A single amino acid change and truncated TM are sufficient for simian immunodeficiency virus to enter cells using CCR5 in a CD4-independent pathway

被引:14
作者
Bonavia, A [1 ]
Bullock, BT [1 ]
Gisselman, KM [1 ]
Margulies, BJ [1 ]
Clements, JE [1 ]
机构
[1] Johns Hopkins Univ, Sch Med, Dept Comparat Med, Retrovirus Biol Lab, Baltimore, MD 21205 USA
关键词
CD4; independence; lentivirus; simian immunodeficiency virus; virus receptor; CCR5; transmembrane;
D O I
10.1016/j.virol.2005.07.001
中图分类号
Q93 [微生物学];
学科分类号
071005 ; 100705 ;
摘要
Entry of HIV and SIV into susceptible cells is mediated by CD4 and chemokine receptors, which act as coreceptors. To study cell entry of SIV, we constructed a cell line, xKLuSIV, derived from non-susceptible human K562 cells, that express the firefly luciferase reporter gene under control of a minimal SIV long terminal repeat (LTR). Using these susceptible cells, we studied the entry of a well-characterized molecularly cloned macrophage-tropic SIV. xKLuSIV cells that express rhesus macaque CD4 and/or the rhesus chemokine receptor CCR5 are susceptible to infection with the macrophage-tropic, neuroviruilent strain SIV/17E-Fr, but only xKLuSIV cells expressing both CCR5 and CD4 were susceptible to infection by the macrophage-tropic, non-neurovirulent strain SIV/17E-Cl. CCR5-dependent, CD4-independent infection by SIV/17E-Fr was abrogated by pre-incubation of the cells with AOP-RANTES, a ligand for CCR5. In addition to viral entry occurring by a CD4-independent mechanism, neutralization of SIV/17E-Fr with rhesus mAbs from 3 different neutralization groups blocked entry into xKLuSIV cells by both CD4-dependent and -independent mechanisms. Triggering the env glycoprotein of SIV-17EFr with soluble CD4 had no significant effect in infectivity, but triggering of the same glycoprotein of SIV/17E-Cl allowed it to enter cells in a CD4-independent fashion. Using mutant molecular clones, we studied the determinants for CD4 independence, all of which are confined to the env gene. We report here that truncation of the TM at amino acid 764 and changing a single amino acid (R751G) in the SIV envelope transmembrane protein (TM) conferred the observed CD4-independent phenotype. Our data suggest that the envelope from the neurovirulent SIV/17E-Fr interacts with CCR5 in a CD4-independent manner, and changes in the TM protein of this virus are important components that contribute to neurovirulence in SIV (c) 2005 Elsevier Inc. All rights reserved.
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收藏
页码:12 / 23
页数:12
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