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Antimicrobial Synergy Testing by the Inkjet Printer-assisted Automated Checkerboard Array and the Manual Time-kill Method
Published on: April 18, 2019
Synergistic antibacterial action of the iron complex and ampicillin against Staphylococcus aureus
Ludmila Kosaristanova1, Martin Rihacek1, Frantiska Sucha1
1Department of Chemistry and Biochemistry, Faculty of AgriSciences, Mendel University in Brno, Brno, Czech Republic.
Objectives:
Resistance to antibiotics among bacteria of clinical importance, including Staphylococcus aureus, is a serious problem worldwide and the search for alternatives is needed. Some metal complexes have antibacterial properties and when combined with antibiotics, they may increase bacterial sensitivity to antimicrobials. In this study, we synthesized the iron complex and tested it in combination with ampicillin (Fe16 + AMP) against S. aureus.
Methods:
An iron complex (Fe16) was synthesized and characterized using spectroscopy methods. Confirmation of the synergistic effect between the iron complex (Fe16) and ampicillin (AMP) was performed using ζ-potential, infrared spectra and FICI index calculated from the minimum inhibitory concentration (MIC) from the checkerboard assay. Cytotoxic properties of combination Fe16 + AMP was evaluated on eukaryotic cell line. Impact of combination Fe16 + AMP on chosen genes of S. aureus were performed by Quantitative Real-Time PCR.
Results:
The MIC of Fe16 + AMP was significantly lower than that of AMP and Fe16 alone. Furthermore, the infrared spectroscopy revealed the change in the ζ-potential of Fe16 + AMP. We demonstrated the ability of Fe16 + AMP to disrupt the bacterial membrane of S. aureus and that likely allowed for better absorption of AMP. In addition, the change in gene expression of bacterial efflux pumps at the sub-inhibitory concentration of AMP suggests an insufficient import of iron into the bacterial cell. At the same time, Fe16 + AMP did not have any cytotoxic effects on keratinocytes.
Conclusions:
Combined Fe16 + AMP therapy demonstrated significant synergistic and antimicrobial effects against S. aureus. This study supports the potential of combination therapy and further research.
Insights
This study shows that combining an iron complex (Fe16) with ampicillin (AMP) effectively kills Staphylococcus aureus. This combination therapy offers a promising new strategy against antibiotic-resistant bacteria.
Area of Science:
- Microbiology
- Materials Science
- Biochemistry
Background:
- Antibiotic resistance in bacteria like Staphylococcus aureus is a global health crisis.
- Metal complexes are being explored as potential antimicrobial agents or adjuncts to existing antibiotics.
- Synergistic effects between metal complexes and antibiotics could enhance bacterial sensitivity to antimicrobial treatments.
Purpose of the Study:
- To synthesize and characterize an iron complex (Fe16).
- To evaluate the synergistic antimicrobial activity of Fe16 in combination with ampicillin (AMP) against S. aureus.
- To investigate the mechanism of action and safety profile of the Fe16 + AMP combination.
Main Methods:
- Synthesis and spectroscopic characterization of the iron complex (Fe16).
- Checkerboard assay to determine the Fractional Inhibitory Concentration Index (FICI) and Minimum Inhibitory Concentration (MIC).
- Evaluation of membrane disruption, gene expression of efflux pumps, and cytotoxicity on keratinocytes.
Main Results:
- The Fe16 + AMP combination exhibited significantly lower MIC values compared to AMP or Fe16 alone.
- Spectroscopic analysis indicated changes in ζ-potential and infrared spectra, suggesting interaction and potential membrane disruption.
- The combination showed no cytotoxicity on eukaryotic cells, while impacting bacterial gene expression related to iron import and efflux pumps.
Conclusions:
- The combined Fe16 + AMP therapy demonstrates significant synergistic and antimicrobial effects against S. aureus.
- Fe16 enhances ampicillin's efficacy, potentially by disrupting the bacterial membrane and improving drug uptake.
- This combination therapy holds promise as a strategy to combat antibiotic resistance, warranting further investigation.
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