Functional and genetic analysis of coreceptor usage by dualtropic HIV-1 subtype C isolates

被引:11
|
作者
Singh, Ashika [1 ]
Page, Taryn [1 ]
Moore, Penny L. [2 ]
Allgaier, Rachel L. [1 ,3 ]
Hiramen, Keshni [1 ]
Coovadia, Hoosen M. [1 ,4 ]
Walker, Bruce D. [1 ,3 ]
Morris, Lynn [2 ]
Ndung'u, Thumbi [1 ,3 ]
机构
[1] Univ KwaZulu Natal, Doris Duke Med Res Inst, HIV Pathogenesis Programme, Nelson R Mandela Sch Med, ZA-4001 Durban, South Africa
[2] Natl Inst Communicable Dis, AIDS Virus Res Unit, Johannesburg, Gauteng, South Africa
[3] MIT & Harvard, Ragon Inst MGH, Charlestown, MA USA
[4] Univ KwaZulu Natal, Dept Paediat & Child Hlth, Nelson R Mandela Sch Med, Durban, South Africa
基金
新加坡国家研究基金会; 美国国家卫生研究院;
关键词
HIV-1 subtype C; Dualtropism; Coreceptor usage; Envelope; V3; loop; CXCR4; IMMUNODEFICIENCY-VIRUS TYPE-1; CHEMOKINE RECEPTORS; DISEASE PROGRESSION; CCR5; GP120; ENTRY; SEQUENCES; VARIANTS; TROPISM; FITNESS;
D O I
10.1016/j.virol.2009.07.021
中图分类号
Q93 [微生物学];
学科分类号
071005 ; 100705 ;
摘要
It is widely documented that a complete switch from the predominant CCR5 (R5) to CXCR4 (X4) phenotype is less common for HIV-1 Subtype C (HIV-1C) compared to other major subtypes. We investigated whether clualtropic HIV-1C isolates represented dualtropic, mixed R5 and X4 clones or both. Thirty of 35 functional HIV-1 env clones generated by bulk PCR amplification from peripheral blood mononuclear cells (PBMCs) infected with seven clualtropic HIV-1C isolates utilized CXCR4 exclusively. Five of 35 clones displayed dualtropism. Endpoint dilution of one isolate did not yield a substantial proportion of R5-monotropic env clones. Sequence-based predictive algorithms showed that env sequences from PBMCs, CXCR4 or CCR5-expressing cell lines were indistinguishable and all possessed X4/dualtropic characteristics. We describe HIV-1C CXCR4-tropic env sequence features. Our results suggest a dramatic loss of CCR5 monotropism as dualtropism emerges in HIV-1 C which has important implications for the use of coreceptor antagonists in therapeutic strategies for this subtype. (C) 2009 Elsevier Inc. All rights reserved.
引用
收藏
页码:56 / 67
页数:12
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