Qin Liuxing, Rao Tingting, Li Xiangmin, Chen Huanchun, Qian Ping
National Key Laboratory of Agricultural Microbiology, Hubei Hongshan Laboratory, Huazhong Agricultural University, Wuhan, Hubei 430070, PR China; Laboratory of Animal Virology, College of Veterinary Medicine, Huazhong Agricultural University, Wuhan 430070, PR China.
National Key Laboratory of Agricultural Microbiology, Hubei Hongshan Laboratory, Huazhong Agricultural University, Wuhan, Hubei 430070, PR China; Laboratory of Animal Virology, College of Veterinary Medicine, Huazhong Agricultural University, Wuhan 430070, PR China; Key Laboratory of Development of Veterinary Diagnostic Products, Ministry of Agriculture, Wuhan 430070, PR China; Key Laboratory of Preventive Veterinary Medicine in Hubei Province, The Cooperative Innovation Center for Sustainable Pig Production, Wuhan 430070, PR China.
Virus Res. 2023 Oct 15;336:199210. doi: 10.1016/j.virusres.2023.199210. Epub 2023 Sep 1.
Numerous studies have documented that the interaction of viral and cellular proteins is essential in the viral life cycle. In our previous study, to screen cellular proteins that take part in the life cycle of JEV, cellular proteins that interacted with JEV NS3 were identified by Co-immunoprecipitation coupled with mass spectrometry analysis (Co-IP-MS), the results showed that ILF2, DnaJA1, DnaJA2, CKB, TUFM, and PABPC1 that putatively interact with NS3. Another candidate protein, DnaJA2, which interacted with JEV NS3 protein, was selected for further study. Overexpression of DnaJA2 increased JEV infection. Conversely, the knockdown of DnaJA2 suppressed JEV infection. Furthermore, DnaJA2 interacted with NS5 besides NS3 and colocalized with viral dsRNA. Additionally, the level of viral NS3 protein expression was higher in cells overexpressing DnaJA2 than in cells with empty vector expression, whereas DnaJA2 knockdown resulted in NS3 protein degradation, which was subsequently restored by MG132 treatment. Further analysis revealed that the C-terminal of DnaJA2 was a critical domain for interaction with NS3 and promoted JEV infection. Collectively, our study identified DnaJA2 as an essential host factor required for JEV infection, potentially representing a novel therapeutic target for the development of antiviral therapies against JEV.
大量研究表明,病毒蛋白与细胞蛋白的相互作用在病毒生命周期中至关重要。在我们之前的研究中,为了筛选参与日本脑炎病毒(JEV)生命周期的细胞蛋白,通过免疫共沉淀结合质谱分析(Co-IP-MS)鉴定了与JEV NS3相互作用的细胞蛋白,结果显示ILF2、DnaJA1、DnaJA2、CKB、TUFM和PABPC1可能与NS3相互作用。另一种与JEV NS3蛋白相互作用的候选蛋白DnaJA2被选作进一步研究对象。DnaJA2的过表达增加了JEV感染。相反,敲低DnaJA2可抑制JEV感染。此外,DnaJA2除了与NS3相互作用外,还与NS5相互作用并与病毒双链RNA共定位。另外,过表达DnaJA2的细胞中病毒NS3蛋白表达水平高于空载体表达的细胞,而敲低DnaJA2导致NS3蛋白降解,随后用MG132处理可恢复。进一步分析表明,DnaJA2的C末端是与NS3相互作用并促进JEV感染的关键结构域。总之,我们的研究确定DnaJA2是JEV感染所需的必需宿主因子,可能代表针对JEV开发抗病毒疗法的新治疗靶点。