Role of CgTpo4 in Polyamine and Antimicrobial Peptide Resistance: Determining Virulence in Candida glabrata

Int J Mol Sci. 2021 Jan 29;22(3):1376. doi: 10.3390/ijms22031376.

Abstract

Candida glabrata is an emerging fungal pathogen whose success depends on its ability to resist antifungal drugs but also to thrive against host defenses. In this study, the predicted multidrug transporter CgTpo4 (encoded by ORF CAGL0L10912g) is described as a new determinant of virulence in C. glabrata, using the infection model Galleria mellonella. The CgTPO4 gene was found to be required for the C. glabrata ability to kill G. mellonella. The transporter encoded by this gene is also necessary for antimicrobial peptide (AMP) resistance, specifically against histatin-5. Interestingly, G. mellonella's AMP expression was found to be strongly activated in response to C. glabrata infection, suggesting AMPs are a key antifungal defense. CgTpo4 was also found to be a plasma membrane exporter of polyamines, especially spermidine, suggesting that CgTpo4 is able to export polyamines and AMPs, thus conferring resistance to both stress agents. Altogether, this study presents the polyamine exporter CgTpo4 as a determinant of C. glabrata virulence, which acts by protecting the yeast cells from the overexpression of AMPs, deployed as a host defense mechanism.

Keywords: AMP resistance; Candida glabrata; CgTpo4; Galleria mellonella; polyamine resistance; virulence.

MeSH terms

  • Antifungal Agents / metabolism
  • Antifungal Agents / pharmacology
  • Candida glabrata / drug effects
  • Candida glabrata / genetics*
  • Candida glabrata / metabolism
  • Candida glabrata / pathogenicity
  • Candidiasis / drug therapy
  • Candidiasis / metabolism
  • Candidiasis / microbiology*
  • Drug Resistance, Fungal
  • Fungal Proteins / genetics*
  • Fungal Proteins / metabolism
  • Gene Expression Regulation, Fungal
  • Genes, Fungal
  • Histatins / metabolism
  • Histatins / pharmacology
  • Humans
  • Multidrug Resistance-Associated Proteins / genetics*
  • Multidrug Resistance-Associated Proteins / metabolism
  • Polyamines / metabolism
  • Polyamines / pharmacology*
  • Pore Forming Cytotoxic Proteins / metabolism
  • Pore Forming Cytotoxic Proteins / pharmacology*
  • Virulence

Substances

  • Antifungal Agents
  • Fungal Proteins
  • Histatins
  • Multidrug Resistance-Associated Proteins
  • Polyamines
  • Pore Forming Cytotoxic Proteins