Interrelationship between HIV-1 Fitness and Mutation Rate

被引:31
|
作者
Dapp, Michael J. [1 ,3 ,4 ]
Heineman, Richard H. [1 ,2 ]
Mansky, Louis M. [1 ,2 ,3 ,4 ,5 ]
机构
[1] Univ Minnesota, Inst Mol Virol, Acad Hlth Ctr, Minneapolis, MN 55455 USA
[2] Univ Minnesota, Sch Dent, Minnesota Craniofacial Res Training Program, Dept Diagnost & Biol Sci, Minneapolis, MN 55455 USA
[3] Univ Minnesota, Acad Hlth Ctr, Ctr Drug Design, Minneapolis, MN 55455 USA
[4] Univ Minnesota, Sch Med, Pharmacol Grad Program, Minneapolis, MN 55455 USA
[5] Univ Minnesota, Sch Med, Dept Microbiol, Minneapolis, MN 55455 USA
关键词
retrovirus; lentivirus; evolution; mutation; fitness; IMMUNODEFICIENCY-VIRUS TYPE-1; RESISTANT REVERSE-TRANSCRIPTASE; DYNAMICS IN-VIVO; ESCHERICHIA-COLI; DNA-SYNTHESIS; LETHAL MUTAGENESIS; REPLICATION FIDELITY; RNA VIRUSES; POLYMERASE FIDELITY; DISEASE PROGRESSION;
D O I
10.1016/j.jmb.2012.10.009
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
Differences in replication fidelity, as well as mutator and antimutator strains, suggest that virus mutation rates are heritable and prone to natural selection. Human immunodeficiency virus type 1 (HIV-1) has many distinct advantages for the study of mutation rate optimization given the wealth of structural and biochemical data on HIV-1 reverse transcriptase (RT) and mutants. In this study, we conducted parallel analyses of mutation rate and viral fitness. In particular, a panel of 10 RT mutants-most having drug resistance phenotypes-was analyzed for their effects on viral fidelity and fitness. Fidelity differences were measured using single-cycle vector assays, while fitness differences were identified using ex vivo head-to-head competition assays. As anticipated, virus mutants possessing either higher or lower fidelity had a corresponding loss in fitness. While the virus panel was not chosen randomly, it is interesting that it included more viruses possessing a mutator phenotype rather than viruses possessing an antimutator phenotype. These observations provide the first description of an interrelationship between HIV-1 fitness and mutation rate and support the conclusion that nnutator and antimutator phenotypes correlate with reduced viral fitness. In addition, the findings here help support a model in which fidelity comes at a cost of replication kinetics and may help explain why retroviruses like HIV-1 and RNA viruses maintain replication fidelity near the extinction threshold. (C) 2012 Elsevier Ltd. All rights reserved.
引用
收藏
页码:41 / 53
页数:13
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