Burns D P, Desrosiers R C
New England Regional Primate Research Center, Harvard Medical School, Southborough, Massachusetts 01772.
J Virol. 1991 Apr;65(4):1843-54. doi: 10.1128/JVI.65.4.1843-1854.1991.
Genetic and antigenic variation may be one means by which lentiviruses that cause AIDS avoid elimination by host immune responses. Genetic variation in the envelope gene (env) was studied by comparing the nucleotide sequences of 27 clones obtained from two rhesus monkeys infected with molecularly cloned simian immunodeficiency virus. All 27 clones differed from each other and differed from the input clone in the gp120 (SU) portion of the envelope gene. Nucleotide substitutions were shown to accumulate with time at an average rate of 8.5 per 1,000 per year in SU. Surprisingly, the majority of nucleotide substitutions (81%) resulted in amino acid changes. Variation in SU was not random but occurred predominantly in five discrete regions. Within these variable regions, a remarkable 98% of the nucleotide substitutions changed the amino acid. These results demonstrate that extensive sequence variability accumulates in vivo after infection with molecularly cloned virus and that selection occurs in vivo for changes in distinct variable regions in env.
基因和抗原变异可能是导致艾滋病的慢病毒逃避宿主免疫反应清除的一种方式。通过比较从两只感染了分子克隆的猴免疫缺陷病毒的恒河猴获得的27个克隆的核苷酸序列,研究了包膜基因(env)的基因变异。所有27个克隆彼此不同,并且在包膜基因的gp120(SU)部分与输入克隆不同。核苷酸替换显示以每年每1000个平均8.5的速率随时间积累在SU中。令人惊讶的是,大多数核苷酸替换(81%)导致氨基酸变化。SU中的变异不是随机的,而是主要发生在五个离散区域。在这些可变区域内,高达98%的核苷酸替换改变了氨基酸。这些结果表明,感染分子克隆病毒后体内会积累广泛的序列变异性,并且在体内会选择env中不同可变区域的变化。