aureus, and contributed considerably to biofilm formation in some clinical isolates (Otto, 2008). The dispersal stage involves the overproduction of proteases that are controlled by the quorum-sensing system agr, whereby single cell or cell clusters are detached from biofilms (Boles & Horswill, 2008). Besides, phenol-soluble modulins may also be involved (Otto, 2008). To date, several factors such as glucose (Mack et al., 1992), urea (Hjelm & Lundell-Etherden, 1991), Fe2+ (Deighton & Borland, 1993; Elci et al., 1995), EDTA (Banin et al., 2006), ethanol

(Knobloch et al., 2001), antibiotics (Rachid et al., 2000b; Hoffman et al., 2005; Yakandawala et al., 2007), anaerobiosis (Cramton et al., 2001), osmolarity and temperature (Rachid et al., 2000a), have been reported to affect S. aureus biofilm formation. Glucose plays an inductive role in the transcription of ica, while the detailed mechanism remains unknown selleck compound (Dobinsky et al., 2003). Our study has revealed that the presence of thiols affected the glucose Ribociclib supplier metabolism in S. aureus, and PIA biosynthesis was reduced significantly. Bacterial strains used in this study are listed in Supporting Information, Table S1. For routine cultivation, S. aureus and S. epidermidis strains were grown at 37 °C in tryptone

soy broth (TSB) medium (0.25% glucose, Oxido) with aeration at 37 °C. Bacterial cells at stationary phase were inoculated into 96-well polystyrene culture plates (Corning, Costar) with a dilution of 1 : 200 Molecular motor for a 12-h cultivation to form biofilms as described previously (Lim et al., 2004). The supernatant was removed and the plates were washed twice with distilled water. The biofilms were then fixed and stained with staining buffer containing

2% crystal violet and 4% formaldehyde for 5 min. The stained biofilms were washed again to remove the unbound stain and allowed to dry at room temperature for the determination of A490 nm (ELX800 Universal Microplate Reader, Bio-Tek). Staphylococcus aureus NCTC8325 was grown in TSB medium to stationary phase at 37 °C with shaking. Stationary phase cells (250 μL) were inoculated into 50 mL fresh TSB, TSB supplemented with 10 mM dithiothreitol, TSB supplemented with 20 mM cysteine and TSB supplemented with 40 mM β-mercaptoethanol (BME) respectively. The cell densities were determined by measuring OD600 nm (DU730 Nucleic Acid/Protein Analyzer, Beckman Coulter) per 60 min for 8 h. The primary attachment assay was preformed as described previously (Knobloch et al., 2001). Staphylococcus aureus NCTC8325 was precultivated in TSB, TSB supplemented with 10 mM dithiothreitol or TSB supplemented with 20 mM BME to stationary phase. Bacterial cells were then diluted into the respective medium with appropriate densities in 24-well cell culture plates, and incubated at 37 °C for an hour.