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从纤维素基质中洗脱肠道病毒 RNA 的优化方法。

An optimized method for elution of enteroviral RNA from a cellulose-based substrate.

机构信息

Shandong Provincial Key Laboratory of Infectious Diseases Control and Prevention, Shandong Center for Disease Control and Prevention, 16992 Jingshi Road, Jinan 250014, China.

出版信息

J Virol Methods. 2012 Dec;186(1-2):62-7. doi: 10.1016/j.jviromet.2012.08.016. Epub 2012 Sep 6.

Abstract

The Flinders Technology Australia (FTA) Elute Card is a commercial product that facilitates the collection, transport, archiving and processing of nucleic acids from a wide variety of biological samples at room temperature. While the cards have been designed so that sterile/deionized water can elute DNA easily, they are not suitable for some less stable RNAs. This study was undertaken to determine the optimal conditions such as the buffer type, buffer pH and incubation temperature for the elution of enteroviral RNA from FTA Elute Cards prior to quantitative analysis using real-time PCR (qPCR) or consensus degenerate hybrid oligonucleotide primer VP1 RT-semi nested PCR (CODEHOP VP1 RT-snPCR). TE-1 (pH 8.0), rather than sterile water, was the best buffer for high efficiency elution of enteroviral RNA at 95°C. However, as the estimated recovery rate of viral RNA eluted from the cards averaged to be only 6.1%, enterovirus assays using FTA elution should be considered qualitative, especially at low virus titers, and therefore the results of the assay should be interpreted carefully.

摘要

澳大利亚弗林德斯技术公司(FTA)洗脱卡是一种商业产品,可在室温下从各种生物样本中收集、运输、存档和处理核酸。虽然这些卡片的设计使得无菌/去离子水可以轻松洗脱 DNA,但它们并不适合一些不太稳定的 RNA。本研究旨在确定最佳条件,如缓冲液类型、缓冲液 pH 值和孵育温度,以便在使用实时 PCR(qPCR)或共识简并杂交寡核苷酸引物 VP1 RT-半巢式 PCR(CODEHOP VP1 RT-snPCR)对 FTA 洗脱卡中的肠道病毒 RNA 进行定量分析之前进行洗脱。TE-1(pH8.0)而不是无菌水,是在 95°C 下高效洗脱肠道病毒 RNA 的最佳缓冲液。然而,由于从卡片中洗脱的病毒 RNA 的估计回收率平均仅为 6.1%,因此使用 FTA 洗脱进行肠道病毒检测应被视为定性检测,特别是在病毒滴度较低的情况下,因此应仔细解释检测结果。

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