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Clusters of acute respiratory illness associated with human enterovirus 68--Asia, Europe, and United States, 2008-2010.与人类肠道病毒 68 相关的急性呼吸道疾病集群-亚洲、欧洲和美国,2008-2010 年。
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Comparative evaluation of the Seegene Seeplex RV15 and real-time PCR for respiratory virus detection.比较赛沛 Seeplex RV15 与实时 PCR 检测呼吸道病毒的效果。
J Med Virol. 2011 Aug;83(8):1469-75. doi: 10.1002/jmv.22125.
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Application of TaqMan low-density arrays for simultaneous detection of multiple respiratory pathogens.TaqMan 低密度基因芯片在同时检测多种呼吸道病原体中的应用。
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Viral infections of the lower respiratory tract: old viruses, new viruses, and the role of diagnosis.下呼吸道病毒感染:旧病毒、新病毒及诊断的作用。
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Comparative evaluation of Taqman real-time PCR and semi-nested VP1 PCR for detection of enteroviruses in clinical specimens.Taqman 实时 PCR 和半巢式 VP1 PCR 检测临床标本中肠道病毒的比较评估。
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快速诊断呼吸道病原体多重实时 RT-PCR 检测与内部单重检测在全面检测人类呼吸道病毒中的比较。

Comparison of fast-track diagnostics respiratory pathogens multiplex real-time RT-PCR assay with in-house singleplex assays for comprehensive detection of human respiratory viruses.

机构信息

Division of Viral Diseases, Centers for Disease Control and Prevention, Atlanta, GA, USA.

出版信息

J Virol Methods. 2012 Nov;185(2):259-66. doi: 10.1016/j.jviromet.2012.07.010. Epub 2012 Jul 11.

DOI:10.1016/j.jviromet.2012.07.010
PMID:22796035
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC7119496/
Abstract

Fast-track Diagnostics respiratory pathogens (FTDRP) multiplex real-time RT-PCR assay was compared with in-house singleplex real-time RT-PCR assays for detection of 16 common respiratory viruses. The FTDRP assay correctly identified 26 diverse respiratory virus strains, 35 of 41 (85%) external quality assessment samples spiked with cultured virus and 232 of 263 (88%) archived respiratory specimens that tested positive for respiratory viruses by in-house assays. Of 308 prospectively tested respiratory specimens selected from children hospitalized with acute respiratory illness, 270 (87.7%) and 265 (86%) were positive by FTDRP and in-house assays for one or more viruses, respectively, with combined test results showing good concordance (K=0.812, 95% CI=0.786-0.838). Individual FTDRP assays for adenovirus, respiratory syncytial virus and rhinovirus showed the lowest comparative sensitivities with in-house assays, with most discrepancies occurring with specimens containing low virus loads and failed to detect some rhinovirus strains, even when abundant. The FTDRP enterovirus and human bocavirus assays appeared to be more sensitive than the in-house assays with some specimens. With the exceptions noted above, most FTDRP assays performed comparably with in-house assays for most viruses while offering enhanced throughput and easy integration by laboratories using conventional real-time PCR instrumentation.

摘要

快速诊断呼吸道病原体(FTDRP)多重实时 RT-PCR 检测法与内部单重实时 RT-PCR 检测法相比,可用于检测 16 种常见呼吸道病毒。FTDRP 检测法正确识别了 26 种不同的呼吸道病毒株,41 份外部质量评估样本中,35 份(85%)用培养病毒接种的样本和 263 份(88%)存档呼吸道样本中,232 份(88%)经内部检测法检测为呼吸道病毒阳性的样本。在 308 份从因急性呼吸道疾病住院的儿童中前瞻性检测的呼吸道样本中,FTDRP 和内部检测法分别对 270 份(87.7%)和 265 份(86%)样本检测出一种或多种病毒呈阳性,两种检测方法的联合检测结果具有良好的一致性(K=0.812,95%CI=0.786-0.838)。FTDRP 腺病毒、呼吸道合胞病毒和鼻病毒检测法与内部检测法相比敏感性最低,大多数差异出现在病毒载量低的样本中,并且未能检测到一些鼻病毒株,即使样本中病毒含量丰富也未能检测到。FTDRP 肠道病毒和人类博卡病毒检测法与内部检测法相比,在某些样本中似乎更敏感。除了上述例外情况,大多数 FTDRP 检测法与内部检测法相比,对大多数病毒的检测性能相当,同时提高了检测通量,并方便了使用常规实时 PCR 仪器的实验室进行整合。