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首页> 外文期刊>Applied and Environmental Microbiology >Identification and grouping of mycoplasmalike organisms associated with grapevine yellows and clover phyllody diseases based on immunological and molecular analyses.
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Identification and grouping of mycoplasmalike organisms associated with grapevine yellows and clover phyllody diseases based on immunological and molecular analyses.

机译:基于免疫学和分子分析,鉴定与葡萄黄和三叶草叶状病相关的支原体样生物并进行分组。

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摘要

Immunofluorescent staining, dot blot hybridization, PCR, random amplified polymorphic DNA (RAPD) markers, and restriction fragment length polymorphism wee used to study the genetic relatedness among mycoplasmalike organisms (MLOs) associated with several geographically diverse grapevine yellows diseases (CA1, CH1, SA1, and SA2 from Bologna, Italy; GYU from Udine, Italy; GYR from Rome, Italy; and GYG from Germany). The relationship between these and MLOs associated with clover phyllody diseases in Italy (CPhB and CPhC) and Canada (CPhCa) was also examined. Two monoclonal antibodies reacted with MLOs of GYU-, CPhB-, and CPhC-infected periwinkles. Dot blot hybridization with two cloned GYU DNA fragments, GYD-1 and GYD-2 inserts, showed that both hybridized with DNAs of GYU-, CPhB-, and CPhC-infected periwinkles but not with those of GYR and CPhCa. In addition, GYD-1 insert hybridized with DNAs of CA1, CH1, SA1, SA2, and GYG. Three primer pairs were developed in PCR experiments for this study. By using primer set GYD2P1F and GYD2P1R, a 600-bp DNA fragment was amplified only when DNAs from GYU-, CPhB-, and CPhC-infected plants were used as templates. With the primer pair GYD2P1F and GYD2P2R, a 550-bp DNA fragment was amplified from GYU, CPhB, CPhC, and GYG. The primer pair GYD1P1F and GYD1P2R, on the other hand, could amplify all isolates, although the patterns of PCR products were not identical for all isolates.(ABSTRACT TRUNCATED AT 250 WORDS)
机译:免疫荧光染色,斑点印迹杂交,PCR,随机扩增多态性DNA(RAPD)标记和限制性片段长度多态性用于研究与几种地理上不同的葡萄黄病(CA1,CH1,SA1)相关的支原体样生物(MLO)的遗传相关性。 ,以及来自意大利博洛尼亚的SA2;来自意大利乌迪内的GYU;来自意大利罗马的GYR;以及来自德国的GYG)。还检查了这些与意大利(CPhB和CPhC)和加拿大(CPhCa)的三叶草叶状疾病相关的MLO之间的关系。两种单克隆抗体与感染GYU-,CPhB-和CPhC的长春花的MLO发生反应。与两个克隆的GYU DNA片段(GYD-1和GYD-2插入片段)的斑点印迹杂交表明,两者均与感染GYU-,CPhB-和CPhC的长春的DNA杂交,但不与GYR和CPhCa的DNA杂交。此外,GYD-1插入片段与CA1,CH1,SA1,SA2和GYG的DNA杂交。在这项研究的PCR实验中开发了三个引物对。通过使用引物组GYD2P1F和GYD2P1R,仅当将GYU-,CPhB-和CPhC感染植物的DNA用作模板时,才能扩增600 bp的DNA片段。使用引物对GYD2P1F和GYD2P2R,从GYU,CPhB,CPhC和GYG扩增了550 bp的DNA片段。另一方面,引物对GYD1P1F和GYD1P2R可以扩增所有分离株,尽管所有分离株的PCR产物的模式都不相同(摘要截短为250字)。

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