MICs were determined for each strain using the broth microdilution method described previously116 (link) and adapted to the specific growth conditions of C. acnes. Specifically, C. acnes strains grown on Schaedler agar plates were inoculated into 2 mL of 0.45% saline solution (Air Life, Carefusion, CA, USA) to obtain turbidity of 0.5 ± 0.1 McFarland turbidity standard (approximately 108 CFU/mL). Samples were diluted at 1:100 in BHI, and 100 μL of bacterial suspension, were seeded into a sterile 96-multiwell polystyrene plate containing different antibiotics at variable concentrations (Corning Inc., Corning, NY, USA). Serial two-fold dilutions of the amoxicillin/clavulanic acid, ampicillin, benzylpenicillin, clindamycin, doxycycline, ertapenem, imipenem, meropenem, moxifloxacin, piperacillin/tazobactam, tigecycline, vancomycin were prepared. After the antibiotic treatment, viable cells were determined by plate counting for the CFU/mL determination. The MIC was defined as the lowest concentration of an antibiotic preventing bacterial growth. Experiments were conducted in triplicate.
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