Cyclophilin a modulates processing of human immunodeficiency virus type 1 p55Gag:: Mechanism for antiviral effects of cyclosporin A

被引:47
作者
Streblow, DN
Kitabwalla, M
Malkovsky, M
Pauza, CD
机构
[1] Univ Wisconsin, Dept Pathol & Lab Med, Madison, WI 53706 USA
[2] Univ Wisconsin, Dept Med Microbiol & Immunol, Madison, WI 53706 USA
关键词
D O I
10.1006/viro.1998.9155
中图分类号
Q93 [微生物学];
学科分类号
071005 ; 100705 ;
摘要
The molecular chaperone cyclophilin A (Cyp A) modulates human immunodeficiency virus type 1 (HIV-1) infectivity through its interactions with Gag structural proteins. The molecular mechanism for CypA in HIV-1 replication is not known. We studied chaperone effects on Gag precursor processing using cyclosporin A (CsA) to bind CypA and prevent its interaction with p55(Gag). CsA treatment inhibited p55(Gag) processing in extracellular virus-like particles produced from COS cells. We confirmed the effect of CsA on Gag processing by examining virions produced from CEMx174 cells infected with HIV-1(LAI). Particles accumulated in the presence of CsA displayed mostly immature virion morphology and lacked condensed capsids. CsA has a direct effect on HIV-1 Gag processing that implicates CypA as having an important role in the maturation of HIV-I particles. (C) 1998 Academic Press.
引用
收藏
页码:197 / 202
页数:6
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