Characterization of CXCR4-using HIV-1 during primary infection by ultra-deep pyrosequencing

J Antimicrob Chemother. 2013 Dec;68(12):2875-81. doi: 10.1093/jac/dkt290. Epub 2013 Jul 18.

Abstract

Objectives: R5 viruses have long been thought to account for almost all strains present in primary HIV-1 infections (PHIs), but recent studies using sensitive phenotypic assays have revealed that 3%-6.4% of subjects also harbour CXCR4-using viruses. Phenotypic assays provide only qualitative results: the presence or absence of CXCR4-using viruses. We have therefore used ultra-deep pyrosequencing (UDS) to determine the frequency of CXCR4-using viruses among HIV-1 quasispecies.

Methods: We first screened 200 patients for HIV-1 tropism using a sensitive phenotypic assay during PHI and identified 11 infected with an R5X4 dual/mixed (D/M) virus population. We then used UDS of the V3 env region with the geno2pheno algorithm (false positive rate = 5.75) to identify the HIV-1 quasispecies.

Results: CXCR4-using viruses were detected in all but 1 of the 11 patients by UDS, and accounted for 0.2%-100% of the virus populations. The frequency of CXCR4-using viruses was <20% in six subjects and 100% in four subjects. Virus populations containing 100% CXCR4-using variants during PHI persisted for at least 1-2 years after the acute phase. The CCR5 Δ32 heterozygous genotype was similarly prevalent in patients infected with D/M (27%) and R5 (15%) viruses.

Conclusions: UDS and the phenotype were concordant for determining HIV-1 coreceptor usage. UDS analysis indicated large differences in the percentage of CXCR4-using viruses in the HIV-1 quasispecies during PHI. Further studies should examine the impact of the proportion of CXCR4-using viruses on disease prognosis.

Keywords: HIV envelope protein gp120; HIV quasispecies; HIV tropism; V3 genotype; chemokine receptor.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Adult
  • Female
  • Genetic Variation
  • HIV Envelope Protein gp120 / genetics
  • HIV Infections / virology*
  • HIV-1 / classification
  • HIV-1 / genetics*
  • HIV-1 / physiology*
  • High-Throughput Nucleotide Sequencing*
  • Humans
  • Male
  • RNA, Viral / genetics*
  • Receptors, CXCR4 / metabolism*
  • Receptors, HIV / metabolism
  • Viral Tropism*
  • Young Adult

Substances

  • CXCR4 protein, human
  • HIV Envelope Protein gp120
  • RNA, Viral
  • Receptors, CXCR4
  • Receptors, HIV
  • gp120 protein, Human immunodeficiency virus 1