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An HIV-1 integrase genotype assay for the detection of drug resistance mutations

机译:用于检测耐药性突变的HIV-1整合酶基因型检测

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Background: The integrase inhibitors (e.g. Raltegravir) are a new class of antiretroviral drugs that have recently become available for the treatment of patients with multi-drug resistant HIV-1 within Australia. The emergence of mutations that confer resistance to the integrase inhibitors has been observed in vivo; however, no commercial genotyping assay is currently available to screen for resistance to these drugs. Methods: The HIV-1 integrase gene was amplified from plasma-derived HIV-1 viral RNA via reverse transcription-polymerase chain reaction and genotype determined via population DNA sequencing. Drug resistance mutations and polymorphisms were detected using the Stanford University online HIV database. Assay sensitivity and reproducibility were determined using clinical and laboratory-derived samples. Results: Our in-house assay was capable of genotyping the integrase gene from all samples tested (n = 30) of HIV-1 subtypes B, C, D, F, CFR01_AE and CRF02_AG and can amplify the integrase region from plasma samples containing as few as 50 HIV RNA copies/mL. The assay is highly reproducible (average nucleotide concordance = 99.6%, n = 4) and is capable of detecting resistance-associated mutations. Conclusions:This assay is suitable for routine drug resistance screening of plasma samples from HIV-infected patients receiving integrase inhibitor antiretroviral drugs and also serves as a useful research tool.
机译:背景:整合酶抑制剂(例如Raltegravir)是一类新型的抗逆转录病毒药物,最近已在澳大利亚境内用于治疗具有多重耐药性HIV-1的患者。在体内已经观察到了赋予对整合酶抑制剂抗性的突变。但是,目前尚无商业基因分型分析可用于筛选对这些药物的耐药性。方法:通过逆转录-聚合酶链反应从血浆来源的HIV-1病毒RNA中扩增HIV-1整合酶基因,并通过群体DNA测序确定基因型。使用斯坦福大学在线HIV数据库检测了耐药性突变和多态性。使用临床和实验室衍生的样品确定测定的灵敏度和可重复性。结果:我们的内部分析能够对所有测试的HIV-1 B,C,D,F,CFR01_AE和CRF02_AG亚型的所有样本(n = 30)中的整合酶基因进行基因分型,并且可以从含有以下成分的血浆样本中扩增整合酶区域少至50个HIV RNA拷贝/ mL。该测定具有高度可重复性(平均核苷酸一致性= 99.6%,n = 4),并且能够检测与耐药相关的突变。结论:该测定方法适合常规检测接受整合酶抑制剂抗逆转录病毒药物的HIV感染患者的血浆样品,也可作为有用的研究工具。

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