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Development of a duplex SYBR Green I-based quantitative real-time PCR assay for the rapid differentiation of goose and Muscovy duck parvoviruses

机译:双向基于SYBR Green I的定量实时PCR分析方法的开发,用于快速区分鹅和番鸭细小病毒

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Waterfowl parvoviruses, including goose parvovirus (GPV) and Muscovy duck parvovirus (MDPV), can cause seriously diseases in geese and ducks. Developing a fast and precise diagnosis assay for these two parvoviruses is particularly important. A duplex SYBR Green I-based quantitative real-time PCR assay was developed for the simultaneous detection and differentiation of GPV and MDPV. The assay yielded melting curves with specific single peak (Tm?=?87.3?±?0.26?°C or Tm?=?85.4?±?0.23?°C) when GPV or MDPV was evaluated, respectively. When both parvoviruses were assessed in one reaction, melting curves with specific double peaks were yielded. This duplex quantitative RT-PCR can be used to rapid identify of GPV and MDPV in field cases and artificial trials, which make it a powerful tool for diagnosing, preventing and controlling waterfowl parvovirus infections.
机译:水禽细小病毒,包括鹅细小病毒(GPV)和番鸭细小病毒(MDPV),可导致鹅和鸭的严重疾病。为这两种细小病毒开发一种快速而精确的诊断分析方法尤其重要。开发了一种基于SYBR Green I的双向实时荧光定量PCR检测试剂盒,用于同时检测和区分GPV和MDPV。分别评估GPV或MDPV时,该测定法产生了具有特定单峰的解链曲线(Tmα=α87.3α±α0.26°C或Tmα=α85.4α±α0.23°C)。当在一个反应​​中评估两种细小病毒时,会产生具有特定双峰的解链曲线。这种双重定量RT-PCR可用于在野外病例和人工试验中快速鉴定GPV和MDPV,使其成为诊断,预防和控制水禽细小病毒感染的有力工具。

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