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Nucleic Acid Sequence-Based Amplification Assays for Rapid Detection of West Nile and St. Louis Encephalitis Viruses

机译:快速检测西尼罗河和圣路易斯脑炎病毒的核酸序列为基础的扩增方法

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摘要

The development and application of nucleic acid sequence-based amplification (NASBA) assays for the detection of West Nile (WN) and St. Louis encephalitis (SLE) viruses are reported. Two unique detection formats were developed for the NASBA assays: a postamplification detection step with a virus-specific internal capture probe and electrochemiluminescence (NASBA-ECL assay) and a real-time assay with 6-carboxyfluorescein-labeled virus-specific molecular beacon probes (NASBA-beacon assay). The sensitivities and specificities of these NASBA assays were compared to those of a newly described standard reverse transcription (RT)-PCR and TaqMan assays for SLE virus and to a previously published TaqMan assay for WN virus. The NASBA assays demonstrated exceptional sensitivities and specificities compared to those of virus isolation, the TaqMan assays, and standard RT-PCR, with the NASBA-beacon assay yielding results in less than 1 h. These assays should be of utility in the diagnostic laboratory to complement existing diagnostic testing methodologies and as a tool in conducting flavivirus surveillance in the United States.
机译:据报道,用于检测西尼罗河(WN)和圣路易斯脑炎(SLE)病毒的基于核酸序列的扩增(NASBA)分析方法的开发和应用。针对NASBA分析开发了两种独特的检测格式:使用病毒特异性内部捕获探针和电化学发光的扩增后检测步骤(NASBA-ECL分析)和使用6-羧基荧光素标记的病毒特异性分子信标探针进行实时检测( NASBA信标测定)。将这些NASBA测定的灵敏度和特异性与新描述的SLE病毒的标准逆转录(RT)-PCR和TaqMan测定以及先前公布的WN病毒TaqMan测定的灵敏度和特异性进行了比较。与病毒分离,TaqMan测定和标准RT-PCR相比,NASBA测定具有出色的灵敏度和特异性,NASBA信标测定在不到1小时的时间内即可得出结果。这些测定法应在诊断实验室中有用,以补充现有的诊断测试方法,并作为在美国进行黄病毒监测的工具。

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