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An oxylipin signal confers protection against antifungal echinocandins in pathogenic aspergilli.

Dante G CaliseSung Chul ParkJin Woo BokGustavo Henrique GoldmanNancy P Keller
Published in: Nature communications (2024)
Aspergillus fumigatus is the leading causative agent of life-threatening invasive aspergillosis in immunocompromised individuals. One antifungal class used to treat Aspergillus infections is the fungistatic echinocandins, semisynthetic drugs derived from naturally occurring fungal lipopeptides. By inhibiting beta-1,3-glucan synthesis, echinocandins cause both fungistatic stunting of hyphal growth and repeated fungicidal lysis of apical tip compartments. Here, we uncover an endogenous mechanism of echinocandin tolerance in A. fumigatus whereby the inducible oxylipin signal 5,8-diHODE confers protection against tip lysis via the transcription factor ZfpA. Treatment of A. fumigatus with echinocandins induces 5,8-diHODE synthesis by the fungal oxygenase PpoA in a ZfpA dependent manner resulting in a positive feedback loop. This protective 5,8-diHODE/ZfpA signaling relay is conserved among diverse isolates of A. fumigatus and in two other Aspergillus pathogens. Our findings reveal an oxylipin-directed growth program-possibly arisen through natural encounters with native echinocandin producing fungi-that enables echinocandin tolerance in pathogenic aspergilli.
Keyphrases
  • candida albicans
  • transcription factor
  • cell wall
  • dna binding
  • signaling pathway
  • single cell
  • gene expression
  • multidrug resistant
  • drug induced
  • genome wide identification
  • intensive care unit
  • bacillus subtilis