Abstract

Fusarium graminearum is a destructive wheat pathogen. No fully resistant cultivars are available. Knowledge concerning the molecular weapons of F. graminearum to achieve infection remains limited. Here, we report that deletion of the putative secondary metabolite biosynthesis gene cluster fg3_54 compromises the pathogen’s ability to infect wheat through cell-to-cell penetration. Ectopic expression of fgm4, a pathway-specific bANK-like regulatory gene, activates the transcription of the fg3_54 cluster in vitro. We identify a linear, C- terminally reduced and d-amino acid residue-rich octapeptide, fusaoctaxin A, as the product of the two nonribosomal peptide synthetases encoded by fg3_54. Chemically-synthesized fusaoctaxin A restores cell-to-cell invasiveness in fg3_54-deleted F. graminearum, and enables colonization of wheat coleoptiles by two Fusarium strains that lack the fg3_54 homolog and are nonpathogenic to wheat. In conclusion, our results identify fusaoctaxin A as a virulence factor required for cell-to-cell invasion of wheat by F. graminearum.

Highlights

  • Fusarium graminearum is a destructive wheat pathogen

  • Using laser microdissection combined with microarray analysis, we have previously identified nrps[5], nrps[9] and six adjacent genes that are located in a 54 kb region and coexpressed during infecting coleoptiles of wheat seedlings[33]

  • We characterized fusaoctaxin A, an unusual non-ribosomal octapeptide that is selectively produced by F. graminearum in planta, which serves as a new virulence factor during wheat infection

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Summary

Introduction

Fusarium graminearum is a destructive wheat pathogen. No fully resistant cultivars are available. Sources for Fusarium head blight resistance are limited, and far only one resistance gene, PFT, has been identified in wheat[6], and no fully resistant cultivars are yet available[1,7]. Graminearum that directly interact with and impact host plant cells remains limited, with only a secreted lipase FGL114 and trichothecene secondary metabolites (deoxynivalenol and nivalenol)[15,16] having been identified to date. As in many other fungi, F. graminearum possesses genes that are involved in secondary metabolite biosynthesis (SMB) These genes are organized into clusters[21], and many of them encode classic SMB-related enzymes such as non-ribosomal peptide synthetases (NRPS), polyketide synthases (PKS), or terpene cyclases (TC). Based on the number of gene clusters identified, F. graminearum has the potential to produce more kinds of secondary metabolites that contribute to virulence

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