Assessments of intra- and inter-host diversity of hepatitis C virus using Next Generation Sequencing and Mass spectrometry

Zoya Dimitrova, David S. Campo, S. Ramachandran, Gilberto Vaughan, L. Ganova-Raeva, Yulin Lin, J. Forbi, G. Xia, P. Skums, B. Pearlman, Y. Khudyakov
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引用次数: 3

Abstract

Recent advances in sequencing methods allow the analysis of an unprecedented number of viral variants from infected patients and present a novel opportunity for understanding viral evolution, drug resistance and immune escape. In the present paper, we compared three technologies for amplicon analysis: (i) Next Generation Sequencing; (ii) Clonal sequencing using End-point Limiting-dilution for isolation of individual sequence variants followed by Real-Time PCR and sequencing; and (iii) Mass spectrometry of base-specific cleavage reactions of a target sequence. Hypervariable region 1 of hepatitis C virus was analyzed using these three technologies to assess diversity and genetic relatedness of intra-host viral populations in specimens obtained from 38 patients. Estimates of population heterogeneity varied among technologies. However, all three technologies were equally accurate in identification of genetic relatedness among viral strains, supporting their application in molecular epidemiology for tracking viral variants and detecting transmission events.
使用下一代测序和质谱法评估丙型肝炎病毒宿主内和宿主间的多样性
测序方法的最新进展允许分析来自感染患者的空前数量的病毒变体,并为了解病毒进化,耐药性和免疫逃逸提供了新的机会。在本文中,我们比较了三种扩增子分析技术:(i)下一代测序;(ii)克隆测序,使用终点限制稀释法分离单个序列变异,然后进行实时荧光定量PCR和测序;(iii)目标序列碱基特异性裂解反应的质谱分析。使用这三种技术分析了38例患者标本中丙型肝炎病毒的高变区1,以评估宿主内病毒种群的多样性和遗传相关性。对人口异质性的估计因技术而异。然而,这三种技术在鉴定病毒株之间的遗传相关性方面同样准确,支持它们在分子流行病学中用于跟踪病毒变异和检测传播事件的应用。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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