首页> 外文期刊>Canadian Journal of Plant Pathology: Revue Canadienne de phytopathologie >Incidence and molecular characterization of a 16SrI-B phytoplasma strain associated with Vitis vinifera leaf yellowing and reddening in the west of Iran
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Incidence and molecular characterization of a 16SrI-B phytoplasma strain associated with Vitis vinifera leaf yellowing and reddening in the west of Iran

机译:伊朗西部肺炎叶片变黄和红细胞变黄与抗炎植物叶和红肿的发病率和分子表征

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Leaf yellowing and reddening symptoms on Vitis vinifera vines were observed in different grapevine nurseries in the province of Kurdistan in the west of Iran during 2016-2017. Total DNA was extracted from 27 symptomatic and four symptomless plants and tested for the presence of phytoplasma DNA by nested polymerase chain reaction (PCR) using P1/P7 and R16F2n/R16R2 primer pairs. PCR amplicons of about 1.8 and 1.2 kb in size were obtained from all symptomatic V. vinifera but not from symptomless plants. Restriction fragment length polymorphism (RFLP) profiles of R16F2n/R2 amplicons using AluI, HhaI, HpaII, RsaI, TaqI, KpnI, HaeIII and Sau3AI restriction enzymes were identical to each other and to those obtained from 16SrI phytoplasmas, indicating that the phytoplasmas associated with grapevine yellowing and reddening were members of the 16SrI group. A R16F2n/R16R2 16S rDNA sequence of Kurdistan V. vinifera yellowing and reddening strain (KVvY) was submitted to GenBank as accession number MH638316. The Blast analysis of KVvY showed 100% sequence identity with those of the 'Candidatus Phytoplasma asteris'-related strains. Phylogenetic analysis confirmed that the phytoplasma associated with KVvY clustered within the 16SrI phytoplasma clade closer to the Onion yellows mild strain (OY-M), a 16SrI-B phytoplasma. Restriction analysis using iPhyClassifier confirmed that virtual RFLP patterns of the KVvY were identical (similarity coefficient 1.00) to the reference pattern of 16Sr group I, subgroup B (GenBank accession AP006628).
机译:在2016 - 2017年伊朗西部的Kurdistan省的不同葡萄苗圃中观察到​​葡萄葡萄族葡萄藤的叶子变黄和变红症状。从27个症状和四种症状植物中提取总DNA,并使用P1 / P7和R16F2N / R16R2引物对通过嵌套聚合酶链反应(PCR)测试植物DNA的存在。大小约为1.8和1.2 kB的PCR扩增子是从所有症状V.Vinifera获得的,而不是来自症状的植物。使用Alui,Hai,HPaii,Rsai,Taqi,Kpni,Haeiii和Sau3ai限制酶R16F2N / R2扩增子的限制性片段长度多态性(RFLP)谱彼此相同,并与16SRI植物获得的那些相同,表明植物相关联的植物葡萄葡萄葡萄和变红是16SRI集团的成员。 Kurdistan V.Vinifera黄化和葡萄酒株(KVVY)的R16F2N / R16R2 16S RDNA序列提交给GenBank作为登录号MH638316。 KVVY的爆炸分析显示了100%的序列同一性与“Candidatus植物的植物相关菌株”。系统发育分析证实,与kVvy相关的植物组聚集在16sri植物的岩土内,更接近洋葱黄色菌株(OY-M),A 16SRI-B植物。使用iphyclassifer的限制性分析证实了KVVY的虚拟RFLP模式与16SR组I,子组B(GenBank Rescession AP006628)的参考模式相同(相似度系数1.00)。

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