Molecular identification, cloning and characterization of transmitted/founder HIV-1 subtype A, D and A/D infectious molecular clones

被引:57
作者
Baalwa, Joshua [1 ]
Wang, Shuyi [3 ]
Parrish, Nicholas F. [3 ]
Decker, Julie M. [4 ]
Keele, Brandon F. [5 ]
Learn, Gerald H. [3 ]
Yue, Ling [6 ]
Ruzagira, Eugene [7 ]
Ssemwanga, Deogratius [7 ]
Kamali, Anatoli [7 ]
Amornkul, Pauli N. [8 ]
Price, Matt A. [8 ]
Kappes, John C. [4 ]
Karita, Etienne [6 ]
Kaleebu, Pontiano [7 ]
Sanders, Eduard [8 ]
Gilmour, Jill [8 ]
Allen, Susan [9 ]
Hunter, Eric [6 ]
Montefiori, David C. [10 ]
Haynes, Barton F. [10 ]
Cormier, Emmanuel [8 ]
Hahn, Beatrice H. [3 ]
Shaw, George M. [2 ,3 ]
机构
[1] Univ Alabama Birmingham, Dept Pathol, Birmingham, AL 35294 USA
[2] Univ Penn, Perelman Sch Med, Dept Med, Philadelphia, PA 19104 USA
[3] Univ Penn, Dept Microbiol, Philadelphia, PA 19104 USA
[4] Univ Alabama Birmingham, Dept Med, Birmingham, AL 35294 USA
[5] SAIC Frederick Inc, AIDS & Canc Virus Program, Frederick Natl Lab Canc Res, Ft Detrick, MD 21702 USA
[6] Emory Univ, Dept Pathol, Atlanta, GA 30322 USA
[7] Uganda Virus Res Inst, Med Res Council Program AIDS, Entebbe, Uganda
[8] Int AIDS Vaccine Initiat, New York, NY 10004 USA
[9] Emory Univ, Dept Global Hlth, Atlanta, GA 30322 USA
[10] Duke Univ, Sch Med, Duke Human Vaccine Inst, Durham, NC 27710 USA
关键词
HIV-1; Transmitted/founder virus; Single genome sequencing; transmission; HIV-1 subtype A; HIV-1 subtype D; Neutralizing antibodies; HUMAN-IMMUNODEFICIENCY-VIRUS; FASTER DISEASE PROGRESSION; GP41 CYTOPLASMIC TAIL; 2ND CODING EXON; TYPE-1; SUBTYPE; HETEROSEXUAL TRANSMISSION; NEUTRALIZING ANTIBODIES; GENOTYPIC CHARACTERISTICS; ENVELOPE GLYCOPROTEINS; CORECEPTOR TROPISM;
D O I
10.1016/j.virol.2012.10.009
中图分类号
Q93 [微生物学];
学科分类号
071005 ; 100705 ;
摘要
We report the molecular identification, cloning and initial biological characterization of 12 full-length HIV-1 subtype A, D and AID recombinant transmitted/founder (T/F) genomes. T/F genomes contained intact canonical open reading frames and all TIP viruses were replication competent in primary human T-cells, although subtype D virus replication was more efficient (p <0.05). All 12 viruses utilized CCR5 but not CXCR4 as a co-receptor for entry and exhibited a neutralization profile typical of tier 2 primary virus strains, with significant differences observed between subtype A and D viruses with respect to sensitivity to monoclonal antibodies VRC01, PG9 and PG16 and polyclonal subtype C anti-HIV IgG (p <0.05 for each). The present report doubles the number of T/F HIV-1 clones available for pathogenesis and vaccine research and extends their representation to include subtypes A, B, C and D. (C) 2012 Elsevier Inc. All rights reserved.
引用
收藏
页码:33 / 48
页数:16
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