Sakai H, Shibata R, Sakuragi J, Sakuragi S, Kawamura M, Adachi A
Institute for Virus Research, Kyoto University, Japan.
J Virol. 1993 Mar;67(3):1663-6. doi: 10.1128/JVI.67.3.1663-1666.1993.
A highly sensitive single-round infection assay using a bacterial chloramphenicol acetyltransferase was developed to analyze an early stage of human immunodeficiency virus type 1 replication. By a combination of transfection and single-round infection assay, a virus with a vif mutation, depending on host cells from which the virus was derived, was demonstrated to be defective at the early phase of infection cycle. Analysis of viral proteins synthesized in cells indicated that incorporation of the Env surface protein into virions of the vif mutant, again in a cell-dependent way, was greatly restricted. Taken together, it is concluded that the Vif protein acts through modulation of the Env protein in the virions, directly or indirectly, to enhance viral infectivity in a certain cell type.
利用细菌氯霉素乙酰转移酶开发了一种高灵敏度的单轮感染检测方法,用于分析1型人类免疫缺陷病毒复制的早期阶段。通过转染和单轮感染检测相结合,发现携带vif突变的病毒,根据其来源的宿主细胞不同,在感染周期的早期存在缺陷。对细胞中合成的病毒蛋白进行分析表明,Env表面蛋白以细胞依赖的方式掺入vif突变体病毒颗粒的过程受到极大限制。综上所述,得出结论:Vif蛋白通过直接或间接调节病毒颗粒中的Env蛋白,在特定细胞类型中增强病毒感染性。