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dc.contributor.authorWatson, BNJ
dc.contributor.authorPursey, E
dc.contributor.authorGandon, S
dc.contributor.authorWestra, ER
dc.date.accessioned2024-04-02T09:29:29Z
dc.date.issued2023-09-15
dc.date.updated2024-03-28T16:08:42Z
dc.description.abstractOrganisms have evolved a range of constitutive (always active) and inducible (elicited by parasites) defence mechanisms, but we have limited understanding of what drives the evolution of these orthogonal defence strategies. Bacteria and their phages offer a tractable system to study this: Bacteria can acquire constitutive resistance by mutation of the phage receptor (surface mutation, sm) or induced resistance through their CRISPR-Cas adaptive immune system. Using a combination of theory and experiments, we demonstrate that the mechanism that establishes first has a strong advantage because it weakens selection for the alternative resistance mechanism. As a consequence, ecological factors that alter the relative frequencies at which the different resistances are acquired have a strong and lasting impact: High growth conditions promote the evolution of sm resistance by increasing the influx of receptor mutation events during the early stages of the epidemic, whereas a high infection risk during this stage of the epidemic promotes the evolution of CRISPR immunity, since it fuels the (infection-dependent) acquisition of CRISPR immunity. This work highlights the strong and lasting impact of the transient evolutionary dynamics during the early stages of an epidemic on the long-term evolution of constitutive and induced defences, which may be leveraged to manipulate phage resistance evolution in clinical and applied settings.en_GB
dc.description.sponsorshipNatural Environment Research Council (NERC)en_GB
dc.description.sponsorshipEuropean Research Council (ERC)en_GB
dc.description.sponsorshipBiotechnology and Biological Sciences Research Council (BBSRC)en_GB
dc.identifier.citationVol. 21(9), article e3002122en_GB
dc.identifier.doihttps://doi.org/10.1371/journal.pbio.3002122
dc.identifier.grantnumberNE/S001921/1en_GB
dc.identifier.grantnumberERC-STG-2016-714478en_GB
dc.identifier.grantnumberBB/X010600/1en_GB
dc.identifier.urihttp://hdl.handle.net/10871/135657
dc.identifierORCID: 0000-0003-0968-8334 (Watson, Bridget Nora Janice)
dc.identifierORCID: 0000-0003-4396-0354 (Westra, Edze Rients)
dc.language.isoenen_GB
dc.publisherPublic Library of Science (PLoS)en_GB
dc.relation.urlhttps://doi.org/10.5281/zenodo.8193506en_GB
dc.relation.urlhttps://www.ncbi.nlm.nih.gov/pubmed/37713428en_GB
dc.rights© 2023 Watson et al. This is an open access article distributed under the terms of the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are credited.en_GB
dc.subjectBacteriophagesen_GB
dc.titleTransient eco-evolutionary dynamics early in a phage epidemic have strong and lasting impact on the long-term evolution of bacterial defencesen_GB
dc.typeArticleen_GB
dc.date.available2024-04-02T09:29:29Z
dc.contributor.editorBank, C
dc.identifier.issn1544-9173
exeter.article-numbere3002122
exeter.place-of-publicationUnited States
dc.descriptionThis is the final version. Available on open access from Public Library of Science (PLoS) via the DOI in this recorden_GB
dc.descriptionData Availability: Data and code are available online https://doi.org/10.5281/zenodo.8193506en_GB
dc.identifier.eissn1545-7885
dc.identifier.journalPLoS Biologyen_GB
dc.rights.urihttps://creativecommons.org/licenses/by/4.0/en_GB
dcterms.dateAccepted2023-08-07
rioxxterms.versionVoRen_GB
rioxxterms.licenseref.startdate2023-09-15
rioxxterms.typeJournal Article/Reviewen_GB
refterms.dateFCD2024-04-02T09:26:48Z
refterms.versionFCDVoR
refterms.dateFOA2024-04-02T09:29:38Z
refterms.panelAen_GB
refterms.dateFirstOnline2023-09-15


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© 2023 Watson et al. This is an open access article distributed under the terms of the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are credited.
Except where otherwise noted, this item's licence is described as © 2023 Watson et al. This is an open access article distributed under the terms of the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are credited.