Hawaii 7981 tomato (Lycopersicon esculentum Mill,), resistant to race T3 of
the bacterial spot pathogen [Xanthomonas campestris pv. vesicatoria (Doidg
e) Dye], was crossed to the susceptible tomato inbred, FIa, 7060, and subse
quently F-2 and backcross seed were obtained. These generations were plante
d in the field, inoculated with the race T3 pathogen and evaluated for dise
ase severity over two summer seasons. Data were tested for goodness-of-fit
to a model based on control by the incompletely dominant gene Xv3 that conf
ers hypersensitivity. The F-1 was intermediate in disease severity to the p
arents for both seasons. When data were combined over both seasons, the bac
kcrosses fit the expected I:I ratios although each deviated from the expect
ed ratio in one of the 2 years tested. The F-2 did not fit the expected 1:2
:1 ratio in either pear or when data from the two years were combined due t
o a deficiency of resistant plants. Thirty-three F-2 plants representing an
array of disease severities and hypersensitivity reactions were selected i
n the second season and their F-3 progeny were inoculated and evaluated for
disease severity. Hawaii 7981 was significantly more resistant than the 12
most resistant F-3 selections even though all expressed hypersensitivity.
A hypersensitive F-3 With intermediate field resistance was crossed to Hawa
ii 7981 and subsequently, F-2 and backcross generations were obtained. Thes
e generations were field inoculated with the race T3 pathogen and evaluated
for disease severity. Hawaii 7981 was significantly more resistant than th
e F-3 parent as in the previous year. The data did not fit an additive-domi
nance model and epistatic interactions were significant. Thus, it appears t
hat field resistance to race T3 of bacterial spot found in Hawaii 7981 is c
onferred quantitatively by Xv3 and other resistance genes. Breeding implica
tions are discussed.