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dc.rights.licenseopenen_US
hal.structure.identifierMicrobiologie Fondamentale et Pathogénicité [MFP]
dc.contributor.authorMONTESPAN, Charlotte
dc.contributor.authorMARVIN, Shauna A
hal.structure.identifierMicrobiologie Fondamentale et Pathogénicité [MFP]
dc.contributor.authorAUSTIN, Sisley
dc.contributor.authorBURRAGE, Andrew M
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.authorFAURE, Muriel
dc.contributor.authorCAMPELL, Edward M
dc.contributor.authorSCHNEIDER, Carola
dc.contributor.authorREIMER, Rudolph
dc.contributor.authorGRÜNEWALD, Kay
dc.contributor.authorWIETHOFF, Christopher M
hal.structure.identifierMicrobiologie Fondamentale et Pathogénicité [MFP]
dc.contributor.authorWODRICH, Harald
dc.date.accessioned2023-11-03T14:59:53Z
dc.date.available2023-11-03T14:59:53Z
dc.date.issued2017-02-01
dc.identifier.issn1553-7374en_US
dc.identifier.urihttps://oskar-bordeaux.fr/handle/20.500.12278/184588
dc.description.abstractEnCells employ active measures to restrict infection by pathogens, even prior to responses from the innate and humoral immune defenses. In this context selective autophagy is activated upon pathogen induced membrane rupture to sequester and deliver membrane fragments and their pathogen contents for lysosomal degradation. Adenoviruses, which breach the endosome upon entry, escape this fate by penetrating into the cytosol prior to autophagosome sequestration of the ruptured endosome. We show that virus induced membrane damage is recognized through Galectin-8 and sequesters the autophagy receptors NDP52 and p62. We further show that a conserved PPxY motif in the viral membrane lytic protein VI is critical for efficient viral evasion of autophagic sequestration after endosomal lysis. Comparing the wildtype with a PPxY-mutant virus we show that depletion of Galectin-8 or suppression of autophagy in ATG5-/- MEFs rescues infectivity of the PPxY-mutant virus while depletion of the autophagy receptors NDP52, p62 has only minor effects. Furthermore we show that wildtype viruses exploit the autophagic machinery for efficient nuclear genome delivery and control autophagosome formation via the cellular ubiquitin ligase Nedd4.2 resulting in reduced antigenic presentation. Our data thus demonstrate that a short PPxY-peptide motif in the adenoviral capsid permits multi-layered viral control of autophagic processes during entry.
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.enAdenovirus Infections
dc.subject.enHuman
dc.subject.enAmino Acid Motifs
dc.subject.enAnimals
dc.subject.enAutophagy
dc.subject.enBlotting
dc.subject.enWestern
dc.subject.enCapsid Proteins
dc.subject.enCell Line
dc.subject.enEnzyme-Linked Immunosorbent Assay
dc.subject.enEnzyme-Linked Immunospot Assay
dc.subject.enFlow Cytometry
dc.subject.enFluorescent Antibody Technique
dc.subject.enGalectins
dc.subject.enHumans
dc.subject.enImage Processing
dc.subject.enComputer-Assisted
dc.subject.enMice
dc.subject.enMicroscopy
dc.subject.enConfocal
dc.subject.enMicroscopy
dc.subject.enElectron
dc.subject.enTransmission
dc.subject.enVirus Internalization
dc.title.enMulti-layered control of Galectin-8 mediated autophagy during adenovirus cell entry through a conserved PPxY motif in the viral capsid.
dc.title.alternativePLoS Pathogen_US
dc.typeArticle de revueen_US
dc.subject.halSciences du Vivant [q-bio]/Microbiologie et Parasitologieen_US
dc.identifier.pubmed28192531en_US
bordeaux.journalPLoS Pathogensen_US
bordeaux.pagee1006217en_US
bordeaux.volume13en_US
bordeaux.hal.laboratoriesMFP (Laboratoire Microbiologie Fondamentale et Pathogénicité) - UMR 5234en_US
bordeaux.issue2en_US
bordeaux.institutionCNRSen_US
bordeaux.peerReviewedouien_US
bordeaux.inpressnonen_US
bordeaux.import.sourcepubmed
hal.identifierhal-04269898
hal.version1
hal.date.transferred2023-11-03T14:59:57Z
hal.popularnonen_US
hal.audienceInternationaleen_US
hal.exporttrue
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=2017-02-01&rft.volume=13&rft.issue=2&rft.spage=e1006217&rft.epage=e1006217&rft.eissn=1553-7374&rft.issn=1553-7374&rft.au=MONTESPAN,%20Charlotte&MARVIN,%20Shauna%20A&AUSTIN,%20Sisley&BURRAGE,%20Andrew%20M&ROGER,%20Benoit&rft.genre=article


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