The Cryptococcus neoformans MAP kinase Mpk1 regulates cell integrity in response to antifungal drugs and loss of calcineurin function

Mol Microbiol. 2003 Jun;48(5):1377-87. doi: 10.1046/j.1365-2958.2003.03508.x.

Abstract

Cell wall integrity is crucial for fungal growth, development and stress survival. In the model yeast Saccharomyces cerevisiae, the cell integrity Mpk1/Slt2 MAP kinase and calcineurin pathways monitor cell wall integrity and promote cell wall remodelling under stress conditions. We have identified the Cryptococcus neoformans homologue of the S. cerevisiae Mpk1/Slt2 MAP kinase and have characterized its role in the maintenance of cell integrity in response to elevated growth temperature and in the presence of cell wall synthesis inhibitors. C. neoformans Mpk1 is required for growth at 37 degrees C in vitro, and this growth defect is suppressed by osmotic stabilization. C. neoformans mutants lacking Mpk1 are attenuated for virulence in the mouse model of cryptococcosis. Phosphorylation of Mpk1 is induced in response to perturbations of cell wall biosynthesis by the antifungal drugs nikkomycin Z (a chitin synthase inhibitor), caspofungin (a beta-1,3-glucan synthase inhibitor), or FK506 (a calcineurin inhibitor), and mutants lacking Mpk1 display enhanced sensitivity to nikkomycin Z and caspofungin. Lastly, we show that calcineurin and Mpk1 play complementing roles in regulating cell integrity in C. neoformans. Our studies demonstrate that pharmacological inhibition of the cell integrity pathway would enhance the activity of antifungal drugs that target the cell wall.

Publication types

  • Research Support, U.S. Gov't, P.H.S.

MeSH terms

  • Animals
  • Antifungal Agents / pharmacology*
  • Calcineurin / metabolism*
  • Calcineurin Inhibitors
  • Cell Wall / chemistry
  • Cell Wall / drug effects
  • Cell Wall / metabolism*
  • Cryptococcosis / microbiology
  • Cryptococcus neoformans / drug effects*
  • Cryptococcus neoformans / enzymology*
  • Cryptococcus neoformans / growth & development
  • Cryptococcus neoformans / pathogenicity
  • Culture Media
  • Enzyme Inhibitors / pharmacology
  • Female
  • Fungal Proteins / genetics
  • Fungal Proteins / metabolism
  • Gene Expression Regulation, Fungal*
  • Mice
  • Mice, Inbred DBA
  • Mitogen-Activated Protein Kinases / genetics
  • Mitogen-Activated Protein Kinases / metabolism*
  • Saccharomyces cerevisiae Proteins / genetics
  • Temperature
  • Virulence

Substances

  • Antifungal Agents
  • Calcineurin Inhibitors
  • Culture Media
  • Enzyme Inhibitors
  • Fungal Proteins
  • Saccharomyces cerevisiae Proteins
  • Mitogen-Activated Protein Kinases
  • SLT2 protein, S cerevisiae
  • Calcineurin