Figure 8 Transcription of virulence factors. atl, coa, hla, spa and hld transcription was monitored over growth in strains Newman and ΔsecDF. Ethidium bromide-stained 16S rRNA is shown as an indication of RNA loading. Discussion Efflux pumps play an important role in S. aureus resistance, virulence and pathogenicity. Yet the impact of the RND family of efflux pumps in staphylococcal resistance and fitness is still open (reviewed in [41]). To our knowledge, this is the first study

to evaluate their role in S. aureus. We found SecDF to click here contribute probably in part indirectly to resistance against several substances, including β-lactams and glycopeptides, making it an interesting target for increasing the efficacy of these standard antibiotics. In contrast Sa2056 and Sa2339 seemed not to be required for growth and resistance under the conditions tested. Banerjee et al. recently had found a conservative amino

acid mutation in Sa2056 in a high-level β-lactam resistant mecA-negative strain [42]. However in that strain PBP4 and Sa0013 were also mutated and the exact reason for the observed resistance phenotype was not identified. Resistance against cell wall active antibiotics and cell separation is dependent on a tightly balanced regulation of cell wall synthetic and hydrolytic enzymes, including their timely localization to the septum [43, 44]. The amount of PBPs 1-4 and PBP2a was learn more apparently not influenced, suggesting that other factors important for cell division and β-lactam resistance were affected. The increased hydrolytic activity in the secDF mutant may explain

the observed Gemcitabine in vitro differences in cell wall production and separation. Overproduction of a hydrolase has been observed to PF299 mw affect formation of the FtsZ-ring in Mycobacterium tuberculosis [45]. This cytoskeleton structure recruits the other cell division proteins to the site of future cell separation. A similar indirect effect in the secDF mutant might have lead to an incorrect localization of the cell division machinery, including PBPs (for a general review see [46]), thereby causing reduced resistance against the cell wall active antibiotics oxacillin and vancomycin. The difference in Atl processing might have impeded proper cell separation in addition. Like E. coli and B. subtilis secDF mutants [6, 24], the S. aureus secDF mutant displayed a cold-sensitive phenotype. In E. coli and B. subtilis SecDF has furthermore been shown to participate in membrane integration and secretion of proteins [6, 24, 47]. In S. aureus many physiological functions were affected by the secDF deletion. Analysis of the secretion of classical S. aureus virulence factors containing a Sec-type signal peptide revealed a complex picture. Coagulase and proteases were reduced in the supernatant in the secDF mutant.