Primary CCR5 only using HIV-1 isolates does not accurately represent the in vivo replicating quasi-species

被引:18
作者
Aasa-Chapman, Marlen M. I.
Aubin, Keith
Williams, Ian
McKnight, Aine
机构
[1] UCL, Wohl Virion Ctr, Div Infect & Immun, London W1T 4JF, England
[2] UCL, Ctr Sexual Hlth & HIV Res, London WC1E 6AU, England
基金
英国医学研究理事会; 英国惠康基金;
关键词
HIV-1; gp120; coreceptors; CCR3; CCR5; primary isolates;
D O I
10.1016/j.virol.2006.04.002
中图分类号
Q93 [微生物学];
学科分类号
071005 ; 100705 ;
摘要
Most HIV-1 isolates depend on CCR5 or CXCR4 to infect target cells, and efficient use of other coreceptors; is rare. We cloned HIV-1 envelopes from virus at acute infection and found that most use CCR3 efficiently. This result contradicts prevailing data, suggesting that CCR3 usage is rare. We hypothesized that direct isolation into PBMC biases selection of viruses that use CCR5 and not CCR3. We therefore compared coreceptor use of isolates obtained by PBMC coculture with envelopes cloned directly from patient blood samples, which should represent actively replicating species. Viruses derived by cloning generally used CCR3 and CCR5 with equally efficiently. In contrast, we found that viruses isolated by PBMC coculture largely, or exclusively, used CCR5. Regardless of whether CCR3 use contributes to HIV-1 transmission or pathogenesis, our results demonstrate that 'primary isolates' generated by PBMC culture are unlikely to accurately represent the in vivo replicating quasi-species. (c) 2006 Elsevier Inc. All rights reserved.
引用
收藏
页码:489 / 496
页数:8
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