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Antiviral drug resistance as an adaptive process
被引:152
作者:
Irwin, Kristen K.
[1
,2
]
Renzette, Nicholas
[3
]
Kowalik, Timothy F.
[3
]
Jensen, Jeffrey D.
[1
,2
]
机构:
[1] Ecole Polytech Fed Lausanne, Sch Life Sci, Lausanne, Switzerland
[2] SIB, Lausanne, Switzerland
[3] Univ Massachusetts, Sch Med, Dept Microbiol & Physiol Syst, Worcester, MA 01605 USA
基金:
欧洲研究理事会;
瑞士国家科学基金会;
关键词:
antiviral resistance;
genetic barrier;
mutagenesis;
fluctuating selection;
compensatory mutation;
cost of adaptation;
HEPATITIS-C VIRUS;
HUMAN INFLUENZA-A;
IN-VITRO;
CONFERRING RESISTANCE;
REVERSE-TRANSCRIPTASE;
REPLICATIVE CAPACITY;
MOLECULAR ADAPTATION;
LETHAL MUTAGENESIS;
RECOMBINATION RATE;
ERROR CATASTROPHE;
D O I:
10.1093/ve/vew014
中图分类号:
Q93 [微生物学];
学科分类号:
071005 ;
100705 ;
摘要:
Antiviral drug resistance is a matter of great clinical importance that, historically, has been investigated mostly from a viro-logical perspective. Although the proximate mechanisms of resistance can be readily uncovered using these methods, larger evolutionary trends often remain elusive. Recent interest by population geneticists in studies of antiviral resistance has spurred new metrics for evaluating mutation and recombination rates, demographic histories of transmission and compartmentalization, and selective forces incurred during viral adaptation to antiviral drug treatment. We present up-to-date summaries on antiviral resistance for a range of drugs and viral types, and review recent advances for studying their evolutionary histories. We conclude that information imparted by demographic and selective histories, as revealed through population genomic inference, is integral to assessing the evolution of antiviral resistance as it pertains to human health.
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