Cell-dependent requirement of human immunodeficiency virus type 1 Vif protein for maturation of virus particles
Author(s) -
Hiroyuki Sakai,
Riri Shibata,
Jun-ichi Sakuragi,
Sayuri Sakuragi,
M Kawamura,
Akio Adachi
Publication year - 1993
Publication title -
journal of virology
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 2.617
H-Index - 292
eISSN - 1070-6321
pISSN - 0022-538X
DOI - 10.1128/jvi.67.3.1663-1666.1993
Subject(s) - biology , chloramphenicol acetyltransferase , virology , virus , infectivity , viral replication , transfection , mutant , viral protein , viral entry , viral transformation , cell , mutation , cell culture , reporter gene , gene , gene expression , genetics
A highly sensitive single-round infection assay using a bacterial chloramphenicol acetyltransferase was developed to analyze an early stage of human immunodeficiency virus type 1 replication. By a combination of transfection and single-round infection assay, a virus with a vif mutation, depending on host cells from which the virus was derived, was demonstrated to be defective at the early phase of infection cycle. Analysis of viral proteins synthesized in cells indicated that incorporation of the Env surface protein into virions of the vif mutant, again in a cell-dependent way, was greatly restricted. Taken together, it is concluded that the Vif protein acts through modulation of the Env protein in the virions, directly or indirectly, to enhance viral infectivity in a certain cell type.
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