Modeling Pseudomonas aeruginosa-Staphylococcus aureus interactions in zebrafish to assess the host inflammatory

Floriane Costes1, Flore Nilly1, Aurélia Rousset2

  • 1Laboratory of Pathogens and Host Immunity (LPHI), CNRS, Inserm, Université de Montpellier, Montpellier, 34095, France.

Scientific Reports
|July 4, 2025
PubMed

Insights

Zebrafish models chronic co-infections by Staphylococcus aureus and Pseudomonas aeruginosa. This study shows zebrafish can model polymicrobial interactions and host immune responses seen in human cystic fibrosis patients.

Area of Science:

  • Microbiology
  • Immunology
  • Infectious Diseases

Background:

  • Polymicrobial infections, particularly Staphylococcus aureus and Pseudomonas aeruginosa co-infections, are common in chronic diseases like cystic fibrosis (CF).
  • Understanding how bacterial interactions (competitive vs. coexistent) influence host response in these chronic infections is crucial.
  • Relevant in vivo models are needed to study these complex polymicrobial dynamics and host immune interactions.

Purpose of the Study:

  • To establish and validate a zebrafish (Danio rerio) co-infection model for studying Staphylococcus aureus and Pseudomonas aeruginosa interactions.
  • To investigate how bacterial interaction states (competitive or coexistent) affect the host innate immune response in vivo.
  • To compare the host response in zebrafish larvae with that observed in human lung epithelial cells.

Main Methods:

  • Developed a wound infection method in zebrafish larvae to model co-infections with P. aeruginosa and S. aureus.
  • Utilized a trio of bacterial strains co-isolated from a cystic fibrosis patient to mimic clinical scenarios.
  • Monitored inflammatory response by measuring cytokine expression at the infection site and in whole larvae using RT-qPCR.

Main Results:

  • The zebrafish co-infection model successfully recapitulated in vitro observed competitive and coexistent bacterial interactions.
  • Monoinfections elicited a stronger inflammatory response with P. aeruginosa compared to S. aureus.
  • Co-infection modulated the inflammatory response, with bacterial interaction states showing a slight impact on cytokine profiles, mirroring human lung cell responses.

Conclusions:

  • Zebrafish embryos provide a relevant and powerful in vivo model for studying persistent polymicrobial co-infections involving P. aeruginosa and S. aureus.
  • This model offers unique opportunities to investigate the host innate immune response dynamics in complex co-infection scenarios.
  • Findings suggest zebrafish models can effectively bridge the gap between in vitro observations and human disease pathology in chronic infections.

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