首页> 外文期刊>Journal of Virological Methods >Differential detection of porcine reproductive and respiratory syndrome virus genotypes by a fluorescence melting curve analysis using peptide nucleic acid probe-mediated one-step real-time RT-PCR
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Differential detection of porcine reproductive and respiratory syndrome virus genotypes by a fluorescence melting curve analysis using peptide nucleic acid probe-mediated one-step real-time RT-PCR

机译:使用肽核酸探针介导的一步实时RT-PCR,荧光熔化曲线分析荧光熔化曲线分析的差异检测荧光熔化曲线分析

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摘要

Peptide nucleic acids (PNAs), artificially synthesized DNA analogues, hybridize strongly with DNA and are useful for fluorescence melting curve analyses (FMCA) based on the thermal denaturation of the probe-target duplex. In this study, we developed a PNA-based one-step real-time RT-PCR assay for the differential and qualitative detection of the porcine reproductive and respiratory syndrome virus genotypes PRRSV1 and PRRSV2. The specificity of the assay was analyzed in silico using previously reported primers and probes and was subsequently verified using Korean PRRSV panels and clinical samples. Seven clinical samples showing low curves with high Ct values were confirmed as negative by FMCA. The sensitivities of one-step real-time PCR for PRRSV1 and PRRSV2 were 15 and 11 copies, respectively, and the results were in 100% agreement with those of conventional RT-PCR combined with nested PCR using clinical samples. Therefore, the assay is highly specific for the detection of current PRRSV1 and PRRSV2 without non-specific amplification by FMCA.
机译:肽核酸(PNA),人工合成的DNA类似物,用DNA强烈杂交,可用于基于探针 - 目标双链体的热变性的荧光熔化曲线分析(FMCA)。在这项研究中,我们开发了一种基于PNNA的一步实时RT-PCR测定,用于猪生殖和呼吸综合征病毒基因型PRRSv1和PRRSV2的差异和定性检测。使用先前报道的引物和探针在硅中分析测定的特异性,随后使用韩国PRRSV面板和临床样品进行验证。七个显示具有高CT值的低曲线的临床样本被FMCA确认为阴性。 PRRSV1和PRRSV2的一步实时PCR的敏感性分别为15和11份,结果与使用临床样品与常规RT-PCR联合巢式PCR的常规RT-PCR协议100%。因此,测定对于检测电流PRRSv1和PRRSV2的测定非常具体,而不通过FMCA进行非特异性扩增。

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