First demonstration of a lack of viral sequence evolution in a nonprogressor, defining replication-incompetent HIV-1 infection

被引:56
作者
Wang, B
Mikhail, M
Dyer, WB
Zaunders, JJ
Kelleher, AD
Saksena, NK [1 ]
机构
[1] Univ Sydney, Westmead Hosp, Westmead Millennium Inst, Ctr Virus Res,Retroviral Genet Lab, Westmead, NSW 2145, Australia
[2] Australian Red Cross Blood Serv, Tissue Typing Dept, Viral Immunol Lab, Sydney, NSW 2000, Australia
[3] St Vincents Hosp, Ctr Immunol, Darlinghurst, NSW 2010, Australia
[4] UNSW, NCHECR, Darlinghurst, NSW 2010, Australia
基金
英国医学研究理事会;
关键词
Human Immunodeficiency virus type 1; long-term nonprogressor; G-A hypermutation; stop codon; sequence evolution; replication incompetence;
D O I
10.1016/S0042-6822(03)00159-4
中图分类号
Q93 [微生物学];
学科分类号
071005 ; 100705 ;
摘要
It is universally acknowledged that genetic diversity is a hallmark of HIV-1 infection, and it is one of the traits that has considerably hampered the development of an effective vaccine. In a study of full-length HIV-1 genomic sequences (>9 kb), we show unique evidence for complete absence of viral evolution in an individual with truly nonprogressive infection. Gross gene defects were not detected, but the state of replication incompetence was attributed to the presence of stop codons in the structural genes gag p17 and p24 and in pol RT, which emerged as a consequence of G-A hypermutation. These inactivating mutations may have occurred early, soon after infection, during the clonal stage of primary viral replication, since these are the sole archival strains present today. This genetic homogeneity, with <1% variation between strains over an 8-year period, suggests that only limited proviral integration events occurred in this patient. Further study on the antigenic properties of this strain may assist in the development of HIV vaccines and therapeutics. (C) 2003 Elsevier Science (USA). All rights reserved.
引用
收藏
页码:135 / 150
页数:16
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