首页> 外文期刊>Journal of Phytopathology >Molecular Characterization of Sclerospora graminicola, the Incitant of Pearl Millet Downy Mildew Using ISSR Markers
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Molecular Characterization of Sclerospora graminicola, the Incitant of Pearl Millet Downy Mildew Using ISSR Markers

机译:使用ISSR标记对粟米霜霉病的诱因的菌核菌的分子表征

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The DNA polymorphism among 22 isolates of Sclerospora graminicola, the causal agent of downy mildew disease of pearl millet was assessed using 20 inter simple sequence repeats (ISSR) primers. The objective of the study was to examine the effectiveness of using ISSR markers for unravelling the extent and pattern of genetic diversity in 22 S. graminicola isolates collected from different host cultivars in different states of India. The 19 functional ISSR primers generated 410 polymorphic bands and revealed 89% polymorphism and were able to distinguish all the 22 isolates. Polymorphic bands used to construct an unweighted pair group method of averages (UPGMA) dendrogram based on Jaccard's co-efficient of similarity and principal coordinate analysis resulted in the formation of four major clusters of 22 isolates. The standardized Nei genetic distance among the 22 isolates ranged from 0.0050 to 0.0206. The UPGMA clustering using the standardized genetic distance matrix resulted in the identification of four clusters of the 22 isolates with bootstrap values ranging from 15 to 100. The 3D-scale data supported the UPGMA results, which resulted into four clusters amounting to 70% variation among each other. However, comparing the two methods show that sub clustering by dendrogram and multi dimensional scaling plot is slightly different. All the S. graminicola isolates had distinct ISSR genotypes and cluster analysis origin. The results of ISSR fingerprints revealed significant level of genetic diversity among the isolates and that ISSR markers could be a powerful tool for fingerprinting and diversity analysis in fungal pathogens.
机译:使用20个简单序列重复序列(ISSR)引物评估了22种分离菌株(Sclerospora graminicola)的DNA多态性,这是珍珠粟霜霉病病的病原体。这项研究的目的是检验使用ISSR标记揭示从印度不同州的不同寄主品种中收集的22株葡萄沙门氏菌菌株遗传多样性的程度和模式的有效性。 19个功能性ISSR引物产生410个多态性条带,显示89%的多态性,能够区分所有22个分离物。基于Jaccard相似性系数和主坐标分析的多态性条带用于构建均值的非加权成对组方法(UPGMA)树状图,从而形成了22个分离株的四个主要簇。 22个分离株之间的标准化Nei遗传距离范围为0.0050至0.0206。使用标准遗传距离矩阵对UPGMA进行聚类,结果鉴定出22个分离株中的四个聚类,其自举值介于15到100之间。3D规模数据支持UPGMA结果,结果导致四个聚类之间的变异率为70%彼此。但是,比较这两种方法表明,通过树状图和多维比例尺图进行子聚类略有不同。所有的葡萄球菌都具有不同的ISSR基因型和聚类分析起源。 ISSR指纹图谱的结果显示了分离株之间遗传多样性的显着水平,并且ISSR标记可能是真菌病原体指纹图谱和多样性分析的强大工具。

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