| Literature DB >> 28877473 |
Florine E M Scholte1, Marko Zivcec1, John V Dzimianski2, Michelle K Deaton2, Jessica R Spengler1, Stephen R Welch1, Stuart T Nichol1, Scott D Pegan2, Christina F Spiropoulou1, Éric Bergeron3.
Abstract
Antiviral responses are regulated by conjugation of ubiquitin (Ub) and interferon-stimulated gene 15 (ISG15) to proteins. Certain classes of viruses encode Ub- or ISG15-specific proteases belonging to the ovarian tumor (OTU) superfamily. Their activity is thought to suppress cellular immune responses, but studies demonstrating the function of viral OTU proteases during infection are lacking. Crimean-Congo hemorrhagic fever virus (CCHFV, family Nairoviridae) is a highly pathogenic human virus that encodes an OTU with both deubiquitinase and deISGylase activity as part of the viral RNA polymerase. We investigated CCHFV OTU function by inactivating protease catalytic activity or by selectively disrupting its deubiquitinase and deISGylase activity using reverse genetics. CCHFV OTU inactivation blocked viral replication independently of its RNA polymerase activity, while deubiquitinase activity proved critical for suppressing the interferon responses. Our findings provide insights into viral OTU functions and support the development of therapeutics and vaccines. Published by Elsevier Inc.Entities:
Keywords: Bunyavirus; Crimean-Congo hemorrhagic fever; innate immunity; interferon; interferon stimulated gene-15; reverse genetics; ubiquitin; ubiquitin specific protease; virus replication
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Year: 2017 PMID: 28877473 PMCID: PMC5616139 DOI: 10.1016/j.celrep.2017.08.040
Source DB: PubMed Journal: Cell Rep Impact factor: 9.423