Mass Spectrometry-Based Metabolomics Reveals a Concurrent Action of Several Chemical Mechanisms in Arabidopsis-Fusarium oxysporum Compatible and Incompatible Interactions.
Kourosh HooshmandEnoch Narh KudjordjieMogens NicolaisenOliver FiehnInge S FomsgaardPublished in: Journal of agricultural and food chemistry (2020)
Fusarium oxysporum is a destructive root-infecting plant pathogen that causes significant yield losses in many economically important crop species. Hence, a deeper understanding of pathogen infection strategies is needed. With liquid chromatography-tandem mass spectrometry and gas chromatography-time of flight mass spectrometry platforms, we analyzed the metabolic changes in a time-course experiment with Arabidopsis accessions either resistant (Col-0) or susceptible (Ler-0) to isolates of Fusarium oxysporum forma specialis matthioli infection. We showed a concurrent effect of Fusarium-derived polyols and the mycotoxin beauvericin in the suppression of the immune response of susceptible hosts. A significant increase in oxidized glutathione in the resistant host was probably associated with effective reactive oxygen species-mediated resistance responses. Through a combination of targeted and untargeted metabolomics, we demonstrated the concurrent action of several Arabidopsis defense systems as well as the concurrent action of several virulence systems in the fungal attack of susceptible Arabidopsis.
Keyphrases
- mass spectrometry
- gas chromatography
- transcription factor
- liquid chromatography tandem mass spectrometry
- liquid chromatography
- cell wall
- locally advanced
- simultaneous determination
- high resolution mass spectrometry
- reactive oxygen species
- solid phase extraction
- immune response
- high performance liquid chromatography
- tandem mass spectrometry
- capillary electrophoresis
- plant growth
- gas chromatography mass spectrometry
- high resolution
- escherichia coli
- candida albicans
- squamous cell carcinoma
- climate change
- pseudomonas aeruginosa
- antimicrobial resistance
- staphylococcus aureus
- inflammatory response