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dc.contributor.authorCitores González, Lucía 
dc.contributor.authorValletta, Mariangela
dc.contributor.authorSingh, Vikram Pratap
dc.contributor.authorPedone, Paolo Vincenzo
dc.contributor.authorIglesias Álvarez, María del Rosario 
dc.contributor.authorFerreras Rodríguez, José Miguel 
dc.contributor.authorChambery, Angela
dc.contributor.authorRusso, Rosita
dc.date.accessioned2023-11-14T09:43:37Z
dc.date.available2023-11-14T09:43:37Z
dc.date.issued2022
dc.identifier.citationInternational Journal of Molecular Sciences, 2022, Vol. 23, Nº. 2, 680es
dc.identifier.issn1422-0067es
dc.identifier.urihttps://uvadoc.uva.es/handle/10324/62924
dc.descriptionProducción Científicaes
dc.description.abstractPenicillium digitatum is a widespread pathogen responsible for the postharvest decay of citrus, one of the most economically important crops worldwide. Currently, chemical fungicides are still the main strategy to control the green mould disease caused by the fungus. However, the increasing selection and proliferation of fungicide-resistant strains require more efforts to explore new alternatives acting via new or unexplored mechanisms for postharvest disease management. To date, several non-chemical compounds have been investigated for the control of fungal pathogens. In this scenario, understanding the molecular determinants underlying P. digitatum’s response to biological and chemical antifungals may help in the development of safer and more effective non-chemical control methods. In this work, a proteomic approach based on isobaric labelling and a nanoLC tandem mass spectrometry approach was used to investigate molecular changes associated with P. digitatum’s response to treatments with α-sarcin and beetin 27 (BE27), two proteins endowed with antifungal activity. The outcomes of treatments with these biological agents were then compared with those triggered by the commonly used chemical fungicide thiabendazole (TBZ). Our results showed that differentially expressed proteins mainly include cell wall-degrading enzymes, proteins involved in stress response, antioxidant and detoxification mechanisms and metabolic processes such as thiamine biosynthesis. Interestingly, specific modulations in response to protein toxins treatments were observed for a subset of proteins. Deciphering the inhibitory mechanisms of biofungicides and chemical compounds, together with understanding their effects on the fungal physiology, will provide a new direction for improving the efficacy of novel antifungal formulations and developing new control strategies.es
dc.format.mimetypeapplication/pdfes
dc.language.isoenges
dc.publisherMDPIes
dc.rights.accessRightsinfo:eu-repo/semantics/openAccesses
dc.rights.urihttp://creativecommons.org/licenses/by/4.0/*
dc.subjectPenicillium digitatumes
dc.subjectProteomicses
dc.subjectProteómicaes
dc.subjectRibosome inactivating proteines
dc.subjectRibosomes - Structurees
dc.subjectProteins - Synthesises
dc.subjectRibotoxines
dc.subjectFungies
dc.subjectMolds (Fungi)es
dc.subjectCitruses
dc.subjectCítricoses
dc.subjectPlant pathologyes
dc.subjectEnfermedades de las plantases
dc.subjectFungal diseases of plantses
dc.subjectBiochemistryes
dc.subjectMolecular biologyes
dc.titleDeciphering molecular determinants underlying Penicillium digitatum’s response to biological and chemical antifungal agents by tandem mass tag (TMT)-based high-resolution LC-MS/MSes
dc.typeinfo:eu-repo/semantics/articlees
dc.rights.holder© 2022 The Authorses
dc.identifier.doi10.3390/ijms23020680es
dc.relation.publisherversionhttps://www.mdpi.com/1422-0067/23/2/680es
dc.identifier.publicationfirstpage680es
dc.identifier.publicationissue2es
dc.identifier.publicationtitleInternational Journal of Molecular Scienceses
dc.identifier.publicationvolume23es
dc.peerreviewedSIes
dc.description.projectMinistero dell'Università e della Ricerca (MIUR) de Italia , project PON “Research and Innovation 2014–2020” - (Grant AIM 1890997-2)es
dc.description.projectMISE, project NUTRABEST PON I&C 2014–2020 - (Grant F/200050/01–03/X45)es
dc.description.projectJunta de Castilla y León, Consejería de Educación - (Grant VA033G19)es
dc.identifier.essn1422-0067es
dc.rightsAtribución 4.0 Internacional*
dc.type.hasVersioninfo:eu-repo/semantics/publishedVersiones
dc.subject.unesco2302.27 Proteínases
dc.subject.unesco3108.05 Hongoses
dc.subject.unesco2414.09 Mohoses
dc.subject.unesco2302 Bioquímicaes
dc.subject.unesco2302.21 Biología Moleculares


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