Dimitrov D S, Willey R L, Sato H, Chang L J, Blumenthal R, Martin M A
Section on Membrane Structure and Function, National Cancer Institute, Bethesda, Maryland 20892.
J Virol. 1993 Apr;67(4):2182-90. doi: 10.1128/JVI.67.4.2182-2190.1993.
Tissue culture infections of CD4-positive human T cells by human immunodeficiency virus type 1 (HIV-1) proceed in three stages: (i) a period following the initiation of an infection during which no detectable virus is produced; (ii) a phase in which a sharp increase followed by a peak of released progeny virions can be measured; and (iii) a final period when virus production declines. In this study, we have derived equations describing the kinetics of HIV-1 accumulation in cell culture supernatants during multiple rounds of infection. Our analyses indicated that the critical parameter affecting the kinetics of HIV-1 infection is the infection rate constant k = Inn/ti, where n is the number of infectious virions produced by one cell (about 10(2)) and ti is the time required for one complete cycle of virus infection (typically 3 to 4 days). Of particular note was our finding that the infectivity of HIV-1 during cell-to-cell transmission is 10(2) to 10(3) times greater than the infectivity of cell-free virus stocks, the inocula commonly used to initiate tissue culture infections. We also demonstrated that the slow infection kinetics of an HIV-1 tat mutant is not due to a longer replication time but reflects the small number of infectious particles produced per cycle.
1型人类免疫缺陷病毒(HIV-1)对CD4阳性人类T细胞的组织培养感染过程分为三个阶段:(i)感染开始后的一段时间,在此期间检测不到病毒产生;(ii)一个阶段,在此阶段可测量到释放的子代病毒颗粒急剧增加然后达到峰值;以及(iii)病毒产生下降的最后阶段。在本研究中,我们推导了描述多轮感染期间HIV-1在细胞培养上清液中积累动力学的方程。我们的分析表明,影响HIV-1感染动力学的关键参数是感染率常数k = Inn/ti,其中n是一个细胞产生的感染性病毒颗粒数量(约10²),ti是病毒感染一个完整周期所需的时间(通常为3至4天)。特别值得注意的是,我们发现HIV-1在细胞间传播期间的感染性比无细胞病毒储备(通常用于启动组织培养感染的接种物)的感染性大10²至10³倍。我们还证明,HIV-1 tat突变体的缓慢感染动力学不是由于复制时间更长,而是反映了每个周期产生的感染性颗粒数量较少。