Antagonistic effect of Pseudomonas aeruginosa on Candida auris

Ana Beatriz N Macedo1, Daniele de Figuerêdo Silva1, Anthony G J Medeiros1

  • 1Departamento de Microbiologia e Parasitologia, Universidade Federal do Rio Grande do Norte, Natal, Rio Grande do Norte, Brazil.

PubMed
Abstract

Insights

Pseudomonas aeruginosa inhibits Candida auris growth through secreted molecules, a fungistatic effect partially reversed by iron. This interaction is crucial for understanding hospital-acquired infections.

Area of Science:

  • Microbiology
  • Infectious Diseases
  • Medical Mycology

Background:

  • Candida auris and Pseudomonas aeruginosa are significant pathogens in healthcare settings, contributing to hospital-acquired infections (HAIs).
  • These microbes often coexist in similar ecological niches, yet their interspecies communication mechanisms remain poorly understood.
  • Understanding their interactions is vital for developing effective infection control strategies.

Purpose of the Study:

  • To investigate the in vitro interaction between Candida auris and Pseudomonas aeruginosa.
  • To determine the effect of Pseudomonas aeruginosa on Candida auris growth and viability.
  • To explore the role of secreted molecules and iron availability in this interaction.

Main Methods:

  • Co-culture experiments of C. auris and P. aeruginosa in various media with and without iron supplementation.
  • Fluorescence microscopy to assess C. auris viability.
  • Evaluation of cell-free P. aeruginosa supernatants on C. auris growth.

Main Results:

  • P. aeruginosa significantly inhibited C. auris growth in a fungistatic manner, with viability maintained.
  • Inhibition persisted for up to 72 hours and was observed across different media.
  • Iron supplementation partially restored C. auris growth, and cell-free supernatants confirmed the role of secreted molecules.

Conclusions:

  • P. aeruginosa secretes fungistatic molecules that inhibit C. auris growth.
  • Iron availability modulates this inhibitory effect.
  • Findings provide a basis for further research into secreted compounds and clinical implications of co-infections.

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