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现场条件下样本制备评估及一种用于新城疫病毒快速现场检测的便携式实时 RT-PCR 检测方法。

Assessment of Preparation of Samples Under the Field Conditions and a Portable Real-Time RT-PCR Assay for the Rapid On-Site Detection of Newcastle Disease Virus.

机构信息

Department of Virology, Immunobiology and Parasitology, National Veterinary Institute, Uppsala, Sweden.

The OIE Collaborating Centre for the Biotechnology-based Diagnosis of Infectious Diseases in Veterinary Medicine, Uppsala, Sweden.

出版信息

Transbound Emerg Dis. 2016 Apr;63(2):e245-50. doi: 10.1111/tbed.12261. Epub 2014 Sep 11.

DOI:10.1111/tbed.12261
PMID:25209697
Abstract

Newcastle disease virus (NDV), also known as virulent forms of avian paramyxovirus serotype 1 (AMPV-1), is the causative agent of Newcastle disease affecting many species of birds and causing heavy losses to the poultry industry worldwide. Early, rapid and sensitive detection of the viruses or the viral nucleic acids is very important for disease diagnosis and control. This study aimed to evaluate sample preparation under field conditions and the application of a real-time RT-PCR method in the portable T-COR4 platform for the rapid, on-site detection of NDV on a farm. In the laboratory setting, the portable real-time RT-PCR assay had a similar performance compared with that obtained with a larger, stationary Rotor Gene real-time thermocycler. In the field conditions, viral nucleic acids were manually extracted just outside of animal units with minimal equipment and real-time RT-PCR detection was performed with the portable thermocycler T-COR4 placed in a nearby room. The portable assay at the farm detected viral RNA in 15 samples and reached an agreement of 83% (39/47) when the same RNA preparations were tested in the Rotor Gene thermocycler under the laboratory setting. The results demonstrated the feasibility of performing field detection but also the need to improve and further simplify sample preparation procedures.

摘要

新城疫病毒(NDV),也称为禽副黏病毒 1 型(AMPV-1)的强毒形式,是引起新城疫的病原体,影响多种鸟类,给全球家禽业造成重大损失。早期、快速和灵敏地检测病毒或病毒核酸对于疾病诊断和控制非常重要。本研究旨在评估现场条件下的样品制备和实时 RT-PCR 方法在便携式 T-COR4 平台上的应用,以快速、现场检测农场中的 NDV。在实验室条件下,与较大的固定式 Rotor Gene 实时热循环仪相比,便携式实时 RT-PCR 检测具有相似的性能。在现场条件下,在动物单位外使用最少的设备手动提取病毒核酸,并在附近房间内放置的便携式热循环仪 T-COR4 上进行实时 RT-PCR 检测。便携式检测在 15 个样本中检测到了病毒 RNA,当在实验室条件下在 Rotor Gene 热循环仪中测试相同的 RNA 制剂时,达到了 83%(39/47)的一致性。结果表明进行现场检测是可行的,但需要改进和进一步简化样品制备程序。

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Field-Deployable Reverse Transcription-Insulated Isothermal PCR (RT-iiPCR) Assay for Rapid and Sensitive Detection of Foot-and-Mouth Disease Virus.用于快速灵敏检测口蹄疫病毒的现场可部署逆转录绝缘等温PCR(RT-iiPCR)检测法
Transbound Emerg Dis. 2017 Oct;64(5):1610-1623. doi: 10.1111/tbed.12554. Epub 2016 Sep 3.