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Targeting Biofilm Associated Staphylococcus aureus Using Resazurin Based Drug-susceptibility Assay
Published on: May 5, 2016
Synergistic combination of baicalein and rifampicin against Staphylococcus aureus biofilms
Rajeshwari Muniyasamy1, I Manjubala1
1School of Biosciences and Technology, Vellore Institute of Technology, Vellore, India.
Abstract:
Staphylococcus aureus, a Gram-positive bacterium, is a predominant pathogen associated with various infections. The rapid emergence of antibiotic resistance has intensified the challenge of managing fracture-related infections in severe osteoporotic patients. Rifampicin, a potent antimicrobial agent employed against fracture and implant-related infections, necessitates combination therapies due to its susceptibility to antibiotic resistance. In this study, we explored the potential of baicalein, a bioactive flavonoid from Oroxylum indicum and Scutellaria baicalensis, in combination with rifampicin against S. aureus biofilms invitro. The minimum inhibitory concentration of baicalein and rifampicin were determined as 500 μg/mL and 12.5 ng/mL respectively. The synergistic activity of baicalein and rifampicin was determined by the fractional inhibitory concentration index (FICI) using checkerboard assay. The results showed the FICI of baicalein and rifampicin was lesser than 0.5, demonstrating synergistic effect. Furthermore, the efficacy of baicalein and rifampicin, both individually and in combination, was evaluated for biofilm inhibition and eradication. Scanning electron microscopy and confocal laser microscopy also confirmed that the synergistic combinations effectively removed most of the biofilms and partially killed pre-formed biofilms. In conclusion, the findings demonstrate that baicalein is as effective as rifampicin in inhibiting and eradicating S. aureus biofilms. Their combination exhibits synergistic effect, enhancing their bactericidal effect in completely eradicating S. aureus biofilms. The findings of this research underscore the research potential of combining baicalein and rifampicin as a novel therapeutic strategy against S. aureus biofilms, offering a promising direction for future research in the treatment of fracture-related S. aureus infections.
Insights
This study found that baicalein and rifampicin work together synergistically to effectively inhibit and eradicate Staphylococcus aureus biofilms. This combination therapy shows promise for treating biofilm-related infections, especially in antibiotic-resistant cases.
Area of Science:
- Microbiology
- Pharmacology
- Biochemistry
Background:
- Staphylococcus aureus is a major cause of infections, with rising antibiotic resistance complicating treatment.
- Fracture-related infections in osteoporotic patients are particularly challenging to manage.
- Rifampicin is effective against these infections but requires combination therapy to prevent resistance.
Purpose of the Study:
- To investigate the synergistic potential of baicalein and rifampicin against Staphylococcus aureus biofilms in vitro.
- To evaluate the efficacy of this combination in inhibiting and eradicating S. aureus biofilms.
Main Methods:
- Determined minimum inhibitory concentrations (MICs) for baicalein and rifampicin.
- Utilized checkerboard assay to calculate the fractional inhibitory concentration index (FICI) for synergy.
- Employed scanning electron microscopy (SEM) and confocal laser microscopy to assess biofilm inhibition and eradication.
Main Results:
- Baicalein and rifampicin demonstrated synergistic activity with an FICI < 0.5.
- The combination therapy effectively inhibited and eradicated S. aureus biofilms.
- Microscopy confirmed significant biofilm removal and bacterial killing by the synergistic combination.
Conclusions:
- Baicalein exhibits comparable efficacy to rifampicin in inhibiting and eradicating S. aureus biofilms.
- The combination of baicalein and rifampicin shows synergistic effects, enhancing bactericidal activity.
- This combination represents a promising novel therapeutic strategy for S. aureus biofilm infections, particularly in fracture-related contexts.

