Utilization of a publicly available diversity panel in genomic prediction of Fusarium head blight resistance traits in wheat.

Fusarium head blight (FHB) is an economically and environmentally concerning disease of wheat (Triticum aestivum L). A two-pronged approach of marker-assisted selection coupled with genomic selection has been suggested when breeding for FHB resistance. A historical dataset comprised of entries in the Southern Uniform Winter Wheat Scab Nursery (SUWWSN) from 2011 to 2021 was partitioned and used in genomic prediction. Two traits were curated from 2011 to 2021 in the SUWWSN: percent Fusarium damaged kernels (FDK) and deoxynivalenol (DON) content. Heritability was estimated for each trait-by-environment combination. A consistent set of check lines was drawn from each year in the SUWWSN, and k-means clustering was performed across environments to assign environments into clusters. Two clusters were identified as FDK and three for DON. Cross-validation on SUWWSN data from 2011 to 2019 indicated no outperforming training population in comparison to the combined dataset. Forward validation for FDK on the SUWWSN 2020 and 2021 data indicated a predictive accuracy r ≈ 0.58 $r \approx 0.58$ and r ≈ 0.53 $r \approx 0.53$ , respectively. Forward validation for DON indicated a predictive accuracy of r ≈ 0.57 $r \approx 0.57$ and r ≈ 0.45 $r \approx 0.45$ , respectively. Forward validation using environments in cluster one for FDK indicated a predictive accuracy of r ≈ 0.65 $r \approx 0.65$ and r ≈ 0.60 $r \approx 0.60$ , respectively. Forward validation using environments in cluster one for DON indicated a predictive accuracy of r ≈ 0.67 $r \approx 0.67$ and r ≈ 0.60 $r \approx 0.60$ , respectively. These results indicated that selecting environments based on check performance may produce higher forward prediction accuracies. This work may be used as a model for utilizing public resources for genomic prediction of FHB resistance traits across public wheat breeding programs.

Mapping of powdery mildew resistance gene Pm53 introgressed from Aegilops speltoides into soft red winter wheat.

KEY MESSAGE: A powdery mildew resistance gene was introgressed from Aegilops speltoides into winter wheat and mapped to chromosome 5BL. Closely linked markers will permit marker-assisted selection for the resistance gene. Powdery mildew of wheat (Triticum aestivum L.) is a major fungal disease in many areas of the world, caused by Blumeria graminis f. sp. tritici (Bgt). Host plant resistance is the preferred form of disease prevention because it is both economical and environmentally sound. Identification of new resistance sources and closely linked markers enable breeders to utilize these new sources in marker-assisted selection as well as in gene pyramiding. Aegilops speltoides (2n = 2x = 14, genome SS), has been a valuable disease resistance donor. The powdery mildew resistant wheat germplasm line NC09BGTS16 (NC-S16) was developed by backcrossing an Ae. speltoides accession, TAU829, to the susceptible soft red winter wheat cultivar 'Saluda'. NC-S16 was crossed to the susceptible cultivar 'Coker 68-15' to develop F2:3 families for gene mapping. Greenhouse and field evaluations of these F2:3 families indicated that a single gene, designated Pm53, conferred resistance to powdery mildew. Bulked segregant analysis showed that multiple simple sequence repeat (SSR) and single nucleotide polymorphism (SNP) markers specific to chromosome 5BL segregated with the resistance gene. The gene was flanked by markers Xgwm499, Xwmc759, IWA6024 (0.7 cM proximal) and IWA2454 (1.8 cM distal). Pm36, derived from a different wild wheat relative (T. turgidum var. dicoccoides), had previously been mapped to chromosome 5BL in a durum wheat line. Detached leaf tests revealed that NC-S16 and a genotype carrying Pm36 differed in their responses to each of three Bgt isolates. Pm53 therefore appears to be a new source of powdery mildew resistance.

MlAG12: a Triticum timopheevii-derived powdery mildew resistance gene in common wheat on chromosome 7AL.

Wheat powdery mildew is an economically important disease in cool and humid environments. Powdery mildew causes yield losses as high as 48% through a reduction in tiller survival, kernels per head, and kernel size. Race-specific host resistance is the most consistent, environmentally friendly and, economical method of control. The wheat (Triticum aestivum L.) germplasm line NC06BGTAG12 possesses genetic resistance to powdery mildew introgressed from the AAGG tetraploid genome Triticum timopheevii subsp. armeniacum. Phenotypic evaluation of F(3) families derived from the cross NC06BGTAG12/'Jagger' and phenotypic evaluation of an F(2) population from the cross NC06BGTAG12/'Saluda' indicated that resistance to the 'Yuma' isolate of powdery mildew was controlled by a single dominant gene in NC06BGTAG12. Bulk segregant analysis (BSA) revealed simple sequence repeat (SSR) markers specific for chromosome 7AL segregating with the resistance gene. The SSR markers Xwmc273 and Xwmc346 mapped 8.3 cM distal and 6.6 cM proximal, respectively, in NC06BGTAG12/Jagger. The multiallelic Pm1 locus maps to this region of chromosome 7AL. No susceptible phenotypes were observed in an evaluation of 967 F(2) individuals in the cross NC06BGTAG12/'Axminster' (Pm1a) which indicated that the NC06BGTAG12 resistance gene was allelic or in close linkage with the Pm1 locus. A detached leaf test with ten differential powdery mildew isolates indicated the resistance in NC06BGTAG12 was different from all designated alleles at the Pm1 locus. Further linkage and allelism tests with five other temporarily designated genes in this very complex region will be required before giving a permanent designation to this gene. At this time the gene is given the temporary gene designation MlAG12.