Prehaustorial local resistance to coffee leaf rust in a Mexican cultivar involves expression of salicylic acid-responsive genes
Edgar Couttolenc-Brenis,
Gloria L. Carrión,
Luc Villain,
Fernando Ortega-Escalona,
Daniel Ramírez-Martínez,
Martín Mata-Rosas,
Alfonso Méndez-Bravo
Affiliations
Edgar Couttolenc-Brenis
Red de Manejo Biotecnológico de Recursos, Instituto de Ecología, A.C., Xalapa, Veracruz, México
Gloria L. Carrión
Red de Biodiversidad y Sistemática de Hongos, Instituto de Ecología, A.C., Xalapa, Veracruz, México
Luc Villain
La Recherche Agronomique pour le Développement, UMR, RPB, CIRAD, Montpellier, France
Fernando Ortega-Escalona
Red de Ecología Funcional, Instituto de Ecología, A.C., Xalapa, Veracruz, México
Daniel Ramírez-Martínez
Escuela Nacional de Estudios Superiores Unidad Morelia, Universidad Nacional Autónoma de México, Morelia, Michoacán, México
Martín Mata-Rosas
Red de Manejo Biotecnológico de Recursos, Instituto de Ecología, A.C., Xalapa, Veracruz, México
Alfonso Méndez-Bravo
CONACYT-Escuela Nacional de Estudios Superiores Unidad Morelia, Laboratorio Nacional de Análisis y Síntesis Ecológica, Universidad Nacional Autónoma de México, Morelia, Michoacán, México
Background In Mexico, coffee leaf rust (CLR) is the main disease that affects the Arabica coffee crop. In this study, the local response of two Mexican cultivars of Coffea arabica (Oro Azteca and Garnica) in the early stages of Hemileia vastatrix infection was evaluated. Methods We quantified the development of fungal structures in locally-infected leaf disks from both cultivars, using qRT-PCR to measure the relative expression of two pathogenesis recognition genes (CaNDR1 and CaNBS-LRR) and three genes associated with the salicylic acid (SA)-related pathway (CaNPR1, CaPR1, and CaPR5). Results Resistance of the cv. Oro Azteca was significantly higher than that of the cv. Garnica, with 8.2% and 53.3% haustorial detection, respectively. In addition, the non-race specific disease resistance gene (CaNDR1), a key gene for the pathogen recognition, as well as the genes associated with SA, CaNPR1, CaPR1, and CaPR5, presented an increased expression in response to infection by H. vastatrix in cv. Oro Azteca if comparing with cv. Garnica. Our results suggest that Oro Azteca’s defense mechanisms could involve early recognition of CLR by NDR1 and the subsequent activation of the SA signaling pathway.