Moon C D, Tapper B A, Scott B
Institute of Molecular BioSciences, Massey University, Palmerston North, New Zealand.
Appl Environ Microbiol. 1999 Mar;65(3):1268-79. doi: 10.1128/AEM.65.3.1268-1279.1999.
Epichloë endophytes are a group of filamentous fungi that include both sexual (Epichloë) and asexual (Neotyphodium) species. As a group they are genetically diverse and form both antagonistic and mutualistic associations with temperate grasses. We report here on the development of a microsatellite-based PCR system for fingerprinting this group of fungi with template isolated from either culture or infected plant material. M13mp19 partial genomic libraries were constructed for size-fractionated genomic DNA from two endophyte strains. These libraries were screened with a mixture of DIG-labeled dinucleotide and trinucleotide repeat probes. Positive clones were sequenced, and nine unique microsatellite loci were identified. An additional microsatellite was serendipitously identified in the 3' untranscribed region of the 3-hydroxy-3-methylglutaryl coenzyme A (HMG CoA) reductase gene from N. lolii Lp19. Primers were designed for each locus and a panel of endophytes, from different taxonomic groupings, was screened to determine the degree of polymorphism. On the basis of these results a multiplex assay was developed for strain identification with fluorescently labeled primers for five of these loci. Using this system the size of the products amplified can be precisely determined by automated analysis, and an allele profile for each strain can be readily generated. The assay was shown to resolve endophyte groupings to the level of known isozyme phenotype groupings. In a blind test the assay was used successfully to identify a set of endophytes in planta. A reference database of allele sizes has been established for the panel of endophytes examined, and this will be expanded as new strains are analyzed.
Epichloë内生真菌是一类丝状真菌,包括有性(Epichloë)和无性(Neotyphodium)物种。作为一个群体,它们在遗传上具有多样性,并与温带禾本科植物形成拮抗和互利共生关系。我们在此报告一种基于微卫星的PCR系统的开发,该系统用于对从培养物或受感染植物材料中分离的模板的这组真菌进行指纹识别。构建了M13mp19部分基因组文库,用于来自两个内生真菌菌株的大小分级基因组DNA。用DIG标记的二核苷酸和三核苷酸重复探针混合物筛选这些文库。对阳性克隆进行测序,鉴定出9个独特的微卫星位点。在来自N. lolii Lp19的3-羟基-3-甲基戊二酰辅酶A(HMG CoA)还原酶基因的3'非转录区意外鉴定出另一个微卫星。为每个位点设计引物,并筛选来自不同分类组的一组内生真菌,以确定多态性程度。基于这些结果,开发了一种多重分析方法,用于用荧光标记的引物对其中五个位点进行菌株鉴定。使用该系统,扩增产物的大小可以通过自动分析精确确定,并且可以很容易地生成每个菌株的等位基因图谱。该分析方法被证明可以将内生真菌分组解析到已知同工酶表型分组的水平。在一项盲测中,该分析方法成功用于鉴定植物中的一组内生真菌。已经为所检查的内生真菌组建立了等位基因大小的参考数据库,并且随着新菌株的分析,该数据库将得到扩展。