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dc.rights.licenseopenen_US
hal.structure.identifierMicrobiologie Fondamentale et Pathogénicité [MFP]
dc.contributor.authorKOMATSU, Tetsuro
dc.contributor.authorWILL, Hans
dc.contributor.authorNAGATA, Kyosuke
hal.structure.identifierMicrobiologie Fondamentale et Pathogénicité [MFP]
dc.contributor.authorWODRICH, Harald
dc.date.accessioned2023-11-13T13:27:28Z
dc.date.available2023-11-13T13:27:28Z
dc.date.issued2016-04-22
dc.identifier.issn1090-2104en_US
dc.identifier.urihttps://oskar-bordeaux.fr/handle/20.500.12278/184736
dc.description.abstractEnRecent studies involving several viral systems have highlighted the importance of cellular intrinsic defense mechanisms through nuclear antiviral proteins that restrict viral propagation. These factors include among others components of PML nuclear bodies, the nuclear DNA sensor IFI16, and a potential restriction factor PHF13/SPOC1. For several nuclear replicating DNA viruses, it was shown that these factors sense and target viral genomes immediately upon nuclear import. In contrast to the anticipated view, we recently found that incoming adenoviral genomes are not targeted by PML nuclear bodies. Here we further explored cellular responses against adenoviral infection by focusing on specific conditions as well as additional nuclear antiviral factors. In line with our previous findings, we show that neither interferon treatment nor the use of specific isoforms of PML nuclear body components results in co-localization between incoming adenoviral genomes and the subnuclear domains. Furthermore, our imaging analyses indicated that neither IFI16 nor PHF13/SPOC1 are likely to target incoming adenoviral genomes. Thus our findings suggest that incoming adenoviral genomes may be able to escape from a large repertoire of nuclear antiviral mechanisms, providing a rationale for the efficient initiation of lytic replication cycle.
dc.language.isoENen_US
dc.subject.enAdenoviridae
dc.subject.enAdenoviridae Infections
dc.subject.enCell Line
dc.subject.enTumor
dc.subject.enDNA-Binding Proteins
dc.subject.enFluorescent Antibody Technique
dc.subject.enIndirect
dc.subject.enGenome
dc.subject.enViral
dc.subject.enHost-Pathogen Interactions
dc.subject.enHumans
dc.subject.enInterferons
dc.subject.enMicroscopy
dc.subject.enFluorescence
dc.subject.enNeutrophils
dc.subject.enNuclear Proteins
dc.subject.enPhosphoproteins
dc.subject.enTranscription Factors
dc.subject.enVirus Replication
dc.title.enImaging analysis of nuclear antiviral factors through direct detection of incoming adenovirus genome complexes.
dc.title.alternativeBiochem Biophys Res Communen_US
dc.typeArticle de revueen_US
dc.identifier.doi10.1016/j.bbrc.2016.03.078en_US
dc.subject.halSciences du Vivant [q-bio]/Microbiologie et Parasitologieen_US
dc.identifier.pubmed27012198en_US
bordeaux.journalBiochemical and Biophysical Research Communicationsen_US
bordeaux.page200-205en_US
bordeaux.volume473en_US
bordeaux.hal.laboratoriesMFP (Laboratoire Microbiologie Fondamentale et Pathogénicité) - UMR 5234en_US
bordeaux.issue1en_US
bordeaux.institutionCNRSen_US
bordeaux.peerReviewedouien_US
bordeaux.inpressnonen_US
bordeaux.import.sourcepubmed
hal.identifierhal-04282406
hal.version1
hal.date.transferred2023-11-13T13:27:30Z
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=Biochemical%20and%20Biophysical%20Research%20Communications&rft.date=2016-04-22&rft.volume=473&rft.issue=1&rft.spage=200-205&rft.epage=200-205&rft.eissn=1090-2104&rft.issn=1090-2104&rft.au=KOMATSU,%20Tetsuro&WILL,%20Hans&NAGATA,%20Kyosuke&WODRICH,%20Harald&rft.genre=article


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