Genome-wide association analysis of Septoria tritici blotch for adult plant resistance in elite bread wheat (Triticum aestivum L) genotypes

对优良面包小麦(Triticum aestivum L)基因型进行全基因组关联分析,以研究小麦颖枯病对成株的抗性

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Abstract

Septoria tritici blotch (STB) is a predominant foliar disease of wheat, caused by the pathogen Zymoseptoria tritici. This disease can lead to substantial yield losses warranting control by using expensive fungicides. One effective method of STB control is the utilization of resistant wheat varieties. In this particular study, a panel comprising of 186 bread wheat genotypes was assessed for their adult plant resistance (APR) to STB. Field trials were conducted across five environments in Ethiopia during the 2022 and 2023 growing seasons under natural infestation conditions. The association panel was genotyped using 20K single nucleotide polymorphism (SNP) markers. To determine the relationship between genetic markers and STB resistance, a mixed linear model (MLM) analysis was performed using the statgen GWAS R software package. Heritability estimates for STB resistance ranged from 0.39 to 0.95, underscoring the genetic variability and the potential for selection. The study identified 52 marker-trait associations (MTAs) for STB resistance at maturity (SDSM) and 62 MTAs at heading (SDSH). Chromosome 5A contains a high concentration of MTAs that confer resistance to STB, hosting multiple significant MTAs, including four consistently associated markers ('Kukri_c10033_724', 'RAC875_rep_c116420_103', 'TG0019', and 'RAC875_c30566_230'). Additionally, chromosomes 1B, 2B, 5B, and 7A were found to harbor important MTAs, contributing to resistance across various environments. Notably, two QTLs, qtSTB23 (5A) and qtSTB38 (7B), exhibited stability across multiple environments, making them robust candidates for breeding programs. Furthermore, novel resistance loci on chromosome 2A were discovered, offering new opportunities for enhancing resistance. Therefore, these findings provide an opportunity for improving STB resistance through gene stacking using marker-assisted selection (MAS).

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