| Abstract: | Resistance in apple is evaluated by needle–inoculation of succulent shoot tips with 106–107 cells of a virulent isolate of Erwinia amylovora (Burr.) Winslow et al. (the incitant of fireblight) and measurement of the resulting cortical lesion when extension is complete. Data are now available on practically all commercial cultivars, some of which have a useful level of resistance. Some newer cultivars, particularly those with resistance to scab (Venluria inaequalis Cooke] Wint.) derived from Malus floribunda, have good resistance to E. amylovora. A very high level of resistance is present in Asiatic Malus species, including M. x robusta, M. x sublo–bata, M. x atrosanguinea, and M. prunifolia, and in the North American species M. fusca. This type of resistance appears to be inherited polygenically, and because of its detectability in young seedlings can be used conveniently in breeding. Objectives of pear breeding programs are aimed at developing superior fruit quality combined with resistance to fireblight, psylla, and Fabraea leaf spot. Many high quality cultivars of Pyrus communis are extremely susceptible to E. amylovora and sensitivity appears to be controlled by a dominant gene Se. A high level of resistance is present in P. ussuriensis but varies considerably between clonal selections of other Pyrus species. Pear seedlings from controlled pollinations are artificially inoculated in the glasshouse with a similar bacterial suspension as used for apples, and only the most resistant ones are selected and planted in the field for future evaluation. In Beltsville, heritability studies of crosses between non–sensitive parents have indicated that selection for resistance within progenies results in a high degree of genetic gain. Interspecific hybridization has an advantage over P. communis crosses mainly when insect or fungus resistance is required. |
