Liu Z Q, Wood C, Levy J A, Cheng-Mayer C
Department of Microbiology, University of Kansas, Lawrence 66045-2103.
J Virol. 1990 Dec;64(12):6148-53. doi: 10.1128/JVI.64.12.6148-6153.1990.
Human immunodeficiency virus type 1 (HIV-1) strains isolated from the central nervous system (CNS) may represent a subgroup that displays a host cell tropism different from those isolated from peripheral blood and lymph nodes. One CNS-derived isolate, HIV-1SF128A, which can be propagated efficiently in primary macrophage culture but not in any T-cell lines, was molecularly cloned and characterized. Recombinant viruses between HIV-1SF128A and the peripheral blood isolate HIV-1SF2 were generated in order to map the viral gene(s) responsible for the macrophage tropism. The env gene sequences of the two isolates are about 91.1% homologous, with variations scattered mainly in the hypervariable regions of gp120. Recombinant viruses that have acquired the HIV-1SF128A env gene display HIV-1SF128A tropism for macrophages. Furthermore, the gp120 variable domains, V1, V2, V4, and V5, the CD4-binding domain, and the gp41 fusion domain are not directly involved in determining macrophage tropism.
从中枢神经系统(CNS)分离出的1型人类免疫缺陷病毒(HIV-1)毒株可能代表了一个亚组,其表现出与从外周血和淋巴结分离出的毒株不同的宿主细胞嗜性。一种源自中枢神经系统的分离株HIV-1SF128A,它能在原代巨噬细胞培养物中高效繁殖,但不能在任何T细胞系中繁殖,已被进行分子克隆和特性分析。为了确定负责巨噬细胞嗜性的病毒基因,构建了HIV-1SF128A与外周血分离株HIV-1SF2之间的重组病毒。这两种分离株的env基因序列约有91.1%同源,差异主要分散在gp120的高变区。获得HIV-1SF128A env基因的重组病毒表现出HIV-1SF128A对巨噬细胞的嗜性。此外,gp120可变区V1、V2、V4和V5、CD4结合域以及gp41融合域并不直接参与决定巨噬细胞嗜性。