Fusion of the upstream vpu sequences to the env of simian human immunodeficiency virus (SHIVKU-1bMC33) results in the synthesis of two envelope precursor proteins, increased numbers of virus particles associated with the cell surface and is pathogenic for pig-tailed macaques

Abstract

Previous studies have shown that the gene coding for the Vpu protein of the human immunodeficiency virus type 1 (HIV-1) is 5′ to the env gene, is in a different reading frame, and overlaps the env by 90 nucleotides. In this study, we examined the processing of the Env protein as well as the maturation and infectivity of a virus (SHIV Vpenv ) in which a single nucleotide was removed at the vpu–env junction, fusing the first 162 bases of vpu to the env ORF. Pulse-chase analysis revealed that SHIV Vpenv -infected cells gave rise to two precursor glycoprotein species (gp160 and gp175). Immune precipitation results also revealed that an anti-Vpu serum could immune precipitate the gp175 precursor, suggesting that the amino-terminal Vpu sequence was fused to the Env protein. Growth curves revealed that the SHIV Vpenv -inoculated cultures released approximately three times more p27 into the culture medium than parental SHIV KU-1bMC33 . Electron microscopy revealed that while both viruses matured at the cell plasma membrane, significantly higher quantities of virus particles were cell associated on SHIV Vpenv -infected cells compared to cultures inoculated with parental SHIV KU-1bMC33 . Furthermore, virus was observed maturing into intracellular vesicles of SHIV Vpenv -infected cells. To assess the pathogenicity of SHIV Vpenv , three pig-tailed macaques were inoculated with the SHIV Vpenv and monitored for 6 months for CD4 + T cell levels, viral loads, and the stability of the deletion at the vpu–env junction. Our results indicated that SHIV Vpenv caused a severe CD4 + T cell loss in all three macaques within weeks of inoculation. Sequence analysis of the vpu gene analyzed from sequential PBMC samples derived from macaques revealed that this mutation was stable during the period of rapid CD4 + T cell loss. Sequence analysis showed that with increasing time of infection, the one base pair deletion was repaired in all three macaques inoculated with SHIV Vpenv with the reversion occurring at 10 weeks in macaque CT1G and at 12 weeks in macaque CP3R and CT1R. These results indicate that fusion of the first 54 amino acids of Vpu to Env results in intracellular maturation of virus, and accumulation of virus within intracellular vesicles as well as on the cell plasma membrane. Our results indicate that while fusion of the vpu gene to env results in a virus that is still pathogenic for pig-tailed macaques, there is a selective pressure to maintain the vpu and env genes in separate reading frames.