Pre-Screening HIV-1 Reverse Transcriptase Resistance Mutations in Subtype B Patients Using a Novel Multiplex Primer Extension Assay

被引:3
作者
Jakobsen, Martin Roelsgaard [1 ]
Aggerholm, Anni [1 ]
Jorgensen, Louise Bruun [2 ]
Laursen, Alex [1 ]
Ostergaard, Lars [1 ]
机构
[1] Aarhus Univ Hosp, Dept Infect Dis, DK-8200 Aarhus N, Denmark
[2] Statens Serum Inst, Dept Virol, DK-2300 Copenhagen S, Denmark
关键词
HIV-1; Drug Resistance; Minority mutation; Genotyping; Primer extension; IMMUNODEFICIENCY-VIRUS TYPE-1; OLIGONUCLEOTIDE LIGATION ASSAY; DRUG-RESISTANCE; ANTIRETROVIRAL THERAPY; GENOTYPIC RESISTANCE; DNA; POPULATIONS; PERSISTENCE; INHIBITORS; COPIES/ML;
D O I
10.2174/157016209788680615
中图分类号
R392 [医学免疫学]; Q939.91 [免疫学];
学科分类号
100102 ;
摘要
Antiretroviral therapy is standard treatment for HIV-infected patients. Such therapy has decreased mortality and morbidity, but treatment success is often jeopardized by the emergence of viral drug resistance. Moreover, in recent years there has been a reported rise in the incidence of transmitted drug resistance, highlighting the importance of pretreatment resistance screening. In this report, we describe the development and utility of a sensitive multiplex approach for detecting mutations conferring drug resistance to HIV-1 reverse transcriptase inhibitors. This protocol, termed HIV-SNaPshot, utilizes a multiplex primer extension assay with capillary electrophoresis reporting altered nucleotides at nine important drug resistance mutation positions. Mutations were successfully detected to levels of 5% in viral quasispecies populations. Furthermore, although developed and optimised for HIV-1 subtype B, drug resistance mutations could also be detected in most non-B subtypes. Comparison of the HIV-SNaPshot with the commercial Viroseq genotyping system in 10 patients gave similar results, but importantly, additional resistance mutations were identified in several patients by the HIV-SNaPshot assay. Thus, the HIV-SNaPshot is a method capable to support standard genotyping for the determination of minority HIV-1 resistance mutations, with equivalent and perhaps greater sensitivity than Viroseq.
引用
收藏
页码:398 / 409
页数:12
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