The transmembrane protein Sho1 cooperates with the mucin Msb2 to regulate invasive growth and plant infection in Fusarium oxysporum

Mol Plant Pathol. 2015 Aug;16(6):593-603. doi: 10.1111/mpp.12217. Epub 2014 Dec 15.

Abstract

In the vascular wilt pathogen Fusarium oxysporum, the mitogen-activated protein kinase (MAPK) Fmk1 is essential for plant infection. The mucin-like membrane protein Msb2 regulates a subset of Fmk1-dependent functions. Here, we examined the role of the tetraspan transmembrane protein Sho1 as an additional regulator of the Fmk1 pathway and determined its genetic interaction with Msb2. Targeted Δsho1 mutants were generated in wild-type and Δmsb2 backgrounds to test possible interactions between the two genes. The mutants were examined for hyphal growth under different stress conditions, phosphorylation of the MAPK Fmk1 and an array of Fmk1-dependent virulence functions. Similar to Msb2, Sho1 was required for the activation of Fmk1 phosphorylation, as well as Fmk1-dependent gene expression and invasive growth functions, including extracellular pectinolytic activity, cellophane penetration, plant tissue colonization and virulence on tomato plants. Δsho1 mutants were hypersensitive to the cell wall-perturbing compound Calcofluor White, and this phenotype was exacerbated in the Δmsb2 Δsho1 double mutant. These results highlight that Sho1 and Msb2 have partially overlapping functions upstream of the Fmk1 MAPK cascade, to promote invasive growth and plant infection, as well as cell wall integrity, in F. oxysporum.

Keywords: Fusarium oxysporum; fungal plant pathogen; invasive growth; mitogen-activated protein kinase; virulence.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Fungal Proteins / metabolism
  • Fungal Proteins / physiology*
  • Fusarium / pathogenicity*
  • Gene Expression Regulation, Fungal
  • Molecular Sequence Data
  • Plant Development
  • Plants / microbiology*
  • Protein Binding
  • Virulence

Substances

  • Fungal Proteins

Associated data

  • GENBANK/NCU08067