Ott D E, Nigida S M, Henderson L E, Arthur L O
AIDS Vaccine Program, Program Resources Inc./DynCorp, National Cancer Institute, Frederick Cancer Research and Development Center, Maryland 21702-1201.
J Virol. 1995 Apr;69(4):2443-50. doi: 10.1128/JVI.69.4.2443-2450.1995.
We have isolated seven single-cell clones from an H9 culture infected with human immunodeficiency virus type 1 strain MN so that a stable producer of virus could be obtained. DNAs from these clones were examined by Southern blot analysis and found to contain between one and four proviruses per clone. One of these cell lines, Clone 4, produced high levels of replication-competent virus and contained two proviruses. Southern blot analysis of DNAs from Clone 4 revealed that, after extended culture, some of the cells had acquired additional proviruses, presumably by superinfection. Analysis of Clone 4 single-cell subclones isolated from a late-passage culture found that 14 out of 20 (70%) subclones were reinfected and that 8 out of 20 (40%) were reinfected more than once. Fluorescence-activated cell sorter analysis showed that surface CD4 levels on Clone 4 cells were appropriately down-regulated. Our results indicate that while there is significant interference to superinfection in the Clone 4 culture, it is not absolute and that superinfected cells accumulate in the culture over time in the presence of high virus exposure and extensive cell-to-cell contact. Given our data, it seems likely that superinfection can occur in vivo within the lymphoid reservoirs that harbor human immunodeficiency virus type 1 during the clinically latent period and may contribute to disease progression.
我们从感染了1型人类免疫缺陷病毒MN株的H9培养物中分离出7个单细胞克隆,以便获得稳定的病毒生产者。通过Southern印迹分析检测这些克隆的DNA,发现每个克隆含有1至4个前病毒。其中一个细胞系,克隆4,产生高水平的具有复制能力的病毒,并且含有两个前病毒。对克隆4的DNA进行Southern印迹分析表明,在长期培养后,一些细胞获得了额外的前病毒,推测是通过重复感染。对从晚期传代培养物中分离出的克隆4单细胞亚克隆进行分析发现,20个亚克隆中有14个(70%)被再次感染,20个中有8个(40%)被多次再次感染。荧光激活细胞分选分析表明,克隆4细胞表面的CD4水平被适当下调。我们的结果表明,虽然在克隆4培养物中对重复感染有显著干扰,但并非绝对,并且在高病毒暴露和广泛的细胞间接触的情况下,随着时间的推移,重复感染的细胞在培养物中积累。根据我们的数据,重复感染似乎可能在临床潜伏期携带1型人类免疫缺陷病毒的淋巴样储存库内发生,并可能导致疾病进展。