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Molecular Assays for Detection of Human Metapneumovirus

机译:用于检测人间质肺病毒的分子检测

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The recent description of the respiratory pathogen human metapneumovirus (hMPV) has highlighted a deficiency in current diagnostic techniques for viral agents associated with acute lower respiratory tract infections. We describe two novel approaches to the detection of viral RNA by use of reverse transcriptase PCR (RT-PCR). The PCR products were identified after capture onto a solid-phase medium by hybridization with a sequence-specific, biotinylated oligonucleotide probe. The assay was applied to the screening of 329 nasopharyngeal aspirates sampled from patients suffering from respiratory tract disease. These samples were negative for other common microbial causes of respiratory tract disease. We were able to detect hMPV sequences in 32 (9.7%) samples collected from Australian patients during 2001. To further reduce result turnaround times we designed a fluorogenic TaqMan oligoprobe and combined it with the existing primers for use on the LightCycler platform. The real-time RT-PCR proved to be highly reproducible and detected hMPV in an additional 6 out of 62 samples (9.6%) tested during the comparison of the two diagnostic approaches. We found the real-time RT-PCR to be the test of choice for future investigation of samples for hMPV due to its speed, reproducibility, specificity, and sensitivity.
机译:呼吸道病原体人类肺炎病毒(hMPV)的最新描述突出了当前与急性下呼吸道感染相关的病毒制剂的诊断技术的缺陷。我们描述了两种通过使用逆转录酶PCR(RT-PCR)检测病毒RNA的新方法。通过与序列特异性生物素化寡核苷酸探针杂交捕获到固相培养基上后,鉴定出PCR产物。该测定法用于筛查从患有呼吸道疾病的患者中采集的329鼻咽抽吸物。这些样品对呼吸道疾病的其他常见微生物原因均呈阴性。我们能够在2001年期间从澳大利亚患者那里采集的32个样本(9.7%)中检测到hMPV序列。为了进一步减少结果的周转时间,我们设计了荧光TaqMan寡聚探针并将其与现有引物结合使用,以用于LightCycler平台。实时RT-PCR被证明是高度可重复的,并且在两种诊断方法的比较中,在所测试的62个样本中,另外6个样本(9.6%)中检测到hMPV。由于其速度,可重复性,特异性和敏感性,我们发现实时RT-PCR成为hMPV样品未来研究的选择测试。

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