Antibiotics were used at the following concentrations: erythromycin, 10 μg mL−1, and tetracycline, 3 μg mL−1. The sensitivity

check details of P. gingivalis strains to H2O2 was tested as described previously (Henry et al., 2008). Briefly, P. gingivalis strains were grown to the early log phase (OD600 nm∼0.2) in BHI broth. H2O2 at a final concentration of 0.25 mM was then added to the cultures and further incubated at 37 °C for 24 h. The OD600 nm was measured at 3-h intervals over a 24-h period. Cell cultures without H2O2 were used as controls. Long PCR-based fusion of several fragments was performed as described previously (Shevchuk et al., 2004). The primers used in this study are listed in Table 2. One kilobase flanking fragments both upstream and downstream of the target genes were PCR amplified from chromosomal DNA of P. gingivalis W83. The ermF cassette was amplified from the pVA2198 (Fletcher et al., 1995) plasmid with

oligonucleotide primers that contained overlapping nucleotides for the upstream and downstream fragments. These three fragments were fused together using the forward primer of the upstream fragment and the reverse primer of the downstream fragment. The fusion PCR program consisted of 1 cycle of 5 min at 94 °C, followed by 30 cycles of 30 s at 94 °C, 30 s at 55 °C, and 4 min at 68 °C, with a final extension of 5 min at 68 °C. This PCR-fused fragment was used to transform P. gingivalis W83 by electroporation selleck chemical as described previously (Abaibou et al., 2001). The cells were plated on a BHI agar containing 10 μg mL−1 of erythromycin and incubated at 37 °C for 7 days. The correct gene replacement in the erythromycin-resistant mutants was confirmed by colony PCR and DNA sequencing. A DNA fragment containing the PG0162 ORF with an upstream regulatory region was amplified from chromosomal DNA

of P. gingivalis W83 using the primer sets PG0162_Com_F pheromone and PG_0162_Com_R (Table 2). A BamHI restriction site was designed at the 5′ end of both primers to facilitate the subcloning of the PCR fragment. Both pT-COW (Gardner et al., 1996) and the BamHI-digested PCR fragment were ligated together and used to transform Escherichia coli DH5α. The purified recombined plasmid designated pFLL350a was used to transform P. gingivalis FLL350 (PG0162∷ermF) by electroporation. The transformants were selected on BHI agar plates with erythromycin and tetracycline. Hemolytic activity was determined as reported previously (Vanterpool et al., 2004). Briefly, bacterial cells from 24 h cultures were harvested by centrifugation (10 000 g for 10 min), washed three times with phosphate-buffered saline (PBS, 0.147 M NaCl, 0.01 M sodium phosphate, pH 7.4), and then resuspended to a final OD600 nm of 1.5. Sheep erythrocytes (Hemostat Laboratories, Dixon, CA) were harvested by centrifugation (4400 g for 20 min) and washed with PBS until the supernatant was visibly free of hemoglobin pigment.