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Identification of alternative amino acid substitutions in drug-resistant variants of the HIV-1 reverse transcriptase
被引:11
|作者:
Berkhout, Ben
Back, Nicole K. T.
de Ronde, Anthony
Jurriaans, Suzanne
Bakker, Margreet
Parkin, Neil T.
van der Hoek, Lia
机构:
[1] Univ Amsterdam, Acad Med Ctr, Dept Human Retrovirol, NL-1105 AZ Amsterdam, Netherlands
[2] Monogram Biosci, San Francisco, CA USA
来源:
关键词:
drug resistance mutations;
evolution;
HIV-1;
reverse transcriptase;
D O I:
10.1097/01.aids.0000237367.56864.75
中图分类号:
R392 [医学免疫学];
Q939.91 [免疫学];
学科分类号:
100102 ;
摘要:
Objective/design: To identify new drug-resistance-associated mutations in the HIV-1 reverse transcriptase (RT) protein, we screened the RT sequence database of our hospital for alternative amino acid substitutions at known RT drug-resistance positions. Method: The genotypic database used for this analysis contained 1322 RT sequences from 1015 patients. We analysed this RT database with a focus on alternative mutations at RT positions known to be involved in drug resistance. The patterns of drug resistance associated with these alternative mutations were investigated in a separate database containing genotype and drug-susceptibility results. Results: We identified multiple alternative resistance-associated mutations at amino acid positions 44, 62, 67, 69, 70, 74, 75, 103, 181, 190, 210, and 219 in RT. Phenotypic analysis indicated that drug-resistance properties of the alternative Y181V and L741 mutants are similar, but not identical, to that of the well-known Y181C and L74V mutations. Conclusion: This initial survey indicates that many resistance-associated phenomena can be distilled from existing data. These findings endorse a more extensive analysis by computerized methods. (c) 2006 Lippincott Williams & Wilkins.
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页码:1515 / 1520
页数:6
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