Lee Jaikoo, Lee Sangsun, Young J Peter W
Korea National University of Education, Chungbuk, Korea.
FEMS Microbiol Ecol. 2008 Aug;65(2):339-49. doi: 10.1111/j.1574-6941.2008.00531.x. Epub 2008 Jul 9.
A set of PCR primers that should amplify all subgroups of arbuscular mycorrhizal fungi (AMF, Glomeromycota), but exclude sequences from other organisms, was designed to facilitate rapid detection and identification directly from field-grown plant roots. The small subunit rRNA gene was targeted for the new primers (AML1 and AML2) because phylogenetic relationships among the Glomeromycota are well understood for this gene. Sequence comparisons indicate that the new primers should amplify all published AMF sequences except those from Archaeospora trappei. The specificity of the new primers was tested using 23 different AMF spore morphotypes from trap cultures and Miscanthus sinensis, Glycine max and Panax ginseng roots sampled from the field. Non-AMF DNA of 14 plants, 14 Basidiomycota and 18 Ascomycota was also tested as negative controls. Sequences amplified from roots using the new primers were compared with those obtained using the established NS31 and AM1 primer combination. The new primers have much better specificity and coverage of all known AMF groups.
设计了一组聚合酶链式反应(PCR)引物,该引物应能扩增丛枝菌根真菌(AMF,球囊菌门)的所有亚群,但排除其他生物的序列,以便于直接从田间种植的植物根系中进行快速检测和鉴定。新引物(AML1和AML2)靶向小亚基rRNA基因,因为对于该基因,球囊菌门内的系统发育关系已得到充分了解。序列比较表明,新引物应能扩增除来自特拉普古生孢囊霉(Archaeospora trappei)以外的所有已发表的AMF序列。使用来自诱捕培养物的23种不同AMF孢子形态型以及从田间采集的芒草(Miscanthus sinensis)、大豆(Glycine max)和人参(Panax ginseng)根系对新引物的特异性进行了测试。还测试了14种植物、14种担子菌门和18种子囊菌门的非AMF DNA作为阴性对照。将使用新引物从根系中扩增的序列与使用已确立的NS31和AM1引物组合获得的序列进行比较。新引物对所有已知AMF群体具有更好的特异性和覆盖率。