首页> 外文期刊>Journal of Plant Protection Research >Characterization of Phytoplasmas Related to Aster Yellows Group Infecting Annual Plants in Iran, Based on the Studies of 16S rRNA and RP Genes
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Characterization of Phytoplasmas Related to Aster Yellows Group Infecting Annual Plants in Iran, Based on the Studies of 16S rRNA and RP Genes

机译:基于16S rRNA和RP基因的研究,与感染伊朗年青植物的翠菊组相关的植原体的特征

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Several annual field crops, vegetables, ornamentals, oilseed crops, and weeds showing phytoplasma diseases symptoms were collected to detect phytoplasmas related to ‘Candidatus Phytoplasma asteris’. The collecting was done in the central regions of Iran. For general detection of phytoplasmas, 16S rRNA gene fragments were amplified using phytoplasma universal primer pair P1/P7 in polymerase chain reaction (PCR) followed by primer pair R16F2n/R16R2 in nested PCR. Then, for finer detection of phytoplasmas related to ‘Ca. P. asteris’, DNA samples were used to extend the rp and tuf gene fragments by PCR using aster yellows group specific primer pairs rp(I)F1A/rp(I)R1A and fTufAy/rTufAy, respectively. Restriction fragment lenght polymorphism (RFLP) analysis of rp gene fragments using digestion with AluI, MseI, and Tsp509I restriction enzymes indicated that aster yellows group related phytoplasmas in these Iranian regions, belong to rpI-B subgroups. Sequence analysis of partial 16S rRNA and rp genes from representative phytoplasma isolates confirmed the RFLP results. This research is the first report of annual plants infected with phytoplasmas related to subgroup rpI-B in Iran.
机译:收集了数种表现出植物原虫病症状的一年生大田作物,蔬菜,观赏植物,油料作物和杂草,以检测与“紫and病”有关的植物原虫。收集工作在伊朗中部地区进行。为了对植物质体进行常规检测,在聚合酶链反应(PCR)中使用植物质体通用引物对P1 / P7扩增16S rRNA基因片段,然后在巢式PCR中扩增引物对R16F2n / R16R2。然后,为了更好地检测与'Ca相关的植物质浆。 DNA样本被用于分别使用翠菊黄族特异性引物对rp(I)F1A / rp(I)R1A和fTufAy / rTufAy进行PCR扩增rp和tuf基因片段。使用AluI,MseI和Tsp509I限制性内切酶消化对rp基因片段进行的限制性片段长度多态性(RFLP)分析表明,这些伊朗地区的翠菊黄族相关植原体属于rpI-B亚组。来自代表性植原体分离物的部分16S rRNA和rp基因的序列分析证实了RFLP结果。这项研究是伊朗感染了与rpI-B亚组相关的植物原质的一年生植物的第一份报告。

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