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dc.contributor.authorWestra, ER
dc.contributor.authorLevin, BR
dc.date.accessioned2021-07-07T07:12:11Z
dc.date.issued2020-10-29
dc.description.abstractArticles on CRISPR commonly open with some variant of the phrase “these short palindromic repeats and their associated endonucleases (Cas) are an adaptive immune system that exists to protect bacteria and archaea from viruses and infections with other mobile genetic elements.” There is an abundance of genomic data consistent with the hypothesis that CRISPR plays this role in natural populations of bacteria and archaea, and experimental demonstrations with a few species of bacteria and their phage and plasmids show that CRISPR-Cas systems can play this role in vitro. Not at all clear are the ubiquity, magnitude, and nature of the contribution of CRISPR-Cas systems to the ecology and evolution of natural populations of microbes and the strength of selection mediated by different types of phage and plasmids to the evolution and maintenance of CRISPR-Cas systems. In this perspective, with the aid of heuristic mathematical–computer simulation models, we explore the a priori conditions under which exposure to lytic and temperate phage and conjugative plasmids will select for and maintain CRISPR-Cas systems in populations of bacteria and archaea. We review the existing literature addressing these ecological and evolutionary questions and highlight the experimental and other evidence needed to fully understand the conditions responsible for the evolution and maintenance of CRISPR-Cas systems and the contribution of these systems to the ecology and evolution of bacteria, archaea, and the mobile genetic elements that infect them.en_GB
dc.description.sponsorshipNatural Environment Research Council (NERC)en_GB
dc.description.sponsorshipBiotechnology and Biological Sciences Research Council (BBSRC)en_GB
dc.description.sponsorshipEuropean Research Council (ERC)en_GB
dc.description.sponsorshipUS National Institutes of General Medical Scienceen_GB
dc.description.sponsorshipEmory Universityen_GB
dc.identifier.citationVol. 117 (45), pp. 27777 - 27785en_GB
dc.identifier.doi10.1073/pnas.1915966117
dc.identifier.grantnumberNE/M018350/1en_GB
dc.identifier.grantnumberBB/N017412/1en_GB
dc.identifier.grantnumberERC-STG-2016-714478–EVOIMMECHen_GB
dc.identifier.grantnumberGM091875-17en_GB
dc.identifier.grantnumber1R35 GM136407-01en_GB
dc.identifier.urihttp://hdl.handle.net/10871/126328
dc.language.isoenen_GB
dc.publisherNational Academy of Sciencesen_GB
dc.rights© 2020 the Author(s). Published by PNAS. This open access article is distributed under Creative Commons Attribution License 4.0 (CC BY).en_GB
dc.subjectCRISPR-Casen_GB
dc.subjectbacteriaen_GB
dc.subjectphageen_GB
dc.subjectevolutionen_GB
dc.titleIt is unclear how important CRISPR-Cas systems are for protecting natural populations of bacteria against infections by mobile genetic elementsen_GB
dc.typeArticleen_GB
dc.date.available2021-07-07T07:12:11Z
dc.identifier.issn0027-8424
dc.descriptionThis is the final version. Available on open access from the National Academy of Sciences via the DOI in this recorden_GB
dc.descriptionData Availability: All study data are included in the article and SI Appendix.en_GB
dc.identifier.journalProceedings of the National Academy of Sciences (PNAS)en_GB
dc.rights.urihttps://creativecommons.org/licenses/by/4.0/en_GB
dcterms.dateAccepted2020-09-11
rioxxterms.versionVoRen_GB
rioxxterms.licenseref.startdate2020-10-29
rioxxterms.typeJournal Article/Reviewen_GB
refterms.dateFCD2021-07-07T07:05:23Z
refterms.versionFCDVoR
refterms.dateFOA2021-07-07T07:14:44Z
refterms.panelAen_GB


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© 2020 the Author(s). Published by PNAS. This open access article is distributed under Creative Commons Attribution License 4.0 (CC BY).
Except where otherwise noted, this item's licence is described as © 2020 the Author(s). Published by PNAS. This open access article is distributed under Creative Commons Attribution License 4.0 (CC BY).