Shankarappa R, Gupta P, Learn G H, Rodrigo A G, Rinaldo C R, Gorry M C, Mullins J I, Nara P L, Ehrlich G D
Department of Pathology, University of Pittsburgh, Pennsylvania 15261, USA.
Virology. 1998 Feb 15;241(2):251-9. doi: 10.1006/viro.1997.8996.
Sequence variation displayed by the human immunodeficiency virus type 1 (HIV-1) has been proposed to be linked to the pathogenesis of acquired immunodeficiency syndrome (AIDS). To assess viral evolution during the course of infection, we evaluated sequence variability in the env variable domains in four HIV-1-infected individuals exhibiting differing profiles of CD4+ T cell decline when followed from seroconversion until the development of AIDS or loss of followup. Proviral sequences encoding the V3-V5 region of gp 120 were obtained following PCR amplification of peripheral blood mononuclear cell DNA and cloning. Virus in each patient was relatively homogeneous early in infection and then diverged with time, more consistently at its nonsynonymous sites. Just prior to or coincident with a rapid decline in CD4+ T cell numbers, sequences were found with basic amino acid substitutions clustered within and downstream of the gp 120 V3 domain. Within the constraints of the current data set, we conclude that the virus appears to continually accumulate changes in its amino acid sequences well into the time of marked CD4+ T cell decline.
人类免疫缺陷病毒1型(HIV-1)所表现出的序列变异被认为与获得性免疫缺陷综合征(AIDS)的发病机制有关。为了评估感染过程中的病毒进化,我们对4名HIV-1感染个体的env可变区序列变异性进行了评估,这些个体从血清转化开始随访,直至发展为AIDS或失访,呈现出不同的CD4+ T细胞下降情况。通过对外周血单核细胞DNA进行PCR扩增和克隆,获得了编码gp120 V3-V5区域的前病毒序列。每位患者体内的病毒在感染早期相对均一,随后随时间发生分化,在非同义位点的变化更为一致。就在CD4+ T细胞数量快速下降之前或同时,发现序列中存在碱性氨基酸替代,这些替代集中在gp120 V3结构域及其下游。在当前数据集的限制范围内,我们得出结论,在明显的CD4+ T细胞下降时期,病毒似乎在其氨基酸序列中持续积累变化。