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首页> 外文期刊>Mycopathologia >Virulence Analysis and Oligonucleotide Fingerprinting to Detect Diversity Among Indian Isolates of Fusarium oxysporum f. sp. ciceris Causing Chickpea Wilt
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Virulence Analysis and Oligonucleotide Fingerprinting to Detect Diversity Among Indian Isolates of Fusarium oxysporum f. sp. ciceris Causing Chickpea Wilt

机译:毒力分析和寡核苷酸指纹图谱检测尖酸镰刀菌印度分离株之间的多样性。 sp。导致鹰嘴豆枯萎的西塞里斯

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Virulence analysis of 64 isolates of Fusarium oxysporum f. sp. ciceris causing chickpea wilt collected from major chickpea growing states of India on 14 varieties, including 10 international differentials revealed that the isolates from each state were highly variable. Based on the reactions on international differentials, more than one race was found to be prevalent in every state. Majority of the isolates were not matched with the race specific reactions. Therefore, some of the cultivars, namely, GPF 2, DCP 92-3, and KWR 108 should be included as new differentials to obtain clear-cut differential responses. Randomly amplified polymorphic DNA (RAPD), inter-simple sequence repeat (ISSR), and simple sequence repeat (SSR) markers were used to assess the genetic diversity of these isolates. Unweighted paired group method with arithmetic average (UPGMA) cluster analysis was used to divide the isolates into distinct clusters. The clusters generated by RAPD grouped all isolates into three categories at 25% genetic similarity and into two major categories at 30% genetic similarity. ISSR and SSR analyses also grouped all the isolates into two major categories. Majority of the isolates from Punjab and a few from Rajasthan were grouped in one category while the isolates from all other states were grouped in another suggesting the existence of diverse genetic populations of the pathogen at the same location. Some of the RAPD (OPM 6, OPI 9, P 17, OPN 4, OPF 1, P 17, P 21, and SC 1), ISSR (ISSR 7, ISSR 11, and ISSR 12) and SSR (MB 17) markers clearly distinguished area specific isolates.
机译:枯萎镰刀菌64株毒力分析。 sp。从印度主要鹰嘴豆生长州收集到的导致鹰嘴豆萎的西塞里斯有14个变种,包括10种国际差异表明,每个州的分离株变化很大。根据对国际差异的反应,发现在每个州都盛行一种以上的种族。大多数分离物与种族特异性反应不匹配。因此,应将某些品种,即GPF 2,DCP 92-3和KWR 108包括在内,作为新的差异,以获得明确的差异响应。随机扩增的多态性DNA(RAPD),简单序列间重复(ISSR)和简单序列重复(SSR)标记用于评估这些分离株的遗传多样性。使用算术平均值(UPGMA)聚类分析的非加权配对组方法将分离株分为不同的聚类。 RAPD产生的簇将所有分离株分为遗传相似度为25%的三类和两大遗传相似度为30%的大类。 ISSR和SSR分析还将所有分离株分为两大类。来自旁遮普邦的大多数分离株和来自拉贾斯坦邦的少数分离株被归为一类,而来自所有其他州的分离株被归为另一类,这表明在同一位置存在病原体的多种遗传种群。一些RAPD(OPM 6,OPI 9,P 17,OPN 4,OPF 1,P 17,P 21和SC 1),ISSR(ISSR 7,ISSR 11和ISSR 12)和SSR(MB 17)标记清楚地区分的分离株。

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