Tang S, Poulin L, Levy J A
Cancer Research Institute, University of California, School of Medicine, San Francisco 94143-0128.
J Gen Virol. 1992 Apr;73 ( Pt 4):933-9. doi: 10.1099/0022-1317-73-4-933.
Human immunodeficiency virus type 1 (HIV-1) infection of the CD4+ SupT and CEM cell lines, blocked in cell replication by the polymerase alpha inhibitor aphidicolin (APC), was studied. The APC-treated cells showed a lack of viral production, but the presence of single cell killing. High levels of unintegrated viral DNA forms were found in the infected APC-treated cells as compared with untreated cells. Moreover, an increased rate of viral replication occurred in the remaining viable cells following removal of APC. The results indicate that HIV-1 entry and reverse transcription can take place in cells blocked in the S phase of the cell cycle. Replication of infectious progeny virions appears to require de novo cell division. Finally, accumulation of viral DNA in cells during APC treatment can result in cytopathological effects and subsequent enhancement of virus production.
研究了1型人类免疫缺陷病毒(HIV-1)对CD4+ SupT和CEM细胞系的感染情况,这些细胞系被聚合酶α抑制剂阿非科林(APC)阻断了细胞复制。经APC处理的细胞显示没有病毒产生,但存在单细胞杀伤现象。与未处理的细胞相比,在经APC处理的受感染细胞中发现了高水平的未整合病毒DNA形式。此外,去除APC后,剩余存活细胞中的病毒复制速率增加。结果表明,HIV-1的进入和逆转录可以在细胞周期S期被阻断的细胞中发生。感染性子代病毒颗粒的复制似乎需要重新进行细胞分裂。最后,在APC处理期间细胞中病毒DNA的积累可导致细胞病理效应并随后增强病毒产生。