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首页> 外文期刊>Journal of Clinical Microbiology >Assessment of a Novel Automatic Real-Time PCR Assay on the Cobas 4800 Analyzer as a Screening Platform for Hepatitis C Virus Genotyping in Clinical Practice: Comparison with Massive Sequencing
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Assessment of a Novel Automatic Real-Time PCR Assay on the Cobas 4800 Analyzer as a Screening Platform for Hepatitis C Virus Genotyping in Clinical Practice: Comparison with Massive Sequencing

机译:作为临床实践中丙型肝炎病毒基因分型筛选平台的Cobas 4800分析仪对新型自动实时PCR分析的评估:与大规模测序的比较

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The unequivocal identification of hepatitis C virus (HCV) subtypes 1a/1b and genotypes 2 to 6 is required for optimizing the effectiveness of interferon-free, direct-acting antiviral therapies. We compared the performance of a new real-time HCV genotyping assay used on the Cobas 4800 system (C4800) with that of high-resolution HCV subtyping (HRCS). In total, 502 samples were used, including 184 samples from chronic HCV patients (from routine laboratory activity during April 2016), 5 stored samples with double HCV genotype infections for testing the limitations of the method, and 313 samples from a screening protocol implemented in our hospital (from May to August 2016) based on the new method to further determine its genotyping accuracy. A total of 282 samples, including 171 from April 2016 (the 13 remaining had too low of a viral load for HRCS), 5 selected with double infections, and 106 from screening, were analyzed by both methods, and 220 were analyzed only by the C4800. The C4800 correctly subtyped 125 of 126 1a/1b samples, and the 1 remaining sample was reported as genotype 1. The C4800 correctly genotyped 38 of 45 non-1a/1b samples (classified by HRCS), and it reported the remaining 7 samples as indeterminate. One hundred two of 106 non-1a/1b genotype samples that were identified using the C4800 for screening were confirmed by HRCS. In the 4 remaining samples, 3 were correctly reported as genotype 1 (without defining the subtype) and 1 was reported as indeterminate. None of the samples were misgenotyped. Four of 7 samples with double HCV infections were correctly genotyped by the C4800. Excluding the 5 selected double-infected samples, the C4800 showed 95.7% concordant results for genotyping HCVs 2 to 6 and 1a/1b subtyping, and 99.2% concordance for subtyping 1a/1b single infections in clinical samples. To improve laboratory workflow, we propose using the C4800 as a first-line test for HCV genotyping and 1a/1b classification, followed by transferring non-1a/1b samples to a center where HRCS is available, if further characterization is needed.
机译:明确鉴定丙型肝炎病毒(HCV)亚型1a / 1b和基因型2至6是优化无干扰素,直接作用抗病毒疗法的有效性所必需的。我们将Cobas 4800系统(C4800)上使用的新型实时HCV基因分型测定与高分辨率HCV亚型(HRCS)的性能进行了比较。总共使用了502个样本,其中包括184例来自慢性HCV患者的样本(来自2016年4月的常规实验室活动),5个具有双重HCV基因型感染的储存样本以测试该方法的局限性,以及313项来自于我院(2016年5月至2016年8月)根据新方法进一步确定其基因分型准确性。两种方法共分析了282个样品,包括2016年4月的171个样品(剩余的13个样品的HRCS病毒载量太低),5个样品被双重感染选择和106个筛查样品进行了分析,而220个样品仅通过两种方法进行了分析。 C4800。 C4800对126个1a / 1b样本中的125个正确地进行了亚型分析,其余1个样本被报告为基因型1。C4800对45个非1a / 1b样本(按HRCS分类)中的38个样本进行了正确的基因分型。不定。 HRCS确认了使用C4800进行筛选的106个非1a / 1b基因型样本中的102个。在剩下的4个样本中,有3个被正确报告为基因型1(未定义亚型),有1个被报告为不确定型。没有样品被错误分型。 C4800正确地对双重HCV感染的7个样本中的4个进行了基因分型。除5个选定的双重感染样本外,C4800在临床样本中对HCV 2至6和1a / 1b亚型进行基因分型显示95.7%的一致性结果,对1a / 1b单一感染亚型进行分类的结果为99.2%。为了改善实验室工作流程,我们建议使用C4800作为HCV基因分型和1a / 1b分类的一线测试,如果需要进一步表征,则将非1a / 1b样品转移到可提供HRCS的中心。

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