黄瓜种质资源抗疫病鉴定及遗传多样性分析

    Resistance identification and genetic diversity analysis of cucumber germplasm resources to Phytophthora disease

    • 摘要:
      目的 评价世界各地的不同黄瓜Cucumis sativus L.种质资源对疫病的抗性及遗传多样性,为黄瓜抗性育种提供依据和参考。
      方法 采用人工接种黄瓜疫霉菌Phytophthora melonis的方法对这些资源进行了抗性评价,并对90份黄瓜种质资源的重要农艺性状进行统计,进一步利用全基因组设计200对SSR引物对其进行分子标记筛选及遗传多样性分析。
      结果 不同类型黄瓜材料对疫病抗性水平有显著差异,其中,高抗材料4份,抗病材料10份,多为华南型黄瓜;感病材料38份,高感材料38份。SSR分析表明,45对引物在90份黄瓜资源中共扩增出142个等位基因,变幅为2~4个,平均每对引物扩增的等位基因数为3.22,有效等位基因数在1.0225~3.0840之间,平均为1.6684;Nei’s遗传多样性指数在0.0610~1.1728之间,平均为0.5816;种群平均Shannon多样性指数为0.2402;遗传相似系数在 0.0556~1.0000 之间,平均相似系数为 0.5783。聚类分析表明,在遗传相似系数为0.5500处,90份黄瓜种质可分为9类,抗性资源集中在Ⅰ、Ⅱ和Ⅺ类,多为华南型黄瓜。
      结论 通过对90份黄瓜材料进行人工接种疫霉菌,鉴定出抗性材料14份。筛选出45对多态性高的SSR引物,可有效对90份黄瓜种质材料进行聚类分析。本研究可为筛选、评价优良黄瓜种质资源及黄瓜抗性育种提供材料和理论基础。

       

      Abstract:
      Objective This study aimed to evaluate the resistance to blight disease and genetic diversity of different cucumber (Cucumis sativus L.) germplasm resources from around the world, providing a basis and reference for cucumber resistance breeding.
      Method The resistance of these resources was evaluated by artificial inoculation with Phytophthora melonis. The important agronomic traits of 90 cucumber germplasm resources were recorded. Two hundred pairs of SSR primers were designed based on the whole genome to screen molecular markers and analyze genetic diversity.
      Result Different types of cucumber materials had significant differences in blight disease resistance. There were 4 highly resistant materials and 10 resistant materials, most of which were South China type cucumbers. There were 38 susceptible materials and 38 highly susceptible materials. The results of SSR analysis showed that a total of 142 alleles were amplified from 90 cucumber resources using 45 primer pairs, with a range from 2 to 4 alleles and an average of 3.22 alleles amplified per a pair of primers. The effective allele number ranged from 1.0225 to 3.0840 with an average of 1.6684. The Nei’s genetic diversity index ranged from 0.0610 to 1.1728 with an average of 0.5816. The average Shannon diversity index was 0.2402. The genetic similarity coefficient ranged from 0.0556 to 1.0000 with an average of 0.5783. The cluster analysis showed that at the genetic similarity coefficient of 0.5500, these 90 cucumber germplasms could be clustered into 9 groups. The resistant germplasm resources were concentrated in groups Ⅰ, Ⅱ and Ⅺ, predominantly South China type cucumbers.
      Conclusion Through artificial inoculation of 90 cucumber materials with P. melonis, 14 resistant materials were identified. The 45 SSR primer pairs with high polymorphism were screened out, which could effectively cluster 90 cucumber germplasm materials. This study provides the materials and theoretical basis for screening and evaluating excellent cucumber germplasm resources and resistance breeding.

       

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