An evolutionarily diverged mitochondrial protein controls biofilm growth and virulence in Candida albicans

PLoS Biol. 2021 Mar 15;19(3):e3000957. doi: 10.1371/journal.pbio.3000957. eCollection 2021 Mar.

Abstract

A forward genetic screening approach identified orf19.2500 as a gene controlling Candida albicans biofilm dispersal and biofilm detachment. Three-dimensional (3D) protein modeling and bioinformatics revealed that orf19.2500 is a conserved mitochondrial protein, structurally similar to, but functionally diverged from, the squalene/phytoene synthases family. The C. albicans orf19.2500 is distinguished by 3 evolutionarily acquired stretches of amino acid inserts, absent from all other eukaryotes except a small number of ascomycete fungi. Biochemical assays showed that orf19.2500 is required for the assembly and activity of the NADH ubiquinone oxidoreductase Complex I (CI) of the respiratory electron transport chain (ETC) and was thereby named NDU1. NDU1 is essential for respiration and growth on alternative carbon sources, important for immune evasion, required for virulence in a mouse model of hematogenously disseminated candidiasis, and for potentiating resistance to antifungal drugs. Our study is the first report on a protein that sets the Candida-like fungi phylogenetically apart from all other eukaryotes, based solely on evolutionary "gain" of new amino acid inserts that are also the functional hub of the protein.

Publication types

  • Research Support, N.I.H., Extramural

MeSH terms

  • Biofilms / growth & development*
  • Candida albicans / genetics*
  • Candida albicans / growth & development
  • Computational Biology / methods
  • Fungal Proteins / metabolism
  • Gene Expression Regulation, Fungal / genetics
  • Genes, Mitochondrial / genetics
  • Genes, Mitochondrial / physiology
  • Mitochondrial Proteins / genetics*
  • Mitochondrial Proteins / metabolism
  • Models, Biological
  • Phylogeny
  • Virulence / genetics

Substances

  • Fungal Proteins
  • Mitochondrial Proteins