Lawrence Tidakbi, Hongliang Wang, Amy Bernardo, Paul St Amand, Allan Fritz, Guorong Zhang, Myron Bruce, Jessica L Rupp Noller, Gina Brown-Guedira, Guihua Bai, John Fellers, Mary J Guttieri, Katherine W Jordan
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引用次数: 0
Abstract
Fusarium head blight (FHB), primarily caused by Fusarium graminearum in North America, is a devastating disease in bread wheat (Triticum aestivum L.). The characteristic mycotoxin production and reduced grain fill cause several million metric tons of annual crop and economic losses. Exome capture-generated single nucleotide polymorphisms (SNPs) from 269 winter wheat breeding lines and cultivars representing most U.S. wheat-growing regions, were associated with FHB resistance using a genome-wide association study (GWAS). The panel was evaluated for FHB symptoms in the Rocky Ford FHB nursery (Manhattan, KS) across three field seasons. Significant variation was observed for FHB incidence (INC, %), area under the disease progress curve (AUDPC), Fusarium-damaged kernels (FDK, %), and deoxynivalenol (DON, ppm). Data analysis revealed significant FHB disease trait correlations (r = 0.32-0.70) across years and moderate broad-sense heritability (H2) estimates (0.65-0.74). We identified 22 significant loci representing priority breeding targets combating FHB damage. Many loci reside within proximity to previously identified native quantitative trait loci (QTL). A 1BL haplotype from the soft winter wheat cultivar 'Jamestown' reduced AUDPC and FDK by 25% and DON by 18%, demonstrating FHB resistance in an environment different from its native environment. We developed KASP assays to identify this resistance haplotype, and five other target SNPs for future incorporation in breeding pipelines increasing FHB resistance. Our findings highlight breeding progress demonstrated by the increased frequency of many resistant alleles in adapted varieties and breeding lines and emphasizes pyramiding native FHB resistance regions as the next step to prevent FHB losses.
期刊介绍:
G3: Genes, Genomes, Genetics provides a forum for the publication of high‐quality foundational research, particularly research that generates useful genetic and genomic information such as genome maps, single gene studies, genome‐wide association and QTL studies, as well as genome reports, mutant screens, and advances in methods and technology. The Editorial Board of G3 believes that rapid dissemination of these data is the necessary foundation for analysis that leads to mechanistic insights.
G3, published by the Genetics Society of America, meets the critical and growing need of the genetics community for rapid review and publication of important results in all areas of genetics. G3 offers the opportunity to publish the puzzling finding or to present unpublished results that may not have been submitted for review and publication due to a perceived lack of a potential high-impact finding. G3 has earned the DOAJ Seal, which is a mark of certification for open access journals, awarded by DOAJ to journals that achieve a high level of openness, adhere to Best Practice and high publishing standards.