Integrin αvβ3 promotes infection by Japanese encephalitis virus

被引:26
作者
Fan, Wenchun [1 ,2 ]
Qian, Ping [1 ,2 ,3 ]
Wang, Dandan [1 ,2 ]
Zhi, Xianwei [1 ,2 ]
Wei, Yanming [1 ,2 ]
Chen, Huanchun [1 ,2 ,3 ]
Li, Xiangmin [1 ,2 ]
机构
[1] Huazhong Agr Univ, State Key Lab Agr Microbiol, Wuhan 430070, Hubei, Peoples R China
[2] Huazhong Agr Univ, Coll Vet Med, Lab Anim Virol, Wuhan 430070, Hubei, Peoples R China
[3] Huazhong Agr Univ, Cooperat Innovat Ctr Sustainable Pig Prod, Wuhan 430070, Hubei, Peoples R China
基金
中国国家自然科学基金;
关键词
Japanese encephalitis virus; Envelope protein; Integrin alpha v; Integrin beta 3; WEST-NILE-VIRUS; GLYCOPROTEIN DOMAIN-III; ENVELOPE GLYCOPROTEIN; PUTATIVE RECEPTOR; CELLULAR RECEPTOR; ENTRY; PROTEIN; CELLS; BINDING; ALPHA(V)BETA(3);
D O I
10.1016/j.rvsc.2016.12.007
中图分类号
S85 [动物医学(兽医学)];
学科分类号
0906 ;
摘要
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 alpha v and beta 3 on the infection of JEV were evaluated. Reduced expression of integrin alpha v/beta 3 by special shRNA confers 2 to 4-fold inhibition of JEV replication in BHK-21 cells. Meanwhile, antibodies specific for integrin alpha v/beta 3 displayed similar to 58% and similar to 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 beta 3. Moreover, integrin av mediates JEV infection in viral binding stage of life cycle. Therefore, our study suggested that integrin av and beta 3 serve as a host factor associated with JEV entry into the target cells. (C) 2016 Elsevier Ltd. All rights reserved.
引用
收藏
页码:67 / 74
页数:8
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