Development and adhesion of infection structures of the grapevine powdery mildew fungus. U~cinu/a necator (Schw.) Burr.. were investigated during the early stages of leaf colonization. Light microscopy showed that primary appressoria occurred 3.5 h post inoculation (p.i.) and that hyphae on the leaf surface, indicative of successful host colonization, appeared 14 h p.i. Low temperature scanning electron microscopy revealed deposits of extracellular material at the contact zone of fungal structures and plant cuticle, suggesting firm attachment of the pathogen. To investigate whether or not esterase or cutinase activity is involved in establishing the fungus on the host cuticle, histochemical assays and inhibitor studies were performed. Results indicated that esterase activity was associated with conidia and infection structures. A single fungal extracellular protein was identified as a cutinase by its ability to hydrolyze 3H-cutin. Probing Southern blots of genomic DNA of U necalor, Magnaporlhe grisea, and Fusarium so/ani fsp. pisi with the cutinase gene of F so/ani fsp. pisi suggested that the cutinase gene of U necalor shares only limited sequence similarities with the cutinase genes of the other fungi investigated. Adhesion assays showed that the presence of esterase-cutinase inhibitors on the cuticle did not significantly affect adhesion. The role of the enzyme in fungal adhesion is discussed.Key words: grapevine powdery mildew, Vilis vinifera, cutinase, extracellular matrix, cryofixation, low temperature scanning electron microscopy.Resume: Le developpement et l' adhesion 'des structures infectieuses du champignon de I' o"idium de la vigne, Uncinu/a necator (Schw.) Burr., ont ete etudies pendant les premiers stades de la colonisation de la feuille. La microscopie optique a revele un appressorium primaire 3.5 h apres inoculation (p.i.) et un hyphe sur la feuil1e, indiquant le succes de la colonisation. 14 h p.i. En microscopie electronique it balayage des dep6ts de materiel extracellulaire ont pu etre observes sur la zone de contact entre les structures fongiques et la cuticule de la plante, suggerant un attachement ferme du pathogene. Pour rechercher si une activite cutinase ou esterase participait it l'etablissement du champignon sur la cuticule de l'h6te, des etudes histochimiques et avec des inhibiteurs ont ete conduites. Elles ont montre que l'activite esterase etait associee avec les conidies et les structures infectieuses. Une seule protei ne fongique extracel1ulaire a ete identifiee comme une cutinase par sa capacite it hydrolyser de la 3H-cutine. Des Southern blots d' ADN genomique d' U necalor. Magnaporlhe grisea et Fusarium so/ani fsp. pisi utilisant corn me probe le gene de la cutinase de F so/ani fsp. pisi suggerent que le gene de la cutinase d' U necator ne partage que peu de zones de similarite de sequence avec les genes de la cutinase des autres especes etudiees. Des essais d' adhesion ont montre que la presence d' inhibiteurs d' esterase-cutinase sur la cuticule n' affectent pas sig...