Campa Ana, Trabanco Noemí, Ferreira Juan José
First and third authors: Plant Genetics, Area of Horticultural and Forest Crops, SERIDA, Asturias, Spain; and second author: Division of Plant Production (DiSAA), Università degli Studi di Milano, Via Celoria 2, Milan (Italy).
Phytopathology. 2017 Dec;107(12):1515-1521. doi: 10.1094/PHYTO-01-17-0012-R. Epub 2017 Sep 21.
The correct identification of the anthracnose resistance systems present in the common bean cultivars AB136 and MDRK is important because both are included in the set of 12 differential cultivars proposed for use in classifying the races of the anthracnose causal agent, Colletrotrichum lindemuthianum. In this work, the responses against seven C. lindemuthianum races were analyzed in a recombinant inbred line population derived from the cross AB136 × MDRK. A genetic linkage map of 100 molecular markers distributed across the 11 bean chromosomes was developed in this population to locate the gene or genes conferring resistance against each race, based on linkage analyses and χ tests of independence. The identified anthracnose resistance genes were organized in clusters. Two clusters were found in AB136: one located on linkage group Pv07, which corresponds to the anthracnose resistance cluster Co-5, and the other located at the end of linkage group Pv11, which corresponds to the Co-2 cluster. The presence of resistance genes at the Co-5 cluster in AB136 was validated through an allelism test conducted in the F population TU × AB136. The presence of resistance genes at the Co-2 cluster in AB136 was validated through genetic dissection using the F population ABM3 × MDRK, in which it was directly mapped to a genomic position between 46.01 and 47.77 Mb of chromosome Pv11. In MDRK, two independent clusters were identified: one located on linkage group Pv01, corresponding to the Co-1 cluster, and the second located on LG Pv04, corresponding to the Co-3 cluster. This report enhances the understanding of the race-specific Phaseolus vulgaris-C. lindemuthianum interactions and will be useful in breeding programs.
正确识别普通豆品种AB136和MDRK中存在的炭疽病抗性系统很重要,因为这两个品种都包含在拟用于对炭疽病病原菌林氏炭疽菌的小种进行分类的12个鉴别品种之中。在这项研究中,分析了由杂交组合AB136×MDRK衍生的重组自交系群体对7个林氏炭疽菌小种的反应。基于连锁分析和独立性χ检验,在该群体中构建了一张分布于11条豆科染色体上的包含100个分子标记的遗传连锁图谱,以定位赋予对每个小种抗性的一个或多个基因。所鉴定出的炭疽病抗性基因成簇排列。在AB136中发现了两个簇:一个位于连锁群Pv07上,对应于炭疽病抗性簇Co-5;另一个位于连锁群Pv11的末端,对应于Co-2簇。通过在F群体TU×AB136中进行的等位性测试,验证了AB136中Co-5簇处抗性基因的存在。通过使用F群体ABM3×MDRK进行遗传剖析,验证了AB136中Co-2簇处抗性基因的存在,在该群体中该基因被直接定位到染色体Pv11上46.01至47.77 Mb之间的基因组位置。在MDRK中,鉴定出两个独立的簇:一个位于连锁群Pv01上,对应于Co-1簇;另一个位于连锁群Pv04上,对应于Co-3簇。本报告增进了对菜豆与林氏炭疽菌小种特异性互作的理解,将对育种计划有用。