
AT kochbenjaminj thepredictivepowerofphylogenyongrowthratesinsoilbacterialcommunities
AT purcellaliciam thepredictivepowerofphylogenyongrowthratesinsoilbacterialcommunities
AT pettridgejennifer thepredictivepowerofphylogenyongrowthratesinsoilbacterialcommunities
AT wangchao thepredictivepowerofphylogenyongrowthratesinsoilbacterialcommunities
AT hungatebrucea thepredictivepowerofphylogenyongrowthratesinsoilbacterialcommunities
AT morrisseyemberm thepredictivepowerofphylogenyongrowthratesinsoilbacterialcommunities
AT walkupjeth predictivepowerofphylogenyongrowthratesinsoilbacterialcommunities
AT dangchansotheary predictivepowerofphylogenyongrowthratesinsoilbacterialcommunities
AT maurebeccal predictivepowerofphylogenyongrowthratesinsoilbacterialcommunities
AT hayermichaela predictivepowerofphylogenyongrowthratesinsoilbacterialcommunities
AT schwartzegbert predictivepowerofphylogenyongrowthratesinsoilbacterialcommunities
AT stonebramw predictivepowerofphylogenyongrowthratesinsoilbacterialcommunities
AT hofmockelkirstens predictivepowerofphylogenyongrowthratesinsoilbacterialcommunities
AT kochbenjaminj predictivepowerofphylogenyongrowthratesinsoilbacterialcommunities
AT purcellaliciam predictivepowerofphylogenyongrowthratesinsoilbacterialcommunities
AT pettridgejennifer predictivepowerofphylogenyongrowthratesinsoilbacterialcommunities
AT wangchao predictivepowerofphylogenyongrowthratesinsoilbacterialcommunities
AT hungatebrucea predictivepowerofphylogenyongrowthratesinsoilbacterialcommunities
AT morrisseyemberm predictivepowerofphylogenyongrowthratesinsoilbacterialcommunities