Lebreton Lionel, Lucas Philippe, Dugas Françoise, Guillerm Anne-Yvonne, Schoeny Alexandra, Sarniguet Alain
INRA UMR Biologie des Organismes et des Populations appliquée à la Protection des Plantes, Domaine de la Motte, BP 35327, F-35653 Le Rheu Cedex, France.
Environ Microbiol. 2004 Nov;6(11):1174-85. doi: 10.1111/j.1462-2920.2004.00637.x.
A method was developed to assess the genetic structure of Gaeumannomyces graminis var. tritici (Ggt) populations and test the hypothesis of an association between disease level in the field with changes in pathogen populations. A long-term wheat monoculture experiment, established since 1994, generated different take-all epidemics with varying the number of wheat crop successions in the 1999-2000 cropping season. Genetic polymorphism in Ggt populations was investigated over natural, local epidemics. Four populations of 30 isolates were isolated from necrotic wheat roots in a first, third, fourth, and sixth wheat crop in the same year. Each Ggt isolate was characterized with RAPD (Random Amplification Polymorphism DNA) markers and AFLP (Amplified Fragment Length Polymorphism) fingerprinting. Seventeen multilocus genotypes based on the combination of RAPD and AFLP markers were identified among all these populations. The 120 isolates were divided into two main groups, G1 and G2, according to bootstrap values higher than 86%, except for an unique isolate from the third wheat crop. Within each group, populations ranged between 93 and 100% similarity. Both groups included isolates collected from the first, third, fourth or sixth wheat crop. However, G1 group profiles dominated amongst isolates sampled in the first and the sixth wheat crops, whereas G2 group profiles largely dominated amongst isolates collected from the third and fourth wheat crops. Aggressiveness of group G2 (38%) was significantly greater than that of G1 (29.5%). These results suggest that changes in Ggt population structure occur during continuous wheat cropping. The distinction of two Ggt groups provides a simple basis for further spatio-temporal analysis of Ggt population during polyetic take-all decline.
开发了一种方法来评估小麦全蚀病菌变种(Gaeumannomyces graminis var. tritici,Ggt)群体的遗传结构,并检验田间病害水平与病原菌群体变化之间存在关联的假设。自1994年以来建立的长期小麦连作试验,在1999 - 2000种植季节通过改变小麦连作次数产生了不同的全蚀病流行情况。在自然的、局部的病害流行过程中对Ggt群体的遗传多态性进行了研究。在同一年的第一季、第三季、第四季和第六季小麦作物中,从坏死的小麦根部分离出了四个群体,共30个分离株。每个Ggt分离株通过随机扩增多态性DNA(RAPD)标记和扩增片段长度多态性(AFLP)指纹图谱进行特征分析。基于RAPD和AFLP标记的组合,在所有这些群体中鉴定出了17种多位点基因型。除了来自第三季小麦作物的一个独特分离株外,根据自展值高于86%,这120个分离株被分为两个主要组,G1和G2。在每个组内,群体间的相似性在93%至100%之间。两个组都包括从第一季、第三季、第四季或第六季小麦作物中收集的分离株。然而,G1组的图谱在第一季和第六季小麦作物中采集的分离株中占主导地位,而G2组的图谱在从第三季和第四季小麦作物中收集的分离株中占很大比例。G2组的致病力(38%)显著高于G1组(29.5%)。这些结果表明,在连续种植小麦的过程中,Ggt群体结构发生了变化。这两个Ggt组的区分,为在多病程全蚀病衰退期间对Ggt群体进行进一步的时空分析提供了一个简单的基础。