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ABSTRACT: Background
The interaction of HIV-1 and target cells involves sequential binding of the viral gp120 Env protein to the CD4 receptor and a chemokine co-receptor (either CCR5 or CXCR4). CCR5 antagonists have proved to be an effective salvage therapy in patients with CCR5 using variants (R5) but not with variants capable of using CXCR4 (×4) phenotype. Thus, it is critically important to determine cellular tropism of a country's circulating HIV strains to guide a management decision to improve treatment outcome. In this study, we report the prevalence of R5 and ×4 HIV strains in 45 proviral DNA massively parallel sequencing "MPS" data from recently infected Brazilian blood donors.Methods
The MPS data encompassing the tropism-related V3 loop region of the HIV-1 env gene was extr
SUBMITTER: Pessoa R
PROVIDER: S-EPMC4438479 | biostudies-literature | 2015 May
REPOSITORIES: biostudies-literature