Genetic mapping from field tests of qualitative and quantitative resistance to Phytophthora infestans in a population derived from Solanum tuberosum and Solanum berthaultii
Ee. Ewing et al., Genetic mapping from field tests of qualitative and quantitative resistance to Phytophthora infestans in a population derived from Solanum tuberosum and Solanum berthaultii, MOL BREED, 6(1), 2000, pp. 25-36
Under controlled field conditions, a Solanum backcross population segregate
d for resistance to Phytophthora infestans. The population ('BCT') had been
derived previously by crossing the Solanum tuberosum dihaploid USW2230 x S
olanum berthaultii PI473331 to obtain the hybrid M200-30, and then backcros
sing the hybrid to the S. tuberosum dihaploid HH1-9. Resistance was assesse
d from analyses of epidemics in small plots of each individual genotype, an
d data were recorded as area under the disease progress curve (AUDPC). The
parents of the original cross (USW2230 and a selection from PI473331) were
not included in the test, but the hybrid was incompatible and HH1-9 was com
patible with the tester strain of P. infestans (US-8 lineage). Somewhat mor
e than half of the progeny also were incompatible with the tester strain, i
ndicating the presence of an R gene. This gene segregated from the S. berth
aultii parent and mapped 4.8 cm from the RFLP marker TG63 on chromosome 10.
We deduce that the R gene is not R-1, R-2, R-3, R-6, or R-7 and is probabl
y not R-4, R-5, or R-10. Among the remaining, compatible progeny, there was
a wide range of quantitative resistance. All were more resistant than the
susceptible cultivar Superior, and most individuals were much more resistan
t than the moderately resistant cultivar Kennebec. AUDPC values among the s
ub-population of compatible genotypes ranged from about 400 to 1500 units t
he first year and from 400 to 1760 units the second year. At least five qua
ntitative trait loci (QTLs) were detected in this sub-population in both 19
97 and 1998, including one detected through segregation of alleles from bot
h the hybrid parent and the recurrent S. tuberosum parent. A model of main
and epistatic effects explained 56% and 66% of the variation observed for q
uantitative resistance to late blight in 1997 and 1998, respectively. Sever
al of the QTLs for late blight resistance were located in regions of the ge
nome to which QTLs for late maturity have previously been mapped.