College of Veterinary Medicine, South China Agricultural University, 483 Wushan Street, Tianhe District, Guangzhou, Guangdong Province 510642, PR China.
Vet Parasitol. 2010 Dec 15;174(3-4):228-33. doi: 10.1016/j.vetpar.2010.09.005. Epub 2010 Sep 21.
The present study developed and validated a species-specific loop-mediated isothermal amplification (LAMP) assay for the rapid detection and discrimination of Fasciola hepatica and Fasciola gigantica. The LAMP assay is inexpensive, easy to perform and shows rapid reaction, wherein the amplification can be obtained in 45 min under isothermal conditions of 61 °C or 62 °C by employing a set of four species-specific primer mixtures and results can be checked through naked-eye visualization. The optimal assay conditions with no cross-reaction with other closely related trematodes (Clonorchis sinensis, Opisthorchis viverrini, Orientobilharzia turkestanicum and Schistosoma japonicum) as well as within the two Fasciola species were established. The assay was validated by examining F. gigantica DNA in the intermediate host snails and in faecal samples. The results indicated that the LAMP assay is approximately 10(4) times more sensitive than the conventional specific PCR assays. These findings indicate that this Fasciola species-specific LAMP assay may have a potential clinical application for detection and differentiation of Fasciola species, especially in endemic countries.
本研究开发并验证了一种用于快速检测和区分肝片形吸虫和巨片形吸虫的种特异性环介导等温扩增(LAMP)检测方法。LAMP 检测方法成本低廉,易于操作,且反应迅速,在 61°C 或 62°C 的等温条件下,采用四组种特异性引物混合物,可在 45 分钟内获得扩增结果,并且可以通过肉眼观察进行结果检查。该检测方法建立了最佳的反应条件,与其他密切相关的吸虫(华支睾吸虫、肝片形吸虫、麝猫后睾吸虫和日本血吸虫)以及两种肝片形吸虫之间没有交叉反应。该检测方法通过检查中间宿主蜗牛和粪便样本中的巨片形吸虫 DNA 进行了验证。结果表明,LAMP 检测方法的灵敏度比常规的特异性 PCR 检测方法高约 10(4)倍。这些发现表明,这种肝片形吸虫种特异性 LAMP 检测方法可能具有用于检测和区分肝片形吸虫种的潜在临床应用,特别是在流行地区。