Gao F, Robertson D L, Carruthers C D, Li Y, Bailes E, Kostrikis L G, Salminen M O, Bibollet-Ruche F, Peeters M, Ho D D, Shaw G M, Sharp P M, Hahn B H
Department of Medicine and Microbiology, University of Alabama at Birmingham, Birmingham, Alabama 35294, USA.
J Virol. 1998 Dec;72(12):10234-41. doi: 10.1128/JVI.72.12.10234-10241.1998.
Full-length reference clones and sequences are currently available for eight human immunodeficiency virus type 1 (HIV-1) group M subtypes (A through H), but none have been reported for subtypes I and J, which have only been identified in a few individuals. Phylogenetic information for subtype I, in particular, is limited since only about 400 bp of env gene sequences have been determined for just two epidemiologically linked viruses infecting a couple who were heterosexual intravenous drug users from Cyprus. To characterize subtype I in greater detail, we employed long-range PCR to clone a full-length provirus (94CY032.3) from an isolate obtained from one of the individuals originally reported to be infected with this subtype. Phylogenetic analysis of C2-V3 env gene sequences confirmed that 94CY032.3 was closely related to sequences previously classified as subtype I. However, analysis of the remainder of its genome revealed various regions in which 94CY032.3 was significantly clustered with either subtype A or subtype G. Only sequences located in vpr and nef, as well as the middle portions of pol and env, formed independent lineages roughly equidistant from all other known subtypes. Since these latter regions most likely have a common origin, we classify them all as subtype I. These results thus indicate that the originally reported prototypic subtype I isolate 94CY032 represents a triple recombinant (A/G/I) with at least 11 points of recombination crossover. We also screened HIV-1 recombinants with regions of uncertain subtype assignment for the presence of subtype I sequences. This analysis revealed that two of the earliest mosaics from Africa, Z321B (A/G/?) and MAL (A/D/?), contain short segments of sequence which clustered closely with the subtype I domains of 94CY032.3. Since Z321 was isolated in 1976, subtype I as well as subtypes A and G must have existed in Central Africa prior to that date. The discovery of subtype I in HIV-1 hybrids from widely distant geographic locations also suggests a more widespread distribution of this virus subtype, or at least segments of it, than previously recognized.
目前已有8种人类免疫缺陷病毒1型(HIV-1)M组亚型(A至H)的全长参考克隆和序列,但尚未有I型和J型亚型的相关报道,这两种亚型仅在少数个体中被鉴定出来。特别是I型亚型的系统发育信息有限,因为仅针对来自塞浦路斯的一对异性恋静脉吸毒夫妇感染的两种具有流行病学关联的病毒,测定了约400 bp的env基因序列。为了更详细地鉴定I型亚型,我们采用长距离PCR从最初报道感染该亚型的一名个体所获得的分离株中克隆了一个全长前病毒(94CY032.3)。对C2-V3 env基因序列的系统发育分析证实,94CY032.3与先前归类为I型亚型的序列密切相关。然而,对其基因组其余部分的分析显示,94CY032.3在各个区域与A亚型或G亚型显著聚类。仅位于vpr和nef以及pol和env中间部分的序列形成了与所有其他已知亚型大致等距的独立谱系。由于后述这些区域很可能有共同起源,我们将它们全部归类为I型亚型。因此,这些结果表明,最初报道的原型I型亚型分离株94CY032代表一种具有至少11个重组交叉点的三重重组体(A/G/I)。我们还筛选了亚型归属不确定区域的HIV-1重组体,以寻找I型亚型序列的存在情况。该分析表明,来自非洲的最早的两种嵌合体Z321B(A/G/?)和MAL(A/D/?)包含与94CY032.3的I型亚型结构域紧密聚类的短序列片段。由于Z321于1976年分离得到,I型亚型以及A亚型和G亚型在该日期之前必定已存在于中非地区。在来自遥远地理位置的HIV-1杂交体中发现I型亚型也表明,该病毒亚型或至少其部分片段的分布比先前认识的更为广泛。