Ku Karin S, Chodavarapu Ramakrishna K, Martin Ross, Miller Michael D, Mo Hongmei, Svarovskaia Evguenia S
Gilead Sciences, Inc., Foster City, California, USA
Gilead Sciences, Inc., Foster City, California, USA.
J Clin Microbiol. 2016 Jul;54(7):1835-1841. doi: 10.1128/JCM.00238-16. Epub 2016 May 4.
Direct-acting antivirals (DAAs) with activity against multiple genotypes of the hepatitis C virus (HCV) were recently developed and approved for standard-of-care treatment. However, sequencing assays to support HCV genotype 5 and 6 analysis are not widely available. Here, we describe the development of a sequencing assay for the NS3/4A, NS5A, and NS5B genes from HCV genotype 5 and 6 patient isolates. Genotype- and subtype-specific primers were designed to target NS3/4A, NS5A, and NS5B for cDNA synthesis and nested PCR amplification. Amplification was successfully performed for a panel of 32 plasma samples from HCV-infected genotype 5 and 6 patients with sequencing data obtained for all attempted samples. LiPA 2.0 (Versant HCV genotype 2.0) is a reverse hybridization line probe assay that is commonly used for genotyping HCV-infected patients enrolled in clinical studies. Using NS3/4A, NS5A, and NS5B consensus sequences, HCV subtypes were determined that were not available for the initial LiPA 2.0 result for genotype 6 samples. Samples amplified here included the following HCV subtypes: 5a, 6a, 6e, 6f, 6j, 6i, 6l, 6n, 6o, and 6p. The sequencing data generated allowed for the determination of the presence of variants at amino acid positions previously characterized as associated with resistance to DAAs. The simple and robust sequencing assay for genotypes 5 and 6 presented here may lead to a better understanding of HCV genetic diversity and prevalence of resistance-associated variants.
最近开发出了对多种丙型肝炎病毒(HCV)基因型具有活性的直接作用抗病毒药物(DAA)并被批准用于标准治疗。然而,支持HCV基因型5和6分析的测序检测方法尚未广泛应用。在此,我们描述了一种针对HCV基因型5和6患者分离株的NS3/4A、NS5A和NS5B基因的测序检测方法的开发。设计了基因型和亚型特异性引物,以靶向NS3/4A、NS5A和NS5B用于cDNA合成和巢式PCR扩增。对一组来自HCV感染的基因型5和6患者的32份血浆样本成功进行了扩增,并获得了所有尝试样本的测序数据。LiPA 2.0(Versant HCV基因型2.0)是一种反向杂交线性探针检测方法,常用于对参与临床研究的HCV感染患者进行基因分型。利用NS3/4A、NS5A和NS5B共有序列,确定了HCV亚型,而这些亚型在基因型6样本的初始LiPA 2.0结果中无法获得。此处扩增的样本包括以下HCV亚型:5a、6a、6e、6f、6j、6i、6l、6n、6o和6p。所产生的测序数据有助于确定先前被确定为与对DAA耐药相关的氨基酸位置上变异体的存在。本文介绍的针对基因型5和6的简单且可靠的测序检测方法可能有助于更好地了解HCV遗传多样性和耐药相关变异体的流行情况。