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首页> 外文期刊>Applied and Environmental Microbiology >Evaluation of the Genetic Structure of Xylella fastidiosa Populations from Different Citrus sinensis Varieties
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Evaluation of the Genetic Structure of Xylella fastidiosa Populations from Different Citrus sinensis Varieties

机译:中华柑橘不同品种的小木耳种群遗传结构评价

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摘要

Xylella fastidiosa was isolated from sweet orange plants (Citrus sinensis) grown in two orchards in the northwest region of the Brazilian state of S?o Paulo. One orchard was part of a germ plasm field plot used for studies of citrus variegated chlorosis resistance, while the other was an orchard of C. sinensis cv. Pêra clones. These two collections of strains were genotypically characterized by using random amplified polymorphic DNA (RAPD) and variable number of tandem repeat (VNTR) markers. The genetic diversity (HT) values of X. fastidiosa were similar for both sets of strains; however, HTRAPD values were substantially lower than HTVNTR values. The analysis of six strains per plant allowed us to identify up to three RAPD and five VNTR multilocus haplotypes colonizing one plant. Molecular analysis of variance was used to determine the extent to which population structure explained the genetic variation observed. The genetic variation observed in the X. fastidiosa strains was not related to or dependent on the different sweet orange varieties from which they had been obtained. A significant amount of the observed genetic variation could be explained by the variation between strains from different plants within the orchards and by the variation between strains within each plant. It appears, therefore, that the existence of different sweet orange varieties does not play a role in the population structure of X. fastidiosa. The consequences of these results for the management of sweet orange breeding strategies for citrus variegate chlorosis resistance are also discussed.
机译:从木桶中分离出的小木糖是从巴西圣保罗州西北部两个果园里种植的甜橙植物(柑橘)中分离出来的。一个果园是种质资源田间试验图的一部分,用于研究柑橘多样化的抗黄萎病性,而另一个则是中华茶树的果园。佩拉克隆。通过使用随机扩增多态性DNA(RAPD)和可变数目的串联重复序列(VNTR)标记对这两个菌株进行基因型鉴定。两组菌株的X.fastidiosa的遗传多样性(HT)值相似。但是,HTRAPD值明显低于HTVNTR值。对每株植物六种菌株的分析使我们能够鉴定出一株植物中最多的三种RAPD和五种VNTR多基因座单倍型。使用方差的分子分析来确定群体结构解释所观察到的遗传变异的程度。在X.fastidiosa菌株中观察到的遗传变异与获得它们的不同甜橙品种无关或不相关。观察到的大量遗传变异可以通过果园内不同植物的菌株之间的变异以及每种植物内菌株之间的变异来解释。因此,似乎存在不同的甜橙品种在X.fastidiosa的种群结构中不起作用。还讨论了这些结果对柑桔杂色萎黄病抗性甜橙育种策略管理的影响。

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