Abstract

The importance of root and spore surface molecules in the interactions of Fusarium spp. with conifer roots, and cellular localization of proteins presumed to be involved in host defence, were investigated. For adhesion studies, using a combination of fluorescein isothiocyanate (FITC) labelled lectins and high perfomance liquid chromatography (HPLC), several sugars (pinitol, xylitol, galactose, mannose, and glucose) were detected in root surface mucilage. Both artificial substrata and detached living roots were used to evaluate the significance of selective removal of root or spore surface components on the adhesion process. The spores or roots were pretreated with either periodic acid, pronase E, potassium hydroxide or diethyl ether. Pretreatment of the spores with diethyl ether reduced significantly the level of spore adhesion, which suggests that the adhesive component is either a lipid, or is bound to lipid. Since oxidation of carbohydrate reactive sites with periodic acid on the root surface almost completely abolished the development of germ tubes by adherent spores, it was presumed that some of these periodate-sensitive substances serve as a nutrient source for the fungus. On inoculated roots, F. avenaceum and F. culmorum were significantly pathogenic to both Norway spruce and Scots pine seedlings. Cytochemical labelling of sites of accumulation of host defence molecules within infected root tissues using anti-peroxidase demonstrated increased peroxidase activity in host cell walls. With anti-chitinase and anti-glucanase, gold labelling was found mainly on pathogen hyphal walls.Key words: conifer seedlings, adhesion, Fusarium spp., PR proteins, immunolocalization, lectins.

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