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Metabolite profiles based on GC/MS were used to study the temporal dynamics of metabolites in potato leaves following pathogen inoculation. In the polar and non-polar plant extracts a total of 106 consistent peaks were detected, of which 95 metabolites were tentatively identified. Following pathogen inoculation, the abundances of 42 metabolites were significantly increased or decreased, and these metabolites were designated as Pathogenesis-Related (PR) Metabolites. Factor analysis of the abundance of 106 metabolites identified four plant-pathogen interaction functions: (i) homeostasis; (ii) primary defence; (iii) secondary defence; (iv) collapse of primary and secondary defence responses. During the primary and secondary defence phases, dramatic changes in the amino acids, known precursors of several plant defence-related metabolites, were observed. Plausible satellite-networks of metabolic pathways leading to the up-regulation of these families of amino acids and other secondary metabolites, and their potential application for the evaluation of horizontal resistance in potato against the late blight pathogen is discussed.

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A dramatic increase in the incidence of late blight and changes within populations of Phytophthora infestans have been observed in various regions of Canada. In this study, the occurrence of several new genotypes of the pathogen was documented with associated phenotypes that dominated pathogen populations. Genotype US-23, previously detected only among isolates from the United States, dominated in the western Canadian provinces of British Columbia, Alberta (AB), Saskatchewan, and Manitoba (MB). Although isolates of US-23 infect both potato and tomato, these isolates were the only genotype recovered from commercial garden centers in Canada. Isolates of genotype US-8, previously dominant throughout Canada, represented the only genotype detected from the eastern Canadian provinces of New Brunswick and Prince Edward Island. Isolates of other genotypes detected in Canada included US-11 in AB, US-24 in MB, and US-22 in Ontario (ON). An additional genotype was detected in ON which appears to be a derivative of US-22 that may have arisen through sexual reproduction. However, evidence of clonal reproduction dominated among the isolates collected, and opportunities for sexual reproduction were probably limited because of a surprising geographic separation of the A1 and A2 mating types in Canada. Sensitivity of the US-22, US-23, and US-24 isolates to the fungicide metalaxyl, movement of potato seed and transplants, and weather conditions may have contributed to reduced opportunities for contact between the mating types in fields in Canada. All P. infestans isolates were readily distinguished from other related oomycetes with RG57 restriction fragment length polymorphism analysis. Long-distance movement in seed tubers and garden center transplants may have contributed to the rapid spread of the P. infestans genotypes across Canada. Tracking pathogen movement and population composition should improve the ability to predict the genotypes expected each year in different regions of Canada.