parvula Te3T (=DSM 2008=ATCC 10790=JCM 12972) has been published recently (Gronow et al., 2010), which makes this species an attractive model for selleck screening library in-depth analysis of the biology and pathogenesis potential of veillonellae as a group. Another strain, V. parvula PK1910 [formerly Veillonella atypica PK1910 (Hughes et al., 1992), Veillonella spp. PK1910 (Periasamy & Kolenbrander, 2009)], has been the most characterized Veillonella strain in the oral biofilm. The genome of PK1910 was recently sequenced by our group. Analysis of the draft sequence (http://www.oralgen.lanl.gov/) identified many genes homologous to the competence related genes of both gram-positive and gram-negative bacteria

(Qi & Ferretti, 2011), suggesting that this strain might be transformable. The objective of this investigation was to test the transformability of V. parvula PK1910. Using spontaneous and PCR-generated mutations in the rpsL gene, which

confers streptinomycin-resistance, we demonstrated that DNA containing these mutations could be transferred into PK1910 via electroporation and integrated into the chromosome possibly through homologous recombination. To our knowledge, this is the first report of genetic transformation in veillonellae. The bacterial strains and plasmids used in this study are listed in Table 1. Veillonella parvula strain PK1910 was formerly named V. atypica PK1910 or Veillonella spp. PK1910 (Hughes et al., 1992; Periasamy & Kolenbrander, 2009) and is now renamed V. parvula PK1910 based on Ku-0059436 research buy our recent sequence analysis using the rpoB gene (Qi & Ferretti, 2011). Veillonella parvula PK1910 was grown in Todd–Hewitt (TH) broth (Difco) supplemented with 0.6% sodium lactate (THL), or brain heart infusion (BHI) broth (Difco) supplemented with 0.6% sodium lactate (BHIL), or a chemically defined medium (He et al., 2008) without glucose but supplemented with 0.6% sodium lactate and 0.1% peptone (ASSPL). Streptomycin

(Sigma Chemical Co.) was added to the medium at a final concentration of cAMP 1 mg mL−1 for mutant selection. All V. parvula PK1910 cultures were grown anaerobically (85% nitrogen, 5% carbon dioxide, 10% hydrogen) at 37 °C. Escherichia coli cells were grown in Luria–Bertani (LB; Difco) broth with aeration at 37 °C. Escherichia coli strains carrying plasmid was grown in LB containing 100 μg mL−1 ampicillin (Fluka). Veillonella parvula PK1910 overnight culture was plated on THL plates supplemented with 1 mg mL−1 streptomycin and colonies grown on the plates were isolated and purified. Chromosomal DNA was isolated from these mutants, and then the rpsL gene fragment was generated by PCR using primers rpsL-F and rpsL-R (Table 2 and Fig. 1) and sequenced. Veillonella parvula PK1910 cells were grown in THL, BHIL, or ASSPL media to designated growth phases (OD600 nm of 0.15–0.6), and harvested by centrifugation.