| Literature DB >> 30348523 |
Xixi Wang1, Jing Wu2, Yingtong Wu1, Hongjun Chen3, Shoufeng Zhang4, Jinxiang Li5, Ting Xin1, Hong Jia1, Shaohua Hou1, Yitong Jiang1, Hongfei Zhu6, Xiaoyu Guo7.
Abstract
African swine fever virus (ASFV) is a highly pathogenic large DNA virus that causes African swine fever (ASF) in domestic pigs and European wild boars with mortality rate up to 100%. The DP96R gene of ASFV encodes one of the viral virulence factors, yet its action mechanism remains unknown. In this study, we report that DP96R of ASFV China 2018/1 strain subverts type I IFN production in cGAS sensing pathway. DP96R inhibited the cGAS/STING, and TBK1 but not IRF3-5D mediated IFN-β and ISRE promoters activation. Furthermore, DP96R selectively blocked the activation of NF-κB promoter induced by cGAS/STING, TBK1, and IKKβ, but not by overexpression of p65. Moreover, DP96R inhibited phosphorylation of TBK1 stimulated by cGAS/STING activation, and TBK1-induced antiviral response. Finally, truncated mutation analysis demonstrated that the region spanning amino acids 30 to 96 of DP96R was responsible for the inhibitory activity. To our knowledge, this is for the first time that DP96R of ASFV China 2018/1 is reported to negatively regulate type I IFN expression and NF-κB signaling by inhibiting both TBK1 and IKKβ, which plays an important role in virus immune evasion.Entities:
Keywords: ASFV; DP96R; NF-κB; TBK1; Type I IFN; cGAS
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Year: 2018 PMID: 30348523 DOI: 10.1016/j.bbrc.2018.10.103
Source DB: PubMed Journal: Biochem Biophys Res Commun ISSN: 0006-291X Impact factor: 3.575