Bactericidal activity and mechanism of action of copper-sputtered flexible surfaces against multidrug-resistant

Myriam K S Ballo1,2, Sami Rtimi2, Stefano Mancini1

  • 1Department of Fundamental Microbiology, Quartier Unil-Sorge, University of Lausanne, Biophore Building, CH-1015, Lausanne, Switzerland.

Insights

New flexible copper polyester (Cu-PES) surfaces demonstrate rapid antimicrobial activity against multidrug-resistant pathogens. These stable surfaces kill bacteria by disrupting the cell membrane, not via reactive oxygen species.

Area of Science:

  • Materials Science
  • Microbiology
  • Surface Chemistry

Background:

  • Multidrug-resistant (MDR) pathogens pose a significant global health threat.
  • Developing novel antimicrobial surfaces is crucial for infection control.
  • Copper-based materials have shown promise as antimicrobial agents.

Purpose of the Study:

  • To create and characterize flexible copper polyester (Cu-PES) surfaces.
  • To evaluate the antimicrobial efficacy of Cu-PES against a panel of MDR bacteria.
  • To elucidate the mechanism of Cu-PES antimicrobial activity.

Main Methods:

  • Flexible Cu-PES surfaces were fabricated using direct current magnetron sputtering (DCMS).
  • Antimicrobial activity was tested against Gram-positive (MRSA, VRE, MRSE) and Gram-negative (ESBL E. coli, ESBL K. pneumoniae, resistant P. aeruginosa, resistant A. baumannii) MDR strains.
  • Cell viability, membrane integrity, and activity under aerobic/anaerobic conditions were assessed.

Main Results:

  • Cu-PES surfaces exhibited rapid bactericidal activity (≥3 log10 CFU reduction) within 15-30 minutes.
  • Antimicrobial efficacy was maintained under anaerobic conditions and against bacteria with high catalase levels.
  • Killing correlated with loss of cytoplasmic membrane integrity, indicating membrane disruption as the primary mechanism.

Conclusions:

  • Novel, stable, and sustainable antimicrobial Cu-PES surfaces were developed.
  • Cu-PES effectively kills diverse MDR bacteria through disruption of the cytoplasmic membrane.
  • These findings offer new insights into copper-mediated antimicrobial mechanisms for surface applications.

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