Harrison Nigel A, Davis Robert E, Helmick Ericka E
Plant Pathology Department, Research & Education Center, University of Florida, Fort Lauderdale, FL, USA.
Methods Mol Biol. 2013;938:147-58. doi: 10.1007/978-1-62703-089-2_13.
Detection of pathogen DNA by polymerase chain reaction (PCR) assays is the most widely used method for diagnosing phytoplasma diseases. Reliable and efficient detection of phytoplasmas, especially in woody perennial plants, is challenging due to the unusually low abundance and sporadic distribution of phytoplasmas within infected host tissues. Detection success depends largely upon the host species and sampling procedures and, to a lesser extent, on the protocol used for DNA extraction. Here we describe a simple, straightforward, nondestructive stem sampling protocol to confirm phytoplasma infection of palms and other arborescent monocots of large stature. The protocol requires minimal processing of excised tissues and yields phytoplasma DNA preparations in suitable quantity for reliable detection by nested PCR assays.
通过聚合酶链反应(PCR)检测病原体DNA是诊断植原体病害最广泛使用的方法。由于感染宿主组织中的植原体丰度异常低且分布零散,可靠而有效地检测植原体,尤其是在多年生木本植物中,具有挑战性。检测成功很大程度上取决于宿主物种和采样程序,在较小程度上取决于用于DNA提取的方案。在此,我们描述一种简单、直接、非破坏性的茎采样方案,以确认棕榈和其他高大木本单子叶植物的植原体感染情况。该方案对切除的组织所需处理极少,并能产生适量的植原体DNA制剂,以供通过巢式PCR检测进行可靠检测。