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dc.contributor.authorBösl, Korbinian
dc.contributor.authorIanevski, Aleksandr
dc.contributor.authorThan, Thoa T.
dc.contributor.authorAndersen, Petter I.
dc.contributor.authorKuivanen, Suvi
dc.contributor.authorTeppor, Mona
dc.contributor.authorZusinaite, Eva
dc.contributor.authorDumpis, Uga
dc.contributor.authorVitkauskiene, Astra
dc.contributor.authorCox, Rebecca Jane
dc.contributor.authorKallio-Kokko, Hannimari
dc.contributor.authorBergqvist, Anders
dc.contributor.authorTenson, Tanel
dc.contributor.authorMerits, Andres
dc.contributor.authorOksenych, Valentyn
dc.contributor.authorBjørås, Magnar
dc.contributor.authorAnthonsen, Marit Walbye
dc.contributor.authorShum, David H.K.
dc.contributor.authorKaarbø, Mari
dc.contributor.authorVapalahti, Olli
dc.contributor.authorWindisch, Marc P.
dc.contributor.authorSuperti-Furga, Giulio
dc.contributor.authorSnijder, Berend
dc.contributor.authorKainov, Denis
dc.contributor.authorKandasamy, Richard Kumaran
dc.date.accessioned2020-01-15T13:00:35Z
dc.date.available2020-01-15T13:00:35Z
dc.date.created2019-10-07T15:54:48Z
dc.date.issued2019
dc.identifier.citationFrontiers in Immunology. 2019, 10:2186 1-12.nb_NO
dc.identifier.issn1664-3224
dc.identifier.urihttp://hdl.handle.net/11250/2636439
dc.description.abstractViruses are one of the major causes of acute and chronic infectious diseases and thus a major contributor to the global burden of disease. Several studies have shown how viruses have evolved to hijack basic cellular pathways and evade innate immune response by modulating key host factors and signaling pathways. A collective view of these multiple studies could advance our understanding of virus-host interactions and provide new therapeutic perspectives for the treatment of viral diseases. Here, we performed an integrative meta-analysis to elucidate the 17 different host-virus interactomes. Network and bioinformatics analyses showed how viruses with small genomes efficiently achieve the maximal effect by targeting multifunctional and highly connected host proteins with a high occurrence of disordered regions. We also identified the core cellular process subnetworks that are targeted by all the viruses. Integration with functional RNA interference (RNAi) datasets showed that a large proportion of the targets are required for viral replication. Furthermore, we performed an interactome-informed drug re-purposing screen and identified novel activities for broad-spectrum antiviral agents against hepatitis C virus and human metapneumovirus. Altogether, these orthogonal datasets could serve as a platform for hypothesis generation and follow-up studies to broaden our understanding of the viral evasion landscape.nb_NO
dc.language.isoengnb_NO
dc.publisherFrontiers Medianb_NO
dc.relation.urihttps://doi.org/10.3389/fimmu.2019.02186
dc.rightsNavngivelse 4.0 Internasjonal*
dc.rights.urihttp://creativecommons.org/licenses/by/4.0/deed.no*
dc.subjectMolekylær virologinb_NO
dc.subjectMolecular virologynb_NO
dc.titleCommon nodes of virus–host interaction revealed through an integrated network analysisnb_NO
dc.typeJournal articlenb_NO
dc.typePeer reviewednb_NO
dc.description.versionpublishedVersionnb_NO
dc.subject.nsiVDP::Generell immunologi: 478nb_NO
dc.subject.nsiVDP::General immunology: 478nb_NO
dc.source.pagenumber1-12nb_NO
dc.source.volume10:2186nb_NO
dc.source.journalFrontiers in Immunologynb_NO
dc.identifier.doi10.3389/fimmu.2019.02186
dc.identifier.cristin1734621
dc.relation.projectNorges teknisk-naturvitenskapelige universitet: Onsager fellowshipnb_NO
dc.relation.projectAndre: NRF-2017M3A9G6068246nb_NO
dc.relation.projectNorges forskningsråd: 223255nb_NO
dc.relation.projectEU/MOBTT39nb_NO
dc.relation.projectNorges forskningsråd: 263168nb_NO
dc.relation.projectNorges teknisk-naturvitenskapelige universitet: ONSAGER FELLOWSHIPnb_NO
dc.description.localcodeCopyright © 2019 Bösl, Ianevski, Than, Andersen, Kuivanen, Teppor, Zusinaite, Dumpis, Vitkauskiene, Cox, Kallio-Kokko, Bergqvist, Tenson, Merits, Oksenych, Bjørås, Anthonsen, Shum, Kaarbø, Vapalahti, Windisch, Superti-Furga, Snijder, Kainov and Kandasamy. This is an open-access article distributed under the terms of the Creative Commons Attribution License (CC BY). The use, distribution or reproduction in other forums is permitted, provided the original author(s) and the copyright owner(s) are credited and that the original publication in this journal is cited, in accordance with accepted academic practice. No use, distribution or reproduction is permitted which does not comply with these terms.nb_NO
cristin.unitcode194,65,15,0
cristin.unitnameInstitutt for klinisk og molekylær medisin
cristin.ispublishedtrue
cristin.fulltextoriginal
cristin.qualitycode1


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