Screening and Resistance Locus Identification of the Mutant fcrZ22 Resistant to Crown Rot Caused by Fusarium pseudograminearum

• Published in: Plant disease Vol. 108; no. 2; p. 426
• Main Authors: Li, Qiaoyun, Hao, Xiaopeng, Guo, Zhenfeng, Qu, Kefei, Gao, Mingshuang, Song, Gaili, Yin, Zhao, Yuan, Yuhao, Dong, Chunhao, Niu, Jishan, Yin, Guihong
• Format: Journal Article
• Language: English
• Published: United States 01.02.2024
• Subjects: Disease Resistance - genetics; Fusarium - genetics; Plant Breeding; Quantitative Trait Loci; resistance loci; Fusarium crown rot; genetic analysis; resistant mutant; ethyl methane sulfonate
• ISSN: 0191-2917; 1943-7692
• DOI: 10.1094/PDIS-06-23-1195-RE

Crown rot caused by is a devastating wheat disease worldwide. In addition to yield losses, the fungi causing Fusarium crown rot (FCR) also deteriorate the quality and safety of food because of the production of mycotoxins. Planting resistant cultivars is an effective way to control FCR. However, most wheat cultivars are susceptible to FCR. Therefore, development of new sources and detection of loci for FCR resistance are necessary. In the present study, a resistant mutant, , was identified from an ethyl methane sulfonate (EMS)-mutagenized population of the cultivar Zhoumai 22, and then was crossed with the wild type to produce an F population. Genetic analysis of the F population was carried out by the mixed inheritance model of major genes plus polygenes, and 20 resistant and 20 susceptible plants were selected to assemble mixed pools. Combining 660K SNP arrays, the resistance loci were detected by bulked segregant analysis. The resistance to FCR caused by in the F population was in accordance with the "mixed model with two major genes of additive-epistasis effect + additive-dominant polygenes," and the heritability of the major gene was 0.92. Twenty-one loci were detected, which were located on 10 chromosomes, namely, 1B (1), 1D (1), 2A (3), 1B (1), 3A (3), 3B (3), 4A (2), 5A (2), 7A (3), and 7B (2). Among the 21 loci, eight were new loci for FCR resistance. This is the first report of detecting loci for FCR resistance from a mutant. The results of the present study provided excellent germplasm resources for breeding wheat cultivars with FCR resistance and laid the foundation for fine mapping of FCR resistance loci.