Effect of Antibiotic Exposure on Staphylococcus epidermidis Responsible for Catheter-Related Bacteremia

Cassandra Pouget1, Clotilde Chatre2, Jean-Philippe Lavigne1

  • 1Department of Microbiology and Hospital Hygiene, Bacterial Virulence and Chronic Infections, INSERM U1047, CHU Nîmes Univiversity Montpellier, CEDEX 09, 30029 Nîmes, France.

Insights

Sub-inhibitory antibiotic exposure increased biofilm formation and cross-resistance in Staphylococcus epidermidis strains causing catheter-related bacteremia. This antibiotic exposure modified bacterial pathogenicity and promoted the emergence of resistant bacteria.

Area of Science:

  • Microbiology
  • Infectious Diseases
  • Genomics

Background:

  • Coagulase-negative staphylococci (CoNS), particularly Staphylococcus epidermidis, are significant causes of healthcare-associated infections, especially with indwelling medical devices like catheters.
  • Catheter-related bacteremia (CRB) leads to increased healthcare costs and patient mortality.

Purpose of the Study:

  • To investigate the effects of sub-inhibitory antibiotic concentrations on resistance, fitness, and genome evolution in Staphylococcus epidermidis strains causing CRB.
  • To evaluate the impact of 15-day exposure to ceftobiprole, daptomycin, linezolid, and vancomycin.

Main Methods:

  • Antibiogram testing to assess resistance.
  • Biofilm Ring test® and nematode virulence model to evaluate metabolic adaptation and fitness.
  • Whole-genome sequencing (WGS) to determine genomic changes.
  • Biofilm formation experiments to quantify biofilm development.

Main Results:

  • Staphylococcus epidermidis strains exhibited diverse virulence and biofilm formation capabilities.
  • Antibiotic exposure led to increased biofilm formation, indicating adaptation in bacterial fitness.
  • Antibiotic exposure altered genes associated with resistance, inducing cross-resistance between vancomycin, daptomycin, and ceftobiprole.

Conclusions:

  • Sub-inhibitory antibiotic exposure significantly modifies bacterial pathogenicity and promotes the emergence of resistant Staphylococcus epidermidis strains.
  • This adaptation highlights the potential for increased virulence and resistance in bacteria exposed to low antibiotic concentrations in clinical settings.

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