Evolution of human immunodeficiency virus type 1 envelope sequences in infected individuals with differing disease progression profiles

被引:73
作者
Shankarappa, R
Gupta, P
Learn, GH
Rodrigo, AG
Rinaldo, CR
Gorry, MC
Mullins, JI
Nara, PL
Ehrlich, GD
机构
[1] Univ Washington, Dept Microbiol, Seattle, WA 98195 USA
[2] Univ Pittsburgh, Dept Pathol, Pittsburgh, PA 15261 USA
[3] Univ Pittsburgh, Dept Infect Dis & Microbiol, Pittsburgh, PA 15261 USA
[4] Biol Mimet Inc, Frederick, MD 21701 USA
关键词
D O I
10.1006/viro.1997.8996
中图分类号
Q93 [微生物学];
学科分类号
071005 ; 100705 ;
摘要
Sequence Variation displayed by the human immunodeficiency virus type 1 (HIV-1) has been proposed to be linked to the pathogenesis of acquired immunodeficiency syndrome (AIDS). To assess viral evolution during the course of infection, we evaluated sequence variability in the env variable domains in four HIV-1-infected individuals exhibiting differing profiles of CD4(+) T cell decline when followed from seroconversion until the development of AIDS or loss of followup. Proviral sequences encoding the V3-V5 region of gp120 were obtained following PGR amplification of peripheral blood mononuclear cell DNA and cloning. Virus in each patient was relatively homogeneous early in infection and then diverged with time, more consistently at its nonsynonymous sites. Just prior to or coincident with a rapid decline in CD4(+) T cell numbers, sequences were found with basic amino acid substitutions clustered within and downstream of the gp120 V3 domain. Within the constraints of the current dataset, we conclude that the virus appears to continually accumulate changes in its amino acid sequences well into the time of marked CD4(+) T cell decline. (C) 1998 Academic Press.
引用
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页码:251 / 259
页数:9
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