Chen Chang-mu, Cui Shang-jin
Division of Swine Infectious Diseases, State Key Laboratory of Veterinary Biotechnology, Harbin Veterinary Research Institute of Chinese Academy of Agricultural Sciences, Harbin 15001, Heilongjiang, China.
J Virol Methods. 2009 Feb;155(2):122-5. doi: 10.1016/j.jviromet.2008.10.004. Epub 2008 Nov 20.
Loop-mediated isothermal amplification is a novel method for rapid amplification of DNA. It has been adopted widely for the detection of virus because of its simplicity, rapidity, and specificity. A loop-mediated isothermal amplification assay was developed for the detection of porcine parvovirus. Four primers specific for six regions of PPV non-structural protein 1 gene were designed with an online software. After amplifying at a constant temperature of 59-65 degrees C by Bst enzyme, a clear result was visible after 2.5% agarose gel electrophoresis. The sensitivity and specificity of this assay were evaluated by comparison with the polymerase chain reaction. The detection limit of the assay was shown to be equivalent to 5 PPV copies/reaction. Due to its specificity and simplicity, the assay should be a useful diagnostic tool for epidemiologic studies of PPV.
环介导等温扩增是一种用于快速扩增DNA的新方法。由于其简单、快速和特异性,它已被广泛用于病毒检测。开发了一种环介导等温扩增检测方法用于检测猪细小病毒。使用在线软件设计了针对猪细小病毒非结构蛋白1基因六个区域的四条特异性引物。通过Bst酶在59-65℃恒温下扩增后,经2.5%琼脂糖凝胶电泳可见清晰结果。通过与聚合酶链反应比较评估了该检测方法的灵敏度和特异性。该检测方法的检测限显示相当于5个猪细小病毒拷贝/反应。由于其特异性和简单性,该检测方法应成为猪细小病毒流行病学研究的有用诊断工具。