辣椒种质材料疫病抗性鉴评及遗传多样性分析

    Resistance Evaluation and Genetic Diversity Analysis of Phytophthora Disease in Pepper Germplasm Materials

    • 摘要:
      目的 了解辣椒种质材料的疫病抗性水平及材料的遗传多样性,以便为建立辣椒核心种质库和辣椒抗疫病育种改良提供参考。
      方法 采用改良后的辣椒疫病灌根接种法鉴定了96份辣椒种质材料的疫病抗性水平,并利用全基因组筛选出的20个SSR分子标记对其进行遗传多样性分析。
      结果 供试96份辣椒种质材料中,免疫材料仅1份,高抗材料有6份,抗病材料有24份,感病和高感材料分别有53份和12份,与田间表现基本一致。遗传多样性分析结果显示,20个SSR分子标记共检测出79个等位基因位点,每个标记检测到的等位基因数为2~9个,平均等位基因数为3.95个;Shannon信息指数在0.2992~1.9893之间,平均值为0.9513,表明所选用的20个SSR分子标记遗传多态性较高;Nei’s遗传多样性指数在0.1614~0.8440之间,平均值为0.5259,表明材料间遗传多样性高。聚类分析结果显示,在遗传距离0.37处可以将供试材料分为3个大类群,分别包含3、14、79份材料,另外还有8组材料间的遗传距离接近为0。
      结论 改良后的辣椒疫病灌根接种法适用于辣椒疫病鉴定,其结果与田间表现基本一致,且更简便。筛选出的20个SSR分子标记遗传多态性较高,适用于辣椒种质材料的遗传多样性分析。96份辣椒种质材料来源丰富,但存在同质材料,在种质保存时可以适当舍弃部分材料。

       

      Abstract:
      Objective The study was carried out to understand the Phytophthora disease resistance and genetic diversity of pepper germplasm materials, and to provide references for the establishment of core pepper germplasm bank and improvement of pepper Phytophthora disease resistance breeding.
      Method The Phytophthora disease resistance of 96 pepper germplasm materials was evaluated by using modified root irrigation inoculation method and the genetic diversity of them with 20 SSR molecular markers selected from the whole genome were analyzed.
      Result The results show that there was only 1 immune material, 6 highly resistant, 24 resistant, 53 susceptible and 12 highly susceptible materials among the 96 materials, which were basically consistent with the field performance. The results of genetic diversity analysis showed that a total of 79 alleles were detected among 20 SSR markers, with 2-9 alleles per marker and an average of 3.95 alleles. Shannon's index ranged from 0.2992 to 1.9893, with an average of 0.9513, indicating that the genetic polymorphism of the 20 SSR molecular markers selected was high. Nei's genetic diversity index ranged from 0.1614 to 0.8440, with an average of 0.5259, indicating high genetic diversity among materials. Cluster analysis results showed that the tested materials could be divided into three groups at the genetic distance of 0.37, including 3, 14 and 79 materials, respectively. Additionally, the genetic distance among 8 groups of materials was close to 0.
      Conclusion The improved root irrigation inoculation method is suitable for the identification of pepper Phytophthora disease, and the results are basically consistent with those of the field performance. Moreover, it is more convenient. The genetic polymorphisms of the 20 SSR molecular markers selected are high and suitable for genetic diversity analysis of pepper germplasms. The 96 pepper germplasm materials are rich in resources, but there are homogeneous materials, and some materials should be discarded properly during germplasm preservation.

       

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