The triple mutant PS111 grew very poorly and was hypersusceptible to oxacillin. Complementation of PS111 with any of the three LCP proteins considerably improved growth and increased oxacillin resistance, to different extents: SA2103
reduced sedimentation with increasing efficiency from SA2103 levels of biofilm formation (Fig. 4b and c). The strongest biofilm was produced by SA2103 complementation in strain PS144, followed by complementation with SA0908 and then MsrR. To compare the contribution of the staphylococcal LCP proteins to virulence, single and double mutants were tested in a C. elegans killing assay. Nematode killing was most strongly attenuated in msrR mutants, followed buy Opaganib by sa0908 mutants, while sa2103 deletion had no apparent effect on virulence. In double mutants, sa0908 or sa2103 deletion, combined with msrR deletion, reduced virulence even further (Fig. 5). The Fenbendazole three S. aureus membrane proteins with a conserved extracellular LCP domain clearly play an important role in septum formation and cell division. The deletion of the individual MsrR, SA0908 and SA2103 proteins had small, but distinct effects on growth and cell envelope properties; however, the triple mutant lacking all three proteins was barely viable, growth was severely impaired and temperature sensitive and cells formed large amorphous complexes containing multiple incomplete septa. Phenotypically, the triple mutant cells were similar to those of an S. pneumoniae LytR mutant (Johnsborg & Havarstein, 2009), supporting the hypothesis that LCP genes are essential for optimal, ordered cell division. Optimal cell growth and separation is achieved through the highly coordinated actions of cell wall synthesis and hydrolysis enzymes (Antignac et al., 2007). The extremely low levels of induced autolysis in the triple mutant, indicating impaired murein hydrolase function, correspond with the TEM pictures showing irregular placement of division septa and failure of cell separation. Related posts: