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Reverse transcription loop-mediated isothermal amplification for rapid and sensitive detection of nervous necrosis virus in groupers

机译:反转录环介导的等温扩增用于石斑鱼中神经坏死病毒的快速灵敏检测

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摘要

The reverse transcription loop-mediated isothermal amplification (RT-LAMP) method is a sensitive nucleic acid diagnostic method that can amplify rapidly a target template; it can be applied for the diagnosis of viral disease in grouper aquaculture. In this study, two outer and two inner primers were designed from nervous necrosis virus (NNV) coat protein gene sequence. The reaction temperature and time for the detection of NNV were optimized at 65 super(o)C for 60min. The detection limit of RT-LAMP is 10 super(-) super(6) NNV-RNA from infected groupers, and more sensitive than the one-step RT-PCR and nested RT-PCR. The combination of RNA rapid extraction and RT-LAMP, the process can be completed within 2h. Thus, the RT-LMAP is a rapid, sensitive, specific and efficient method for detection of NNV in groupers.
机译:逆转录环介导的等温扩增(RT-LAMP)方法是一种灵敏的核酸诊断方法,可以快速扩增靶标模板。可用于石斑鱼养殖中病毒病的诊断。在这项研究中,从神经坏死病毒(NNV)外壳蛋白基因序列设计了两个外部和两个内部引物。用于检测NNV的反应温度和时间在65 super(o)C下优化60分钟。 RT-LAMP的检出限为感染石斑鱼的10个super(-)super(6)NNV-RNA,并且比单步RT-PCR和嵌套式RT-PCR灵敏度更高。 RNA快速提取和RT-LAMP的结合,可在2h内完成该过程。因此,RT-LMAP是一种快速,灵敏,特异且有效的方法,可用于检测石斑鱼中的NNV。

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