Significant changes in integrase-associated HIV-1 replication capacity between early and late isolates

被引:4
作者
Capel, Elena [1 ]
Parera, Mariona [1 ]
Clotet, Bonaventura [1 ]
Angel Martinez, Miguel [1 ]
机构
[1] Hosp Badalona Germans Trias & Pujol, Fundacio IrsiCaixa, Badalona 08916, Spain
关键词
HIV; Integrase; Diversification; Fitness; IMMUNODEFICIENCY-VIRUS TYPE-1; CD4 CELL COUNTS; DRUG SUSCEPTIBILITY; ELITE CONTROLLERS; RESISTANT HIV-1; FITNESS; PROTEASE; GAG; VIRULENCE; EVOLUTION;
D O I
10.1016/j.virol.2013.06.023
中图分类号
Q93 [微生物学];
学科分类号
071005 ; 100705 ;
摘要
During the human immunodeficiency virus type 1 (HIV-1) pandemic, continuous, extensive genetic diversification of the virus has been observed. To study the effect of HIV-1 diversification on integrase-associated viral replication capacity (RC), 94 HIV-1 subtype B integrase sequences from two groups of antiretroviral-naive viruses isolated 15 y apart were amplified and recombined with an HIV-1 infectious clone. Viral RC was determined by infecting a T cell line with a long terminal repeat-driven green fluorescent protein reporter. Significant differences in integrase-mediated RC were observed between recombinant viruses from early and late isolates (p = 0.0286). Integrases from late isolates had significantly lower sequence conservation scores compared to an ancestral subtype B sequence (p < 0.0001). Integrase amino acid polymorphisms S17N, I72V, S119P, and D256E were associated with a lower ex vivo viral RC. These results suggest that integrase sequence diversification has affected ex vivo HIV-1 RC. (c) 2013 Elsevier Inc. All rights reserved.
引用
收藏
页码:274 / 281
页数:8
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