A kiwellin disarms the metabolic activity of a secreted fungal virulence factor

Nature. 2019 Jan;565(7741):650-653. doi: 10.1038/s41586-018-0857-9. Epub 2019 Jan 16.

Abstract

Fungi-induced plant diseases affect global food security and plant ecology. The biotrophic fungus Ustilago maydis causes smut disease in maize (Zea mays) plants by secreting numerous virulence effectors that reprogram plant metabolism and immune responses1,2. The secreted fungal chorismate mutase Cmu1 presumably affects biosynthesis of the plant immune signal salicylic acid by channelling chorismate into the phenylpropanoid pathway3. Here we show that one of the 20 maize-encoded kiwellins (ZmKWL1) specifically blocks the catalytic activity of Cmu1. ZmKWL1 hinders substrate access to the active site of Cmu1 through intimate interactions involving structural features that are specific to fungal Cmu1 orthologues. Phylogenetic analysis suggests that plant kiwellins have a versatile scaffold that can specifically counteract pathogen effectors such as Cmu1. We reveal the biological activity of a member of the kiwellin family, a widely conserved group of proteins that have previously been recognized only as important human allergens.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Antigens, Plant / metabolism*
  • Chorismate Mutase / antagonists & inhibitors
  • Chorismate Mutase / chemistry
  • Chorismate Mutase / metabolism
  • Chorismic Acid / metabolism
  • Models, Molecular
  • Phylogeny
  • Plant Diseases / immunology
  • Plant Diseases / microbiology*
  • Salicylic Acid / immunology
  • Ustilago / enzymology
  • Ustilago / metabolism*
  • Ustilago / pathogenicity*
  • Virulence Factors / metabolism*
  • Zea mays / immunology
  • Zea mays / metabolism*
  • Zea mays / microbiology*

Substances

  • Antigens, Plant
  • Virulence Factors
  • Chorismate Mutase
  • Chorismic Acid
  • Salicylic Acid