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Detection and differentiation of virulent and avirulent strains of Newcastle disease virus by real-time PCR.

机译:实时PCR检测和鉴别新城疫病毒的强毒株和无毒株。

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A rapid diagnostic method based on the melting curve SYBR Green I real-time PCR analysis was developed to detect and differentiate Newcastle disease virus (NDV) strains. Degenerated primers based on the cleavage site sequence of the F0 gene were designed to detect specific sequences characteristic of virulent and avirulent strains of NDV. Eighteen strains of NDV from four lineages were identified and grouped into virulent and avirulent strains. Peaks on the melting temperature graph with melting temperature values between 80.00 and 83.80 degrees C were observed for lentogenic (avirulent) strains. Tm values higher than 83.80 were observed for virulent (mesogenic and velogenic) strains. The detection limit of real-time PCR was 2x102 plasmid copies per reaction or 102 EID50 for velogenic strains and 103 EID50 for lentogenic strains. The results obtained in this study demonstrate the possible applications for melting curve real-time PCR analysis in laboratory practice for the diagnosis and differentiation of avirulent and virulent strains of Newcastle disease virus.
机译:建立了基于熔解曲线SYBR Green I实时PCR分析的快速诊断方法,以检测和区分新城疫病毒(NDV)菌株。设计了基于F0基因切割位点序列的简并引物,以检测NDV毒力和无毒力菌株的特异序列。鉴定了来自四个谱系的18个NDV菌株,并将其分为有毒力和无毒力的菌株。观察到了在慢熔温度曲线上的峰值,熔化温度值在80.00到83.80摄氏度之间。对于有毒(介基因和速生)菌株,观察到的 T m 值高于83.80。实时PCR的检出限为每个反应2x10 2 质粒拷贝或速溶菌株10 2 EID 50 和10 3 EID 50 用于慢变菌株。这项研究中获得的结果表明,在实验室实践中,熔解曲线实时PCR分析可用于诊断和鉴别新城疫病毒的无毒力和强毒力菌株。

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