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dc.rights.licenseopenen_US
dc.contributor.authorZHANG, Wenli
dc.contributor.authorMESE, Kemal
dc.contributor.authorSCHELLHORN, Sebastian
dc.contributor.authorBAHLMANN, Nora
dc.contributor.authorMACH, Nicolas
dc.contributor.authorBUNZ, Oskar
dc.contributor.authorDHINGRA, Akshay
dc.contributor.authorHAGE, Elias
dc.contributor.authorLAFON, Marie-Edith
hal.structure.identifierMicrobiologie Fondamentale et Pathogénicité [MFP]
dc.contributor.authorWODRICH, Harald
dc.contributor.authorHEIM, Albert
dc.contributor.authorEHRHARDT, Anja
dc.date.accessioned2024-09-30T10:02:52Z
dc.date.available2024-09-30T10:02:52Z
dc.date.issued2020-09-02
dc.identifier.issn1422-0067en_US
dc.identifier.urihttps://oskar-bordeaux.fr/handle/20.500.12278/202026
dc.description.abstractEnRecently an increasing number of new adenovirus types associated with type-dependent pathogenicity have been identified. However, identification of these clinical isolates represents the very first step to characterize novel pathogens. For deeper analyses, these adenoviruses need to be further characterized in basic virology experiments or they could be applied in translational research. To achieve this goal, it is essential to get genetic access and to enable genetic modification of these novel adenovirus genomes (deletion, insertion, and mutation). Here we demonstrate a high-throughput approach to get genetic access to new adenoviruses via homologous recombination. We first defined the cloning conditions regarding homology arm-length and input adenoviral genome amounts. Then we cloned four naturally occurring adenoviruses (Ad70, Ad73, Ad74, and Ad75) into easy-to-manipulate plasmids and genetically modified them by reporter gene insertion. Three recombinant adenoviruses (Ad70, Ad73, and Ad74) containing a reporter cassette were successfully reconstituted. These novel reporter-labeled adenoviruses were further characterized using the inserted luciferase reporter with respect to receptor usage, presence of anti-adenovirus antibodies, and tropism in vitro. The identified receptor usage, the relatively low prevalence of anti-adenovirus antibodies, and the various cancer cell line transduction pattern are important features of these new pathogens providing essential information for their therapeutic application.
dc.language.isoENen_US
dc.rightsAttribution 3.0 United States*
dc.rights.urihttp://creativecommons.org/licenses/by/3.0/us/*
dc.subject.enAdenoviruses
dc.subject.enHuman
dc.subject.enCloning
dc.subject.enMolecular
dc.subject.enGenes
dc.subject.enReporter
dc.subject.enGenetic Vectors
dc.subject.enGenome
dc.subject.enViral
dc.subject.enHigh-Throughput Screening Assays
dc.subject.enHomologous Recombination
dc.subject.enHumans
dc.title.enHigh-Throughput Cloning and Characterization of Emerging Adenovirus Types 70, 73, 74, and 75.
dc.title.alternativeInt J Mol Scien_US
dc.typeArticle de revueen_US
dc.identifier.doi10.3390/ijms21176370en_US
dc.subject.halSciences du Vivant [q-bio]/Microbiologie et Parasitologieen_US
dc.identifier.pubmed32887347en_US
bordeaux.journalInternational Journal of Molecular Sciencesen_US
bordeaux.volume21en_US
bordeaux.hal.laboratoriesMFP (Laboratoire Microbiologie Fondamentale et Pathogénicité) - UMR 5234en_US
bordeaux.issue17en_US
bordeaux.institutionCNRSen_US
bordeaux.peerReviewedouien_US
bordeaux.inpressnonen_US
bordeaux.import.sourcepubmed
hal.identifierhal-04714407
hal.version1
hal.date.transferred2024-09-30T10:02:55Z
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=International%20Journal%20of%20Molecular%20Sciences&rft.date=2020-09-02&rft.volume=21&rft.issue=17&rft.eissn=1422-0067&rft.issn=1422-0067&rft.au=ZHANG,%20Wenli&MESE,%20Kemal&SCHELLHORN,%20Sebastian&BAHLMANN,%20Nora&MACH,%20Nicolas&rft.genre=article


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