To proactively establish a model system to investigate ramoplanin-resistance mechanisms in S. aureus, Aurora Kinase inhibitor we subjected the NCTC 8325-4 strain to increasing concentrations of ramoplanin, generating strain RRSA16, which had a significantly decreased susceptibility to ramoplanin (Tables 1 and 2). To our knowledge, this is the first report of ramoplanin resistance in clinical or laboratory settings. Ramoplanin treatment is thought to induce lysis by inhibiting the formation of a new cell wall while autolytic enzymes responsible for cell wall turnover remain active, degrading the cell wall. Degradation of the cell wall leads to lysis caused by turgor pressure. When RRSA16 was exposed

to ramoplanin, rapid lysis did not occur (Fig. 2b), likely contributing to the delayed bactericidal effect (Fig. 1b). The Triton X-100-induced autolysis assay demonstrated that autolytic enzymes had decreased activity in RRSA16 compared with its progenitor strain NCTC 8325-4 (Fig. 4). Both the thickened cell wall layer (Fig. 3) and the decreased activity of autolytic enzymes in RRSA16 likely contribute to the observed loss of lysis following ramoplanin treatment and may contribute to the decreased susceptibility of RRSA16 to ramoplanin. However, it is unlikely that decreased autolytic activity was solely responsible for ramoplanin resistance as the R16-18d strain generated

by passage of RRSA16 for 18 days in drug-free media had autolytic

activity similar to that of NCTC 8325-4 (Fig. 4) while its ramoplanin MIC was approximately four times higher than that of NCTC 8325-4 (Table 2). An interesting finding EGFR inhibitors cancer of this study was that RRSA16 possessed a vancomycin MIC of 9 μg mL−1, a level commensurate with VISA. VISA-type-resistant strains display the phenotypes of a thickened cell wall (Hanaki et al., 1998a, b; Cui et al., 2003; Howden et al., 2006), reduced autolytic activity (Pfeltz et al., 2000; Sieradzki & Tomasz, 2003; Howden et al., 2006), reduced peptidoglycan cross-linking and increased production of soluble N-acyl-d-Ala-d-Ala containing Urease peptidoglycan fragments that are ligands for vancomycin (Sieradzki & Tomasz, 1997, 1999; Cui et al., 2003; Sieradzki & Tomasz, 2003; Cui et al., 2006). VISA-type resistance cannot be attributed to the acquisition of a mobile genetic element nor can it be attributed to the mutation of a single gene. Rather, VISA-type resistance arises from multiple mutations in many loci by a gradual adaptive process (Mwangi et al., 2007; Howden et al., 2008; Neoh et al., 2008; Cui et al., 2009). In this study, we have demonstrated that RRSA16 had the VISA phenotypes of reduced autolytic activity (Fig. 4) and a thickened cell wall (Fig. 3). We suspect that increased cell wall material, combined with reduced autolytic enzyme activity, contributed to the increased ramoplanin resistance of RRSA16.