Bruce C, Clegg C, Featherstone A, Smith J, Oram J
Centre for Applied Microbiology and Research, Public Health Laboratory Service, Porton Down, Salisbury, England.
AIDS Res Hum Retroviruses. 1993 Apr;9(4):357-63. doi: 10.1089/aid.1993.9.357.
DNA sequences encoding the surface glycoprotein gp120 of the human immunodeficiency virus type 1 (HIV-1) were amplified by the polymerase chain reaction (PCR) from peripheral blood mononuclear cells obtained from a Ugandan AIDS patient. The PCR-amplified DNA was cloned into a phagemid vector and nine clones sequenced. The gp120 sequences of the proviruses were similar to that of the Zairian isolate HIV-JY1 and unlike that of another Ugandan provirus, U455. Six of the clones were closely related to each other (maximum nucleotide sequence divergence 1.9%), and had a V3 amino acid sequence similar to that frequently seen in recent isolates from Uganda. Two others formed a second group that diverged from the first by an average of 6.0% at the nucleotide level, resulting in a 12.5% divergence of amino acid sequence. These divergent clones had extensive amino acid sequence changes not only in the V3 region, which was highly atypical, but also in V1 and V4, and to a lesser extent in V2 and V5. A further proviral clone had a sequence intermediate between those of the other two groups of clones.
通过聚合酶链反应(PCR)从一名乌干达艾滋病患者的外周血单核细胞中扩增出编码人类免疫缺陷病毒1型(HIV-1)表面糖蛋白gp120的DNA序列。将PCR扩增的DNA克隆到噬菌粒载体中,并对9个克隆进行测序。前病毒的gp120序列与扎伊尔分离株HIV-JY1的序列相似,与另一个乌干达前病毒U455的序列不同。其中6个克隆彼此密切相关(最大核苷酸序列差异为1.9%),其V3氨基酸序列与最近从乌干达分离出的毒株中常见的序列相似。另外两个克隆形成了第二组,在核苷酸水平上与第一组平均相差6.0%,导致氨基酸序列差异为12.5%。这些不同的克隆不仅在高度非典型的V3区域有广泛的氨基酸序列变化,在V1和V4区域也有变化,在V2和V5区域变化较小。另一个前病毒克隆的序列介于其他两组克隆之间。