Components of partial disease resistance detected using a detached leaf assay in CIMMYT Fusarium head blight resistant wheat germplasm

One hundred and nineteen entries from the CIMMYT International Wheat and Maize Improvement Centre 2004/05 Fusarium head blight (FHB) resistance screening nursery were evaluated as possible sources of novel components of partial disease resistance (PDR), against FHB and Microdochium nivale snow mould, detected using a detached leaf assay. In addition the FHB resistant cvs Arina, Alsen and Frontana and 21 European wheat genotypes were included for comparison. There was wide variation among CIMMYT entries for the PDR components incubation period, latent period and lesion length (P < 0.001) and European lines for incubation and latent periods (P < 0.001). The CIMMYT entries with the longest latent periods were not superior to cv. Arina, the best European source of this PDR component identified to date. Notably the CIMMYT lines exhibiting the longest latent periods had Aegilops squarrosa (878) in their pedigree, indicating that Ae. squarrosa (878) may be a source of enhanced resistance detected by latent period. Macroscopic observation suggested that the underlying mechanisms contributing to latent period may differ among the CIMMYT germplasm and European sources of long latent period such as cv. Arina. Among the CIMMYT germplasm, incubation period was only weakly correlated with latent period (r = 0.25; P < 0.01); this also was the case among European genotypes (r = 0.36; P < 0.05) supporting previous findings that these PDR components are largely under separate genetic control. However, the correlation was higher on a subset of the most resistant and susceptible lines for latent period (r = 0.73 and r = 0.44; incubated at 10 °C and 15 °C, respectively). While a number of the European lines had latent periods that were comparable to cv. Arina many were significantly shorter indicating potential for improvement in this PDR component. Adaptations to the experimental design utilized in the present experiments for the efficient evaluation of large numbers of genotypes utilizing the detached leaf assay are discussed.