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南非葡萄藤中植原体的首次报道。

First Report of Phytoplasmas in Grapevine in South Africa.

作者信息

Botti S, Bertaccini A

机构信息

DiSTA, Plant Pathology, Alma Mater Studiorum, University of Bologna, viale Fanin 42, 40127 Bologna, Italy.

出版信息

Plant Dis. 2006 Oct;90(10):1360. doi: 10.1094/PD-90-1360B.

Abstract

In April 2006, grapevine plants with typical symptoms of yellows (GY) were observed in some South African vineyards. The affected plants showed premature yellowing or reddening and downward rolling of leaves. In some cases, these symptoms were associated with extensive lack of cane lignification that was undistinguishable from yellows symptoms reported in grapevine in the major viticultural areas of the world. Nucleic acids were extracted separately from 0.1 g of fresh leaf midribs and cane phloem scrapes from three symptomatic and three asymptomatic grapevine plants, cv. Shiraz, and from three symptomatic plants, cv. Cabernet, collected from three different locations using Qiagen (Milan, Italy) DNAeasy Plant Mini Kit. A nested polymerase chain reaction (PCR) assay was employed for phytoplasma detection with 2.5 μl of the extracted DNA. Direct and nested PCR assays were performed with P1/P7 (2) and R16F2/R2 (1) universal primer pairs, respectively, obtaining the expected products only from phloem scrapes of the symptomatic plant samples cv. Shiraz. Restriction fragment length polymorphism (RFLP) analyses of R16F2/R2 amplicons with TruI and Tsp509I restriction enzymes, discriminating among phytoplasma ribosomal group and subgroups, showed profiles corresponding to those of "Candidatus Phytoplasma aurantifolia" (ribosomal subgroup 16SrII-B) in all three positive samples. A Stolbur phytoplasma profile (ribosomal subgroup 16SrXII-A) was also observed in one of those samples, indicating the presence of mixed phytoplasma infection (1). Sequencing of the obtained amplicons confirmed the RFLP phytoplasma identification; in particular 16SrXII-A could be the same phytoplasma associated with the 'Bois Noir' disease reported in grapevine; the 1601-bp sequence of 16SrII-B phytoplasma showed 98% similarity to U15442, i.e., to the phytoplasma associated with lime witches'-broom disease in Oman ("Ca. P. aurantifolia") confirming RFLP results. To our knowledge, this is the first report of phytoplasmas in grapevine in South Africa. References: (1) I.-M. Lee et al. Phytopathology 85:728, 1995. (2) B. Schneider et al. Pages 369-380 in: Molecular and Diagnostic Procedures in Mycoplasmology Vol. I. Academic Press Inc., 1995.

摘要

2006年4月,在南非一些葡萄园里发现了具有典型黄化症状(GY)的葡萄植株。受影响的植株叶片过早黄化或变红,并向下卷曲。在某些情况下,这些症状与广泛的茎杆木质化缺失有关,这与世界主要葡萄种植区报道的葡萄黄化症状难以区分。使用Qiagen(意大利米兰)DNAeasy的植物小提试剂盒,分别从3株有症状和3株无症状的设拉子葡萄植株以及从3个不同地点采集的3株有症状的赤霞珠葡萄植株的0.1克新鲜叶片中脉和茎杆韧皮部刮屑中提取核酸。采用巢式聚合酶链反应(PCR)检测法,用2.5微升提取的DNA检测植原体。直接PCR和巢式PCR检测分别使用P1/P7(2)和R16F2/R2(1)通用引物对,仅从有症状的设拉子葡萄植株样本的韧皮部的刮屑中获得预期产物。用TruI和Tsp509I限制性内切酶对R16F的2/R2扩增产物进行限制性片段长度多态性(RFLP)分析,区分植原体核糖体组和亚组,结果显示,所有3个阳性样本的图谱均与“柑桔黄龙病菌”(核糖体亚组16SrII-B)相符。在其中一个样本中还观察到了一种翠菊黄化植原体图谱(核糖体亚组16Sr的XII-A),表明存在混合植原体感染(1)。对获得的扩增产物进行测序,证实了RFLP对植原体的鉴定结果;特别是16SrXII-A可能与葡萄中报道的“黑色木痘病”相关的是同一种植原体;16SrII-B植原体的1601bp序列与U15442有98%的相似性,即与阿曼的酸橙丛枝病相关的植原体(“柑桔黄龙病菌”)相似,这也证实了RFLP的结果。据我们所知,这是南非葡萄中植原体的首次报道。参考文献:(1)I.-M. Lee等人的《植物病理学》85:728,1的995年。(2)B. Schneider等人的《支原体学的分子和诊断程序》第一卷第369 -的380页,学术出版社,1995年。

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