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首页> 外文期刊>Journal of Plant Pathology >Genetic diversity of Pseudomonas syringae pv. syringae strains, causing bacterial stem blight disease of alfalfa in the Kurdistan province of Iran.
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Genetic diversity of Pseudomonas syringae pv. syringae strains, causing bacterial stem blight disease of alfalfa in the Kurdistan province of Iran.

机译:丁香假单胞菌的遗传多样性。丁香香兰菌株,在伊朗库尔德斯坦省造成苜蓿细菌性枯萎病。

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摘要

In 2008 and 2009, 66 isolates of Pseudomonas syringae pv. syringae were obtained from infected alfalfa leaf tissues collected from various locations of the Kurdistan province of Iran. These strains, together with the Pseudomonas syringae pv. syringae reference strain were tested for the presence of the syrP gene and were also phenotypically characterized. According to phenotypic properties, 87% and 13% of the strains belonged to LOPAT group 1a and 1b, respectively. Genetic diversity of all strains was assessed by repetitive sequence-based polymerase chain reaction (rep-PCR) using REP (repetitive extragenic palindromic), ERIC (enterobacterial repetitive intergenic consensus) and BOX primer sets. Cluster analysis of rep-PCR revealed three groups at a similarity level of 50%. Group 1 of rep-PCR including all strains belongs to LOPAT group 1a, whereas group 2 and 3 comprise strains of LOPAT group 1a and 1b. A specific band corresponding to syrP gene was produced by 84% of the strains belonging to LOPAT group 1a. Strains belonging to LOPAT group 1b produced only non-specific bands.
机译:在2008年和2009年,有66株丁香假单胞菌分离株。丁香香兰是从从伊朗库尔德斯坦省各地采集的紫花苜蓿叶组织中提取的。这些菌株与丁香假单胞菌一起。测试了丁香参考菌株中syrP基因的存在,并对其表型进行了表征。根据表型特性,分别有87%和13%的菌株属于LOPAT 1a和1b组。使用REP(重复性外基因回文),ERIC(细菌重复性基因间共识)和BOX引物组,通过基于重复序列的聚合酶链反应(rep-PCR)评估所有菌株的遗传多样性。 rep-PCR的聚类分析显示三组的相似度为50%。包括所有菌株的rep-PCR组1属于LOPAT组1a,而组2和3包括LOPAT组1a和1b。属于LOPAT 1a组的菌株中有84%产生了与syrP基因相对应的特异性条带。属于LOPAT 1b组的菌株仅产生非特异性条带。

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