| Literature DB >> 7609029 |
X F Yu1, Z Wang, C Beyrer, D D Celentano, C Khamboonruang, E Allen, K Nelson.
Abstract
Primary human immunodeficiency virus type 1 (HIV-1) isolates were obtained from 22 patients with AIDS from northern Thailand, where HIV-1 is transmitted primarily through the heterosexual route. Viral sequences were determined for the 22 patients with AIDS, and all were subtype E HIV-1 on the basis of sequence analysis of a region from the envelope protein gp120. Syncytium-inducing (SI) viruses were detected for 16 of 22 patients with AIDS by using MT-2 cells. Characteristics of amino acid sequences in V3 which have not been reported previously for subtype B SI HIV-1 were associated with the subtype E HIV-1 SI phenotype. The SI viruses from our study population contain predominantly a GPGR or GPGH motif at the tip of the V3 loop, in contrast to the previously described subtype E HIV-1 from Thailand which contained predominantly GPGQ. All the SI viruses lost a potential N-linked glycosylation site in V3 which is highly conserved among previously described subtype E HIV-1 isolates from asymptomatic patients from Thailand. HIV-1 envelope sequences including V3 from some patients with AIDS were significantly more divergent than viruses from asymptomatic patients in Thailand characterized 2 years ago or earlier. These results suggest that emergence of subtype E SI HIV-1 variants is associated with the development of AIDS, as it is for subtype B HIV-1. The divergence of subtype E HIV-1 in patients with AIDS as the disease progresses, and the divergence of subtype E HIV-1 in the infected population as the epidemic continues in Thailand, may have important implications for vaccine development.Entities:
Keywords: Acquired Immunodeficiency Syndrome; Asia; Developing Countries; Diseases; Examinations And Diagnoses; Genetic Technics; Hiv; Hiv Infections; Laboratory Examinations And Diagnoses; Laboratory Procedures; Research Report; Southeastern Asia; Thailand; Vaccines; Viral Diseases
Mesh:
Year: 1995 PMID: 7609029 PMCID: PMC189267 DOI: 10.1128/JVI.69.8.4649-4655.1995
Source DB: PubMed Journal: J Virol ISSN: 0022-538X Impact factor: 5.103