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The effect of hydrogen peroxide on the viability of tomato cells and of the fungal pathogen Cladosporium fulvum
Institution:1. Departamento de Recursos del Mar, Centro de Investigación y de Estudios Avanzados del Instituto Politécnico Nacional, Unidad Mérida, Km. 6 Antigua Carretera a Progreso, Cordemex, 97310 Mérida, Yucatán, Mexico;2. Oceanography Department and Geochemical and Environmental Research Group, Texas A&M University, 833 Graham Road, College Station, TX 77845, USA;3. Departamento de Ecología, Facultad de Medicina, Veterinaria y Zootecnia, Campus de Ciencias Biológicas y Agropecuarias, Universidad Autónoma de Yucatán, Km 15.5 Carretera Mérida Xmatkuil, CP 97100 Mérida, Yucatán, Mexico;4. Consejo Nacional de Ciencia y Tecnología (CONACYT), Mexico
Abstract:An oxidative burst was previously demonstrated to be induced in tomato plants by race specific elicitors of the fungal pathogen Cladosporium fulvum . The in planta levels of H2O2estimated to occur during elicitor treatment, were compared with the levels required to show toxicity to host cells and to the fungal pathogen. Injection of Cf-9 tomato leaves with 100 m m H2O2caused an insignificant degree of necrosis and 1m H2O2was required to cause complete leaf necrosis comparable to that induced by the AVR9 elicitor. Assays with Cf-5 tomato cell suspensions confirmed the low toxicity of H2O2to tomato cells but, as expected, the addition of Fe2+with H2O2(or with intercellular fluids containing AVR5 elicitor) enhanced cell death as determined by the Evans Blue assay. Germination and germ tube growth of conidia of C. fulvum were significantly retarded by 4–5 m m H2O2, and at higher concentrations, death of germ tubes was observed (ED50=22 m m), as determined by the fluorescein diacetate assay. The addition of Fe2+with H2O2had little effect on fungal growth or viability in vitro . These results suggest that the amount of H2O2accumulating during an elicitor-induced response in leaves may be sufficient to affect fungal colonization but not to affect viability of host cells unless the Fe2+status in the apoplast is in some way altered by the elicitor to facilitate OH.production via the Fenton reaction.
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