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Development of Methods for Detection and Quantification of Avian Influenza and Newcastle Disease Viruses in Compost by Real-Time Reverse Transcription Polymerase Chain Reaction and Virus Isolation.

机译:通过实时逆转录聚合酶链反应和病毒分离检测和量化堆肥中禽流感和新城疫病毒的方法的开发。

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Composting has been used for disposal of poultry carcasses and manure following outbreaks caused by avian influenza virus (AIV) and Newcastle disease virus (NDV), but methods are needed to test for survival of the viruses in compost to ensure biosecurity. Methods developed in the present study include extracting viruses from compost and purifying viral RNA. The extracted viruses were detected by virus isolation using embryonated chicken eggs, and the purified RNA was detected by real-time reverse transcription PCR (RRT-PCR). The virus isolation and the RRT-PCR methods were evaluated with 3 compost preparations that were produced from chicken manure mixed with corn silage, wood shavings, or wheat straw. The detection limits of both methods were 1,700 and 1,000 embryo lethal doses of AIV and NDV per gram of compost, respectively. The copy number of viral RNA quantified by RRT-PCR was highly correlated with the amount of virus in compost. The results suggested that the RRT-PCR method may be used as an alternative to the virus isolation method for rapid detection and accurate quantification of AIV and NDV in compost.
机译:在禽流感病毒(AIV)和新城疫病毒(NDV)引起暴发后,堆肥已被用于处理禽畜尸体和粪便,但是需要一些方法来测试堆肥中病毒的存活率以确保生物安全。本研究开发的方法包括从堆肥中提取病毒和纯化病毒RNA。提取的病毒通过使用胚胎鸡蛋的病毒分离进行检测,纯化的RNA通过实时逆转录PCR(RRT-PCR)检测。使用从鸡粪中掺入玉米青贮饲料,刨花或麦秸的3种堆肥制剂对病毒分离和RRT-PCR方法进行了评估。两种方法的检出限分别为每克堆肥1,700和1,000胚胎致死剂量的AIV和NDV。通过RRT-PCR定量的病毒RNA的拷贝数与堆肥中的病毒数量高度相关。结果表明,RRT-PCR方法可作为病毒分离方法的替代方法,用于快速检测和准确定量堆肥中的AIV和NDV。

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