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一种新型肠道病毒和肠道病毒/鼻病毒多重一步实时 PCR 的验证及临床应用

A novel enterovirus and parechovirus multiplex one-step real-time PCR-validation and clinical experience.

机构信息

Department of Microbiological Diagnostics and Virology, Statens Serum Institut, Artillerivej 5, 2300 Copenhagen S, Denmark; Department of Infectious Diseases, University Hospital Odense, Odense, Denmark.

出版信息

J Virol Methods. 2013 Nov;193(2):359-63. doi: 10.1016/j.jviromet.2013.06.038. Epub 2013 Jul 8.

Abstract

As the number of new enteroviruses and human parechoviruses seems ever growing, the necessity for updated diagnostics is relevant. We have updated an enterovirus assay and combined it with a previously published assay for human parechovirus resulting in a multiplex one-step RT-PCR assay. The multiplex assay was validated by analysing the sensitivity and specificity of the assay compared to the respective monoplex assays, and a good concordance was found. Furthermore, the enterovirus assay was able to detect 42 reference strains from all 4 species, and an additional 9 genotypes during panel testing and routine usage. During 15 months of routine use, from October 2008 to December 2009, we received and analysed 2187 samples (stool samples, cerebrospinal fluids, blood samples, respiratory samples and autopsy samples) were tested, from 1546 patients and detected enteroviruses and parechoviruses in 171 (8%) and 66 (3%) of the samples, respectively. 180 of the positive samples could be genotyped by PCR and sequencing and the most common genotypes found were human parechovirus type 3, echovirus 9, enterovirus 71, Coxsackievirus A16, and echovirus 25. During 2009 in Denmark, both enterovirus and human parechovirus type 3 had a similar seasonal pattern with a peak during the summer and autumn. Human parechovirus type 3 was almost invariably found in children less than 4 months of age. In conclusion, a multiplex assay was developed allowing simultaneous detection of 2 viruses, which can cause similar clinical symptoms.

摘要

随着新肠道病毒和人类肠道病毒的数量似乎不断增加,更新诊断方法是必要的。我们更新了肠道病毒检测方法,并将其与之前发表的人类肠道病毒检测方法相结合,形成了一种多重一步 RT-PCR 检测方法。该多重检测方法通过分析与各自单重检测方法相比的敏感性和特异性进行了验证,发现具有良好的一致性。此外,肠道病毒检测方法能够检测到来自所有 4 个种的 42 个参考株,以及在小组测试和常规使用期间额外的 9 种基因型。在 2008 年 10 月至 2009 年 12 月的 15 个月常规使用期间,我们收到并分析了来自 1546 名患者的 2187 份样本(粪便样本、脑脊液、血液样本、呼吸道样本和尸检样本),在 171 份(8%)和 66 份(3%)样本中分别检测到肠道病毒和肠道病毒,180 份阳性样本可通过 PCR 和测序进行基因分型,最常见的基因型为人类肠道病毒 3 型、柯萨奇病毒 9 型、肠道病毒 71 型、柯萨奇病毒 A16 型和肠道病毒 25 型。在 2009 年丹麦,肠道病毒和人类肠道病毒 3 型具有相似的季节性模式,夏季和秋季达到高峰。人类肠道病毒 3 型几乎总是在 4 个月以下的儿童中发现。总之,开发了一种多重检测方法,可以同时检测到两种可能引起类似临床症状的病毒。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/c44d/7119552/59c0943afed3/gr1.jpg

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