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Ozone-Induced Biochemical and Molecular Changes in Vitis vinifera Leaves and Responses to Botrytis cinerea Infections

To investigate how plants cope with multi-stress conditions, we analyzed the biochemical and molecular changes of Vitis vinifera leaves subjected to single or sequential double stresses (infection by Botrytis cinerea (Bc) and ozone (O(3), 100 ppb for 3 h) treatment). In Bc(+)/O(3)(−) leaves, the hyd...

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Detalles Bibliográficos
Autores principales: Modesti, Margherita, Marchica, Alessandra, Pisuttu, Claudia, Risoli, Samuele, Pellegrini, Elisa, Bellincontro, Andrea, Mencarelli, Fabio, Tonutti, Pietro, Nali, Cristina
Formato: Online Artículo Texto
Lenguaje:English
Publicado: MDPI 2023
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9952442/
https://www.ncbi.nlm.nih.gov/pubmed/36829902
http://dx.doi.org/10.3390/antiox12020343
Descripción
Sumario:To investigate how plants cope with multi-stress conditions, we analyzed the biochemical and molecular changes of Vitis vinifera leaves subjected to single or sequential double stresses (infection by Botrytis cinerea (Bc) and ozone (O(3), 100 ppb for 3 h) treatment). In Bc(+)/O(3)(−) leaves, the hydrogen peroxide (H(2)O(2)) induction (observed at 12 and 24 h from the end of treatment (FET)) triggered a production of ethylene (Et; +35% compared with Bc(−)/O(3)(−) leaves), which was preceded by an increase of salicylic acid (SA; +45%). This result confirms a crosstalk between SA- and Et-related signaling pathways in lesion spread. The ozone induced an early synthesis of Et followed by jasmonic acid (JA) and SA production (about 2-fold higher), where Et and SA signaling triggered reactive oxygen species production by establishing a feedback loop, and JA attenuated this cycle by reducing Et biosynthesis. In Bc(+) + O(3)(+) leaves, Et peaked at 6 and 12 h FET, before SA confirmed a crosstalk between Et- and SA-related signaling pathways in lesion propagation. In O(3)(+) + Bc(+) leaves, the H(2)O(2) induction triggered an accumulation of JA and Et, demonstrating a synergistic action in the regulation of defence reactions. The divergence in these profiles suggests a rather complex network of events in the transcriptional regulation of genes involved in the systemic acquired resistance.