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Use of Botanicals to Suppress Different Stages of the Life Cycle of Fusarium graminearum.

  • Drakopoulos D Ecological Plant Protection in Arable Crops, Research Division Plant Protection, Agroscope, 8046 Zurich, Switzerland.
  • Luz C Food Chemistry and Toxicology, Faculty of Pharmacy, University of Valencia, 46100 Burjassot, Spain.
  • Torrijos R Food Chemistry and Toxicology, Faculty of Pharmacy, University of Valencia, 46100 Burjassot, Spain.
  • Meca G Food Chemistry and Toxicology, Faculty of Pharmacy, University of Valencia, 46100 Burjassot, Spain.
  • Weber P Ecological Plant Protection in Arable Crops, Research Division Plant Protection, Agroscope, 8046 Zurich, Switzerland.
  • Bänziger I Ecological Plant Protection in Arable Crops, Research Division Plant Protection, Agroscope, 8046 Zurich, Switzerland.
  • Voegele RT Department of Phytopathology, Institute of Phytomedicine, Faculty of Agricultural Sciences, University of Hohenheim, 70599 Stuttgart, Germany.
  • Six J Sustainable Agroecosystems, Institute of Agricultural Sciences, Department of Environmental Systems Science, ETH Zurich, 8092 Zurich, Switzerland.
  • Vogelgsang S Ecological Plant Protection in Arable Crops, Research Division Plant Protection, Agroscope, 8046 Zurich, Switzerland.
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  • 2019-10-11
Published in:
  • Phytopathology. - 2019
Fusarium graminearum
biological control
botanicals
disease control
mycology
Antifungal Agents
Fusarium
Mycotoxins
Plant Diseases
Plant Extracts
Spores, Fungal
English Fusarium head blight (FHB) is one of the most important cereal diseases worldwide, causing yield losses and contamination of harvested products with mycotoxins. Fusarium graminearum is one of the most common FHB-causing species in wheat and barley cropping systems. We assessed the ability of different botanical extracts to suppress essential stages of the fungal life cycle using three strains of F. graminearum (FG0410, FG2113, and FG1145). The botanicals included aqueous extracts from white mustard (Sinapis alba) seed flour (Pure Yellow Mustard [PYM] and Tillecur [Ti]) as well as milled Chinese galls (CG). At 2% concentration (wt/vol), PYM and Ti completely inhibited growth of mycelium of all F. graminearum strains whereas, at 1%, CG reduced the growth by 65 to 83%, depending on the strain. While PYM and Ti reduced the germination of both conidia and ascospores at 2% (wt/vol), CG was only effective in reducing conidia germination. Perithecia formation of FG0410 but not FG2113 was suppressed by all botanicals. Moreover, application of botanicals on mature perithecia led to a two- to fourfold reduction in discharge of ascospores. Using liquid chromatography (LC) with diode array detection, we quantified the principal glucosinolate component sinalbin of PYM and Ti. LC time-of-flight mass spectrometry was used to demonstrate that the bioactive matrix of CG contains different gallotannins as well as gallic and tannic acids. Possible antifungal mechanisms of the botanical matrices are discussed. The results of this study are promising and suggest that PYM, Ti, and CG should be explored further for efficacy at managing FHB.[Formula: see text] Copyright © 2019 The Author(s). This is an open access article distributed under the CC BY-NC-ND 4.0 International license.
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  • English
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https://sonar.ch/global/documents/2964
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