Zhao Qin, Miao Chang, Chen Yi-Ting, Zhu Long-Yue, Zhang Ya-Ting, Luo Sai-Qi, Wang Yu-Luo, Zhu Zhu-Ming, Han Xinfeng, Wen Yiping, Wu Rui, Du Senyan, Yan Qi-Gui, Huang Xiaobo, Zhao Shan, Lang Yi-Fei, Wang Yiping, Zheng Yi, Zhao Fei, Cao San-Jie
Research Center for Swine Diseases, College of Veterinary Medicine, Sichuan Agricultural University, Chengdu 611130, China.
National Demonstration Center for Experimental Animal Education, Sichuan Agricultural University, Chengdu 611130, China.
Microorganisms. 2024 Aug 31;12(9):1804. doi: 10.3390/microorganisms12091804.
Although the (JEV) infects various cell types, its receptor molecules are still not clearly understood. In our laboratory's prior research, Rab4b was identified as a potential host factor that facilitates JEV infection in PK15 cells, utilizing a genome-wide CRISPR/Cas9 knockout library (PK-15-GeCKO). To further explore the effect of Rab4b on JEV replication, we used the knockout PK15 cell line using the CRISPR/Cas9 technology and overexpressing the PK15 cell line, with IFA, RT-qPCR, and Western blot to study the effect of Rab4b on viral replication in the whole life cycle of the JEV. The results show that the knockout of inhibited the replication of the JEV in PK15 cells, and the overexpression of promoted the replication of the JEV in PK15 cell lines. Furthermore, we demonstrated for the first time that host factor Rab4b facilitates the adsorption, internalization, assembly, and release of the JEV, thereby promoting JEV replication. This study enriches the regulatory network between the JEV and host factors and lays the experimental foundation for further understanding of the function of the Rab4b protein.
虽然日本脑炎病毒(JEV)可感染多种细胞类型,但其受体分子仍未完全明确。在我们实验室之前的研究中,利用全基因组CRISPR/Cas9敲除文库(PK-15-GeCKO),Rab4b被鉴定为促进JEV在PK15细胞中感染的潜在宿主因子。为进一步探究Rab4b对JEV复制的影响,我们利用CRISPR/Cas9技术构建了Rab4b基因敲除的PK15细胞系以及Rab4b过表达的PK15细胞系,通过间接免疫荧光法(IFA)、实时定量聚合酶链反应(RT-qPCR)和蛋白质免疫印迹法(Western blot)研究Rab4b对JEV全生命周期病毒复制的影响。结果显示,Rab4b基因敲除抑制了JEV在PK15细胞中的复制,而Rab4b过表达则促进了JEV在PK15细胞系中的复制。此外,我们首次证明宿主因子Rab4b促进了JEV的吸附、内化、组装和释放,从而促进JEV的复制。本研究丰富了JEV与宿主因子之间的调控网络,为进一步了解Rab4b蛋白的功能奠定了实验基础。