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dc.contributor.authorØrpetveit, Irene
dc.contributor.authorKüntziger, Thomas
dc.contributor.authorSindre, Hilde
dc.contributor.authorRimstad, Espen
dc.contributor.authorDannevig, Birgit H
dc.date.accessioned2015-10-20T10:52:37Z
dc.date.available2015-10-20T10:52:37Z
dc.date.issued2012
dc.identifier.citationVirology Journal. 2012 Oct 05;9(1):228
dc.identifier.urihttp://hdl.handle.net/10852/46999
dc.description.abstractBackground The aquatic birnavirus infectious pancreatic necrosis virus (IPNV) causes infectious pancreatic necrosis (IPN), a severe disease in farmed salmonid fish. IPNV has a very broad host range and infects many different species of fish as well as molluscs and crustaceans. Investigation of the host reservoir of a virus may reveal important molecular mechanisms governing the infection processes such as receptors and entry mechanisms. In the present work we have studied whether IPNV is able to infect cells with different mammalian origin. Results IPNV bound in a specific manner to a membrane protein of the rabbit kidney cell line RK-13 as shown by the use of a virus overlay protein binding assay (VOPBA). Six different mammalian cell lines were inoculated with IPNV and incubated in parallels at different temperatures. At 7 days post inoculation (dpi), IPNV was detected by indirect immunofluorescent antibody test (IFAT) in all the cell lines. Confocal microscopy confirmed intracellular presence of the virus. No apparent cytopathic effect (cpe) was observed in any of the cultures, and no viral replication was demonstrated with real-time RT-PCR. Conclusion Our results show that IPNV is able to enter into a wide range of mammalian cells, and virus entry is most likely receptor mediated. We found no indication of IPNV replication in any of the mammalian cell lines tested.
dc.language.isoeng
dc.rightsØrpetveit et al.; licensee BioMed Central Ltd.
dc.rightsAttribution 2.0 Generic
dc.rights.urihttp://creativecommons.org/licenses/by/2.0/
dc.titleInfectious pancreatic necrosis virus (IPNV) from salmonid fish enters, but does not replicate in, mammalian cells
dc.typeJournal article
dc.date.updated2015-10-20T10:52:38Z
dc.creator.authorØrpetveit, Irene
dc.creator.authorKüntziger, Thomas
dc.creator.authorSindre, Hilde
dc.creator.authorRimstad, Espen
dc.creator.authorDannevig, Birgit H
dc.identifier.doihttp://dx.doi.org/10.1186/1743-422X-9-228
dc.identifier.urnURN:NBN:no-51155
dc.type.documentTidsskriftartikkel
dc.type.peerreviewedPeer reviewed
dc.identifier.fulltextFulltext https://www.duo.uio.no/bitstream/handle/10852/46999/1/12985_2012_Article_2007.pdf
dc.type.versionPublishedVersion
cristin.articleid228


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