Frolov I, Schlesinger S
Department of Molecular Microbiology, Washington University School of Medicine, St. Louis, Missouri 63110-1093.
J Virol. 1994 Mar;68(3):1721-7. doi: 10.1128/JVI.68.3.1721-1727.1994.
Infection of BHK cells by Sindbis virus leads to rapid inhibition of host cell protein synthesis and cytopathic effects (CPE). We have been studying these events to determine whether the expression of a specific viral gene is required and, in the present study, have focused our attention on the role of the structural proteins--the capsid protein and the two membrane glycoproteins. We tested a variety of Sindbis viruses and Sindbis virus replicons (virus particles containing an RNA that is self-replicating but with some or all of the viral structural protein genes deleted) for their abilities to inhibit host cell protein synthesis and cause CPE in infected BHK cells. Our results show that shutoff of host cell protein synthesis occurred in infected BHK cells when no viral structural proteins were synthesized and also under conditions in which the level of the viral subgenomic RNA was too low to be detected. These results support the conclusion that the early steps in viral gene expression are the ones required for the inhibition of host cell protein synthesis in BHK cells. In contrast, the Sindbis viruses and Sindbis virus replicons were clearly distinguished by the time at which CPE became evident. Viruses that synthesized high levels of the two membrane glycoproteins on the surface of the infected cells caused a rapid (12 to 16 h postinfection) appearance of CPE, and those that did not synthesize the glycoprotein spikes showed delayed (30 to 40 h) CPE.
辛德毕斯病毒感染BHK细胞会导致宿主细胞蛋白质合成迅速受到抑制,并产生细胞病变效应(CPE)。我们一直在研究这些事件,以确定是否需要特定病毒基因的表达,在本研究中,我们将注意力集中在结构蛋白——衣壳蛋白和两种膜糖蛋白的作用上。我们测试了多种辛德毕斯病毒和辛德毕斯病毒复制子(含有自我复制RNA但部分或全部病毒结构蛋白基因缺失的病毒颗粒)在感染BHK细胞时抑制宿主细胞蛋白质合成和引起CPE的能力。我们的结果表明,当没有合成病毒结构蛋白时,以及在病毒亚基因组RNA水平低到无法检测的条件下,感染的BHK细胞中宿主细胞蛋白质合成均会停止。这些结果支持了这样的结论,即病毒基因表达的早期步骤是BHK细胞中抑制宿主细胞蛋白质合成所必需的。相比之下,辛德毕斯病毒和辛德毕斯病毒复制子在CPE明显出现的时间上有明显区别。在感染细胞表面合成高水平两种膜糖蛋白的病毒会导致CPE迅速出现(感染后12至16小时),而那些不合成糖蛋白刺突的病毒则表现出延迟的CPE(30至40小时)。