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An isolate of human immunodeficiency virus type 1 originally classified as subtype I represents a complex mosaic
F Gao1, D L Robertson, C D Carruthers
1Department of Medicine and Microbiology, University of Alabama at Birmingham, Birmingham, Alabama 35294, USA.
Abstract:
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.
Insights
Human Immunodeficiency Virus type 1 (HIV-1) subtype I, previously poorly characterized, is identified as a triple recombinant virus (A/G/I). This finding suggests subtype I existed earlier and was more widespread than previously thought.
Area of Science:
- Virology
- Genetics
- Epidemiology
Background:
- Limited phylogenetic data exists for Human Immunodeficiency Virus type 1 (HIV-1) subtypes I and J.
- Previous characterization of subtype I was based on short env gene sequences from only two individuals.
Purpose of the Study:
- To perform a detailed characterization of HIV-1 subtype I using a full-length provirus clone.
- To investigate the origin and distribution of HIV-1 subtype I.
Main Methods:
- Employed long-range PCR to clone a full-length HIV-1 provirus (94CY032.3).
- Conducted phylogenetic analysis of env gene sequences (C2-V3) and the entire viral genome.
- Screened other HIV-1 recombinants for the presence of subtype I sequences.
Main Results:
- The 94CY032.3 isolate, classified as subtype I, was found to be a triple recombinant (A/G/I) with at least 11 recombination crossover points.
- Specific genomic regions (vpr, nef, middle pol, and env) formed independent lineages classified as subtype I.
- Segments of subtype I sequences were identified in early African HIV-1 mosaic viruses (Z321B, MAL), dating back to 1976.
Conclusions:
- HIV-1 subtype I is a recombinant subtype, likely originating from recombination between subtypes A, G, and I.
- Subtype I, along with subtypes A and G, existed in Central Africa prior to 1976.
- The presence of subtype I in geographically distant HIV-1 hybrids suggests a broader distribution than previously recognized.