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Characterization of minority HIV-1 drug resistant variants in the United Kingdom following the verification of a deep sequencing-based HIV-1 genotyping and tropism assay

机译:在验证了基于深度测序的HIV-1基因型和嗜性分析后在英国鉴定了少数HIV-1耐药变异体

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摘要

BackgroundThe widespread global access to antiretroviral drugs has led to considerable reductions in morbidity and mortality but, unfortunately, the risk of virologic failure increases with the emergence, and potential transmission, of drug resistant viruses. Detecting and quantifying HIV-1 drug resistance has therefore become the standard of care when designing new antiretroviral regimens. The sensitivity of Sanger sequencing-based HIV-1 genotypic assays is limited by its inability to identify minority members of the quasispecies, i.e., it only detects variants present above ~ 20% of the viral population, thus, failing to detect minority variants below this threshold. It is clear that deep sequencing-based HIV-1 genotyping assays are an important step change towards accurately monitoring HIV-infected individuals.
机译:背景技术全球范围内广泛使用抗逆转录病毒药物已导致发病率和死亡率显着降低,但是不幸的是,随着耐药病毒的出现和潜在传播,病毒学失败的风险增加。因此,在设计新的抗逆转录病毒疗法时,检测和量化HIV-1耐药性已成为护理的标准。基于Sanger测序的HIV-1基因型检测方法的敏感性受到其无法识别准种的少数成员的限制,即它只能检测到病毒种群中约20%以上的变异,因此无法检测到低于此水平的少数变异阈。显然,基于深度测序的HIV-1基因分型测定法是朝准确监测HIV感染者迈出的重要一步。

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