Literature DB >> 17411382

HIV type 1 subtype C gag and nef diversity in Southern Africa.

Helba Bredell1, Darren P Martin, Joanne Van Harmelen, Arvind Varsani, Haynes W Sheppard, Richard Donovan, Clive M Gray, Carolyn Williamson.   

Abstract

Several HIV-1 subtype C-specific gag- and/or nef-based vaccines are currently intended for clinical trial in southern Africa. Here we provide sequences of 64 gag and 45 nef genes sampled in Malawi, Zambia, Zimbabwe, and South Africa and assess the degree of southern African HIV-1 diversity that will confront these vaccines. Whereas reasonable phylogenetic evidence exists for geographical clustering of subtype C gag and nef sequences from various other parts of the world, there is little evidence of similar population founder effects in the southern African epidemic. The entire breadth of subtype C diversity is represented in the southern African genes suggesting there may be no advantage in producing region- or country-specific subtype C vaccines. We do not, however, find much evidence of intersubtype recombination in the Southern African genes, implying that the likelihood of vaccine failure due to the emergence of intersubtype recombinants is probably low.

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Year:  2007        PMID: 17411382     DOI: 10.1089/aid.2006.0232

Source DB:  PubMed          Journal:  AIDS Res Hum Retroviruses        ISSN: 0889-2229            Impact factor:   2.205


  14 in total

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8.  Characterization of HIV-1 gag and nef in Cameroon: further evidence of extreme diversity at the origin of the HIV-1 group M epidemic.

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Authors:  Emily Adland; Jonathan M Carlson; Paolo Paioni; Henrik Kløverpris; Roger Shapiro; Anthony Ogwu; Lynn Riddell; Graz Luzzi; Fabian Chen; Thambiah Balachandran; David Heckerman; Anette Stryhn; Anne Edwards; Thumbi Ndung'u; Bruce D Walker; Søren Buus; Philip Goulder; Philippa C Matthews
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