Boulerice F, Bour S, Geleziunas R, Lvovich A, Wainberg M A
Lady Davis Institute, Jewish General Hospital, Montreal, Quebec, Canada.
J Virol. 1990 Apr;64(4):1745-55. doi: 10.1128/JVI.64.4.1745-1755.1990.
Limiting-dilution techniques were employed to derive single-cell clones from U-937 cells that had been chronically infected with human immunodeficiency virus type 1. All clones thus obtained were positive for the presence of viral antigens; however, not all of the clones produced infectious progeny virus, as detected by the presence of reverse transcriptase (RT) activity in culture fluids. Six of these clones were monitored over time to determine whether their phenotype of human immunodeficiency virus type 1 expression was stable. Three clones maintained production of RT activity at a high level and showed a very high percentage of cells positive for viral p24 antigen, as determined by indirect immunofluorescence. The other three clones showed variations in either their levels of RT activity or the number of cells positive for p24, after which they stabilized. Infectious virus could be recovered from only three clones, as assessed by coculture experiments with different cell types. Two other clones were shown to produce noninfectious viruses. Molecular analyses at the DNA, RNA, and protein levels showed extensive variations between the viral isolates recovered from each clone.
采用极限稀释技术从长期感染1型人类免疫缺陷病毒的U - 937细胞中获得单细胞克隆。所有如此获得的克隆病毒抗原检测均呈阳性;然而,并非所有克隆都产生有感染性的子代病毒,这可通过培养液中逆转录酶(RT)活性的存在来检测。对其中6个克隆进行了长期监测,以确定它们1型人类免疫缺陷病毒的表达表型是否稳定。3个克隆维持高水平的RT活性,并且通过间接免疫荧光测定显示,病毒p24抗原阳性细胞的比例非常高。另外3个克隆在RT活性水平或p24阳性细胞数量上表现出变化,之后趋于稳定。通过与不同细胞类型共培养实验评估,仅从3个克隆中可回收有感染性的病毒。另外两个克隆显示产生无感染性的病毒。DNA、RNA和蛋白质水平的分子分析表明,从每个克隆中回收的病毒分离株之间存在广泛差异。