Courgnaud Valérie, Salemi Marco, Pourrut Xavier, Mpoudi-Ngole Eitel, Abela Bernadette, Auzel Philippe, Bibollet-Ruche Frédéric, Hahn Beatrice, Vandamme Anne-Mieke, Delaporte Eric, Peeters Martine
UR36, Institut de Recherche pour le Développement, and University of Montpellier I, France.
J Virol. 2002 Aug;76(16):8298-309. doi: 10.1128/jvi.76.16.8298-8309.2002.
In the present study, we describe a new simian immunodeficiency virus (SIV), designated SIVgsn, naturally infecting greater spot-nosed monkeys (Cercopithecus nictitans) in Cameroon. Together with SIVsyk, SIVgsn represents the second virus isolated from a monkey belonging to the Cercopithecus mitis group of the Cercopithecus genus. Full-length genome sequence analysis of two SIVgsn strains, SIVgsn-99CM71 and SIVgsn-99CM166, revealed that despite the close phylogenetic relationship of their hosts, SIVgsn was highly divergent from SIVsyk. First of all, they differ in their genomic organization. SIVgsn codes for a vpu homologue, so far a unique feature of the members of the SIVcpz/human immunodeficiency virus type 1 (HIV-1) lineage, and detailed phylogenetic analyses of various regions of the viral genome indicated that SIVgsn might be a mosaic of sequences with different evolutionary histories. SIVgsn was related to SIVsyk in Gag and part of Pol and related to SIVcpz in Env, and the middle part of the genome did not cluster significantly with any of the known SIV lineages. When comparing the two SIVgsn Env sequences with that of SIVcpz, a remarkable conservation was seen in the V3 loop, indicating a possible common origin for the envelopes of these two viruses. The habitats of the two subspecies of chimpanzees infected by SIVcpz overlap the geographic ranges of greater spot-nosed monkeys and other monkey species, allowing cross-species transmission and recombination between coinfecting viruses. The complex genomic structure of SIVgsn, the presence of a vpu gene, and its relatedness to SIVcpz in the envelope suggest a link between SIVgsn and SIVcpz and provide new insights about the origin of SIVcpz in chimpanzees.
在本研究中,我们描述了一种新的猿猴免疫缺陷病毒(SIV),命名为SIVgsn,它自然感染喀麦隆的大白鼻长尾猴(Cercopithecus nictitans)。与SIVsyk一起,SIVgsn是从猕猴属的白眉猴组的猴子中分离出的第二种病毒。对两种SIVgsn毒株SIVgsn-99CM71和SIVgsn-99CM166进行的全长基因组序列分析表明,尽管它们的宿主在系统发育上关系密切,但SIVgsn与SIVsyk高度不同。首先,它们在基因组组织上存在差异。SIVgsn编码一个vpu同源物,这是迄今为止SIVcpz/1型人类免疫缺陷病毒(HIV-1)谱系成员的独特特征,对病毒基因组各个区域的详细系统发育分析表明,SIVgsn可能是具有不同进化历史的序列的镶嵌体。SIVgsn在Gag和部分Pol中与SIVsyk相关,在Env中与SIVcpz相关,并且基因组的中间部分与任何已知的SIV谱系均无明显聚类。当将两个SIVgsn Env序列与SIVcpz的Env序列进行比较时,在V3环中观察到显著的保守性,表明这两种病毒的包膜可能有共同的起源。感染SIVcpz的两种黑猩猩亚种的栖息地与大白鼻长尾猴和其他猴类物种的地理范围重叠,这使得共感染病毒之间能够发生跨物种传播和重组。SIVgsn复杂的基因组结构、vpu基因的存在及其在包膜中与SIVcpz的相关性表明SIVgsn与SIVcpz之间存在联系,并为黑猩猩中SIVcpz的起源提供了新的见解。