米丘林斯克国立农业大学苹果无性系砧木抗白粉病的研究

I. N. Shamshin, M. L. Dubrovsky, A. A. Trifonova, K. V. Boris, A. M. Kudryavtsev
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摘要

苹果无性系砧木是现代集约化园艺的基础,为果树栽培提供了快速增产和便利。在高湿条件下生产无性系砧木往往会引起由病原菌白粉病(Podosphaera leucotricha Salm)引起的白粉病。,这大大降低了凳子的生产率。种植抗白粉病的基因型是对抗这种疾病的最适当的方法,可以减少杀菌剂的使用。为了加速寻找耐药形式,已经开发了与耐药基因相关的分子标记。然而,这些标记尚未用于无性系砧木的研究。本研究的目的是对米丘林斯克国立农业大学收集的苹果无性生殖砧木的白粉病抗性进行田间鉴定,并对收集的果实进行Pl-1、Pl-2、Pl-w和Pl-d抗性基因筛选。对80种砧木的白粉病抗性进行了为期三年的实地评估,结果使我们能够区分出从极低抗性到高度抗性的五个主要群体。一组57个品种被列为白粉病抗性品种。利用AT20 SCAR (Pl-1基因)、OPU02 SCAR (Pl- 2基因)、EM DM01 (Pl-d基因)和EM M02 (Pl-w基因)标记寻找耐药基因。Pl-d和Pl-1基因分别在33份(41.25%)和31份(38.75%)中最常见。Pl-w基因仅在2份材料中检测到。用OPU02 SCAR标记鉴定Pl-2基因并没有发现预期大小的片段。30份不同抗白粉病评分的材料均含有Pl-1和Pl-d两个基因,高抗性品种G16和14-1含有Pl-d和Pl-w两个基因的组合。这些材料可作为抗白粉病供体,用于培育新的苹果无性系砧木。
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Powdery mildew resistance of apple clonal rootstocks from the collection of the Michurinsk State Agrarian University
Apple clonal rootstocks are the basis of modern intensive horticulture, providing a rapid increase in yield and convenience of fruit trees cultivation. Production of clonal rootstocks under high humidity often causes powdery mildew infection caused by the pathogenic fungus Podosphaera leucotricha Salm., which significantly reduces the productivity of stoolbed. Growing powdery mildew resistant genotypes is the most appropriate way to combat this disease and allows reducing the use of fungicides. To accelerate the search for resistant forms, molecular markers associated with resistance genes have been developed. However, these markers have not been used to study clonal rootstocks. The aims of the work were the field assessment of powdery mildew resistance of apple clonal rootstocks from the collection of the Michurinsk State Agrarian University and the screening of the collection for Pl-1, Pl-2, Pl-w and Pl-d resistance genes. The results of a three-year field evaluation of powdery mildew resistance of 80 rootstocks allowed us to distinguish five main groups ranging from very low to highly resistant. A group of 57 accessions was classified as powdery mildew resistant. The search for resistance genes was performed using the AT20 SCAR (Pl-1 gene), OPU02 SCAR (Pl- 2 gene), EM DM01 (Pl-d gene), and EM M02 (Pl-w gene) markers. The Pl-d and Pl-1 genes identified in 33 (41.25 %) and 31 (38.75 %) accessions, respectively, were the most common in the collection. The Pl-w gene was detected only in two accessions. Identification of the Pl-2 gene with the OPU02 SCAR marker did not reveal a fragment of the expected size. Thirty accessions with different powdery mildew resistance scores had two genes, Pl-1 and Pl-d, and highly resistant forms G16 and 14-1 had a combination of the Pl-d and Pl-w genes. These accessions can be used as donors of powdery mildew resistance for breeding new apple clonal rootstocks.
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