A subset of world barley collection was used in the identification of sources of resistance and marker-trait association for resistance for bacterial leaf streak

Abstract

The bacterial leaf streak (BLS) disease of barley, caused by Xanthomonas translucens pv. translucens (Xtt), has become increasingly important worldwide in recent years. Inefficacy of chemical control methods leaves deployment of host resistance to be the only option to manage this disease. However, current commercial varieties are mainly susceptible to BLS. Therefore, our goal was to identify sources of resistance from diverse barley germplasms and map associated genetic factors. To do so, we evaluated a subset of the World Barley Core Collection (BCC), consisting of 198 accessions, on their reaction to BLS from 2013 to 2016 under natural or artificially inoculated disease pressures. Ten accessions exhibited consistently low disease severities over four years of evaluations. Using genotype data from the T3/Barley database, genome-wide association studies were conducted to identify marker-trait associations (MTAs) in this barley mini-core panel for BLS resistance. Utilizing four mixed-model analyses (MLM, MLMM, FarmCPU, BLINK), five significant MTAs were consistently identified from at least two mixed model analyses including two in chromosome 2H, and one each in chromosomes 5H, and 7H. Associations in chromosomes 2H and 5H appear to be in the same region with loci identified in a previous association study, reinforcing their potential relevance. The identified resistant barley accessions and associated markers will be valuable inbreeding BLS-resistant barley varieties. Core ideas- A subset of world barley collection was used in the identification of sources of resistance and marker-trait association for resistance for bacterial leaf streak. - Ten accessions consistently showed low disease severity across different years, highlighting their value in BLS resistance breeding. - Five MTAs were consistently identified using different models, with two aligning with previously identified resistance QTLs.