Potential interactions between vancomycin and meropenem in culture-negative periprosthetic joint infection: an in

Liqin Yao1, Youcai Ma2, Rui Liu3

  • 1Orthopedic Center, First Affiliated Hospital of Xinjiang Medical University, Urumqi, 830054, China.

BMC Microbiology
|April 4, 2025
PubMed
Abstract

Insights

The combination of vancomycin (VAN) and meropenem (MEM) showed antagonistic effects against polymicrobial cultures and biofilms in a culture-negative periprosthetic joint infection (CN-PJI) model. This suggests careful antibiotic selection is crucial for treating these challenging infections.

Area of Science:

  • Infectious Diseases
  • Microbiology
  • Pharmacology

Background:

  • Culture-negative periprosthetic joint infections (CN-PJIs) are a significant clinical challenge.
  • Current treatment often involves antibiotic combinations, but their interactions are not well understood.
  • Investigating antibiotic interactions is crucial for optimizing CN-PJI management.

Purpose of the Study:

  • To evaluate the synergistic and antagonistic effects of vancomycin (VAN) and meropenem (MEM) against common pathogens in an in vitro model of CN-PJI.
  • To assess the impact of VAN and MEM combinations on planktonic and biofilm bacterial growth.

Main Methods:

  • Minimum Inhibitory Concentration (MIC), Minimum Bactericidal Concentration (MBC), Minimum Biofilm Inhibitory Concentration (MBIC), and Minimum Biofilm Eradication Concentration (MBEC) were determined for VAN and MEM.
  • Fractional Inhibitory Concentration (FIC) and Fractional Biofilm Eradication Concentration (FBEC) indices were calculated.
  • Effects were tested on Staphylococcus aureus, Staphylococcus epidermidis, and Escherichia coli, alone and in combination, in planktonic and biofilm states.

Main Results:

  • Meropenem (MEM) demonstrated higher activity than vancomycin (VAN) against planktonic bacteria and biofilms.
  • The VAN and MEM combination showed indifferent effects against individual Staphylococci but antagonistic effects against polymicrobial cultures.
  • In biofilms, the VAN and MEM combination was antagonistic against most tested combinations, particularly those involving Staphylococcus aureus.

Conclusions:

  • The combination of VAN and MEM exhibits antagonistic effects in polymicrobial and biofilm settings relevant to CN-PJI.
  • These findings underscore the importance of considering specific bacterial compositions and growth states when selecting antibiotic regimens for CN-PJIs.
  • Further research into antibiotic interactions is necessary to improve treatment strategies for culture-negative infections.