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dc.contributor.authorShi, B
dc.contributor.authorPhilpott, SM
dc.contributor.authorWeiser, B
dc.contributor.authorKuiken, C
dc.contributor.authorBrunner, C
dc.contributor.authorFang, G
dc.contributor.authorFowke, KR
dc.contributor.authorPlummer, FA
dc.contributor.authorRowland-Jones, S
dc.contributor.authorBwayo, JJ
dc.contributor.authorAnzala Aggrey O.
dc.contributor.authorKimani, J
dc.contributor.authorKaul, R
dc.contributor.authorBurger, H
dc.date.accessioned2013-04-26T12:12:23Z
dc.date.available2013-04-26T12:12:23Z
dc.date.issued2004
dc.identifier.citationAIDS Res Hum Retroviruses. 2004 Sep;20(9):1015-8en
dc.identifier.urihttp://www.ncbi.nlm.nih.gov/pubmed/15585089
dc.identifier.urihttp://erepository.uonbi.ac.ke:8080/xmlui/handle/123456789/17125
dc.description.abstractThe 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 designen
dc.language.isoenen
dc.titleConstruction of an infectious HIV type 1 molecular clone from an African patient with a subtype D/C Recombinant Virus.en
dc.typeArticleen
local.publisherWadsworth Center, New York State Department of Health, Albany, New York 12208, USAen


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