Tokunaga K, Kojima A, Kurata T, Ikuta K, Akari H, Koyama A H, Kawamura M, Inubushi R, Shimano R, Adachi A
Department of Pathology, National Institute of Infectious Diseases, Tokyo, Japan.
J Gen Virol. 1998 Oct;79 ( Pt 10):2447-53. doi: 10.1099/0022-1317-79-10-2447.
The growth kinetics of wild-type and nef mutant viruses of human immunodeficiency virus type 1 were comparatively analysed in several human CD4+ cell lines. Delayed replication of nef mutant virus was observed in all cell lines examined. To determine the stage in the virus replication cycle that is affected by Nef, a single-round replication assay was performed. Initially, the expression of marker genes in transfected cells was examined in order to study the role of Nef in the late phase of infection. The results obtained indicated that Nef is dispensable during the transcription to virion production stage. Next, the effect of Nef on the early phase was investigated with a single-round infection. It was demonstrated that Nef is required in the early phase of the virus replication cycle, from virion adsorption to integration. Finally, the infectivity of virus stocks prepared from four cell lines was determined. The relative infectivity of the nef mutant from the four cell lines differed. Taken together, we conclude that Nef acts via modulation of viral particles to enhance virus infectivity in a cell-dependent manner.
在几种人CD4 +细胞系中对1型人类免疫缺陷病毒的野生型和nef突变病毒的生长动力学进行了比较分析。在所检测的所有细胞系中均观察到nef突变病毒的复制延迟。为了确定病毒复制周期中受Nef影响的阶段,进行了单轮复制试验。最初,检测转染细胞中标记基因的表达,以研究Nef在感染后期的作用。获得的结果表明,在转录至病毒体产生阶段,Nef是可有可无的。接下来,通过单轮感染研究Nef对早期阶段的影响。结果表明,在病毒复制周期的早期阶段,从病毒体吸附到整合,Nef是必需的。最后,测定了从四个细胞系制备的病毒株的感染性。来自四个细胞系的nef突变体的相对感染性有所不同。综上所述,我们得出结论,Nef通过调节病毒颗粒以细胞依赖性方式增强病毒感染性。