Zhu Jie, Miao Qiuhong, Tan Yonggui, Guo Huimin, Li Chuanfeng, Chen Zongyan, Liu Guangqing
Shanghai Veterinary Research Institute, Chinese Academy of Agricultural Sciences, Shanghai, 200241, PR China.
Shanghai Veterinary Research Institute, Chinese Academy of Agricultural Sciences, Shanghai, 200241, PR China.
J Virol Methods. 2016 Nov;237:86-91. doi: 10.1016/j.jviromet.2016.09.006. Epub 2016 Sep 5.
Rabbit hemorrhagic disease virus (RHDV) is an important member of the caliciviridae family. Currently, no suitable tissue culture system is available for proliferating RHDV, which limits the study of its pathogenesis. To bypass this obstacle, we established a cell line, RK13-VPg, stably expressing the VPg gene with a lentivirus packaging system in this study. In addition, the recently constructed RHDV replicon in our laboratory provided an appropriate model for studying the pathogenesis of RHDV without in vitro RHDV propagation and culture. Using this RHDV replicon and RK13-VPg cell line, we further demonstrated that the presence of VPg protein is essential for efficient translation of an RHDV replicon. Therefore, the RK13-VPg cell line is a powerful tool for studying the replication and translation mechanisms of RHDV.
兔出血症病毒(RHDV)是杯状病毒科的重要成员。目前,尚无合适的组织培养系统可用于增殖RHDV,这限制了对其发病机制的研究。为绕过这一障碍,我们在本研究中利用慢病毒包装系统建立了稳定表达VPg基因的细胞系RK13-VPg。此外,我们实验室最近构建的RHDV复制子为在无体外RHDV增殖和培养的情况下研究RHDV发病机制提供了合适的模型。利用该RHDV复制子和RK13-VPg细胞系,我们进一步证明VPg蛋白的存在对于RHDV复制子的高效翻译至关重要。因此,RK13-VPg细胞系是研究RHDV复制和翻译机制的有力工具。