Holterman L, Dubbes R, Mullins J, Learn G, Niphuis H, Koornstra W, Koopman G, Kuhn E M, Wade-Evans A, Rosenwirth B, Haaijman J, Heeney J
Department of Virology, Biomedical Primate Research Centre, 2280 GH Rijswijk, The Netherlands.
J Virol. 2001 Oct;75(19):9328-38. doi: 10.1128/JVI.75.19.9328-9338.2001.
End-stage simian immunodeficiency virus (SIV) isolates are suggested to be the most fit of the evolved virulent variants that precipitate the progression to AIDS. To determine if there were common characteristics of end-stage variants which emerge from accelerated cases of AIDS, a molecular clone was derived directly from serum following in vivo selection of a highly virulent SIV isolate obtained by serial end-stage passage in rhesus monkeys (Macaca mulatta). This dominant variant caused a marked cytopathic effect and replicated to very high levels in activated but not resting peripheral blood lymphocytes. Furthermore, although this clone infected but did not replicate to detectable levels in rhesus monocyte-derived macrophages, these cells were able to transmit infection to autologous T cells upon contact. Interestingly, although at low doses this end-stage variant did not use any of the known coreceptors except CCR5, it was able to infect and replicate in human peripheral blood mononuclear cells homozygous for the Delta 32 deletion of CCR5, suggesting the use of a novel coreceptor. It represents the first pathogenic molecular clone of SIV derived from viral RNA in serum and provides evidence that not only the genetic but also the biological characteristics acquired by highly fit late-stage disease variants may be distinct in different hosts.
晚期猿猴免疫缺陷病毒(SIV)分离株被认为是最适应进化出的毒性变体,这些变体促使疾病进展至艾滋病。为了确定从艾滋病加速病例中出现的晚期变体是否具有共同特征,我们通过在恒河猴(猕猴)中进行连续晚期传代获得了一种高毒性SIV分离株,并在体内选择后直接从血清中获得了一个分子克隆。这种优势变体引起了明显的细胞病变效应,并在活化而非静止的外周血淋巴细胞中复制到非常高的水平。此外,尽管该克隆能感染恒河猴单核细胞衍生的巨噬细胞,但无法复制到可检测水平,然而这些细胞在接触后能够将感染传递给自体T细胞。有趣的是,尽管在低剂量时,这种晚期变体除了CCR5外不使用任何已知的共受体,但它能够感染并在CCR5基因Delta 32缺失的纯合人类外周血单核细胞中复制,这表明它使用了一种新的共受体。它代表了首个从血清中的病毒RNA获得的SIV致病分子克隆,并提供了证据表明,不仅高度适应的晚期疾病变体所获得的遗传特征,而且其生物学特征在不同宿主中可能有所不同。