Related Experiment Video
Updated: May 19, 2026

Targeting Biofilm Associated Staphylococcus aureus Using Resazurin Based Drug-susceptibility Assay
Published on: May 5, 2016
Rifampicin fails to eradicate mature biofilm formed by methicillin-resistant Staphylococcus aureus
Keli Cristine Reiter1, Gustavo Enck Sambrano, Bárbara Villa
1Programa de Pós-graduação em Ciências da Saúde, Universidade Federal de Ciências da Saúde de Porto Alegre, Porto Alegre, RS, Brasil. kelicrisr@gmail.com
Introduction:
Antimicrobial activity on biofilms depends on their molecular size, positive charges, permeability coefficient, and bactericidal activity. Vancomycin is the primary choice for methicillin-resistant Staphylococcus aureus (MRSA) infection treatment; rifampicin has interesting antibiofilm properties, but its effectivity remains poorly defined.
Methods:
Rifampicin activity alone and in combination with vancomycin against biofilm-forming MRSA was investigated, using a twofold serial broth microtiter method, biofilm challenge, and bacterial count recovery.
Results:
Minimal inhibitory concentration (MIC) and minimal bactericidal concentration for vancomycin and rifampicin ranged from 0.5 to 1mg/l and 0.008 to 4mg/l, and from 1 to 4mg/l and 0.06 to 32mg/l, respectively. Mature biofilms were submitted to rifampicin and vancomycin exposure, and minimum biofilm eradication concentration ranged from 64 to 32,000 folds and from 32 to 512 folds higher than those for planktonic cells, respectively. Vancomycin (15mg/l) in combination with rifampicin at 6 dilutions higher each isolate MIC did not reach in vitro biofilm eradication but showed biofilm inhibitory capacity (1.43 and 0.56log10 CFU/ml reduction for weak and strong biofilm producers, respectively; p<0.05).
Conclusions:
In our setting, rifampicin alone failed to effectively kill biofilm-forming MRSA, demonstrating stronger inability to eradicate mature biofilm compared with vancomycin.
Insights
Rifampicin showed limited efficacy against biofilm-forming methicillin-resistant Staphylococcus aureus (MRSA). While vancomycin and rifampicin combination inhibited biofilm, neither eradicated mature MRSA biofilms effectively.
Area of Science:
- Microbiology
- Infectious Diseases
- Pharmacology
Background:
- Antimicrobial activity against biofilms is influenced by molecular properties.
- Vancomycin is a standard treatment for methicillin-resistant Staphylococcus aureus (MRSA) infections.
- Rifampicin exhibits potential antibiofilm properties, but its effectiveness requires further definition.
Purpose of the Study:
- To investigate the activity of rifampicin, alone and in combination with vancomycin, against biofilm-forming MRSA.
- To determine the efficacy of these agents in eradicating and inhibiting mature MRSA biofilms.
Main Methods:
- Utilized a twofold serial broth microtiter method for determining antimicrobial concentrations.
- Assessed biofilm challenge and bacterial count recovery to evaluate efficacy.
- Determined Minimum Inhibitory Concentration (MIC), Minimum Bactericidal Concentration (MBC), and Minimum Biofilm Eradication Concentration (MBEC).
Main Results:
- Rifampicin and vancomycin MICs and MBCs were determined for planktonic MRSA.
- MBEC values for mature biofilms were significantly higher (64 to 32,000-fold for rifampicin, 32 to 512-fold for vancomycin) compared to planktonic cells.
- Vancomycin combined with rifampicin demonstrated biofilm inhibitory capacity, reducing bacterial load (1.43 and 0.56 log10 CFU/ml for weak and strong biofilm producers, respectively), but did not achieve in vitro eradication.
Conclusions:
- Rifampicin alone was ineffective in killing biofilm-forming MRSA in this study.
- Rifampicin demonstrated a lower ability to eradicate mature MRSA biofilms compared to vancomycin.
- Combined vancomycin and rifampicin showed biofilm inhibition but not complete eradication of mature MRSA biofilms.
Related Concept Videos
Mechanism of Antibiotic Resistance in MRSA
Clinical Significance of Antibiotic Resistance
Inhibitors of Bacterial Protein Synthesis
Development of Antibiotic Resistance
