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Affordable in-house antiretroviral drug resistance assay with good performance in non-subtype B HIV-1

机译:负担得起的内部抗逆转录病毒药物耐药性检测,在非亚型B HIV-1中表现良好

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摘要

The introduction of antiretroviral (ARV) therapy in resource-poor settings is effective in suppressing HIV-1 replication and prolonging life of infected individuals. This has led to a demand for affordable HIV-1 drug resistance assays, since treatment failure due to development of drug resistance is common. This study developed and evaluated an affordable "in-house" genotyping assay to monitor HIV-1 drug resistance in Africa, particularly South Africa. An "in-house" assay using automated RNA extraction, and subtype C specific PCR and sequencing primers was developed and successfully evaluated 396 patient samples (viral load ranges 1000-1.6 million RNA copies/ml). The "in-house" assay was validated by comparing sequence data and drug resistance profiles from 90 patient and 10 external quality control samples to data from the ViroSeq HIV-1 Genotyping kit. The "in-house" assay was more efficient, amplifying all 100 samples, compared to 91 samples using Viroseq. The "in house" sequences were 99.2% homologous to the ViroSeq sequences, and identical drug resistance mutation profiles were observed in 96 samples. Furthermore, the "in-house" assay genotyped 260 of 295 samples from seven African sites, where 47% were non-subtype C. Overall, the newly validated "in-house" drug resistance assay is suited for use in Africa as it overcomes the obstacle of subtype diversity
机译:在资源贫乏地区引入抗逆转录病毒(ARV)治疗可有效抑制HIV-1复制并延长感染者的寿命。这导致对负担得起的HIV-1耐药性分析的需求,因为由于耐药性的发展导致治疗失败很常见。这项研究开发并评估了一种可负担的“内部”基因分型测定法,以监测非洲特别是南非的HIV-1耐药性。开发了使用自动RNA提取,C型特异性PCR和测序引物的“内部”检测方法,并成功评估了396例患者样品(病毒载量范围为1000-160万个RNA拷贝/ ml)。通过比较来自90个患者和10个外部质量控制样品的序列数据和耐药性谱与来自ViroSeq HIV-1基因分型试剂盒的数据进行比较,验证了“内部”分析的有效性。与使用Viroseq的91个样品相比,“内部”分析效率更高,可扩增所有100个样品。 “内部”序列与ViroSeq序列同源性为99.2%,在96个样品中观察到相同的耐药性突变谱。此外,“内部”分析对来自七个非洲地点的295个样品中的260个进行了基因分型,其中47%是非亚型。总体而言,新验证的“内部”耐药性分析适用于非洲,因为它克服了亚型多样性的障碍

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