Consiglio per la Ricerca in Agricoltura e l'analisi dell'Economia agraria (CREA)-Centro di Ricerca Difesa e Certificazione (CREA-DC), Rome, Italy.
Methods Mol Biol. 2022;2316:163-179. doi: 10.1007/978-1-0716-1464-8_15.
Amplification of different nucleic acid targets in the same reaction (multiplex polymerase chain reaction) is challenging but an extremely useful tool especially for viroid diagnosis. In the amplification mixtures, several pairs of primers work together in the same conditions to detect different targets. Here, we describe the development and use of a multiplex reverse transcription polymerase chain reaction protocol highlighting the most crucial factors that can significantly affect the quality of the method. First, particular attention must be paid to primer design. Then, the amplification mixture and temperature conditions must be calibrated precisely to avoid cross reactivity or loss in sensitivity. Finally, the detection system of the amplification results must allow a specific identification of the amplified target(s).
在同一反应中扩增不同的核酸靶标(多重聚合酶链反应)具有挑战性,但却是一种非常有用的工具,特别是在类病毒诊断方面。在扩增混合物中,几对引物在相同的条件下共同作用以检测不同的靶标。在这里,我们描述了一种多重逆转录聚合酶链反应方案的开发和使用,强调了可能显著影响方法质量的最关键因素。首先,必须特别注意引物设计。然后,必须精确校准扩增混合物和温度条件,以避免交叉反应或灵敏度降低。最后,扩增结果的检测系统必须允许对扩增的靶标进行特异性识别。