Fan Wenchun, Qian Ping, Wang Dandan, Zhi Xianwei, Wei Yanming, Chen Huanchun, Li Xiangmin
State Key Laboratory of Agricultural Microbiology, Huazhong Agricultural University, Wuhan, Hubei 430070, PR China; Laboratory of Animal Virology, College of Veterinary Medicine, Huazhong Agricultural University, Wuhan, Hubei 430070, PR China.
State Key Laboratory of Agricultural Microbiology, Huazhong Agricultural University, Wuhan, Hubei 430070, PR China; Laboratory of Animal Virology, College of Veterinary Medicine, Huazhong Agricultural University, Wuhan, Hubei 430070, PR China; The Cooperative Innovation Center for Sustainable Pig Production, Huazhong Agricultural University, Wuhan, Hubei 430070, PR China.
Res Vet Sci. 2017 Apr;111:67-74. doi: 10.1016/j.rvsc.2016.12.007. Epub 2016 Dec 28.
Japanese encephalitis virus (JEV) is a mosquito-borne flavivirus that is one of the major causes of viral encephalitis diseases worldwide. The JEV envelope protein facilitates viral entry, and its domain III contains an Arg-Gly-Asp (RGD) motif, that may modulate JEV entry through the RGD-binding integrin. In this study, the roles of integrin αv and β3 on the infection of JEV were evaluated. Reduced expression of integrin αv/β3 by special shRNA confers 2 to 4-fold inhibition of JEV replication in BHK-21 cells. Meanwhile, antibodies specific for integrin αv/β3 displayed ~58% and ~33% inhibition of JEV infectivity and RGD-specific peptides produced ~36% of inhibition. Expression of E protein and JEV RNA loads were clearly increased in CHO cells transfected with cDNA encoding human integrin β3. Moreover, integrin αv mediates JEV infection in viral binding stage of life cycle. Therefore, our study suggested that integrin αv and β3 serve as a host factor associated with JEV entry into the target cells.
日本脑炎病毒(JEV)是一种由蚊子传播的黄病毒,是全球病毒性脑炎疾病的主要病因之一。JEV包膜蛋白促进病毒进入,其结构域III包含一个精氨酸-甘氨酸-天冬氨酸(RGD)基序,该基序可能通过RGD结合整合素来调节JEV的进入。在本研究中,评估了整合素αv和β3对JEV感染的作用。通过特殊的短发夹RNA(shRNA)降低整合素αv/β3的表达,可使BHK-21细胞中JEV复制受到2至4倍的抑制。同时,针对整合素αv/β3的特异性抗体对JEV感染性的抑制率约为58%,RGD特异性肽的抑制率约为36%。在转染了编码人整合素β3的cDNA的CHO细胞中,E蛋白的表达和JEV RNA载量明显增加。此外,整合素αv在病毒生命周期的结合阶段介导JEV感染。因此,我们的研究表明,整合素αv和β3作为与JEV进入靶细胞相关的宿主因子。