Localized coevolution between microbial predator and prey alters community-wide gene expression and ecosystem function

dc.contributor.authorHogle Shane L
dc.contributor.authorRuusulehto Liisa
dc.contributor.authorCairns Johannes
dc.contributor.authorHultman Jenni
dc.contributor.authorHiltunen Teppo
dc.contributor.organizationfi=ekologia ja evoluutiobiologia|en=Ecology and Evolutionary Biology |
dc.contributor.organizationfi=fysiologia ja genetiikka|en=Physiology and Genetics|
dc.contributor.organization-code1.2.246.10.2458963.20.70712835001
dc.contributor.organization-code2606402
dc.converis.publication-id177967180
dc.converis.urlhttps://research.utu.fi/converis/portal/Publication/177967180
dc.date.accessioned2025-08-28T00:29:24Z
dc.date.available2025-08-28T00:29:24Z
dc.description.abstract<p>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.<br></p>
dc.identifier.eissn1751-7370
dc.identifier.jour-issn1751-7362
dc.identifier.olddbid205801
dc.identifier.oldhandle10024/188828
dc.identifier.urihttps://www.utupub.fi/handle/11111/33253
dc.identifier.urlhttps://www.nature.com/articles/s41396-023-01361-9
dc.identifier.urnURN:NBN:fi-fe2023030730173
dc.language.isoen
dc.okm.affiliatedauthorHogle, Shane
dc.okm.affiliatedauthorHiltunen, Teppo
dc.okm.affiliatedauthorCairns, Johannes
dc.okm.discipline1181 Ecology, evolutionary biologyen_GB
dc.okm.discipline1183 Plant biology, microbiology, virologyen_GB
dc.okm.discipline1181 Ekologia, evoluutiobiologiafi_FI
dc.okm.discipline1183 Kasvibiologia, mikrobiologia, virologiafi_FI
dc.okm.internationalcopublicationnot an international co-publication
dc.okm.internationalityInternational publication
dc.okm.typeA1 ScientificArticle
dc.publisherNature Publishing Group
dc.publisher.countryUnited Kingdomen_GB
dc.publisher.countryBritanniafi_FI
dc.publisher.country-codeGB
dc.relation.doi10.1038/s41396-023-01361-9
dc.relation.ispartofjournalISME Journal
dc.source.identifierhttps://www.utupub.fi/handle/10024/188828
dc.titleLocalized coevolution between microbial predator and prey alters community-wide gene expression and ecosystem function
dc.year.issued2023

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