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Title: Inhibition of cGAS-STING-TBK1 signaling pathway by DP96R of ASFV China 2018/1

Journal Article · · Biochemical and Biophysical Research Communications
 [1];  [1];  [1];  [2];  [3];
  1. Institute of Animal Science, Chinese Academy of Agricultural Sciences, Beijing 100193 (China)
  2. Shanghai Veterinary Research Institute, Chinese Academy of Agricultural Sciences, Shanghai 200241 (China)
  3. Institute of Military Veterinary Medicine, Academy of Military Medical Sciences, Changchun 130000 (China)

Highlights: • DP96R is an inhibitor of cGAS-triggered type I IFNs induction and NF-κB activation. • DP96R inhibits the phosphorylation of TBK1 and TBK1-mediated antiviral responses. • The C-terminal domain of DP96R is responsible for its inhibitory effects. 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.

OSTI ID:
23137145
Journal Information:
Biochemical and Biophysical Research Communications, Vol. 506, Issue 3; Other Information: Copyright (c) 2018 Elsevier Inc. All rights reserved.; Country of input: International Atomic Energy Agency (IAEA); ISSN 0006-291X
Country of Publication:
United States
Language:
English

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