Harris T S, Sandall L J, Powers T O
J Nematol. 1990 Oct;22(4):518-24.
Polymerase chain reaction (PCR) was used to amplify a specific 1.8-kb sequence of mitochondrial DNA from single juveniles and eggs from 17 populations of Meloidogyne incognita, M. hapla, M. javanica, and M. arenaria. Approximately 2 mug amplified product were produced per reaction. Restriction digestion of the amplified product with HinfI permitted discrimination of clonal lineages of the four species. Meloidogyne javanica, however, could not be separated from M. hapla by the enzymes used in these experiments. Various amplification conditions and nematode lysis procedures were examined in order to optimize the speed and quality of identifications.
采用聚合酶链反应(PCR)从南方根结线虫、北方根结线虫、爪哇根结线虫和花生根结线虫17个种群的单个幼虫和卵中扩增出线粒体DNA的一段特定的1.8kb序列。每个反应大约产生2μg扩增产物。用HinfI对扩增产物进行限制性酶切,可区分这4个物种的克隆谱系。然而,在这些实验中所用的酶无法将爪哇根结线虫与北方根结线虫区分开。为了优化鉴定的速度和质量,对各种扩增条件和线虫裂解程序进行了研究。