Tokunaga K
Section of Serology, Hokkaido University, Sapporo, Japan.
Hokkaido Igaku Zasshi. 1996 May;71(3):345-57.
We comparatively analyzed the replication kinetics of wild-type (wt) and nef mutant human immunodeficiency virus type 1 (HIV-1) in several CD4-positive cell lines, in order to clarify the molecular function of Nef protein. The delayed growth of nef mutant virus was observed at the initial stage of replication in all cell lines examined. This phenomenon was greatly amplified in the absence of vpu gene. In order to determine the infection stage in viral replication cycle which is specifically affected on virus replication rate in the presence of the Nef protein, we first examined the difference between wt and nef mutant viruses in the virus production rate from transfected cells, and found that the both viruses were produced with equal efficiency. This result showed that Nef protein could be dispensable for virion production. Therefore, early infection stages were focused by single-round infection assay, and the nef mutant virus was found to be much less infectious than wt virus. This indicated that the effect of Nef protein was exhibited in the early phase of a virus replication cycle, during viral adsorption to integration. By entry assay using wt and nef mutant virions, it was revealed that the Nef protein was required for efficient viral entry. These data suggest that the Nef protein might play a role in efficient incorporation of the Env protein into the virions, leading to enhanced viral infectivity.
为阐明Nef蛋白的分子功能,我们比较分析了野生型(wt)和nef突变型1型人类免疫缺陷病毒(HIV-1)在几种CD4阳性细胞系中的复制动力学。在所有检测的细胞系中,nef突变病毒在复制初期均出现生长延迟。在没有vpu基因的情况下,这种现象被大大放大。为了确定在存在Nef蛋白时病毒复制周期中对病毒复制速率有特异性影响的感染阶段,我们首先检测了wt病毒和nef突变病毒在转染细胞中病毒产生率的差异,发现两种病毒的产生效率相同。这一结果表明,Nef蛋白对于病毒粒子的产生可能是可有可无的。因此,通过单轮感染试验聚焦于早期感染阶段,发现nef突变病毒的感染性远低于wt病毒。这表明Nef蛋白的作用在病毒复制周期的早期阶段,即病毒吸附到整合过程中表现出来。通过使用wt和nef突变病毒粒子的进入试验,发现Nef蛋白是病毒有效进入所必需的。这些数据表明,Nef蛋白可能在Env蛋白有效掺入病毒粒子中发挥作用,从而导致病毒感染性增强。