c The strain spa typed as t171 had ST720, a single locus variant of ST121 at the yqil locus. Phenotypic detection of slime producing ability onto Congo red agar The different Congo red agar (CRA) screening methods described in the literature were evaluated [16–18]. The choice of the agar medium, either brain heart infusion or trypticase soy, did not influence the morphology. Selleck SB431542 The majority of S. aureus selleckchem strains (91%) displayed colonies with a normal morphology (smooth round colonies), indicating that most strains

were low-slime producers. Without sucrose, all colonies were colored (bright) red to bordeaux red, irrespective of the agar medium used. Addition of sucrose to both agar media resulted in more dark colonies and made the dry crystalline morphology harder to recognize. With sucrose, all colonies on brain heart infusion agar with Congo red were colored red to bordeaux red, while strains on trypticase soy agar with Congo red displayed mostly purple to black colonies. Nuances in color were not corresponding to differences in morphology. MSSA strains showed more often a deviant, dry crystalline (rough) morphology (slime producing positive) than MRSA isolates, 14% (22 of 156) and 0%, respectively. A significant distinction in slime formation was observed between MRSA and MSSA with MSSA associated MLST CCs, i.e. CC7, CC12,

CC15, CC25 and CC121, and with MRSA associated MLST CCs, i.e. CC1, CC5, CC8, CC22, CC30 and CC45 (P < 0.01), as shown in Figure 1a. MSSA associated with MLST CC121 had the highest prevalence of a deviant morphology, 67% (10 of 15) (Figure 1b). Figure 1 Congo Red Agar screening of S. find more aureus isolates. CRA screening for S. aureus with a dry crystalline colony morphology, which was considered indicative for slime formation. (a) The black bar (not visible, 0%) represents MRSA (n = 72), the dark grey bar represents MSSA with MRSA associated MLST CCs (n = 75) and the light grey bar represents MSSA with MSSA associated MLST CCs (n of = 81). Asterisks

denote statistically significant difference P < 0.01 (a) and statistically significant difference of individual CCs versus all other associated MLST CCs (b) P < 0.01. Detection of biofilm biomass with crystal violet staining Under physiologic glucose (0.1%) concentration, 13% (n = 30) of all strains formed a strong biofilm and all these strains were MRSA or had a MRSA associated MLST CC. MRSA and MSSA with MRSA associated MLST CCs, i.e. CC1, CC5, CC8, CC22, CC30 and CC45, were significantly more capable than MSSA with MSSA associated MLST CCs, i.e. CC7, CC12, CC15, CC25 and CC121, to form strong biofilms in the presence of 0.1% glucose (P < 0.01), but not at glucose concentrations of 0.25% and 0.5% (Figure 2). The higher the glucose concentration, the more strains produced biofilm above the A 590 threshold value and were consequently classified as strong biofilm former. At glucose concentrations of 0.25% and 0.