Sung Chia-Hsuan, Lu Jenn-Kan
Animal Health Inspection Division, Bureau of Animal and Plant Health Inspection and Quarantine, 3F, No. 51, Sec. 2, Chungcing S. Road, Taipei City 100, Taiwan.
J Virol Methods. 2009 Aug;159(2):206-10. doi: 10.1016/j.jviromet.2009.03.022. Epub 2009 Apr 2.
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 degrees C for 60min. The detection limit of RT-LAMP is 10(-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.
逆转录环介导等温扩增(RT-LAMP)方法是一种灵敏的核酸诊断方法,能够快速扩增目标模板;可应用于石斑鱼养殖中病毒性疾病的诊断。在本研究中,根据神经坏死病毒(NNV)衣壳蛋白基因序列设计了两条外引物和两条内引物。检测NNV的反应温度和时间优化为65℃60分钟。RT-LAMP的检测限为感染石斑鱼的10(-6) NNV-RNA,比一步法RT-PCR和巢式RT-PCR更灵敏。RNA快速提取与RT-LAMP相结合,整个过程可在2小时内完成。因此,RT-LMAP是一种快速、灵敏、特异且高效的石斑鱼NNV检测方法。