Heidecker G, Lerche N W, Lowenstine L J, Lackner A A, Osborn K G, Gardner M B, Marx P A
J Virol. 1987 Oct;61(10):3066-71. doi: 10.1128/JVI.61.10.3066-3071.1987.
We have isolated a molecular clone of the full-length integrated provirus of simian acquired immune deficiency syndrome retrovirus serotype 1 (SRV-1) from a fatal case of simian acquired immune deficiency syndrome in a juvenile rhesus macaque. An integrated SRV-1 provirus was cloned, sequenced, and found to contain four large open reading frames encoding gag-precursor protein, protease, polymerase, and envelope. The proviral clone was transfected into D17 canine osteosarcoma cells and found to produce infectious virus. A comparison of the sequences of this clone with a noninfectious clone showed 20 differences, resulting in 10 amino acid changes. Also, a cluster of exchanges, short insertions, and deletions in the 5' leader sequences resulted in extension of the tRNA(Lys) primer-binding site from 14 to 19 nucleotides. Virus isolated from transfected cells was shown to be infectious and pathogenic, resulting in disease that followed the same time course and mortality as disease induced by uncloned, in vitro cultivated virus isolated from diseased animals. These results unequivocally show that a type D retrovirus (SRV-1) causes a fatal immunosuppressive syndrome in rhesus monkeys.
我们从一只幼年恒河猴患猿猴获得性免疫缺陷综合征的致命病例中,分离出了猿猴获得性免疫缺陷综合征逆转录病毒1型(SRV - 1)全长整合前病毒的分子克隆。一个整合的SRV - 1前病毒被克隆、测序,发现它包含四个大的开放阅读框,分别编码gag前体蛋白、蛋白酶、聚合酶和包膜蛋白。将该前病毒克隆转染到D17犬骨肉瘤细胞中,发现能产生感染性病毒。将此克隆的序列与一个无感染性的克隆进行比较,发现有20处差异,导致10个氨基酸发生变化。此外,5'前导序列中的一组交换、短插入和缺失导致tRNA(Lys)引物结合位点从14个核苷酸延长到19个核苷酸。从转染细胞中分离出的病毒具有感染性和致病性,所引发疾病的病程和死亡率与从未克隆的、从患病动物体外培养的病毒所引发的疾病相同。这些结果明确表明,一种D型逆转录病毒(SRV - 1)可在恒河猴中引发致命的免疫抑制综合征。