ABSTRACT
Stem rust is one of the most important diseases, threatening global wheat production. Identifying genomic regions associated with resistance to stem rust at the seedling stage may contribute wheat breeders to introduce durably resistant varieties. Genome-wide association study (GWAS) approach was applied to detect stem rust (Sr) resistance genes/QTLs in a set of 282 Iranian bread wheat varieties and landraces. Germplasms evaluated for infection type and latent period in four races of Puccinia graminis f. sp. tritici (Pgt). A total of 3 QTLs for infection type (R2 values from 9.54% to 10.76%) and 4 QTLs for the latent period (R2 values from 8.97% to 12.24%) of studied Pgt races were identified in the original dataset. However, using the imputed SNPs dataset, the number of QTLs for infection type increased to 10 QTLs (R2 values from 8.12% to 11.19%), and for the latent period increased to 44 QTLs (R2 values from 9.47% to 26.70%). According to the results, the Iranian wheat germplasms are a valuable source of resistance to stem rust which can be used in wheat breeding programs. Furthermore, new information for the selection of resistant genotypes against the disease through improving marker-assisted selection efficiency has been suggested.
ABSTRACT
Development and use of resistant wheat cultivars is the most practical and economical approach for the control of Fusarium head blight (FHB). In the present study, a population of recombinant inbred lines derived from the cross between 'AC Brio' (a Canadian bread wheat cultivar moderately susceptible to FHB) and 'TC 67' (an FHB-resistant cultivar derived from Triticum timopheevii) was used to map quantitative trait loci (QTL) for FHB resistance using microsatellite molecular markers. Multiple interval mapping detected several QTL for FHB resistance on the chromosomes 5AL and 6A. The QTL detected in the marker interval of cfd6.1-barc48 on chromosome 5AL explained 10.9, 5.2, and 7.8% of phenotypic variation for disease incidence (type I resistance), disease severity (a combination of type I and type II resistance), and Fusarium-damaged kernels (FDK) (type IV resistance) under field conditions, respectively. The second QTL mapped to 5AL, in the marker interval of cfd39-cfa2185, explained 19.4 and 20.6% of phenotypic variation for FDK under field conditions and disease severity in the greenhouse (type II resistance), respectively. The QTL located on chromosome 6A conferred resistance to disease incidence and severity under field conditions and to disease severity in the greenhouse, explaining 6.8 to 11.8% of phenotypic variation for these traits. Several QTL for agronomic traits were also mapped in this study, including one and two QTL to the chromosomes 2A and 5AL, respectively, all for plant height, and two QTL to chromosome 6A for plant height and flowering date, respectively. The 5AL QTL for FHB resistance mapped in the marker interval of cfd39-cfa2185 in the present study is a novel QTL that originated from T. timopheevii and is reported here for the first time. Further validation of this QTL is required for wheat breeding programs to enhance resistance levels to FHB.
ABSTRACT
Certain Fusarium species cause Fusarium head blight (FHB) in wheat and other small grains. Differences in characteristics of the pathogen species/isolates used in breeding programs may affect reaction of host genotypes, leading to erroneous results. To clarify differences among Fusarium isolates from different geographical zones, the phylogenetic, chemotypic, and pathogenic abilities of 58 isolates collected from three wheat-producing countries (Canada, Mexico, and Iran) were investigated. Phylogenetic relationships among the isolates were characterized using the Tri101 gene sequence. All Canadian and Iranian isolates clustered in one group and were identified as F. graminearum lineage 7 (=F. graminearum sensu stricto) within the F. graminearum (Fg) clade. The isolates from Mexico were identified as either F. graminearum lineage 3 (=Fusarium boothii) within the Fg clade or Fusarium crookwellense. A polymerase chain reaction assay based on the Tri12 gene identified three trichothecene chemotypes of 15-ADON, 3- ADON, and NIV, with 15-ADON being the most common. All F. boothii isolates from Mexico were of the 15-ADON chemotype, while all F. crookwellense isolates were determined to be NIV producers. While we did not find the NIV chemotype among the Canadian isolates, 25.6% of the Iranian isolates were determined to be NIV producers. High level of variation in aggressiveness was also observed among and within the species tested: F. graminearum sensu stricto isolates were the most aggressive, followed by those of F. boothii, and lastly by F. crookwellense. The differences observed among the isolates may explain why wheat lines/cultivars demonstrate different reactions to FHB in different geographical zones.
