Simon L, Lévesque R C, Lalonde M
Centre de Recherche en Biologie Forestière, Faculté de Foresterie et de Géomatique, Université Laval, Sainte-Foy, Québec, Canada.
Appl Environ Microbiol. 1993 Dec;59(12):4211-5. doi: 10.1128/aem.59.12.4211-4215.1993.
A method to identify arbuscular endomycorrhizal fungi based on the amplification of portions of the nuclear gene coding for the small subunit rRNA is presented. By coupling the sensitivity of the polymerase chain reaction and the specificity afforded by taxon-specific primers, a variety of samples can be analyzed, including small amounts of colonized roots. Family-specific primers as well as generic primers are described and can be used to amplify small subunit rRNA fragments from endomycorrhizal fungi by polymerase chain reaction. The amplified products are then subjected to single-strand conformation polymorphism analysis to detect sequence differences. Among the advantages of this approach is the possibility of directly identifying the fungi inside field-collected roots, without having to rely on the fortuitous presence of spores. This technique should have obvious applications in the study of arbuscular endomycorrhizal fungi populations and allow closer examination of their host specificity.
本文介绍了一种基于编码小亚基rRNA的核基因部分片段扩增来鉴定丛枝内生菌根真菌的方法。通过结合聚合酶链反应的灵敏度和分类群特异性引物所提供的特异性,可以分析各种样品,包括少量被侵染的根。文中描述了科特异性引物以及通用引物,可用于通过聚合酶链反应从内生菌根真菌中扩增小亚基rRNA片段。然后对扩增产物进行单链构象多态性分析以检测序列差异。这种方法的优点之一是有可能直接鉴定田间采集根内的真菌,而不必依赖偶然存在的孢子。该技术在丛枝内生菌根真菌种群研究中应有明显的应用,并能更深入地研究它们的宿主特异性。