In this study, we used an improved lipid extraction method to assess the phospholipid composition of S. aureus and performed molecular genetic analyses to evaluate the role of CL in the resistance of S. aureus to high salinity. Results Staphylococcus aureus phospholipid composition The phospholipid composition of S. aureus grown under various conditions was analyzed. Previous NCT-501 research buy studies with specific S. aureus strains under defined conditions have indicated that the CL level increases as the cells enter stationary phase [22] and when cultured under high-salt conditions [20]. In our initial experiments, the CL level varied among the S. aureus strains tested (Additional file 1, Figure S1), probably because

the cell wall reduced the CL extraction efficiency. Pretreatment with lysostaphin (0.1 mg ml-1 for 3 min at 37°C), which degrades the Gly5-bridge

structures in cell walls [26, 27], increased the CL extraction efficiency without affecting the amounts of other phospholipids extracted (Figure 1). With this method, the CL level did not differ significantly among the strains tested (N315, NKSBm, NKSBv, MRSA No. 7, MRSA No. 33, and COL; Additional file 1, Figure S1). Therefore, cells were treated with lysostaphin prior to lipid extraction in all subsequent experiments. Figure 1 Effect of lysostaphin treatment on CL extraction efficiency. Prior to lipid extraction, cells (N315) were incubated for 3 min at 37°C in the FRAX597 nmr presence of lysostaphin at the indicated concentrations. CL: Cardiolipin. PG: Phosphatidylglycerol. LPG: Lysyl-phosphatidylglycerol. The means and standard deviations of relative signal intensities are shown at the bottom. The phospholipid profile obtained in the

present study (Figure 2) was similar to those reported by others [22, 28]. The signal that intensified as cells tuclazepam entered stationary phase (Figs. 2 and 8) was identified as CL based on molecular mass analysis [28]. However, we did not detect a reproducible increase in the CL level in response to the addition of NaCl (Figure 2). This was the case for S. aureus N315 (Figure 2) and strain 8325-4 and its derivatives RN4220 and SH1000 (data not shown). Figure 2 Phospholipid composition of S. aureus N315 under various growth conditions. Cells were grown in LB containing either 0.1% or 15% NaCl, and harvested during the exponential (exp.) or stationary phase. The means and standard deviations of relative signal intensities are shown at the bottom. Molecular genetic analysis of two cardiolipin synthase homologs Figure 3 shows the phospholipid synthesis pathway, modified from a diagram in the KEGG pathway database [29]. A database search identified two S. aureus genes, SA1155 and SA1891, as homologs of B. Bucladesine chemical structure subtilis clsA (CL synthase gene; one of three paralogous genes, clsA, ywjE, and ywiE) [24, 30]. We constructed single and double mutants of SA1155 and SA1891 genes in S. aureus N315.