番茄青枯病菌的分离鉴定及抗病种质筛选

    Isolation and Identification of Tomato Bacterial Wilt Pathogen (Ralstonia solanacearum) and Screening of Disease-Resistant Germplasm

    • 摘要:
      目的 对粤西地区湛江市番茄青枯病高发区的强致病性菌株进行分离鉴定并开展番茄抗病株系筛选,为番茄抗青枯病种质资源开发及新品种选育奠定基础。
      方法 从湛江市广东海洋大学采集染病番茄植株,通过组织分离法获取病原菌,结合形态学、生理生化和分子生物学技术鉴定菌种;采用茎穿刺法和伤根接种法鉴定菌株生理小种和致病性;将强致病力菌株接种至12份番茄抗青枯病优良自交系,验证并复筛性状稳定的抗病材料。
      结果 成功分离出2个菌株,命名为h2和h4,均为革兰氏阴性菌,菌落呈不规则状近圆形,中心淡红、边缘乳白色,具粘性和流动性。h2和h4菌株被鉴定为生化Ⅳ型、1号生理小种,且均扩增出茄科雷尔氏菌(Ralstonia solanacearum)280 bp和演化型Ⅰ的144 bp特异性片段,表明2个菌株也属于演化型Ⅰ型。16S rDNA分析表明,2个菌株与茄科雷尔氏菌聚在同一分支,序列同源性分别为99.51% 和99.65%。2个菌株均有强致病性,且h4菌株致病性强于h2。接种h4菌株4 d,‘中蔬5号’和‘桂砧1号’发病率分别为67.7% 和4.4%,接种6 d时发病率分别为92.2% 和13.3%,均高于h2菌株。利用h4菌株从12份优良自交系筛选出10个抗病株系。
      结论 h2和h4菌株均为革兰氏阴性菌,属于演化型Ⅰ、生化Ⅳ型和生理小种1号。h4菌株致病性强于h2菌株,利用h4菌株筛选出10个高抗株系。

       

      Abstract:
      Objective To isolate and identify strong pathogenic strains in high-incidence area for tomato bacterial wilt in Zhanjiang City, western Guangdong Province, and screen tomato disease-resistant lines, in order to lay the foundation for development of germplasm resources resistant to Ralstonia solanacearum and breeding new tomato cultivars.
      Method Infected tomato plants were collected from Guangdong Ocean University in Zhanjiang City. The pathogenic bacteria were isolated through the tissue isolation method, and identified by combining morphological, physiological, biochemical and molecular biological techniques. The stem puncture method and root-wounding inoculation method were used to identify the physiological races and pathogenicity of the strains. The highly pathogenic strain was inoculated onto 12 elite inbred lines resistant to bacterial wilt to verify and re-screen disease-resistant materials with stable traits.
      Result The isolated strains (h2 and h4) were both Gram-negative bacteria, with colonies exhibiting an irregular, nearly circular shape featuring pale red centers and milky white edges, demonstrating viscous and fluid properties. The strains h2 and h4 were identified as biochemical type Ⅳ, physiological race 1, and both amplified specific fragments of R. solanacearum (280 bp) and evolutionary type Ⅰ (144 bp), indicating that both strains belong to phylotype Ⅰ. 16S rDNA analysis showed that the two strains clustered in the same branch as R. solanacearum, with sequence homologies of 99.51% and 99.65%, respectively. Both strains exhibited strong pathogenicity, with h4 demonstrating higher virulence. At 4 days and 6 days post-inoculation, disease incidence rates in 'ZS-5' and 'GZ-1' inoculated with h4 reached 67.7% and 4.4% (4 d), 92.2% and 13.3% (6 d), respectively, consistently higher than those of h2. Ten disease-resistant lines were screened from 12 elite inbred lines using the strain h4.
      Conclusion Both strains h2 and h4 are Gram-negative bacteria belonging to evolutionary type Ⅰ, biochemical type Ⅳ, and physiological race 1. Strain h4 has stronger pathogenicity than h2, and ten highly resistant lines were selected using strain h4.

       

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