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Resumen
Cassava common mosaic virus (CsCMV) is a potexvirus that impairs chloroplast and metabolism, causing significant yield losses to cassava crops. Crop yield depends on diel rhythms, influencing carbon allocation and growth, and sugar signaling also impacting light–dark rhythms. This study aimed to elucidate the early impact of CsCMV infection on diel carbon allocation, metabolism, and defense mechanisms in both source and sink cassava leaves before [ver mas...]
dc.contributor.authorZanini, Andrea Alejandra
dc.contributor.authorDominguez Muñoz, Martin Ceferino
dc.contributor.authorRodriguez, Marianela
dc.date.accessioned2025-01-22T14:33:40Z
dc.date.available2025-01-22T14:33:40Z
dc.date.issued2025-01
dc.identifier.issn0918-9440
dc.identifier.issn1618-0860 (online)
dc.identifier.otherhttps://doi.org/10.1007/s10265-024-01595-4
dc.identifier.urihttp://hdl.handle.net/20.500.12123/21051
dc.identifier.urihttps://link.springer.com/article/10.1007/s10265-024-01595-4
dc.description.abstractCassava common mosaic virus (CsCMV) is a potexvirus that impairs chloroplast and metabolism, causing significant yield losses to cassava crops. Crop yield depends on diel rhythms, influencing carbon allocation and growth, and sugar signaling also impacting light–dark rhythms. This study aimed to elucidate the early impact of CsCMV infection on diel carbon allocation, metabolism, and defense mechanisms in both source and sink cassava leaves before storage root bulking. Soluble sugar and starch concentrations were examined over a 24-h cycle (16:8 photoperiod) in CsCMV-infected plants. The expression of an array of genes—carbohydrate metabolism, SnRK1 activity marker, defense, circadian marker—was analyzed at ZT6, ZT16 and ZT24/ZT0. In CsCMV-infected source leaves, at ZT6, sucrose increased whereas glucose, fructose and sucrose rose at night. An increase in Suc:hexose ratio and upregulation of SnRK1 activity marker genes and PR1 transcripts were found in infected leaves, suggesting a combination of altered carbon metabolism and defense response mechanisms against the viral infection. GIGANTEA, a clock-controlled gene, showed a reduced expression in infected leaves at ZT6 and ZT24/ ZT0, suggesting a circadian phase shift compared with uninfected control plants. Additionally, starch mobilization transcripts were downregulated at ZT24/ZT0, though starch content remained unchanged during the 24-h cycle. In sink leaves, a transient peak of maltose (ZT6) was observed. Our findings suggest that CsCMV disrupts the plant's natural rhythms of sugar metabolism and allocation. Spikes in sucrose levels may serve as infection signals in the internal daily clock of the plant, influencing plant responses during the cassava-CsCMV interaction.es_AR
dc.formatapplication/pdfes_AR
dc.language.isoenges_AR
dc.publisherSpringeres_AR
dc.relationinfo:eu-repograntAgreement/INTA/2019-PD-E4-I085-001/2019-PD-E4-I085-001/AR./Determinación de los mecanismos de resistencia a enfermedades mediante la caracterización de las interacciones moleculares en sistemas planta-patógeno.es_AR
dc.relationinfo:eu-repograntAgreement/INTA/2023-PD-L03-I084, Estreses bióticos y abióticos en plantas. Estudios fisiológicos y patológicos para el diseño de estrategias de mejoramiento y manejoes_AR
dc.rightsinfo:eu-repo/semantics/restrictedAccesses_AR
dc.rights.urihttp://creativecommons.org/licenses/by-nc-sa/4.0/es_AR
dc.sourceJournal of Plant Research 138 : 131–145 (2025)es_AR
dc.subjectMandiocaes_AR
dc.subjectCassavaeng
dc.subjectRelaciones Fuente Sumideroes_AR
dc.subjectSource-sink Relationseng
dc.subjectFotoperiodismoes_AR
dc.subjectPhotoperiodicityeng
dc.subject.otherCsCMVes_AR
dc.subject.otherPlant-virus interactiones_AR
dc.subject.otherSugar Allocationeng
dc.subject.otherSugar Signaleng
dc.titleExploring sugar allocation and metabolic shifts in cassava plants infected with Cassava common mosaic virus (CsCMV) under long-day photoperiod: diel changes in source and sink leaveseng
dc.typeinfo:ar-repo/semantics/artículoes_AR
dc.typeinfo:eu-repo/semantics/articlees_AR
dc.typeinfo:eu-repo/semantics/publishedVersiones_AR
dc.rights.licenseCreative Commons Attribution-NonCommercial-ShareAlike 4.0 International (CC BY-NC-SA 4.0)es_AR
dc.description.origenInstituto de Fisiología y Recursos Genéticos Vegetaleses_AR
dc.description.filFil: Zanini, Andrea Alejandra. Consejo Nacional de Investigaciones Científicas y Técnicas (CONICET). Unidad de Estudios Agropecuarios; Argentinaes_AR
dc.description.filFil: Zanini, Andrea Alejandra. Instituto Nacional de Tecnología Agropecuaria (INTA). Unidad de Estudios Agropecuarios; Argentinaes_AR
dc.description.filFil: Zanini, Andrea Alejandra. Donald Danforth Plant Science Center; Estados Unidoses_AR
dc.description.filFil: Dominguez Muñoz, Martin Ceferino. Instituto Nacional de Tecnología Agropecuaria (INTA). Estación Experimental Agropecuaria Cerro Azul; Argentinaes_AR
dc.description.filFil: Rodriguez, Marianela. Instituto Nacional de Tecnología Agropecuaria (INTA). Unidad de Estudios Agropecuarios; Argentina
dc.description.filFil: Rodriguez, Marianela. Consejo Nacional de Investigaciones Científicas y Técnicas (CONICET). Unidad de Estudios Agropecuarios; Argentina
dc.description.filFil: Rodriguez, Marianela. Instituto Nacional de Tecnología Agropecuaria (INTA). Instituto de Fisiología y Recursos Genéticos Vegetales; Argentina
dc.subtypecientifico


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