首页> 外文期刊>Journal of Virological Methods >End-point limiting-dilution real-time PCR assay for evaluation of hepatitis C virus quasispecies in serum: Performance under optimal and suboptimal conditions.
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End-point limiting-dilution real-time PCR assay for evaluation of hepatitis C virus quasispecies in serum: Performance under optimal and suboptimal conditions.

机译:用于评估血清丙型肝炎病毒准种的终点限制稀释实时PCR分析:在最佳和次最佳条件下的性能。

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摘要

An approach for determination of hepatitis C virus (HCV) quasispecies by end-point limiting-dilution real-time PCR (EPLD-PCR) is described. It involves isolation of individual coexisting sequence variants of the hypervariable region 1 (HVR1) of the HCV genome from serum specimens using a limiting-dilution protocol. EPLD-PCR applied to an HCV outbreak study provided insights into the epidemiological relationships between incident and chronic cases. When applied to samples from a longitudinal study of infected patients, HVR1 sequences from each sampling time-point were observed to group as distinct phylogenetic clusters. Melting peak analysis conducted on EPLD-PCR products generated from these patients could be used for evaluation of HVR1 sequence heterogeneity without recourse to clonal sequencing. Further, to better understand the mechanism of single-molecule PCR, experiments were conducted under optimal and suboptimal annealing temperatures. Under all temperature conditions tested, HVR1 variants from the major phylogenetic clusters of quasispecies could be amplified, revealing that successful HVR1 quasispecies analysis is not contingent to dilution of starting cDNA preparations to a single-molecule state. It was found that EPLD-PCR conducted at suboptimal annealing temperatures generated distributions of unique-sequence variants slightly different from the distribution obtained by PCR conducted at the optimal temperature. Hence, EPLD-PCR conditions can be manipulated to access different subpopulations of HCV HVR1 quasispecies, thus, improving the range of the quasispecies detection. Although EPLD-PCR conducted at different conditions detect slightly different quasispecies populations, as was shown in this study, the resulted samples of quasispecies are completely suitable for molecular epidemiological investigation in different clinical and epidemiological settings.
机译:描述了一种通过终点限制稀释实时荧光定量PCR(EPLD-PCR)测定丙型肝炎病毒(HCV)准种的方法。它涉及使用极限稀释方案从血清样本中分离出HCV基因组高变区1(HVR1)的各个共存序列变体。应用于HCV爆发研究的EPLD-PCR提供了有关事件与慢性病例之间流行病学关系的见解。当将其用于来自受感染患者的纵向研究的样本时,观察到每个采样时间点的HVR1序列归为不同的系统发生簇。对从这些患者产生的EPLD-PCR产物进行的熔解峰分析可用于评估HVR1序列异质性,而无需进行克隆测序。此外,为了更好地理解单分子PCR的机理,在最佳和次优退火温度下进行了实验。在测试的所有温度条件下,可以扩增来自准种的主要系统发生簇的HVR1变体,这表明成功的HVR1准种分析并不取决于将起始cDNA制剂稀释到单分子状态。发现在次优退火温度下进行的EPLD-PCR产生的独特序列变异的分布与在最佳温度下进行的PCR获得的分布略有不同。因此,可以操作EPLD-PCR条件以访问HCV HVR1准种的不同亚群,从而提高了准种检测的范围。如本研究所示,尽管在不同条件下进行的EPLD-PCR检测到的准种种群略有不同,但所得的准种样品完全适合在不同的临床和流行病学环境中进行分子流行病学调查。

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