首页> 外文期刊>Clinical microbiology and infection: European Society of Clinical Microbiology and Infectious Diseases >Qualitative multiplex RT-PCR for simultaneous detection of hepatitis C virus and human immunodeficiency virus in plasma samples.
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Qualitative multiplex RT-PCR for simultaneous detection of hepatitis C virus and human immunodeficiency virus in plasma samples.

机译:定性多重RT-PCR同时检测血浆样品中的丙型肝炎病毒和人类免疫缺陷病毒。

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Abstract This report describes the development of a one-tube multiplex reverse transcriptase (RT)-PCR assay for the simultaneous detection of hepatitis C virus (HCV) and human immunodeficiency virus (HIV) in plasma samples. The assay was evaluated with two panels of HCV- and HIV-1-positive samples, as well as negative plasma specimens. Extraction and amplification of HCV and HIV-1 RNA from plasma samples were performed in a single reaction, and amplified genomes were detected with specific probes. Serial dilutions of the HCV and HIV-1 first World Health Organization International Standards were used to evaluate the sensitivity of the method. Two RNA controls were constructed to determine inter-assay variations and the sensitivity of the amplification step. The assay had good specificity and detected all the genotypes and subtypes tested. The analytical sensitivity of the entire assay was 100 IU/mL for HCV and 200 IU/mL for HIV-1, while the amplification step detected ten copies/reaction for HCV and 20 copies/reaction for HIV-1. The multiplex assay allowed the simultaneous extraction, amplification and detection of two virus genomes, thereby providing an important practical advantage and an efficient approach for analysing individual and pooled plasma donations.
机译:摘要本报告描述了一种用于同时检测血浆样品中丙型肝炎病毒(HCV)和人免疫缺陷病毒(HIV)的单管多重逆转录酶(RT)-PCR测定法的开发。用两个小组的HCV-和HIV-1阳性样品以及阴性血浆标本评估了该测定。在单个反应中进行血浆样品中HCV和HIV-1 RNA的提取和扩增,并用特异性探针检测扩增的基因组。 HCV和HIV-1第一次世界卫生组织国际标准的系列稀释液用于评估该方法的敏感性。构建了两个RNA对照以确定测定间差异和扩增步骤的敏感性。该测定法具有良好的特异性,并检测了所有测试的基因型和亚型。整个测定的分析灵敏度对HCV为100 IU / mL,对HIV-1为200 IU / mL,而扩增步骤检测到HCV为10拷贝/反应,HIV-1为20拷贝/反应。多重测定允许同时提取,扩增和检测两个病毒基因组,从而提供了重要的实践优势和有效的方法来分析单个和合并的血浆捐赠。

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