State Key Laboratory of Agricultural Microbiology, Huazhong Agricultural University, Wuhan 430070, Hubei, People's Republic of China.
Laboratory of Animal Virology, College of Veterinary Medicine, Huazhong Agricultural University, Wuhan 430070, Hubei, People's Republic of China.
J Immunol. 2020 Mar 1;204(5):1287-1298. doi: 10.4049/jimmunol.1900946. Epub 2020 Jan 29.
Japanese encephalitis virus (JEV) is a mosquito-borne that causes severe neurologic disease in humans. NS1' is a NS1-related protein only reported in the Japanese encephalitis serogroup members of It is produced through programmed -1 ribosomal frameshift in NS2A. Our previous study demonstrated that JEV NS1' could antagonize type I IFN (IFN-I) production, but the mechanism is still unclear. In the current study, we found that JEV NS1' inhibits the expression of MAVS, and knockdown of MAVS hampers inhibition of IFN-β induction by NS1', suggesting that JEV NS1' inhibits IFN-I production by targeting MAVS. This finding is further supported by the result of the in vivo assay that showed the similar mortality caused by NS1'-deficient virus and its wild type virus in MAVS-deficient mice. Based on our previous sequencing results of noncoding RNA in JEV-infected cells, microRNA-22 (miR-22) was identified to be a key regulator for MAVS expression during JEV infection. Furthermore, we demonstrated that JEV NS1' could induce the expression of miR-22 by increasing the binding of transcriptional factors, CREB and c-Rel, to the promoter elements of miR-22. Taken together, our results reveal a novel mechanism by which JEV NS1' antagonizes host MAVS by regulating miR-22, thereby inhibiting the IFN-I production and facilitating viral replication.
日本脑炎病毒(JEV)是一种通过蚊子传播的病毒,可导致人类严重的神经系统疾病。NS1'是一种仅在日本脑炎血清群成员中报道的 NS1 相关蛋白。它是通过 NS2A 中的程序性-1 核糖体移码产生的。我们之前的研究表明,JEV NS1'可以拮抗 I 型干扰素(IFN-I)的产生,但具体机制尚不清楚。在本研究中,我们发现 JEV NS1'抑制了 MAVS 的表达,而 MAVS 的敲低会阻碍 NS1'对 IFN-β诱导的抑制,表明 JEV NS1'通过靶向 MAVS 抑制 IFN-I 的产生。这一发现得到了体内实验结果的进一步支持,该结果表明在 MAVS 缺陷型小鼠中,NS1'-缺陷型病毒及其野生型病毒的死亡率相似。基于我们之前对 JEV 感染细胞中非编码 RNA 的测序结果,鉴定出 microRNA-22(miR-22)是 JEV 感染过程中调控 MAVS 表达的关键调节因子。此外,我们还证明 JEV NS1'可以通过增加转录因子 CREB 和 c-Rel 与 miR-22 启动子元件的结合,诱导 miR-22 的表达。综上所述,我们的研究结果揭示了 JEV NS1'通过调节 miR-22 拮抗宿主 MAVS 的新机制,从而抑制 IFN-I 的产生并促进病毒复制。