Journal: Frontiers in Pharmacology
Article Title: Bakuchiol kills Staphylococcus aureus persisters and potentiates colistin activity against Acinetobacter baumannii persisters
doi: 10.3389/fphar.2025.1592183
Figure Lengend Snippet: Identification of the persister-killing activity of bakuchiol. (A) Screening results from a natural product library. Actively growing MRSA MW2 cells and MRSA MW2 persister cells were treated with 64 μg/mL of each natural product for 4 h. Each treated sample was then inoculated into fresh CaMH and incubated for 18 h, and the optical density at 600 nm (OD 600 ) was measured. Z-scores for regrowth of treated-growing and treated-persister cells were calculated by obtaining the OD 600 value of each sample, subtracting the mean OD 600 of all tested samples, and dividing by the standard deviation (SD) of the OD 600 values from all tested samples. (B) Chemical structure of bakuchiol. (C,D) Viability of MRSA MW2 (C) and VRSA VRS1 (D) persister cells treated with 100× MIC of conventional antibiotics—vancomycin (Van), gentamicin (Gm), ciprofloxacin (Cipro), daptomycin (Dap), and linezolid (Lin)—or the indicated concentrations of bakuchiol (BAK) for 4 h. Data points at the x-axis detection limit represent a CFU count of 2 × 10 2 CFU/mL. Individual data points (n = 3 biologically independent samples) are shown, with error bars representing the mean ± SD.
Article Snippet: The S. aureus strains MW2 BAA-1707 , ATCC 33591, and ATCC 43300; clinical MRSA isolates (HLSA 16278, 17064, 17078, 18380, 18807, 18840, 18883, 18888, 20835, and 21008) ( ); and vancomycin-resistant S. aureus (VRSA) strain VRS1 ( ) were grown in tryptic soy broth (TSB) (BD, Franklin Lakes, NJ, United States).
Techniques: Activity Assay, Incubation, Standard Deviation