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Título
Experimental data supporting "Trichoderma controls bacterial blight caused by Xanthomonas axonopodis pv. passiflorae in Passiflora edulis" [Dataset]
Autor(es)
Palabras clave
Antibacterial activity
Antioxidant Enzymes
Indirect biocontrol
Passion fruit
Reactive Oxygen Species
Systemic defense responses
Clasificación UNESCO
2414 Microbiology
2415 Molecular Biology
31 Agricultural sciences
Fecha de publicación
2026
Editor
Universidad de Salamanca
Citación
Brito ND, de Novaes QS, Hermosa R and Rubio MB (2026). "Trichoderma controls bacterial blight caused by Xanthomonas axonopodis pv. passiflorae in Passiflora edulis". [Dataset]. Universidad de Salamanca.
Resumen
[EN]Several Trichoderma species are recognized as biocontrol agents that can enhance plant defenses against a wide range of biotic and abiotic stresses. However, few studies have investigated Trichoderma activity against bacterial pathogens, and the Xanthomonas axonopodis pv. passiflorae (Xap)-Passiflora edulis pathosystem remains largely unexplored. Here, we analyzed the effects of cell-free filtrates from Trichoderma cultures on the growth of Xap. We also investigated the potential of T. asperellum T25 and T. harzianum T146, when applied to the plant growth substrate, to control bacterial blight caused by Xap in P. edulis, as well as the mechanisms underlying systemic defense responses in the host plant. In the absence of the pathogen, strain T25 promoted the growth of P. edulis plants. Fifty-day-old plants grown in substrate treated or untreated with a Trichoderma strain were inoculated or not with Xap, and changes in the expression of marker genes representative of jasmonic acid (JA) biosynthesis (LOX2), salicylic acid (SA)-dependent (PR1), and ethylene (ET)-dependent (PDF1.2) defense pathways were analyzed at 48 h post-inoculation (hpi) and 14 days post-inoculation (dpi). At 14 dpi, H₂O₂ content and the activities of three antioxidant enzymes -superoxide dismutase, peroxidase, and catalase- were also evaluated. Both Trichoderma strains controlled disease symptoms with similar efficacy. However, at the early stage of the P. edulis-Xap interaction, differential expression of SA- and JA-related genes was detected between T25-pretreated and T146-pretreated plants. Furthermore, at the later stage of the interaction (14 dpi), pretreatment with strain T146 increased ROS levels (measured as H₂O₂ content) in response to Xap, whereas the lowest oxidative levels were observed in plants inoculated with the pathogen alone. Our results demonstrate that T. asperellum and T. harzianum effectively control bacterial blight caused by a virulent Xap strain in P. edulis. This dataset contains the raw and processed laboratory data (comprising 6 excel files) corresponding to the experimental assays described in the study.
Descripción
The repository consists of 6 Excel files containing raw laboratory data and 1 README file detailing variable descriptions and experimental conditions
Asociado a la publicación
URI
DOI
10.71636/3gzj-sc30
10.71636/3GZJ-SC30
Tabla de contenidos
Table 1_Xap_growth
Table 2_Plant_height
Table 3_Incidence_Severity
Table 4_qPCR_48hpi
Table 5_qPCR_14dpi
Table 6_Biochemical_assay
Readme_Dataset_document
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Ficheros en el ítem
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In vitro antibacterial assay
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Greenhouse plant height measurements
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Disease incidence and severity
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LOX2 and PR1 expression at 48 hpi
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LOX2 and PR1 expression at 14 dpi
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H2O2, SOD, POD and CAT assays
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Datasets that support the associated research article
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