首页> 外文期刊>Journal of Virological Methods >Detection of Colorado Tick Fever viral RNA in acute human serum samples by a quantitative real-time RT-PCR assay.
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Detection of Colorado Tick Fever viral RNA in acute human serum samples by a quantitative real-time RT-PCR assay.

机译:通过定量实时RT-PCR分析检测急性人血清样品中的科罗拉多T虫热病毒RNA。

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摘要

A quantitative real-time RT-PCR assay for the detection of Colorado Tick Fever (CTF) viral RNA in human clinical samples is presented. The sensitivity of this assay has been shown to be greater than that of the isolation of virus in Vero cells by standard plaque assay in a direct comparison. The specificity of the CTF quantitative real-time RT-PCR assay was determined by the exclusive detection of CTF viral RNAs when applied to a diverse panel of CTF viral isolates and reference strain agents known to circulate in areas of CTF virus transmission. Lastly, the quantitative real-time RT-PCR assay demonstrated exceptional sensitivity for the detection of CTF viral RNA in acute human serum. The quantitative real-time RT-PCR assay is efficient, sensitive and specific and as such is useful for the detection of CTF viral RNA in the diagnostic or research laboratory.
机译:提出了一种定量实时RT-PCR测定法,用于检测人类临床样品中的科罗拉多T热(CTF)病毒RNA。在直接比较中,已表明该测定法的灵敏度高于通过标准噬斑测定法在Vero细胞中分离病毒的灵敏度。当将CTF病毒RNA应用于多种CTF病毒分离株和已知在CTF病毒传播区域中流通的参考菌株时,通过对CTF病毒RNA的排他性检测,可以确定CTF实时定量RT-PCR检测的特异性。最后,实时荧光定量RT-PCR分析证明了对急性人血清中CTF病毒RNA的检测具有出色的灵敏度。实时定量RT-PCR定量分析是高效,灵敏和特异的,因此可用于诊断或研究实验室中CTF病毒RNA的检测。

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