aureus virulence in silkworms. The LD50 values of the hla-disrupted mutant, hlb-disrupted mutant, hla/hlb double-disrupted mutant, psmα-deleted mutant and psmβ-deleted mutant were similar to those of the Selleck Antiinfection Compound Library parent strain (Table 4). Thus, hla, hlb, psmα and psmβ encoding hemolysins do not contribute to S. aureus virulence in silkworms. In contrast, the LD50 of the agr mutant was 2.5-fold higher than that of the parent strain (Table 4). This confirms previous findings that the agr locus

contributes to S. aureus virulence in silkworms, and suggests that the agr locus functions in silkworms via hla-, hlb-, psmα- and psmβ-independent pathways. Staphylococcus aureus possesses 16 two-component regulatory systems (Cheung et al., 2004). Among them, arlRS and saeRS broadly regulate the expression of virulence genes (Fournier et al., 2001; Liang et al., 2005, 2006). The arlRS-deleted mutant exhibited attenuated virulence in a mouse systemic infection model (Benton et al., 2004). The saeRS-deleted mutant showed attenuated virulence in a mouse pyelonephritis infection model (Liang et al., 2006). We examined whether the arlS Selleck Forskolin and saeS genes of S. aureus contribute to virulence against silkworms. The LD50 values of the arlS- and saeS-disrupted mutants were 2.7- and 1.8-fold higher than

that of the parent strain, respectively (Table 4). This indicates that arlS and saeS contribute to virulence of S. aureus against silkworms. Cell-wall-anchored proteins of S. aureus are reported to contribute to virulence by facilitating bacterial attachment to host tissues or escape from immune systems (Foster 4-Aminobutyrate aminotransferase & Hook, 1998). Sortase A is required for anchoring of various proteins to the cell wall (Mazmanian et al., 1999). A gene-disrupted mutant of srtA encoding sortase A had attenuated virulence in mouse infection models (Table 3) (Jonsson et al., 2002, 2003; Weiss et al., 2004). We tested whether the srtA-disrupted mutant showed decreased virulence in silkworms.

The LD50 of the srtA-disrupted mutant was 3.1-fold higher than that of the parent strain (Table 4). This suggests that the anchoring of cell-wall proteins by sortase A is required for S. aureus virulence in silkworms. Mouse pneumonia (Bubeck Wardenburg et al., 2007) Rabbit corneal infection (O’Callaghan et al., 1997) psmα1 psmα2 psmα3 psmα4 PSMα1, PSMα2, PSMα3, PSMα4 Mouse systemic infection (Wang et al., 2007) Mouse skin infection (Wang et al., 2007) psmβ1 psmβ2 PSMβ1, SMβ2 AgrA, AgrB, AgrC, AgrD, RNAIII SA1842 SA1843 SA1844 Mouse pneumonia (Heyer et al., 2002) Rabbit corneal infection (O’Callaghan et al., 1997) Silkworm (Kaito et al., 2005) C. elegans (Sifri et al., 2003) Manduca sexta (Fleming et al., 2006) NA in Drosophila (Needham et al., 2004) SA1246 SA1247 SA1248 SA0660 SA0661 C. elegans (Bae et al.