FgPEX4 is involved in development, pathogenicity, and cell wall integrity in Fusarium graminearum

Li Zhang1, Lina Wang1, Yuancun Liang2

  • 1Key Laboratory of Agricultural Microbiology, College of Plant Protection, Shandong Agricultural University, Tai'an, 271018, China.

Current Genetics
|January 4, 2019
PubMed

Insights

The FgPEX4 gene is crucial for the development, pathogenicity, and cell wall integrity of Fusarium graminearum. Deleting FgPEX4 impairs fungal growth, toxin production, and defense against oxidative stress.

Area of Science:

  • Fungal Biology
  • Cell Biology
  • Biochemistry

Background:

  • Peroxisomes are vital organelles in eukaryotic cells, performing diverse biological functions.
  • PEX4, a peroxisome assembly protein (peroxin), acts as a ubiquitin-conjugating enzyme.
  • Fusarium graminearum is a significant phytopathogenic fungus responsible for crop diseases and mycotoxin production.

Purpose of the Study:

  • To functionally characterize the role of FgPEX4 in the phytopathogenic fungus Fusarium graminearum.
  • To investigate the impact of FgPEX4 deletion on fungal development, pathogenicity, and cellular processes.

Main Methods:

  • Construction of a FgPEX4 deletion mutant (ΔPEX4) using homologous recombination.
  • Phenotypic analysis of the ΔPEX4 mutant, including growth, conidiation, and perithecia production.
  • Assessment of pathogenicity, deoxynivalenol (DON) production, cell wall integrity, lipid droplet accumulation, and reactive oxygen species (ROS) elimination.
  • Western blot analysis to examine protein phosphorylation (Mgv1).
  • Proteomics analysis to compare protein expression levels between wild-type and ΔPEX4 strains.

Main Results:

  • The ΔPEX4 mutant exhibited reduced mycelial growth, conidiation, and perithecia formation.
  • FgPEX4 deletion led to impaired pathogenicity and significantly reduced deoxynivalenol (DON) production.
  • FgPEX4 is involved in maintaining cell wall integrity, lipid droplet accumulation, and ROS elimination.
  • Western blot showed reduced phosphorylation of Mgv1 in the ΔPEX4 mutant.
  • Proteomics revealed downregulated protein expression in pathways related to biosynthesis, fatty acid metabolism, cell wall synthesis, and redox reactions in ΔPEX4.

Conclusions:

  • FgPEX4 plays a critical role in the development and pathogenicity of Fusarium graminearum.
  • The gene is essential for maintaining cell wall integrity and managing oxidative stress.
  • FgPEX4 influences key metabolic and biosynthetic pathways within the fungus.

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