Abstract

BackgroundThe widespread occurrence of fungicide resistance in fungal plant pathogens requires the development of new compounds with different mode(s) of action (MOA) to avoid cross resistance. This will require a rapid method to identify MOAs.ResultsHere, gas chromatography–mass spectrometry (GC–MS) based metabolic fingerprinting was used to elucidate the MOAs of fungicides. Botrytis cinerea, an important pathogen of vegetables and flowers, can be inhibited by a wide range of chemical fungicides with different MOAs. A sensitive strain of B. cinerea was exposed to EC50 concentrations of 13 fungicides with different known MOAs and one with unknown MOA. The mycelial extracts were analyzed for their “metabolic fingerprint” using GC–MS. A comparison among the GC–MS vector’ profiles of cultures treated with fungicides were performeded. A model based on hierarchical clustering was established which allowed these antifungal compounds to be distinguished and classified coinciding with their MOAs. Thus, metabolic fingerprinting represents a rapid, convenient, and information-rich method for classifying the MOAs of antifungal substances. The biomarkers of fungicide MOAs were also established by an analysis of variance and included succinate for succinate dehydrogenase inhibitors and cystathionine for methionine synthesis inhibitors. Using the metabolic model and the common perturbation of metabolites, the new fungicide SYP-14288 was identified as having the same MOA as fluazinam.ConclusionThis study provides a comprehensive database of the metabolic perturbations of B. cinerea induced by diverse MOA inhibitors and highlights the utility of metabolic fingerprinting for defining MOAs, which will assist in the development and optimization of new fungicides.

Highlights

  • The widespread occurrence of fungicide resistance in fungal plant pathogens requires the development of new compounds with different mode(s) of action (MOA) to avoid cross resistance

  • Metabolome of B. cinerea The B. cinerea mycelia was grown on PDA plates supplemented individually with 14 fungicides (EC50) and dimethyl sulfoxide (DMSO) (0.1% v/v, control) for 3 days

  • Here, we described a comprehensively and quickly exploring approach for determining the MOAs of unknown antifungals using the microbial metabolic fingerprinting models for fungicides with known MOAs

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Summary

Introduction

The widespread occurrence of fungicide resistance in fungal plant pathogens requires the development of new compounds with different mode(s) of action (MOA) to avoid cross resistance This will require a rapid method to identify MOAs. The fungal pathogen Botrytis cinerea causes serious losses in more than 200 crops worldwide. Comparison of the sequence from a carboxinsensitive Ustilago maydis strain of iron-sulphur protein (Ip) subunit of succinate dehydrogenase (Sdh) with that of the Ip allele from a carboxin -resistant strain revealed a two-base difference between the sequences This mutation led to the substitution of a leucine residue for a histidine residue within the third cysteine-rich cluster of the deduced amino-acid sequence of the Ip allele. Fast, robust, and high-throughput screening techniques are required

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