Abstract

Redox sensing is of primary importance for fungi to cope with oxidant compounds found in their environment. Plant pathogens are particularly subject to the oxidative burst during the primary steps of infection. In the budding yeast Saccharomyces cerevisiae, it is the transcription factor Yap1 that mediates the response to oxidative stress via activation of genes coding for detoxification enzymes. In the cereal pathogen Fusarium graminearum, Fgap1 a homologue of Yap1 was identified and its role was investigated. During infection, this pathogen produces mycotoxins belonging to the trichothecenes family that accumulate in the grains. The global regulation of toxin biosynthesis is not completely understood. However, it is now clearly established that an oxidative stress activates the production of toxins by F. graminearum. The involvement of Fgap1 in this activation was investigated. A deleted mutant and a strain expressing a truncated constitutive form of Fgap1 were constructed. None of the mutants was affected in pathogenicity. The deleted mutant showed higher level of trichothecenes production associated with overexpression of Tri genes. Moreover activation of toxin accumulation in response to oxidative stress was no longer observed. Regarding the mutant with the truncated constitutive form of Fgap1, toxin production was strongly reduced. Expression of oxidative stress response genes was not activated in the deleted mutant and expression of the gene encoding the mitochondrial superoxide dismutase MnSOD1 was up-regulated in the mutant with the truncated constitutive form of Fgap1. Our results demonstrate that Fgap1 plays a key role in the link between oxidative stress response and F. graminearum secondary metabolism.

Highlights

  • Fusarium graminearum is the main causal agent of the Fusarium head blight (FHB), a disease that can affect wheat, barley, rice or maize, and potentially causes important economic losses

  • Fgap1 contains the bZip domain and the c-CRD domain containing the nuclear export signal (NES), essential for ap1-like full functions, and the corresponding nucleic sequence can be used for functional analysis of Fgap1

  • We provide for the first time the functional characterization of Fgap1 in F. graminearum

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Summary

Introduction

Fusarium graminearum (teleomorph Gibberella zeae) is the main causal agent of the Fusarium head blight (FHB), a disease that can affect wheat, barley, rice or maize, and potentially causes important economic losses. The occurrence of FHB is often associated with kernel contamination by mycotoxins that are produced in the field by Fusarium. Among the frequently encountered mycotoxins, type B trichothecenes (TCTB) are predominant [1]. Type B trichothecenes consist of deoxynivalenol (DON) and its acetylated C-3 and C-15 derivatives (3ADON and 15ADON, respectively), as well as nivalenol (NIV) and its C-4 acetylated derivative sometimes called fusarenone X (4ANIV or FX). The presence of these mycotoxins in edible grains represents an important problem of food safety [3]. In Europe, maximum acceptable DON levels in food destined for human consumption were established (EC No1126/2007). Grains exceeding the established limits are not permitted for commercialization for human consumption. The best way to restrict trichothecenes content in food is to limit their biosynthesis by the fungus before harvest

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