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Survey and multigene characterization of stolbur phytoplasmas on various plant species in Serbia

机译:塞尔维亚不同植物种类的茎线虫质原体的调查和多基因表征

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摘要

Stolbur phytoplasmas were detected in 116 out of more than 200 samples from nine plant species collected in 2009-2010 in Serbia. Phytoplasmas were detected and identified by restriction fragment length polymorphism (RFLP) analysis of polymerase chainreaction (PCR) amplified 16S rDNA. While all strains were identical on the level of 16S rDNA sequences, one strain represented a unique variant of stolbur phytoplasma with a SNP producing a new Trull restriction site. RFLP analyses of fw/gene amplicons,using Hpall restriction enzyme, showed profiles identical to tuf type II profile in all stolbur phytoplasma strains from Serbia. Seminested PCR for amplification of the rp gene yielded aspecific amplicons with nearly half of the samples examined. However, in the 23 samples which yielded amplicons of expected size, RFLP analysis with Alul restriction enzyme showed profiles with some variations. RFLP analyses of the amplified complete secY gene, using Trull and Alul restriction enzymes, showed profiles indistinguishable from each other. In phylogenetic analyses of secY gene, strains belonging to tuf type I formed a lineage separate from the strains belonging to tuf type II. To our knowledge this is the first report of stolbur phytoplasma in valerian (Valeriana officinalis) adding a new plant species to the already wide natural host range of stolbur phytoplasma.
机译:在2009-2010年从塞尔维亚收集的9种植物的200多种样品中,有116种检出了Stolbur植原体。通过限制性片段长度多态性(RFLP)分析聚合酶链反应(PCR)扩增的16S rDNA来检测和鉴定植原体。尽管所有菌株在16S rDNA序列的水平上都是相同的,但其中一个菌株代表了茎秆植物质体的独特变体,其SNP产生了一个新的Trull限制性位点。使用Hpall限制性内切酶对fw /基因扩增子进行RFLP分析,显示与来自塞尔维亚的所有stolbur植物原虫菌株中的tuf II型谱相同的谱。用半巢式PCR扩增rp基因可产生非特异性扩增子,其中将近一半的样本被检测到。但是,在23个产生预期大小扩增子的样品中,使用Alul限制酶进行的RFLP分析显示出一些变化。使用Trull和Alul限制酶对扩增的完整secY基因进行RFLP分析,结果显示彼此之间无法区分。在secY基因的系统发育分析中,属于I型Tuf的菌株形成了与属于II型Tuf的菌株不同的世系。据我们所知,这是缬草(Sterbur phytoplasma)的首次报道,其为已经很广的天然寄主植物增添了新的植物种类。

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