内部收益率3
坦克结合激酶1
非洲猪瘟病毒
刺
病毒
生物
磷酸化
DNA病毒
IκB激酶
病毒学
基因
突变
先天免疫系统
信号转导
NF-κB
免疫系统
细胞生物学
遗传学
蛋白激酶A
工程类
基因组
航空航天工程
丝裂原活化蛋白激酶激酶
作者
Xixi Wang,Jing Wu,Yingtong Wu,Hongjun Chen,Shoufeng Zhang,Jinxiang Li,Ting Xin,Hong Ji,Shaohua Hou,Yao Jiang,Hongfei Zhu,Xiaoyu Guo
标识
DOI:10.1016/j.bbrc.2018.10.103
摘要
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.
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