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dc.contributor.authorChabas, H
dc.contributor.authorNicot, A
dc.contributor.authorMeaden, S
dc.contributor.authorWestra, ER
dc.contributor.authorTremblay, DM
dc.contributor.authorPradier, L
dc.contributor.authorLion, S
dc.contributor.authorMoineau, S
dc.contributor.authorGandon, S
dc.date.accessioned2019-04-08T12:09:06Z
dc.date.issued2019-03-25
dc.description.abstractThe durability of host resistance is challenged by the ability of pathogens to escape the defence of their hosts. Understanding the variability in the durability of host resistance is of paramount importance for designing more effective control strategies against infectious diseases. Here, we study the durability of various clustered regularly interspaced short palindromic repeats-Cas (CRISPR-Cas) alleles of the bacteria Streptococcus thermophilus against lytic phages. We found substantial variability in durability among different resistant bacteria. Since the escape of the phage is driven by a mutation in the phage sequence targeted by CRISPR-Cas, we explored the fitness costs associated with these escape mutations. We found that, on average, escape mutations decrease the fitness of the phage. Yet, the magnitude of this fitness cost does not predict the durability of CRISPR-Cas immunity. We contend that this variability in the durability of resistance may be because of variations in phage mutation rate or in the proportion of lethal mutations across the phage genome. These results have important implications on the coevolutionary dynamics between bacteria and phages and for the optimal deployment of resistance strategies against pathogens and pests. Understanding the durability of CRISPR-Cas immunity may also help develop more effective gene-drive strategies based on CRISPR-Cas9 technology. This article is part of a discussion meeting issue 'The ecology and evolution of prokaryotic CRISPR-Cas adaptive immune systems'.en_GB
dc.description.sponsorshipNatural Environment Research Council (NERC)en_GB
dc.description.sponsorshipBiotechnology & Biological Sciences Research Council (BBSRC)en_GB
dc.description.sponsorshipEuropean Commissionen_GB
dc.description.sponsorshipEuropean Molecular Biology Organization (EMBO)en_GB
dc.description.sponsorshipLeverhulme Trusten_GB
dc.description.sponsorshipNatural Sciences and Engineering Research Council of Canadaen_GB
dc.identifier.citationVol. 374 (1772), pp. 20180097en_GB
dc.identifier.doi10.1098/rstb.2018.0097
dc.identifier.grantnumberBB/N017412/1en_GB
dc.identifier.grantnumber714478en_GB
dc.identifier.grantnumberNE/M018350/1en_GB
dc.identifier.grantnumberERC-STG-2016-714478 - EVOIMMECHen_GB
dc.identifier.urihttp://hdl.handle.net/10871/36764
dc.language.isoenen_GB
dc.publisherRoyal Societyen_GB
dc.relation.urlhttps://www.ncbi.nlm.nih.gov/pubmed/30905283en_GB
dc.rights(C) 2019 The Author(s) Published by the Royal Society. All rights reserved.en_GB
dc.subjectclustered regularly interspaced short palindromic repeats-Casen_GB
dc.subjectdurability of resistanceen_GB
dc.subjectmutation ratesen_GB
dc.subjectpathogen evolutionen_GB
dc.titleVariability in the durability of CRISPR-Cas immunityen_GB
dc.typeArticleen_GB
dc.date.available2019-04-08T12:09:06Z
dc.identifier.issn0962-8436
exeter.place-of-publicationEnglanden_GB
dc.descriptionThis is the author accepted manuscript. The final version is available from Royal Society via the DOI in this record.en_GB
dc.identifier.journalPhilosophical Transactions B: Biological Sciencesen_GB
dc.rights.urihttp://www.rioxx.net/licenses/all-rights-reserveden_GB
dcterms.dateAccepted2018-12-03
exeter.funder::Natural Environment Research Council (NERC)en_GB
exeter.funder::Biotechnology & Biological Sciences Research Council (BBSRC)en_GB
exeter.funder::European Commissionen_GB
rioxxterms.versionAMen_GB
rioxxterms.licenseref.startdate2018-12-03
rioxxterms.typeJournal Article/Reviewen_GB
refterms.dateFCD2019-04-08T12:03:39Z
refterms.versionFCDAM
refterms.dateFOA2019-04-08T12:09:09Z
refterms.panelAen_GB


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