Kapoor Amit, Jones Morris, Shafer R W, Rhee Soo-Yon, Kazanjian Powel, Delwart Eric L
Department of Medicine, University of California, San Francisco, 94118, USA.
J Virol. 2004 Jul;78(13):7112-23. doi: 10.1128/JVI.78.13.7112-7123.2004.
Drug-resistant viruses may be present as minority variants during early treatment failures or following discontinuation of failed antiretroviral regimens. A limitation of the traditional direct PCR population sequencing method is its inability to detect human immunodeficiency virus type 1 (HIV-1) variants present at frequencies lower than 20%. A drug resistance genotyping assay based on the isolation and DNA sequencing of minority HIV protease variants is presented here. A multiple-codon-specific heteroduplex generator probe was constructed to improve the separation of HIV protease genes varying in sequence at 12 codons associated with resistance to protease inhibitors. Using an RNA molecule as probe allowed the simple sequencing of protease variants isolated as RNA/DNA heteroduplexes with different electrophoretic mobilities. The protease gene RNA heteroduplex generator-tracking assay (RNA-HTA) was tested on plasma quasispecies from 21 HIV-1-infected persons in whom one or more protease resistance mutations emerged during therapy or following initiation of salvage regimens. In 11 of 21 cases, RNA-HTA testing of virus from the first episode of virologic failure identified protease resistance mutations not seen by population-based PCR sequencing. In 8 of these 11 cases, all of the low-frequency drug resistance mutations detected exclusively by RNA-HTA during the first episode became detectable by population-based PCR sequencing at the later time point. Distinct sets of protease mutations could be linked on different genomes in patients with high-frequency protease gene lineages. The enhanced detection of minority drug resistance variants using a sequencing-based assay may improve the efficacy of genotype-assisted salvage therapies.
在早期治疗失败期间或抗逆转录病毒治疗方案失败停药后,耐药病毒可能以少数变异体的形式存在。传统的直接PCR群体测序方法的一个局限性在于其无法检测到频率低于20%的1型人类免疫缺陷病毒(HIV-1)变异体。本文介绍了一种基于少数HIV蛋白酶变异体分离和DNA测序的耐药基因分型检测方法。构建了一种多密码子特异性异源双链体生成探针,以改善在与蛋白酶抑制剂耐药相关的12个密码子处序列不同的HIV蛋白酶基因的分离。使用RNA分子作为探针,可对作为具有不同电泳迁移率的RNA/DNA异源双链体分离的蛋白酶变异体进行简单测序。蛋白酶基因RNA异源双链体生成追踪检测法(RNA-HTA)在21名HIV-1感染者的血浆准种上进行了测试,这些感染者在治疗期间或挽救治疗方案启动后出现了一个或多个蛋白酶耐药突变。在21例中的11例中,对病毒学失败首次发作时的病毒进行RNA-HTA检测,发现了基于群体的PCR测序未发现的蛋白酶耐药突变。在这11例中的8例中,首次发作时仅通过RNA-HTA检测到的所有低频耐药突变在后期时间点通过基于群体的PCR测序变得可检测到。在具有高频蛋白酶基因谱系的患者中,不同的蛋白酶突变组可与不同的基因组相关联。使用基于测序的检测方法增强对少数耐药变异体的检测可能会提高基因型辅助挽救治疗的疗效。