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Macrolide accumulation by Bacteroides fragilis ATCC 25285
1Institute of Anaerobic Bacteriology, Gifu University School of Medicine, Japan.
Antimicrobial Agents and Chemotherapy
|February 1, 1989
Summary
Macrolide antibiotic accumulation in Bacteroides fragilis increases with hydrophobicity, impacting efflux and bacterial susceptibility. This suggests hydrophobic properties drive macrolide uptake in this Gram-negative bacterium.
Area of Science:
- Microbiology
- Pharmacology
- Bacterial Physiology
Background:
- Bacteroides fragilis is a significant Gram-negative bacterium.
- Understanding antibiotic accumulation is crucial for treating infections caused by B. fragilis.
- Macrolide antibiotics are widely used, but their efficacy against certain bacteria can vary.
Purpose of the Study:
- To investigate the accumulation of macrolide antibiotics in Bacteroides fragilis ATCC 25285.
- To determine the relationship between macrolide hydrophobicity and their accumulation, efflux, and antibacterial activity.
- To elucidate the mechanism underlying the susceptibility of B. fragilis to macrolides.
Main Methods:
- Quantification of macrolide antibiotic accumulation in B. fragilis ATCC 25285.
- Measurement of macrolide efflux half-times.
- Determination of Minimum Inhibitory Concentrations (MICs) for different macrolides.
- Correlation analysis between antibiotic hydrophobicity and accumulation/activity.
Main Results:
- Macrolide accumulation in B. fragilis increased with hydrophobicity in the order: erythromycin < josamycin < rokitamycin.
- Efflux half-times of macrolides were prolonged in the same order of increasing hydrophobicity.
- Minimum Inhibitory Concentrations (MICs) of macrolides were correlated with their hydrophobicity.
Conclusions:
- Macrolide antibiotics accumulate in B. fragilis primarily due to their hydrophobic properties.
- Efficient drug accumulation, driven by hydrophobicity, likely contributes to the observed susceptibility of this Gram-negative bacterium to macrolides.
- The findings provide insights into the pharmacokinetics and pharmacodynamics of macrolides in B. fragilis.