A factorial test was conducted to evaluate the potential of screening sweetpotato plants to three pathogens simultaneously. The pathogens were Meloidogyne incognita, Fusarium oxysporum, and Streptomyces ipomoea. The test also involved six sweetpotato cultivars and three evaluation times. Evaluation times were 3, 6, and 9 weeks post inoculation. The symptoms evaluated were vascular necrosis, fibrous root necrosis, and gall and egg mass production. For each of the three pathogens, the ability to separate cultivars with intermediate levels of resistance from those with low levels of resistance decreased as post Inoculation time increased. Simultaneous screening was practical if the goal was to select plants with resistance to all three pathogens. Resistances to individual pathogens could not be identified in plants inoculated with all three pathogens.
R. Mark Hurley, Paul G. Thompson, and Gary W. Lawrence
Kittipat Ukoskit, Paul G. Thompson, Gary W. Lawrence, and Clarence E. Watson
The inheritance of root-knot nematode race 3 [Meloidogyne incognita (Kofoid & White) Chitwood] resistance was studied in 71 progenies of the F1 backcross population produced from the resistant parent `Regal' and the susceptible parent `Vardaman'. The distribution frequency of the progenies measured on total nematode number (eggs + juveniles) indicated a bimodal distribution with a ratio of 4 resistant: 1 susceptible. Based on this phenotypic ratio, the proposed genetic model was duplex polysomic inheritance (RRrrrr = resistant). Bulk segregant analysis in conjunction with the RAPD technique was employed to identify RAPD marker linked to the root knot nematode-resistant gene. Nine of 760 random decamer primers screened showed polymorphic bands. Primer OPI51500 produced a band in the resistant bulk, but not in the susceptible bulk. Estimated recombination frequency of 0.24 between the OPI51500 marker and the root-knot nematode-resistant gene indicated linkage.