| Literature DB >> 33540654 |
Marie Pourcelot1, Rayane Amaral Moraes1, Aurore Fablet1, Emmanuel Bréard1, Corinne Sailleau1, Cyril Viarouge1, Lydie Postic1, Stéphan Zientara1, Grégory Caignard1, Damien Vitour1.
Abstract
Bluetongue virus (BTV), an arbovirus transmitted by Culicoides biting midges, is a major concern of wild and domestic ruminants. While BTV induces type I interferon (alpha/beta interferon [IFN-α/β]) production in infected cells, several reports have described evasion strategies elaborated by this virus to dampen this intrinsic, innate response. In the present study, we suggest that BTV VP3 is a new viral antagonist of the IFN-β synthesis. Indeed, using split luciferase and coprecipitation assays, we report an interaction between VP3 and both the mitochondrial adapter protein MAVS and the IRF3-kinase IKKε. Overall, this study describes a putative role for the BTV structural protein VP3 in the control of the antiviral response.Entities:
Keywords: Bluetongue virus; IKKε; MAVS; VP3; type-I interferons; virus–host interactions
Year: 2021 PMID: 33540654 PMCID: PMC7913109 DOI: 10.3390/v13020230
Source DB: PubMed Journal: Viruses ISSN: 1999-4915 Impact factor: 5.048