• Transformed aubergine plants constitutively expressing the Dm-AMP1 antimicrobial defensin (from Dahlia merckii ) were generated and characterized. • Transgenic plants were selected on kanamycin and screened by polymerase chain reaction analysis. The expression of Dm-AMP1 in plant tissues and its release in root exudates were detected by Western blot analyses. Dm-AMP1 localization was performed by immunohistochemical experiments. • Dm-AMP1 expression ranged from 0.2% to 0.48% of total soluble proteins in primary transformants and from 0.16% to 0.66% in F 2 plants. Transformed clones showed resistance to the pathogenic fungus Botrytis cinerea , whose development on leaves was reduced by 36–100%, with respect to controls. The protein was released in root exudates of the transformed plants and was active in reducing the growth of the co-cultured pathogenic fungus Verticillium albo-atrum , whereas it did not interfere with recognition responses and symbiosis establishment by the arbuscular mycorrhizal fungus Glomus mosseae . • Dm-AMP1 transformants may represent a useful model to study the interactions between genetically modified plants and pathogenic fungi or beneficial nontarget microorganisms.

The antifungal Dm-AMP1 protein from Dahlia merkii expressed in Solanum melongena is released in root exudates and differentially affects pathogenic fungi and mycorrhizal symbiosis

TURRINI, ALESSANDRA;RUFFINI CASTIGLIONE, MONICA;GIOVANNETTI, MANUELA
2004-01-01

Abstract

• Transformed aubergine plants constitutively expressing the Dm-AMP1 antimicrobial defensin (from Dahlia merckii ) were generated and characterized. • Transgenic plants were selected on kanamycin and screened by polymerase chain reaction analysis. The expression of Dm-AMP1 in plant tissues and its release in root exudates were detected by Western blot analyses. Dm-AMP1 localization was performed by immunohistochemical experiments. • Dm-AMP1 expression ranged from 0.2% to 0.48% of total soluble proteins in primary transformants and from 0.16% to 0.66% in F 2 plants. Transformed clones showed resistance to the pathogenic fungus Botrytis cinerea , whose development on leaves was reduced by 36–100%, with respect to controls. The protein was released in root exudates of the transformed plants and was active in reducing the growth of the co-cultured pathogenic fungus Verticillium albo-atrum , whereas it did not interfere with recognition responses and symbiosis establishment by the arbuscular mycorrhizal fungus Glomus mosseae . • Dm-AMP1 transformants may represent a useful model to study the interactions between genetically modified plants and pathogenic fungi or beneficial nontarget microorganisms.
2004
Turrini, Alessandra; Sbrana, C.; Pitto, L.; RUFFINI CASTIGLIONE, Monica; Giorgetti, L.; Briganti, R.; Bracci, T.; Evangelista, M.; Nuti, M. P.; Giovannetti, Manuela
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Utilizza questo identificativo per citare o creare un link a questo documento: https://hdl.handle.net/11568/199546
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