首页> 外文期刊>Journal of Virological Methods >Validation of two real-time RT-PCR methods for foot-and-mouth disease diagnosis: RNA-extraction, matrix effect, uncertainty of measurement and precision
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Validation of two real-time RT-PCR methods for foot-and-mouth disease diagnosis: RNA-extraction, matrix effect, uncertainty of measurement and precision

机译:验证两种实时RT-PCR方法诊断口蹄疫的方法:RNA提取,基质效应,测量不确定度和精度

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Real-time reverse transcription polymerase chain reaction (rRT-PCR) assays are being used routinely for diagnosing foot-and-mouth disease virus (FMDV). Although most laboratories determine analytical and diagnostic sensitivity and specificity, a thorough validation in terms of establishing optimal RNA-extraction conditions, matrix effect, uncertainty of measurement and precision is not performed or reported generally. In this study, different RNA-extraction procedures were compared for two FMDV rRT-PCRs. The NucleoSpin columns available commercially combined high extraction efficiency with ease-of-automation. Furthermore, six different FMDV-negative matrices were spiked with a dilution series of FMDV SAT1 ZIM 25/89. Compared to cell-culture-spiked viral control samples, no matrix effect on the analytical sensitivity was found for blood or foot epithelium. Approximately 1log sub(1) sub(0) reduction in detection limit was noted for faecal and tongue epithelium samples, whereas a 3log sub(1) sub(0) decrease was observed for spleen samples. By testing the same dilution series in duplicate on 10 different occasions, an estimation of uncertainty of measurement and precision was obtained using blood as matrix. Both rRT-PCRs produced highly precise results emphasising their potential to replace conventional virological methods. The uncertainty measurement, as described in this study, proved to be a useful tool to evaluate the probability of making a wrong decision.
机译:实时逆转录聚合酶链反应(rRT-PCR)分析通常用于诊断口蹄疫病毒(FMDV)。尽管大多数实验室确定分析和诊断的敏感性和特异性,但通常不会进行或报告关于建立最佳RNA提取条件,基质效应,测量不确定性和精度的全面验证。在这项研究中,比较了两种FMDV rRT-PCR的不同RNA提取程序。市售的NucleoSpin色谱柱结合了高萃取效率和易于自动化的特点。此外,用FMDV SAT1 ZIM 25/89稀释系列加标了六个不同的FMDV阴性基质。与细胞培养加标的病毒对照样品相比,没有发现基质对血液或足上皮的分析灵敏度有影响。粪便和舌头上皮样品的检出限降低了约1log sub(1)sub(0),而脾脏样品则降低了3log sub(1)sub(0)。通过在10个不同的情况下重复测试相同的稀释系列,可以使用血液作为基质来获得测量不确定度和精确度的估计值。两种rRT-PCR均产生了高度精确的结果,强调了它们替代传统病毒学方法的潜力。如本研究中所述,不确定性度量被证明是评估做出错误决定的可能性的有用工具。

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