Fungicide resistance toward fludioxonil conferred by overexpression of the phosphatase gene MoPTP2 in Magnaporthe oryzae

Mol Microbiol. 2019 Mar;111(3):662-677. doi: 10.1111/mmi.14179. Epub 2019 Jan 21.

Abstract

The fungicide fludioxonil causes hyperactivation of the Hog1p MAPK within the high-osmolarity glycerol signaling pathway essential for osmoregulation in pathogenic fungi. The molecular regulation of MoHog1p phosphorylation is not completely understood in pathogenic fungi. Thus, we identified and characterized the putative MoHog1p-interacting phosphatase gene MoPTP2 in the filamentous rice pathogen Magnaporthe oryzae. We found overexpression of MoPTP2 conferred fludioxonil resistance in M. oryzae, whereas the 'loss of function' mutant ΔMoptp2 was more susceptible toward the fungicide. Additionally, quantitative phosphoproteome profiling of MoHog1p phosphorylation revealed lower phosphorylation levels of MoHog1p in the MoPtp2p overexpression mutant compared to the wild-type strain, whereas MoHog1p phosphorylation increased in the ΔMoptp2 mutant. Furthermore, we identified a set of MoHog1p-dependent genes regulated by the MoPtp2p expression level. Our results indicate that the phosphatase MoPtp2p is involved in the regulation of MoHog1p phosphorylation and that overexpression of the gene MoPTP2 is a novel molecular mechanism of fungicide resistance.

MeSH terms

  • Dioxoles / pharmacology*
  • Drug Resistance, Fungal*
  • Fungal Proteins / analysis
  • Fungicides, Industrial / pharmacology*
  • Gene Deletion
  • Gene Expression
  • Magnaporthe / drug effects*
  • Magnaporthe / genetics*
  • Mitogen-Activated Protein Kinases / metabolism*
  • Oryza / microbiology
  • Phosphoproteins / analysis
  • Phosphorylation
  • Plant Diseases / microbiology
  • Protein Processing, Post-Translational
  • Protein Tyrosine Phosphatases / biosynthesis*
  • Proteome / analysis
  • Pyrroles / pharmacology*

Substances

  • Dioxoles
  • Fungal Proteins
  • Fungicides, Industrial
  • Phosphoproteins
  • Proteome
  • Pyrroles
  • Mitogen-Activated Protein Kinases
  • Protein Tyrosine Phosphatases
  • fludioxonil