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Rapid and Simultaneous Detection of Major Drug Resistance Mutations in Reverse Transcriptase Gene for HIV-1 CRF01_AE CRF07_BC and Subtype B in China Using Sequenom MassARRAY® System

机译:使用SequenomMassARRAY®系统同时快速检测中国HIV-1 CRF01_AECRF07_BC和B亚型逆转录酶基因的主要耐药突变

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摘要

The development of a rapid, high-throughput and cost-effective HIV-1 drug resistance (HIV-DR) testing system is a challenge for areas consisting different HIV-1 strains. In this study, we established a broadly reactive multiplex assay that could simultaneously detect major drug resistance mutations at 8 loci, which are associated with resistance to commonly used nucleoside reverse transcriptase inhibitors (NRTIs) and Non-nucleoside reverse transcriptase inhibitors (NNRTIs), in specimens of HIV-1 CRF01_AE, CRF07_BC and subtype B, the three major circulating strains in China, using the matrix-assisted laser desorption ionization-time of flight mass spectrometry (MALDI-TOF MS) provided by Sequenom MassARRAY® system. To establish the assay, pol gene fragments were prepared from the plasma viral RNA of 159 patients by nested PCR and the presence of wild type and mutant alleles at the 8 loci were analyzed by MALDI-TOF MS. In terms of loci, the detection rate of the alleles was greater than 97% for M41L, K65R, M184V and G190A, 91.2% for K101E/Q/P, 91.2% for T215F/Y, 89.9% for K103N/S and 80.5% for L210W. In terms of individuals, 80% of the alleles were detected in 95.4% CRF01_AE patients, 100% CRF07_BC patients and 83.3% subtype B patients. Importantly, the MALDI-TOF MS results were concordant to the drug resistance profiles of patients obtained from conventional sequencing analysis after excluded the failed detections. Using plasmid templates, the assay was estimated to be sensitive to detect drug resistant variants at level about 20% of the circulating viral population. The capability of this assay to detect mixed viral populations was further verified by two different patient specimens. In conclusion, this study evaluated the use of Sequenom MassARRAY® system for high-throughput detection of HIV-DR mutations towards the commonly used reverse transcriptase inhibitors in China.
机译:快速,高通量和具有成本效益的HIV-1耐药性(HIV-DR)测试系统的开发对于包含不同HIV-1毒株的地区构成了挑战。在这项研究中,我们建立了广泛的反应性多重检测方法,可以同时检测8个基因座上的主要药物耐药性突变,这些突变与对常用核苷逆转录酶抑制剂(NRTIs)和非核苷逆转录酶抑制剂(NNRTIs)的耐药有关。使用SequenomMassARRAY®系统提供的基质辅助激光解吸电离飞行时间质谱仪(MALDI-TOF MS)对HIV-1 CRF01_AE,CRF07_BC和B型(中国三大主要流行株)的标本进行了分析。为了建立测定方法,通过巢式PCR从159位患者的血浆病毒RNA中制备了pol基因片段,并通过MALDI-TOF MS分析了8个基因座上野生型和突变等位基因的存在。就基因座而言,M41L,K65R,M184V和G190A的等位基因检出率大于97%,K101E / Q / P的检出率为91.2%,T215F / Y的检出率为91.2%,K103N / S的检出率为89.9%,80.5%。适用于L210W。就个体而言,在95.4%的CRF01_AE患者,100%的CRF07_BC患者和83.3%的B亚型患者中检出了80%的等位基因。重要的是,在排除失败的检测之后,MALDI-TOF MS结果与从常规测序分析获得的患者的药物耐药性相一致。使用质粒模板,估计该测定法对检测循环病毒种群约20%的耐药变异体敏感。两种不同的患者标本进一步验证了该测定法检测混合病毒种群的能力。总之,本研究评估了SequenomMassARRAY®系统在针对中国常用逆转录酶抑制剂的HIV-DR突变的高通量检测中的应用。

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