Afficher la notice abrégée

dc.rights.licenseopenen_US
hal.structure.identifierMicrobiologie Fondamentale et Pathogénicité [MFP]
dc.contributor.authorPIED, Noemie
hal.structure.identifierMicrobiologie Fondamentale et Pathogénicité [MFP]
dc.contributor.authorDAUSSY, Coralie F
hal.structure.identifierMicrobiologie Fondamentale et Pathogénicité [MFP]
dc.contributor.authorDENIS, Zoé
hal.structure.identifierMicrobiologie Fondamentale et Pathogénicité [MFP]
dc.contributor.authorRAGUES, Jessica
hal.structure.identifierMicrobiologie Fondamentale et Pathogénicité [MFP]
dc.contributor.authorFAURE, Muriel
hal.structure.identifierInstitut Bergonié [Bordeaux]
dc.contributor.authorIGGO, Richard
dc.contributor.authorTSCHAN, Mario P
hal.structure.identifierMicrobiologie Fondamentale et Pathogénicité [MFP]
dc.contributor.authorROGER, Benoit
hal.structure.identifierMicrobiologie Fondamentale et Pathogénicité [MFP]
dc.contributor.authorRAYNE, Fabienne
hal.structure.identifierMicrobiologie Fondamentale et Pathogénicité [MFP]
dc.contributor.authorWODRICH, Harald
dc.date.accessioned2024-10-24T07:29:21Z
dc.date.available2024-09-30T10:28:35Z
dc.date.available2024-10-24T07:29:21Z
dc.date.issued2022-07-01
dc.identifier.issn1553-7374en_US
dc.identifier.urihttps://oskar-bordeaux.fr/handle/20.500.12278/202033.3
dc.description.abstractEnIntracellular pathogens cause membrane distortion and damage as they enter host cells. Cells perceive these membrane alterations as danger signals and respond by activating autophagy. This response has primarily been studied during bacterial invasion, and only rarely in viral infections. Here, we investigate the cellular response to membrane damage during adenoviral entry. Adenoviruses and their vector derivatives, that are an important vaccine platform against SARS-CoV-2, enter the host cell by endocytosis followed by lysis of the endosomal membrane. We previously showed that cells mount a locally confined autophagy response at the site of endosomal membrane lysis. Here we describe the mechanism of autophagy induction: endosomal membrane damage activates the kinase TBK1 that accumulates in its phosphorylated form at the penetration site. Activation and recruitment of TBK1 require detection of membrane damage by galectin 8 but occur independently of classical autophagy receptors or functional autophagy. Instead, TBK1 itself promotes subsequent autophagy that adenoviruses need to take control of. Deletion of TBK1 reduces LC3 lipidation during adenovirus infection and restores the infectivity of an adenovirus mutant that is restricted by autophagy. By comparing adenovirus-induced membrane damage to sterile lysosomal damage, we implicate TBK1 in the response to a broader range of types of membrane damage. Our study thus highlights an important role for TBK1 in the cellular response to adenoviral endosome penetration and places TBK1 early in the pathway leading to autophagy in response to membrane damage.
dc.language.isoENen_US
dc.rightsAttribution 3.0 United States*
dc.rights.urihttp://creativecommons.org/licenses/by/3.0/us/*
dc.subject.enAdenoviridae
dc.subject.enAdenoviridae Infections
dc.subject.enAutophagy
dc.subject.enEndosomes
dc.subject.enGalectins
dc.subject.enHumans
dc.subject.enProtein Serine-Threonine Kinases
dc.title.enTBK1 is part of a galectin 8 dependent membrane damage recognition complex and drives autophagy upon Adenovirus endosomal escape.
dc.title.alternativePLoS Pathogen_US
dc.typeArticle de revueen_US
dc.identifier.doi10.1371/journal.ppat.1010736en_US
dc.subject.halSciences du Vivant [q-bio]/Microbiologie et Parasitologieen_US
dc.identifier.pubmed35857795en_US
bordeaux.journalPLoS Pathogensen_US
bordeaux.pagee1010736en_US
bordeaux.volume18en_US
bordeaux.hal.laboratoriesMFP (Laboratoire Microbiologie Fondamentale et Pathogénicité) - UMR 5234en_US
bordeaux.hal.laboratoriesMFP (Laboratoire Microbiologie Fondamentale et Pathogénicité) - UMR 5234en_US
bordeaux.issue7en_US
bordeaux.institutionCNRSen_US
bordeaux.peerReviewedouien_US
bordeaux.inpressnonen_US
bordeaux.import.sourcepubmed
hal.identifierhal-04714469
hal.version1
hal.date.transferred2024-09-30T10:28:38Z
hal.popularnonen_US
hal.audienceInternationaleen_US
hal.exportfalse
workflow.import.sourcepubmed
dc.rights.ccPas de Licence CCen_US
bordeaux.COinSctx_ver=Z39.88-2004&rft_val_fmt=info:ofi/fmt:kev:mtx:journal&rft.jtitle=PLoS%20Pathogens&rft.date=2022-07-01&rft.volume=18&rft.issue=7&rft.spage=e1010736&rft.epage=e1010736&rft.eissn=1553-7374&rft.issn=1553-7374&rft.au=PIED,%20Noemie&DAUSSY,%20Coralie%20F&DENIS,%20Zo%C3%A9&RAGUES,%20Jessica&FAURE,%20Muriel&rft.genre=article


Fichier(s) constituant ce document

Thumbnail
Thumbnail

Ce document figure dans la(les) collection(s) suivante(s)

Afficher la notice abrégée

VersionItemDateEn bref

*Version sélectionnée