Methods Bacterial strain and cultures A viscous material producing clinical isolate of P. intermedia, which was isolated

from a periodontitis lesion and designated as strain 17 [12], was used in this study. A total of 10 frozen culture stocks of isolated strain 17 were used in this study. Stock cultures of strain 17 in each vial were grown on trypticase soy blood agar plates (BAP) supplemented with 0.5% yeast extract (Difco Laboratories, Detroit, Selleckchem FG4592 MI), hemin (5 mg/l), L-cystine (400 mg/l) and vitamin K1 (10 mg/l) or grown in the enriched-TSB: trypticase soy broth (TSB; BBL Microbiology Systems, Cockeysville, ND) supplemented with 0.5% yeast extract, hemin (5 mg/l), L-cystine (400 mg/l) and vitamin K1 (10 mg/l). Bacterial cultures were grown anaerobically in an anaerobic chamber (ANX-3, Hirasawa, Tokyo, Japan) at 37°C in a 5% CO2, 10% H2, 85% N2 atmosphere. Biofilm phenotype on strain 17 stock cultures The ability to produce viscous materials in culture media and

form meshwork-like structures on cell surfaces were used as Elafibranor price criteria for distinguishing between “”biofilm-forming”" and “”biofilm-non-forming”" as described previously [16]. We first examined whether strain 17 met the criteria for being a biofilm-forming bacterium, since more than a decade has passed when we first described the unique phenotypic characteristic of strain 17 for check details its ability to produce viscous material [12]. Ten culture stocks were plated on BAP respectively and grown for 48 h anaerobically. Single colony from each culture stock was transferred to enriched-TSB and grown for 24 h as the seed culture. One hundred and fifty μl of this seed culture was transferred to enriched-TSB (15 ml) and grown for 48 h. The spent culture medium Forskolin solubility dmso (550 μl) was put into a rotor, and the viscosity was measured as shearing stress between a rotor and a rotor shaft at 50 rpm, 20°C using a rotary viscometer (Toki-sangyo, Tokyo, Japan). To examine cell surface structures, scanning electron microscopy (SEM) was performed. Bacteria grown on BAP for 48 h

were collected on a piece of filter paper (Glass fiber GA55, Toyo Roshi, Tochigi, Japan), fixed with 2% glutaraldehyde in 0.1 M phosphate buffer for 2 h and 1% OsO4 in 0.1 M phosphate buffer for 1 h at 4°C, and dehydrated through an ethanol series and 2-methyl-2-propanol followed by platinum ion coating (E-1030, Hitachi, Tokyo, Japan). Specimens were examined with a scanning electron microscope (S-4800, Hitachi) at an accelerating voltage of 3 kV. During the evaluation for the ability of our stock strain 17 cultures to form biofilms, one of the 10 stocks that we tested was a naturally-occurring variant that lacked the ability to form biofilms. A stock strain, designated as strain 17-2, produced neither viscous materials in culture medium nor cell surface-associated meshwork-like structures was obtained and considered as a biofilm-negative variant.