| Literature DB >> 15585089 |
Binshan Shi1, Sean M Philpott, Barbara Weiser, Carla Kuiken, Cheryl Brunner, Guowei Fang, Keith R Fowke, Francis A Plummer, Sarah Rowland-Jones, Job Bwayo, Aggrey O Anzala, Joshua Kimani, Rupert Kaul, Harold Burger.
Abstract
The majority of HIV-1 infections worldwide occur in Africa, where subtype B viruses are rare and intersubtype recombinants are common. Pathogenesis and vaccine studies need to focus on viruses derived from African patients, and infectious HIV-1 molecular clones can be useful tools. To clone non-B subtypes and recombinant viruses from patients, we cultivated HIV-1 from the plasma of a Kenyan long-term survivor. Viral DNA was cloned into a plasmid, which was transfected into COS cells; progeny virus was propagated in PBMCs. Sequence analyses revealed that both the patient's plasma HIV-1 RNA and the cloned DNA genomes were recombinants between subtypes D and C; subtype C sequences comprised the nef and LTR regions. The cloned virus used the CCR5 coreceptor and did not form syncytia in vitro. This infectious HIV-1 subtype D/C recombinant molecular clone obtained from a Kenyan long-term survivor promises to be useful to study pathogenesis and vaccine design.Entities:
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Year: 2004 PMID: 15585089 DOI: 10.1089/aid.2004.20.1015
Source DB: PubMed Journal: AIDS Res Hum Retroviruses ISSN: 0889-2229 Impact factor: 2.205