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resumen

Resumen
Apple valsa canker, caused by the fungus Valsa ceratosperma, is one of the most destructive diseases of this crop. Conventional fungicide treatments are not effective enough; therefore, it is necessary to develop alternatives for the control of this pathogen. The use of Trichoderma strains as a biocontrol agent is a promising strategy for the environmentally friendly management of this disease. In this study, seven different isolates of Trichoderma spp. [ver mas...]
dc.contributor.authorValetti, Lucio
dc.contributor.authorBernanrdi Lima, Nelson
dc.contributor.authorCazon, Luis Ignacio
dc.contributor.authorCrociara, Clara Sonia
dc.contributor.authorOrtega, Leandro Ismael
dc.contributor.authorPastor, Silvina Estela
dc.date.accessioned2022-10-11T11:31:22Z
dc.date.available2022-10-11T11:31:22Z
dc.date.issued2022-05-27
dc.identifier.issn0929-1873
dc.identifier.issn1573-8469 (online)
dc.identifier.otherhttps://doi.org/10.1007/s10658-022-02529-3
dc.identifier.urihttp://hdl.handle.net/20.500.12123/13082
dc.identifier.urihttps://link.springer.com/article/10.1007/s10658-022-02529-3
dc.description.abstractApple valsa canker, caused by the fungus Valsa ceratosperma, is one of the most destructive diseases of this crop. Conventional fungicide treatments are not effective enough; therefore, it is necessary to develop alternatives for the control of this pathogen. The use of Trichoderma strains as a biocontrol agent is a promising strategy for the environmentally friendly management of this disease. In this study, seven different isolates of Trichoderma spp. were obtained from the rhizospheric soil of healthy apple plants. The antagonistic capacity of the isolates against the pathogen V. ceratosperma was evaluated using the dual culture method and by the production of antibiotic non-volatile compounds. In the dual culture method, the interaction zone was observed by differential interference contrast microscopy and confocal laser scanning microscopy. The isolates RN-13, RN-33, and RN-34 inhibited more than 75% of mycelial growth, whereas RN-19, RN-16, and RN-15 inhibited growth by 65–72% with respect to the control. The mycoparasitic activity was evidenced by the coiling of hyphae around pathogen hyphae, appressorium-like structures, morphological deformations, and disintegration of mycelial walls. Apple shoots inoculated with Trichoderma isolates and then infected with V. ceratosperma showed the antagonist capacity of RN-16, RN-19, RN-15, and RN-18, which produced a significant decrease in the size of the lesion. Overall, the results showed the great potential of Trichoderma as a biocontrol agent against apple tree valsa canker. Further studies of this fungal interaction are required to design effective control strategies for the protection of apple tree orchards from this disease.eng
dc.formatapplication/pdfes_AR
dc.language.isoenges_AR
dc.publisherSpringeres_AR
dc.relationinfo:eu-repograntAgreement/INTA/PNFRU-1105073/AR./Generación y desarrollo de tecnología para la detección, seguimiento, predicción, prevención y control de vectores, plagas emergentes y/o limitantes de la producción frutícola argentina.es_AR
dc.rightsinfo:eu-repo/semantics/restrictedAccesses_AR
dc.sourceEuropean Journal of Plant Pathology 163 : 923–935 (2022)es_AR
dc.subjectAntagonismeng
dc.subjectTrichodermaeng
dc.subjectAppleseng
dc.subjectAntagonismo
dc.subjectValsa
dc.subjectManzana
dc.subjectAgentes de Control Biológico
dc.subjectBiological Control Agentseng
dc.subject.otherBiocontrol Agentseng
dc.subject.otherCanker Diseaseeng
dc.subject.otherMycoparasitismeng
dc.subject.otherValsa ceratosperma
dc.titleMycoparasitic Trichoderma isolates as a biocontrol agent against Valsa ceratosperma, the causal agent of apple valsa cankeres_AR
dc.typeinfo:ar-repo/semantics/artículoes_AR
dc.typeinfo:eu-repo/semantics/articlees_AR
dc.typeinfo:eu-repo/semantics/publishedVersiones_AR
dc.description.origenInstituto de Patología Vegetales_AR
dc.description.filFil: Valetti, Lucio. Instituto Nacional de Tecnología Agropecuaria (INTA). Instituto de Patología Vegetal; Argentinaes_AR
dc.description.filFil: Valetti, Lucio. Consejo Nacional de Investigaciones Científicas y Técnicas. Unidad de Fitopatología y Modelización Agrícola (UFyMA); Argentinaes_AR
dc.description.filFil: Bernanrdi Lima, Nelson. Consejo Nacional de Investigaciones Científicas y Técnicas. Unidad de Fitopatología y Modelización Agrícola (UFyMA); Argentinaes_AR
dc.description.filFil: Bernanrdi Lima, Nelson. Instituto Nacional de Tecnología Agropecuaria (INTA). Instituto de Patología Vegetal; Argentinaes_AR
dc.description.filFil: Cazon, Luis Ignacio. Instituto Nacional de Tecnología Agropecuaria (INTA). Instituto de Patología Vegetal; Argentinaes_AR
dc.description.filFil: Cazon, Luis Ignacio. Universidad Federal de Vicosa. Laboratorio de Epidemiología. Departamento de Fitopatología; Brasiles_AR
dc.description.filFil: Crociara, Clara Sonia. Consejo Nacional de Investigaciones Científicas y Técnicas. Unidad de Fitopatología y Modelización Agrícola (UFyMA); Argentinaes_AR
dc.description.filFil: Crociara, Clara Sonia. Instituto Nacional de Tecnología Agropecuaria (INTA). Instituto de Patología Vegetal; Argentinaes_AR
dc.description.filFil: Ortega, Leandro Ismael. Instituto Nacional de Tecnología Agropecuaria (INTA). Instituto de Fisiología y Recursos Genéticos Vegetales; Argentinaes_AR
dc.description.filFil: Pastor, Silvina Estela. Instituto Nacional de Tecnología Agropecuaria (INTA). Instituto de Patología Vegetal; Argentinaes_AR
dc.description.filFil: Pastor, Silvina Estela. Consejo Nacional de Investigaciones Científicas y Técnicas. Unidad de Fitopatología y Modelización Agrícola (UFyMA); Argentinaes_AR
dc.subtypecientifico


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