Näytä suppeat kuvailutiedot

dc.contributor.authorMäntynen, Sari
dc.contributor.authorLaanto, Elina
dc.contributor.authorOksanen, Hanna M.
dc.contributor.authorPoranen, Minna M.
dc.contributor.authorDíaz-Muñoz, Samuel L.
dc.date.accessioned2021-09-23T05:13:44Z
dc.date.available2021-09-23T05:13:44Z
dc.date.issued2021
dc.identifier.citationMäntynen, S., Laanto, E., Oksanen, H. M., Poranen, M. M., & Díaz-Muñoz, S. L. (2021). Black box of phage–bacterium interactions : exploring alternative phage infection strategies. <i>Open Biology</i>, <i>11</i>(9), Article 210188. <a href="https://doi.org/10.1098/rsob.210188" target="_blank">https://doi.org/10.1098/rsob.210188</a>
dc.identifier.otherCONVID_101137331
dc.identifier.urihttps://jyx.jyu.fi/handle/123456789/77880
dc.description.abstractThe canonical lytic–lysogenic binary has been challenged in recent years, as more evidence has emerged on alternative bacteriophage infection strategies. These infection modes are little studied, and yet they appear to be more abundant and ubiquitous in nature than previously recognized, and can play a significant role in the ecology and evolution of their bacterial hosts. In this review, we discuss the extent, causes and consequences of alternative phage lifestyles, and clarify conceptual and terminological confusion to facilitate research progress. We propose distinct definitions for the terms ‘pseudolysogeny’ and ‘productive or non-productive chronic infection’, and distinguish them from the carrier state life cycle, which describes a population-level phenomenon. Our review also finds that phages may change their infection modes in response to environmental conditions or the physiological state of the host cell. We outline known molecular mechanisms underlying the alternative phage–host interactions, including specific genetic pathways and their considerable biotechnological potential. Moreover, we discuss potential implications of the alternative phage lifestyles for microbial biology and ecosystem functioning, as well as applied topics such as phage therapy.en
dc.format.mimetypeapplication/pdf
dc.language.isoeng
dc.publisherThe Royal Society Publishing
dc.relation.ispartofseriesOpen Biology
dc.rightsCC BY 4.0
dc.subject.otherphage infection
dc.subject.otherbacteriophage
dc.subject.otherchronic infection
dc.subject.othercarrier state
dc.subject.otherpseudolysogeny
dc.titleBlack box of phage–bacterium interactions : exploring alternative phage infection strategies
dc.typearticle
dc.identifier.urnURN:NBN:fi:jyu-202109234952
dc.contributor.laitosBio- ja ympäristötieteiden laitosfi
dc.contributor.laitosDepartment of Biological and Environmental Scienceen
dc.contributor.oppiaineSolu- ja molekyylibiologiafi
dc.contributor.oppiaineBiologisten vuorovaikutusten huippututkimusyksikköfi
dc.contributor.oppiaineCell and Molecular Biologyen
dc.contributor.oppiaineCentre of Excellence in Biological Interactions Researchen
dc.type.urihttp://purl.org/eprint/type/JournalArticle
dc.type.coarhttp://purl.org/coar/resource_type/c_dcae04bc
dc.description.reviewstatuspeerReviewed
dc.relation.issn2046-2441
dc.relation.numberinseries9
dc.relation.volume11
dc.type.versionpublishedVersion
dc.rights.copyright© 2021 The Authors. Published by the Royal Society.
dc.rights.accesslevelopenAccessfi
dc.subject.ysomikrobiologia
dc.subject.ysobakteriofagit
dc.subject.ysoinfektiot
dc.subject.ysovirukset
dc.subject.ysobakteerit
dc.format.contentfulltext
jyx.subject.urihttp://www.yso.fi/onto/yso/p13507
jyx.subject.urihttp://www.yso.fi/onto/yso/p25303
jyx.subject.urihttp://www.yso.fi/onto/yso/p7316
jyx.subject.urihttp://www.yso.fi/onto/yso/p1123
jyx.subject.urihttp://www.yso.fi/onto/yso/p1749
dc.rights.urlhttps://creativecommons.org/licenses/by/4.0/
dc.relation.doi10.1098/rsob.210188
jyx.fundinginformationThis work was supported by the Academy of Finland Postdoctoral Researcher funding for S.M. (grant no. 323426) and for E.L. (grant no. 321985). M.M.P. was funded via Academy of Finland (grant no. 331627), Jane and Aatos Erkko Foundation (grant no. 170046) and Sigrid Jusélius Foundation. H.M.O. was supported by the University of Helsinki and Academy of Finland funding for FINStruct and Instruct Centre FI, part of Biocenter Finland and Instruct-ERIC.
dc.type.okmA2


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