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Localized coevolution between microbial predator and prey alters community-wide gene expression and ecosystem function
Closely interacting microbial species pairs (e.g., predator and prey) can become coadapted via reciprocal natural selection. A fundamental challenge in evolutionary ecology is to untangle how coevolution in small species groups affects and is affected by biotic interactions in diverse communities. W...
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/PMC10030642/ https://www.ncbi.nlm.nih.gov/pubmed/36658394 http://dx.doi.org/10.1038/s41396-023-01361-9 |
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author | Hogle, Shane L. Ruusulehto, Liisa Cairns, Johannes Hultman, Jenni Hiltunen, Teppo |
author_facet | Hogle, Shane L. Ruusulehto, Liisa Cairns, Johannes Hultman, Jenni Hiltunen, Teppo |
author_sort | Hogle, Shane L. |
collection | PubMed |
description | Closely interacting microbial species pairs (e.g., predator and prey) can become coadapted via reciprocal natural selection. A fundamental challenge in evolutionary ecology is to untangle how coevolution in small species groups affects and is affected by biotic interactions in diverse communities. We conducted an experiment with a synthetic 30-species bacterial community where we experimentally manipulated the coevolutionary history of a ciliate predator and one bacterial prey species from the community. Altering the coevolutionary history of the focal prey species had little effect on community structure or carrying capacity in the presence or absence of the coevolved predator. However, community metabolic potential (represented by per-cell ATP concentration) was significantly higher in the presence of both the coevolved focal predator and prey. This ecosystem-level response was mirrored by community-wide transcriptional shifts that resulted in the differential regulation of nutrient acquisition and surface colonization pathways across multiple bacterial species. Our findings show that the disruption of localized coevolution between species pairs can reverberate through community-wide transcriptional networks even while community composition remains largely unchanged. We propose that these altered expression patterns may signal forthcoming evolutionary and ecological change. |
format | Online Article Text |
id | pubmed-10030642 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2023 |
publisher | Nature Publishing Group UK |
record_format | MEDLINE/PubMed |
spelling | pubmed-100306422023-03-23 Localized coevolution between microbial predator and prey alters community-wide gene expression and ecosystem function Hogle, Shane L. Ruusulehto, Liisa Cairns, Johannes Hultman, Jenni Hiltunen, Teppo ISME J Article Closely interacting microbial species pairs (e.g., predator and prey) can become coadapted via reciprocal natural selection. A fundamental challenge in evolutionary ecology is to untangle how coevolution in small species groups affects and is affected by biotic interactions in diverse communities. We conducted an experiment with a synthetic 30-species bacterial community where we experimentally manipulated the coevolutionary history of a ciliate predator and one bacterial prey species from the community. Altering the coevolutionary history of the focal prey species had little effect on community structure or carrying capacity in the presence or absence of the coevolved predator. However, community metabolic potential (represented by per-cell ATP concentration) was significantly higher in the presence of both the coevolved focal predator and prey. This ecosystem-level response was mirrored by community-wide transcriptional shifts that resulted in the differential regulation of nutrient acquisition and surface colonization pathways across multiple bacterial species. Our findings show that the disruption of localized coevolution between species pairs can reverberate through community-wide transcriptional networks even while community composition remains largely unchanged. We propose that these altered expression patterns may signal forthcoming evolutionary and ecological change. Nature Publishing Group UK 2023-01-19 2023-04 /pmc/articles/PMC10030642/ /pubmed/36658394 http://dx.doi.org/10.1038/s41396-023-01361-9 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 Hogle, Shane L. Ruusulehto, Liisa Cairns, Johannes Hultman, Jenni Hiltunen, Teppo Localized coevolution between microbial predator and prey alters community-wide gene expression and ecosystem function |
title | Localized coevolution between microbial predator and prey alters community-wide gene expression and ecosystem function |
title_full | Localized coevolution between microbial predator and prey alters community-wide gene expression and ecosystem function |
title_fullStr | Localized coevolution between microbial predator and prey alters community-wide gene expression and ecosystem function |
title_full_unstemmed | Localized coevolution between microbial predator and prey alters community-wide gene expression and ecosystem function |
title_short | Localized coevolution between microbial predator and prey alters community-wide gene expression and ecosystem function |
title_sort | localized coevolution between microbial predator and prey alters community-wide gene expression and ecosystem function |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10030642/ https://www.ncbi.nlm.nih.gov/pubmed/36658394 http://dx.doi.org/10.1038/s41396-023-01361-9 |
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