Human immunodeficiency virus envelope V1 and V2 regions influence replication efficiency in macrophages by affecting virus spread

Virology. 1995 Oct 20;213(1):70-9. doi: 10.1006/viro.1995.1547.

Abstract

The V3 hypervariable region of the HIV-1 envelope protein is a major determinant of viral tropism for macrophages. However, the replication of macrophage-tropic HIV-1 strains varies considerably in macrophages, and this variability has been linked to the V1 and V2 envelope regions. In the present study, recombinant HIV clones were generated by inserting V1 and V2 sequences from the Ba-L HIV isolate, which has a high macrophage replication level, into the genomic background of a macrophage-tropic clone with a low macrophage replication level. Infection of macrophages with varying multiplicities of infection and direct detection of the number of infected macrophages per culture showed that the Ba-L V1 and V2 envelope sequences enhanced the ability of virus to spread in the cultures. In contrast, macrophage-tropic clones with low replication efficiency infected macrophages initially but showed no evidence of spread to additional cells during the culture period. This effect on virus spread appeared to be macrophage-specific as it was not observed in cultures of T lymphocytes. Comparison of recombinant clones containing V1, V2, and V3 envelope sequences from high-efficiency Ba-L and JR-FL strains indicated that markedly different V1 and V2 sequences could impart the same rapidly spreading phenotype in macrophages.

MeSH terms

  • Amino Acid Sequence
  • Base Sequence
  • CD4-Positive T-Lymphocytes / virology
  • Cells, Cultured
  • DNA Primers / chemistry
  • DNA, Viral / genetics
  • Enzyme-Linked Immunosorbent Assay
  • Genes, env
  • HIV Core Protein p24 / analysis
  • HIV Envelope Protein gp120 / chemistry
  • HIV Envelope Protein gp120 / genetics
  • HIV Envelope Protein gp120 / physiology*
  • HIV-1 / genetics
  • HIV-1 / physiology*
  • HeLa Cells / virology
  • Humans
  • Immunoenzyme Techniques
  • Macrophages / virology*
  • Molecular Sequence Data
  • Phenotype
  • Recombinant Fusion Proteins
  • T-Lymphocytes / virology
  • Virus Replication*

Substances

  • DNA Primers
  • DNA, Viral
  • HIV Core Protein p24
  • HIV Envelope Protein gp120
  • Recombinant Fusion Proteins