Jang Chang Soon, Lim Jin Ha, Seo Mun Won, Song Jeong Young, Kim Hong Gi
Department of Agricultural Biology, Chungnam National University, Daejeon 305-764, Korea.
Mycobiology. 2010 Mar;38(1):33-8. doi: 10.4489/MYCO.2010.38.1.033. Epub 2010 Mar 31.
We have successfully applied the nested PCR to detect Cylindrocarpon destructans, a major pathogen causing root rot disease from ginseng seedlings in our former study. The PCR assay, in this study, was used to detect the pathogen from soils. The nested PCR using internal transcribed spacer (ITS) 1, 4 primer set and Dest 1, 4 primer set maintained the specificity in soils containing various microorganisms. For a soil DNA extraction method targeting chlamydospores, when several cell wall disrupting methods were tested, the combination of lyophilization and grinding with glass beads, which broke almost all the chlamydospores, was the strongest. The DNA extraction method which was completed based on the above was simple and time-saving because of exclusion of unnecessary stages, and efficient to apply in soils. As three ginseng fields whose histories were known were analyzed, the PCR assay resulted as our expectation derived from the field information. The direct PCR method will be utilized as a reliable and rapid tool for detecting and monitoring C. destructans in ginseng fields.
在我们之前的研究中,我们已成功应用巢式PCR检测人参幼苗根腐病的主要病原菌毁灭柱孢菌。在本研究中,PCR检测用于从土壤中检测该病原菌。使用内转录间隔区(ITS)1、4引物组和Dest 1、4引物组的巢式PCR在含有各种微生物的土壤中保持了特异性。对于一种针对厚垣孢子的土壤DNA提取方法,当测试了几种细胞壁破坏方法时,冻干和用玻璃珠研磨的组合破坏了几乎所有厚垣孢子,是最强的方法。基于上述方法完成的DNA提取方法由于排除了不必要的步骤而简单省时,并且在土壤中应用效率高。对三个已知种植历史的人参田进行分析时,PCR检测结果与我们根据田间信息得出的预期一致。直接PCR方法将作为检测和监测人参田毁灭柱孢菌的可靠且快速的工具。