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Silva M. C., Guerra-Guimaraes L., Loureiro A., Nicole Michel. Involvement of peroxidases in the coffee resistance to orange rust (Hemileia vastatrix). Physiological and Molecular Plant Pathology, 2008, 72 (1-3), p. 29-38. ISSN 0885-5765

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Lien direct chez l'éditeur doi:10.1016/j.pmpp.2008.04.004

Titre
Involvement of peroxidases in the coffee resistance to orange rust (Hemileia vastatrix)
Année de publication2008
Type de documentArticle référencé dans le Web of Science WOS:000262669500005
AuteursSilva M. C., Guerra-Guimaraes L., Loureiro A., Nicole Michel.
SourcePhysiological and Molecular Plant Pathology, 2008, 72 (1-3), p. 29-38. ISSN 0885-5765
RésuméCoffea arabica plants with the S(H)5 and S(H)4S(H)5 genotypes were inoculated with isolates of the coffee orange rust (Hemileia vastatrix) races II and VI, in order to establish two incompatible interactions (I-1 and I-2) and a compatible one. Both incompatible interactions were characterized by restricted fungal growth associated with rapid hypersensitive plant cell death, monitored by cell autofluorescence and/or browning. Cytological and biochemical studies were performed to investigate the association of peroxidases (PODs) with coffee resistance to rust. In both incompatible interactions, in contrast with the compatible one, investigations revealed a peak of POD activity prior or at the same time, as the beginning of cell death. During the first peak, the isoenzyme pattern for peroxidases obtained by IEF (isoelectric focusing electrophoresis) showed an increase in activity of anionic and cationic isoenzymes. Cytochemically, POD and H2O2 were localized at the interface between the cuticle and fungal prepenetration structures, and at infection sites. In both incompatible interactions, a later increase in POD activity was determined which can be related to host cell wall lignification. This peak coincided with the one observed in the compatible interaction. Treatments of coffee leaves (I-2 incompatible interaction) with 2,4-dichlorophenol, an activator of peroxidases and other oxidases, significantly increased cell autofluorescence. On the contrary, salicyl hydroxamic acid, an inhibitor of the same enzymes, and diphenyleneiodonium chloride, an inhibitor of NADPH oxidases, decreased cell autofluorescence. These results suggested that POD, NADPH oxidases and eventually other oxidases are involved in the coffee resistance to H. vastatrix.
Plan de classement076
LocalisationFonds IRD [F B010044226]
Identifiant IRDfdi:010044226
Lien permanenthttp://www.documentation.ird.fr/hor/fdi:010044226

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