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Rapid decline of adaptation of Pseudomonas fluorescens to soil biotic environment

Interactions between microbes can both constrain and enhance their adaptation to the environment. However, most studies to date have employed simplified microbial communities and environmental conditions. We determined how the presence of a commercial potting compost microbial community affected ada...

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Autores principales: Gómez, Pedro, Hall, Alex R., Paterson, Steve, Buckling, Angus
Formato: Online Artículo Texto
Lenguaje:English
Publicado: The Royal Society 2022
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8905175/
https://www.ncbi.nlm.nih.gov/pubmed/35259940
http://dx.doi.org/10.1098/rsbl.2021.0593
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author Gómez, Pedro
Hall, Alex R.
Paterson, Steve
Buckling, Angus
author_facet Gómez, Pedro
Hall, Alex R.
Paterson, Steve
Buckling, Angus
author_sort Gómez, Pedro
collection PubMed
description Interactions between microbes can both constrain and enhance their adaptation to the environment. However, most studies to date have employed simplified microbial communities and environmental conditions. We determined how the presence of a commercial potting compost microbial community affected adaptation of the soil bacterium Pseudomonas fluorescens SBW25 in potting compost. Pseudomonas fluorescens clones isolated from populations evolved in both the presence and absence of the community showed similar fitness increases when measured in the absence of the community. This suggests the presence of the community did not constrain adaptation. By contrast, fitness measured in the presence of the community increased for community-evolved populations, but decreased below the ancestral state for populations evolved in the absence of the community. This suggests some, but not all, mutations that were beneficial with respect to the abiotic environment were costly in the presence of the community, with the former selected against in the presence of the community. Whole-genome sequencing supports this interpretation: most mutations underpinning fitness changes were clone-specific, suggesting multiple genetic pathways to adaptation. Such extreme mutational effects have not been observed in comparable in vitro studies, suggesting that caution is needed when extrapolating results from simplified in vitro systems to natural contexts.
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spelling pubmed-89051752022-03-15 Rapid decline of adaptation of Pseudomonas fluorescens to soil biotic environment Gómez, Pedro Hall, Alex R. Paterson, Steve Buckling, Angus Biol Lett Population Ecology Interactions between microbes can both constrain and enhance their adaptation to the environment. However, most studies to date have employed simplified microbial communities and environmental conditions. We determined how the presence of a commercial potting compost microbial community affected adaptation of the soil bacterium Pseudomonas fluorescens SBW25 in potting compost. Pseudomonas fluorescens clones isolated from populations evolved in both the presence and absence of the community showed similar fitness increases when measured in the absence of the community. This suggests the presence of the community did not constrain adaptation. By contrast, fitness measured in the presence of the community increased for community-evolved populations, but decreased below the ancestral state for populations evolved in the absence of the community. This suggests some, but not all, mutations that were beneficial with respect to the abiotic environment were costly in the presence of the community, with the former selected against in the presence of the community. Whole-genome sequencing supports this interpretation: most mutations underpinning fitness changes were clone-specific, suggesting multiple genetic pathways to adaptation. Such extreme mutational effects have not been observed in comparable in vitro studies, suggesting that caution is needed when extrapolating results from simplified in vitro systems to natural contexts. The Royal Society 2022-03-09 /pmc/articles/PMC8905175/ /pubmed/35259940 http://dx.doi.org/10.1098/rsbl.2021.0593 Text en © 2022 The Authors. https://creativecommons.org/licenses/by/4.0/Published by the Royal Society under the terms of the Creative Commons Attribution License http://creativecommons.org/licenses/by/4.0/ (https://creativecommons.org/licenses/by/4.0/) , which permits unrestricted use, provided the original author and source are credited.
spellingShingle Population Ecology
Gómez, Pedro
Hall, Alex R.
Paterson, Steve
Buckling, Angus
Rapid decline of adaptation of Pseudomonas fluorescens to soil biotic environment
title Rapid decline of adaptation of Pseudomonas fluorescens to soil biotic environment
title_full Rapid decline of adaptation of Pseudomonas fluorescens to soil biotic environment
title_fullStr Rapid decline of adaptation of Pseudomonas fluorescens to soil biotic environment
title_full_unstemmed Rapid decline of adaptation of Pseudomonas fluorescens to soil biotic environment
title_short Rapid decline of adaptation of Pseudomonas fluorescens to soil biotic environment
title_sort rapid decline of adaptation of pseudomonas fluorescens to soil biotic environment
topic Population Ecology
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8905175/
https://www.ncbi.nlm.nih.gov/pubmed/35259940
http://dx.doi.org/10.1098/rsbl.2021.0593
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