Jin M J, Hui H, Robertson D L, Müller M C, Barré-Sinoussi F, Hirsch V M, Allan J S, Shaw G M, Sharp P M, Hahn B H
Department of Medicine, University of Alabama at Birmingham 35294.
EMBO J. 1994 Jun 15;13(12):2935-47. doi: 10.1002/j.1460-2075.1994.tb06588.x.
Elucidation of the phylogenetic origins of simian and human immunodeficiency viruses (SIV and HIV) is fundamental to the understanding of HIV pathogenesis and the spread of AIDS worldwide. In this study, we molecularly characterized multiple SIVAGM isolates from four different African green monkey species (vervet, grivet, sabaeus and tantalus monkeys). Phylogenetic analysis of partial (1 kb) env sequences indicated that all SIVAGM strains cluster together, and that they fall into four distinct sequence sub-groups according to their species of origin. However, alignment of long terminal repeat sequences revealed that SIVs from West African sabaeus monkeys contain a structural feature (a duplication of the transactivation response element) thus far only found in otherwise highly divergent lentiviruses infecting sooty mangabeys (SIVSM) and humans (HIV-2). To determine whether there were additional similarities with the SIVSM/HIV-2 group, a full-length replication competent sabaeus provirus was cloned and sequenced. In phylogenetic trees derived from the central and 3' coding regions, the sabaeus virus clustered with SIVAGM isolates from other African green monkey species. However, in trees derived from the 3' half of gag and the adjacent 5' region of pol, the sabaeus virus grouped with the SIVSM/HIV-2 lineage. These results indicated that the sabaeus virus comprised a mosaic genome which must have resulted from recombination of divergent lentiviruses in the distant past. A second, independent sabaeus isolate exhibited similar phylogenetic relationships, suggesting that all West African green monkey viruses share this complex evolutionary history. Taken together, these results indicate that African green monkeys have been infected with SIVAGM for very long periods of time, and that recombination and cross-species transmission in the wild have contributed to the genetic complexity of primate lentiviruses.
阐明猿猴免疫缺陷病毒和人类免疫缺陷病毒(SIV和HIV)的系统发育起源对于理解HIV发病机制以及艾滋病在全球的传播至关重要。在本研究中,我们对来自四种不同非洲绿猴物种(黑长尾猴、灰绿猴、戴安娜须猴和赤腹长尾猴)的多个SIVAGM分离株进行了分子特征分析。对部分(1 kb)env序列的系统发育分析表明,所有SIVAGM毒株聚集在一起,并且根据其起源物种可分为四个不同的序列亚组。然而,长末端重复序列的比对显示,来自西非戴安娜须猴的SIV含有一种结构特征(反式激活应答元件的重复),迄今为止仅在感染乌黑白眉猴(SIVSM)和人类(HIV-2)的其他高度分化的慢病毒中发现。为了确定与SIVSM/HIV-2组是否存在其他相似性,克隆并测序了一个全长具有复制能力的戴安娜须猴原病毒。在源自中央和3'编码区的系统发育树中,戴安娜须猴病毒与来自其他非洲绿猴物种的SIVAGM分离株聚集在一起。然而,在源自gag的3'半部分和pol的相邻5'区域的树中,戴安娜须猴病毒与SIVSM/HIV-2谱系归为一组。这些结果表明,戴安娜须猴病毒包含一个镶嵌基因组,这一定是在遥远的过去由不同慢病毒的重组产生的。第二个独立的戴安娜须猴分离株表现出相似的系统发育关系,表明所有西非绿猴病毒都共享这种复杂的进化历史。综上所述,这些结果表明非洲绿猴感染SIVAGM的时间非常长,并且野生环境中的重组和跨物种传播导致了灵长类慢病毒的遗传复杂性。