Impact of a single amino acid in the variable region 2 of the Old World monkey TRIM5α SPRY (B30.2) domain on anti-human immunodeficiency virus type 2 activity

被引:12
作者
Kono, Ken [1 ]
Bozek, Katarzyna [2 ]
Domingues, Francisco S. [2 ]
Shioda, Tatsuo [1 ]
Nakayama, Emi E. [1 ]
机构
[1] Osaka Univ, Dept Viral Infect, Res Inst Microbial Dis, Suita, Osaka 5650871, Japan
[2] Max Planck Inst Informat, D-66123 Saarbrucken, Germany
关键词
TRIM5; alpha; Human immunodeficiency virus; Baboon; Rhesus monkey; Cynomolgus monkey; MULTIPLE SEQUENCE ALIGNMENT; CYNOMOLGUS MONKEY; ANIMAL-MODEL; RESTRICTION; BABOONS; INFECTION; HIV-1; PATHOGENESIS; DETERMINES; SELECTION;
D O I
10.1016/j.virol.2009.03.004
中图分类号
Q93 [微生物学];
学科分类号
071005 ; 100705 ;
摘要
Variable region 1 (V1) of the SPRY domain of TRIM5 alpha is a major determinant for species-specific virus restriction in primates. We previously reported that a chimeric TRIM5 alpha containing baboon VI in the background of cynomolgus monkey TRIM5 alpha showed potent anti-human immunodeficiency virus type 2 (HIV-2) activity. Since baboons are reportedly sensitive to HIV-2 infection, there was a discrepancy between the ability of baboon TRIM5 alpha V1 to restrict HIV-2 and baboon sensitivity to HIV-2. In the study presented here, we examined the roles of V2 and V3 of the baboon TRIM5 alpha SPRY domain in its anti-HIV-2 activity. A chimeric TRIM5 alpha containing the entire baboon SPRY domain showed weak anti-HIV-2 activity. This attenuation Of activity Was caused by a single serine-to-proline substitution in baboon TRIM5 alpha V2. These findings indicate that the combination of V1 with other variable regions of SPRY is important in anti-HIV-2 activity of primate TRIM5 alpha. (C) 2009 Elsevier Inc. All rights reserved.
引用
收藏
页码:160 / 168
页数:9
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