Shioda T, Levy J A, Cheng-Mayer C
Department of Medicine, University of California, School of Medicine, San Francisco 94143-0128.
Proc Natl Acad Sci U S A. 1992 Oct 15;89(20):9434-8. doi: 10.1073/pnas.89.20.9434.
Human immunodeficiency virus type 1 (HIV-1) strains display a high degree of heterogeneity in their biological properties that correlate with in vivo pathogenesis of the virus. We previously demonstrated that overlapping regions encompassing the third hypervariable domain (V3), within the envelope glycoprotein gp120 determine the tropisms of HIV-1 for T-cell lines and primary macrophages. Studies with mutant viruses carrying one or more amino acid substitutions in the V3 loop have now identified this hypervariable domain as a major determinant for these cellular host range properties. Three to five amino acid changes in this domain, but rarely a single amino acid substitution, can confer macrophage tropism and alter T-cell-line tropism. These findings emphasize the effect on cell tropism of small amino acid differences in the viral envelope and suggest that the overall conformation of the V3 loop plays the major role in determining the ability of HIV-1 to infect T-cell lines and primary macrophages.
1型人类免疫缺陷病毒(HIV-1)毒株在其生物学特性上表现出高度的异质性,这些特性与该病毒的体内发病机制相关。我们之前证明,包膜糖蛋白gp120内包含第三个高变区(V3)的重叠区域决定了HIV-1对T细胞系和原代巨噬细胞的嗜性。对在V3环中携带一个或多个氨基酸替换的突变病毒的研究现已确定,这个高变区是这些细胞宿主范围特性的主要决定因素。该区域中三到五个氨基酸的变化,但很少是单个氨基酸替换,可赋予巨噬细胞嗜性并改变T细胞系嗜性。这些发现强调了病毒包膜中微小氨基酸差异对细胞嗜性的影响,并表明V3环的整体构象在决定HIV-1感染T细胞系和原代巨噬细胞的能力方面起主要作用。