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Molecular Characterization of Phytoplasmas Associated with Potato Purple TopDisease in Iran

机译:伊朗马铃薯紫色TopDisease相关植原体的分子特征

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Potato plants with symptoms suggestive of potatopurple top disease (PPTD) occurred in the central,western and north-western regions of Iran. Polymerasechain reaction (PCR) and nested PCR assays wereperformed using phytoplasma universal primer pairP1/P7 followed by primer pairs R16F2n/R16R2 andfU5/rU3 for phytoplasma detection. Using primerpairs R16F2n/R16R2 and fU5/rU3 in nested PCR,the expected fragments were amplified from 53% ofsymptomatic potatoes. Restriction fragment lengthpolymorphism (RFLP) analysis using AluI, CfoI,EcoRI, KpnI, HindIII, MseI, RsaI and TaqI restrictionenzymes confirmed that different phytoplasmaisolates caused PPTD in several Iranian potato-growingareas. Sequences analysis of partial 16S rRNAgene amplified by nested PCR indicated that'Candidatus Phytoplasma solani', 'Ca. Phytoplasmaastris' and 'Ca. Phytoplasma trifolii' are prevalent inpotato plants showing PPTD symptoms in the productionareas of central, western and north-westernregions of Iran, although 'Ca. Phytoplasma solani' ismore prevalent than other phytoplasmas. This is thefirst report of phytoplasmas related to 'Ca. Phytoplasmaastris', 'Ca. Phytoplasma solani' and 'Ca. Phytoplasmatrifolii' causing PPTD in Iran.
机译:症状提示马铃薯紫色顶病(PPTD)的马铃薯植株出现在伊朗的中部,西部和西北部地区。进行聚合酶链反应(PCR)和巢式PCR分析,方法是使用植物原质通用引物对P1 / P7,然后使用引物对R16F2n / R16R2和fU5 / rU3对植物原质进行检测。使用巢式PCR中的引物对R16F2n / R16R2和fU5 / rU3,从53%的有症状马铃薯中扩增了预期的片段。使用AluI,CfoI,EcoRI,KpnI,HindIII,MseI,RsaI和TaqI限制酶进行的限制性片段长度多态性(RFLP)分析证实,不同的植物溶胞菌在伊朗的几个马铃薯种植区引起PPTD。通过巢式PCR扩增的部分16S rRNA基因的序列分析表明,'Candidatus Phytoplasma solani','Ca。 Phytoplasmaastris”和“Ca。 Trifolii'Phytoplasma trifolii'是在伊朗中部,西部和西北部地区的生产区中表现出PPTD症状的普遍马铃薯植物,尽管是'Ca'。枯萎病比其他枯萎病更为普遍。这是与Ca相关的植物质疏的首次报道。 Phytoplasmaastris”,“ Ca。植原体”和“Ca。 Phytoplasmatrifolii'在伊朗引起PPTD。

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