Mehle Nataša, Prezelj Nina, Hren Matjaž, Boben Jana, Gruden Kristina, Ravnikar Maja, Dermastia Marina
ational Institute of Biology, Ljubljana, Slovenia.
Methods Mol Biol. 2013;938:253-68. doi: 10.1007/978-1-62703-089-2_22.
The real-time PCR detection system for grapevine yellows phytoplasmas described here is composed of two assays for group-specific detection of flavescence dorée (FD) and bois noir (BN) phytoplasmas and a universal phytoplasma assay. It uses hydrolysis minor groove binder probes (TaqMan-MGB). The addition of an assay for amplification of plant DNA co-extracted with phytoplasma DNA provides a further quality control for the DNA extraction and PCR amplification for each sample. The detection system described is reliable, specific, sensitive, and easily applicable to fast, high-throughput diagnosis of grapevine yellows phytoplasmas. In addition to the detection system, an approach for the quantification of phytoplasmas in the sample is described.
本文所述的葡萄黄化植原体实时荧光定量PCR检测系统由用于特异性检测金黄萎病(FD)和黑木病(BN)植原体的两种检测方法以及一种通用植原体检测方法组成。它使用水解小沟结合探针(TaqMan-MGB)。针对与植原体DNA共提取的植物DNA进行扩增的检测方法,为每个样品的DNA提取和PCR扩增提供了进一步的质量控制。所描述的检测系统可靠、特异、灵敏,且易于应用于葡萄黄化植原体的快速、高通量诊断。除了该检测系统外,还描述了一种对样品中植原体进行定量的方法。