State Key Laboratory of Veterinary Etiological Biology, National Foot and Mouth Diseases Reference Laboratory, Lanzhou Veterinary Research Institute, Chinese Academy of Agricultural Sciences, Lanzhou 730046, China.
Collaborative Innovation Center for Viral Immunology, Medical Research Institute, Wuhan University, Wuhan 430072, China.
Sci Rep. 2016 Feb 17;6:21888. doi: 10.1038/srep21888.
Foot-and-mouth disease virus (FMDV) is the etiological agent of FMD, which affects cloven-hoofed animals. The pathophysiology of FMDV has not been fully understood and the evasion of host innate immune system is still unclear. Here, the FMDV non-structural protein 3A was identified as a negative regulator of virus-triggered IFN-β signaling pathway. Overexpression of the FMDV 3A inhibited Sendai virus-triggered activation of IRF3 and the expressions of RIG-I/MDA5. Transient transfection and co-immunoprecipitation experiments suggested that FMDV 3A interacts with RIG-I, MDA5 and VISA, which is dependent on the N-terminal 51 amino acids of 3A. Furthermore, 3A also inhibited the expressions of RIG-I, MDA5, and VISA by disrupting their mRNA levels. These results demonstrated that 3A inhibits the RLR-mediated IFN-β induction and uncovered a novel mechanism by which the FMDV 3A protein evades the host innate immune system.
口蹄疫病毒(FMDV)是口蹄疫的病原体,影响偶蹄类动物。FMDV 的病理生理学尚未完全阐明,其逃避宿主固有免疫系统的机制仍不清楚。本研究中发现,口蹄疫病毒非结构蛋白 3A 是病毒触发 IFN-β 信号通路的负调控因子。3A 的过表达抑制了仙台病毒触发的 IRF3 和 RIG-I/MDA5 的表达。瞬时转染和免疫共沉淀实验表明,FMDV 3A 与 RIG-I、MDA5 和 VISA 相互作用,这依赖于 3A 的 N 端 51 个氨基酸。此外,3A 通过破坏它们的 mRNA 水平来抑制 RIG-I、MDA5 和 VISA 的表达。这些结果表明,3A 抑制了 RLR 介导的 IFN-β 诱导,并揭示了 FMDV 3A 蛋白逃避宿主固有免疫系统的新机制。