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通过核酸扩增检测北美东部和西部马脑炎病毒。

Detection of North American eastern and western equine encephalitis viruses by nucleic acid amplification assays.

作者信息

Lambert Amy J, Martin Denise A, Lanciotti Robert S

机构信息

Division of Vector-Borne Infectious Diseases, National Center for Infectious Diseases, Centers for Disease Control and Prevention, Public Health Service, U.S. Department of Health and Human Services, Fort Collins, Colorado 80521, USA.

出版信息

J Clin Microbiol. 2003 Jan;41(1):379-85. doi: 10.1128/JCM.41.1.379-385.2003.

Abstract

We have developed nucleic acid sequence-based amplification (NASBA), standard reverse transcription PCR (RT-PCR), and TaqMan nucleic acid amplification assays for the rapid detection of North American eastern equine encephalitis (EEE) and western equine encephalitis (WEE) viral RNAs from samples collected in the field and clinical samples. The sensitivities of these assays have been compared to that of virus isolation. While all three types of nucleic acid amplification assays provide rapid detection of viral RNAs comparable to the isolation of viruses in Vero cells, the TaqMan assays for North American EEE and WEE viral RNAs are the most sensitive. We have shown these assays to be specific for North American EEE and WEE viral RNAs by testing geographically and temporally distinct strains of EEE and WEE viruses along with a battery of related and unrelated arthropodborne viruses. In addition, all three types of nucleic acid amplification assays have been used to detect North American EEE and WEE viral RNAs from mosquito and vertebrate tissue samples. The sensitivity, specificity, and rapidity of nucleic acid amplification demonstrate the usefulness of NASBA, standard RT-PCR, and TaqMan assays, in both research and diagnostic settings, to detect North American EEE and WEE viral RNAs.

摘要

我们已开发出基于核酸序列的扩增技术(NASBA)、标准逆转录聚合酶链反应(RT-PCR)以及TaqMan核酸扩增检测法,用于从现场采集的样本和临床样本中快速检测北美东部马脑炎(EEE)和西部马脑炎(WEE)病毒RNA。已将这些检测法的灵敏度与病毒分离法的灵敏度进行了比较。虽然所有这三种核酸扩增检测法都能像在Vero细胞中分离病毒一样快速检测病毒RNA,但用于检测北美EEE和WEE病毒RNA的TaqMan检测法最为灵敏。通过检测来自不同地理区域和时间的EEE和WEE病毒株以及一系列相关和不相关的节肢动物传播病毒,我们已证明这些检测法对北美EEE和WEE病毒RNA具有特异性。此外,所有这三种核酸扩增检测法都已用于检测来自蚊子和脊椎动物组织样本中的北美EEE和WEE病毒RNA。核酸扩增的灵敏度、特异性和快速性证明了NASBA、标准RT-PCR和TaqMan检测法在研究和诊断环境中检测北美EEE和WEE病毒RNA的实用性。

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