Dakouri Abdulsalam, Lamara Mebarek, Karim Md Masud, Wang Jinghe, Chen Qilin, Gossen Bruce D, Strelkov Stephen E, Hwang Sheau-Fang, Peng Gary, Yu Fengqun
Saskatoon Research and Development Centre, Agriculture and Agri-Food Canada, Saskatoon, Canada.
Institut de Recherche Sur Les Forêts (IRF), Université du Québec en Abitibi-Témiscamingue, 445 boul. de l'Université, Rouyn-Noranda, QC, J9X 5E4, Canada.
Sci Rep. 2021 Mar 23;11(1):6599. doi: 10.1038/s41598-021-85836-9.
Genetic resistance is a successful strategy for management of clubroot (Plasmodiophora brassicae) of brassica crops, but resistance can break down quickly. Identification of novel sources of resistance is especially important when new pathotypes arise. In the current study, the reaction of 177 accessions of Brassica napus to four new, virulent pathotypes of P. brassicae was assessed. Each accession was genotyped using genotyping by sequencing to identify and map novel sources of clubroot resistance using mixed linear model (MLM) analysis. The majority of accessions were highly susceptible (70-100 DSI), but a few accessions exhibited strong resistance (0-20 DSI) to pathotypes 5X (21 accessions), 3A (8), 2B (7), and 3D (15), based on the Canadian Clubroot Differential system. In total, 301,753 SNPs were mapped to 19 chromosomes. Population structure analysis indicated that the 177 accessions belong to seven major populations. SNPs were associated with resistance to each pathotype using MLM. In total, 13 important SNP loci were identified, with 9 SNPs mapped to the A-genome and 4 to the C-genome. The SNPs were associated with resistance to pathotypes 5X (2 SNPs), 3A (4), 2B (5) and 3D (6). A Blast search of 1.6 Mb upstream and downstream from each SNP identified 13 disease-resistance genes or domains. The distance between a SNP locus and the nearest resistance gene ranged from 0.04 to 0.74 Mb. The resistant lines and SNP markers identified in this study can be used to breed for resistance to the most prevalent new pathotypes of P. brassicae in Canada.
遗传抗性是甘蓝型油菜作物根肿病(由芸薹根肿菌引起)防治的一种成功策略,但抗性可能会迅速丧失。当新的致病型出现时,鉴定新的抗性来源尤为重要。在本研究中,评估了177份甘蓝型油菜材料对四种新的芸薹根肿菌致病型的反应。利用简化基因组测序对每个材料进行基因分型,通过混合线性模型(MLM)分析来鉴定和定位根肿病抗性的新来源。根据加拿大根肿病鉴别系统,大多数材料高度感病(病情严重度指数为70 - 100),但有少数材料对致病型5X(21份材料)、3A(8份)、2B(7份)和3D(15份)表现出强抗性(病情严重度指数为0 - 20)。总共301,753个单核苷酸多态性(SNP)被定位到19条染色体上。群体结构分析表明,这177份材料属于七个主要群体。利用MLM分析将SNP与对每种致病型的抗性进行关联。总共鉴定出13个重要的SNP位点,其中9个SNP定位到A基因组,4个定位到C基因组。这些SNP与对致病型5X(2个SNP)、3A(4个)、2B(5个)和3D(6个)的抗性相关。对每个SNP上下游1.6 Mb区域进行Blast搜索,鉴定出13个抗病基因或结构域。SNP位点与最近的抗性基因之间的距离在0.04至