Carrillo A, Trowbridge D B, Westervelt P, Ratner L
Department of Medicine, Washington University School of Medicine, St Louis, Missouri 63110.
Virology. 1993 Dec;197(2):817-24. doi: 10.1006/viro.1993.1664.
Determinants responsible for HIV-1 infection of T lymphoid cell lines were identified by functional analysis of chimeric proviral clones derived from T-cell line tropic-(HXB2) and non-T-cell line-tropic isolates (YU2, ADA). Replacement of the HXB2 V3 envelope loop sequence with that derived from YU2 resulted in a virus that is no longer T cell line-tropic. However, the reciprocal replacement using HXB2 V3 loop sequences did not confer upon either ADA or YU2 envelope proteins the ability to infect T cell lines. Furthermore, the resultant viruses were incapable of infection of primary lymphocytes. Single, double, and multiple point mutations made within the V3 loop sequence did not result in change in tropism, although mutations involving residue 275 resulted in a virus that was incapable of infecting primary lymphocytes but retained the ability to infect Jurkat T lymphoid cells. These results suggest that the V3 envelope determinant is necessary for T cell line infection, but other determinant(s) in envelope are also necessary to obtain infectious virus expression.
通过对源自T细胞系嗜性(HXB2)和非T细胞系嗜性分离株(YU2、ADA)的嵌合原病毒克隆进行功能分析,确定了导致HIV-1感染T淋巴细胞系的决定因素。用源自YU2的序列替换HXB2的V3包膜环序列,产生的病毒不再具有T细胞系嗜性。然而,用HXB2的V3环序列进行反向替换,并未赋予ADA或YU2包膜蛋白感染T细胞系的能力。此外,产生的病毒无法感染原代淋巴细胞。在V3环序列中进行的单点、双点和多点突变并未导致嗜性改变,尽管涉及275位残基的突变产生的病毒无法感染原代淋巴细胞,但仍保留感染Jurkat T淋巴细胞的能力。这些结果表明,V3包膜决定因素对于T细胞系感染是必需的,但包膜中的其他决定因素对于获得感染性病毒表达也是必需的。