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Development of a real-time recombinase polymerase amplification assay for rapid and sensitive detection of porcine circovirus 2

机译:开发实时重组酶聚合酶扩增测定,用于快速和敏感性检测猪圆环毒素2

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Porcine diseases associated with porcine circovirus 2 (PCV-2) infection have resulted in significant economic losses worldwide. A real-time recombinase polymerase amplification (RPA) assay was developed to detect PCV-2 using primers and an exo probe specific for the ORF2 gene. The reaction process can be completed in 20 min at 38 degrees C. The assay only detects PCV-2, as there was no cross-reaction with other pathogens important in pigs. Using the PCV-2 genomic DNA as template, the analytical sensitivity of the real-time RPA was 103 copies. The assay performance was evaluated by testing 38 field samples and compared with real-time PCR. The two assays demonstrated a 100% diagnostic agreement, and PCV-2 DNA was detected in 26 samples. The R-2 value of real-time RPA and real-time PCR was 0.954 by linear regression analysis. The real-time RPA assay provides an alternative tool for rapid, simple, and reliable detection of PCV-2, especially in remote and rural areas.
机译:与猪胃肠病毒2(PCV-2)感染相关的猪病导致全球经济损失显着。 制定了实时重组酶聚合酶扩增(RPA)测定以使用对ORF2基因的引物和特异的EXO探针检测PCV-2。 反应过程可以在38℃下在20分钟内完成。测定仅检测PCV-2,因为与猪中的其他病原体没有交叉反应。 使用PCV-2基因组DNA作为模板,实时RPA的分析敏感性为103份。 通过测试38场样品并与实时PCR进行比较来评估测定性能。 两种测定证明了100%的诊断协议,在26个样品中检测到PCV-2 DNA。 通过线性回归分析,实时RPA和实时PCR的R-2值为0.954。 实时RPA测定为PCV-2的快速,简单,可靠地检测,特别是在远程和农村地区提供替代工具。

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