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Real-Time Fluorogenic Reverse Transcription-PCR Assays for Detection of Bacteriophage MS2

机译:实时荧光逆转录PCR检测噬菌体MS2的方法。

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摘要

Bacteriophage MS2 is used in place of pathogenic viruses in a wide variety of studies that range from testing of compounds for disinfecting surfaces to studying environmental transport and fate of pathogenic viruses in groundwater. MS2 is also used as a pathogen simulant in the research, development, and testing (including open air tests) of methods, systems, and devices for the detection of pathogens in both the battlefield and homeland defense settings. PCR is often used as either an integral part of such detection systems or as a reference method to assess the sensitivity and specificity of microbial detection. To facilitate the detection of MS2 by PCR, we describe here a set of real-time fluorogenic reverse transcription-PCR assays. The sensitivity of the assays (performed with primer pairs and corresponding dye-labeled probes) ranged from 0.4 to 40 fg of MS2 genomic RNA (200 to 20,000 genome equivalents). We also demonstrate the usefulness of the primer pairs in assays without dye-labeled probe that included the DNA-binding dye SYBR green. None of the assays gave false-positive results when tested against 400 pg of several non-MS2 nucleic acid targets.
机译:噬菌体MS2被用于代替病原病毒,其研究范围很广,从测试表面消毒的化合物到研究环境运输以及病原病毒在地下水中的命运。 MS2还在研究,开发和测试(包括露天测试)的方法,系统和设备中用作病原体模拟物,以在战场和国土防御环境中检测病原体。 PCR通常用作此类检测系统的组成部分,或用作评估微生物检测灵敏度和特异性的参考方法。为了便于通过PCR检测MS2,我们在这里描述了一组实时荧光逆转录PCR检测方法。测定的灵敏度(用引物对和相应的染料标记探针进行)范围为0.4至40 fg MS2基因组RNA(200至20,000个基因组当量)。我们还证明了引物对在不含染料标记探针(包括DNA结合染料SYBR green)的分析中的有用性。当针对400 pg的几种非MS2核酸靶标进行测试时,没有一种测定法提供假阳性结果。

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