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A Quantitative Real-Time RT-PCR Assay for the Detection of Venezuelan equine encephalitis virus Utilizing a Universal Alphavirus Control RNA

机译:利用通用Alphavirus对照RNA检测委内瑞拉马脑炎病毒的实时定量RT-PCR分析

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摘要

Venezuelan equine encephalitis virus (VEEV) is an Alphavirus from the family Togaviridae that causes epizootic outbreaks in equids and humans in Central and South America. So far, most studies use conventional reverse transcriptase PCR assays for the detection of the different VEEV subtypes. Here we describe the development of a TaqMan quantitative real-time reverse transcriptase PCR assay for the specific detection and quantitation of all VEEV subtypes which uses in parallel a universal equine encephalitis virus control RNA carrying target sequences of the three equine encephalitis viruses. The control RNA was used to generate standard curves for the calculation of copy numbers of viral genome of Eastern equine encephalitis virus (EEEV), Western equine encephalitis virus (WEEV), and VEEV. The new assay provides a reliable high-throughput method for the detection and quantitation of VEEV RNA in clinical and field samples and allows a rapid differentiation from potentially cocirculating EEEV and WEEV strains. The capability to detect all known VEEV variants was experimentally demonstrated and makes this assay suitable especially for the surveillance of VEEV.
机译:委内瑞拉马脑炎病毒(VEEV)是Togaviridae家族的甲型病毒,在中美洲和南美洲引起马匹和人类的流行病暴发。迄今为止,大多数研究都使用常规逆转录酶PCR分析法检测不同的VEEV亚型。在这里,我们描述了TaqMan定量实时逆转录酶PCR检测方法的开发,用于所有VEEV亚型的特异性检测和定量,该方法同时使用携带三种马脑炎病毒目标序列的通用马脑炎病毒控制RNA。对照RNA用于产生标准曲线,用于计算东部马脑炎病毒(EEEV),西部马脑炎病毒(WEEV)和VEEV的病毒基因组的拷贝数。这项新的检测方法为临床和野外样品中VEEV RNA的检测和定量提供了可靠的高通量方法,并可以与潜在的共同循环的EEEV和WEEV菌株快速区分。实验证明了检测所有已知VEEV变体的能力,使该测定特别适合于VEEV的监测。

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