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敏感多重实时 RT-qPCR 检测法用于丝状病毒的检测。

Sensitive Multiplex Real-time RT-qPCR Assay for the Detection of Filoviruses.

出版信息

Health Secur. 2018 Jan/Feb;16(1):14-21. doi: 10.1089/hs.2017.0027. Epub 2018 Jan 19.

Abstract

Filoviruses are important etiological agents of emergent diseases with high mortality rates. Traditionally, filovirus fever diseases have primarily been a burden of African countries; however, global interconnectedness has increased the probability of the worldwide spread of filoviruses. Therefore, national healthcare organizations need tools for managing filovirus risk, including diagnostic kits based on real-time reverse transcription PCR (RT-qPCR), as this is the most suitable method for diagnosing filovirus fever diseases. Here we describe a real-time RT-qPCR assay for filovirus detection. This assay is a further development of our previously reported EBOV (Zaire)-Fl kit. Two sets (FiloA-Fl and FiloB-Fl) of real-time RT-qPCR assays for the detection of filoviruses were developed and evaluated using armored RNA phage particles (ARs) as positive controls. The limit of detection of the assay was 5x10 copies/ml of the AR-positive control for the FiloA-Fl set and 5x10 copies/ml of the AR-positive control for the FiloB-Fl set. Our assay provides a rapid and sensitive tool for detecting filoviruses. The high specificity and sensitivity of the assay make it useful for clinical and epidemiologic investigations in the field of filovirus fever diseases and their etiological agents.

摘要

丝状病毒是具有高死亡率的新兴疾病的重要病原体。传统上,丝状病毒发热疾病主要是非洲国家的负担;然而,全球互联性增加了丝状病毒在全球传播的可能性。因此,国家医疗保健组织需要管理丝状病毒风险的工具,包括基于实时逆转录聚合酶链反应(RT-qPCR)的诊断试剂盒,因为这是诊断丝状病毒发热疾病最适合的方法。在这里,我们描述了一种用于丝状病毒检测的实时 RT-qPCR 检测方法。该检测方法是我们之前报道的 EBOV(扎伊尔)-Fl 试剂盒的进一步发展。开发了两套(FiloA-Fl 和 FiloB-Fl)用于检测丝状病毒的实时 RT-qPCR 检测方法,并使用装甲 RNA 噬菌体颗粒(ARs)作为阳性对照进行了评估。对于 FiloA-Fl 组,该检测方法的检测限为 5x10 个拷贝/ml 的 AR 阳性对照,对于 FiloB-Fl 组,该检测方法的检测限为 5x10 个拷贝/ml 的 AR 阳性对照。我们的检测方法提供了一种快速灵敏的检测丝状病毒的工具。该检测方法具有高特异性和灵敏度,可用于丝状病毒发热疾病及其病原体的临床和流行病学研究。

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