vestibularis, is not plausible. Furthermore, the independent colonization

of bovine mammary and human oral mucosae by a putative ancestor originating from a third environment Protein Tyrosine Kinase inhibitor is not compatible with these phylogenies unless we assume two distinct yet closely related streptococcal ancestors; one that independently colonized the two ecosystems yielding S. thermophilus and S. A-1210477 nmr vestibularis on the one hand, and S. salivarius on the other. Alternatively, the direct or indirect invasion of the bovine mammary mucosa by an ancestor of S. vestibularis originating from the human oral cavity would also be compatible with the S. vestibularis/S. thermophilus sister-relationship. Conclusion The phylogenetic analyses presented in the present paper strongly support the S. vestibularis/S. thermophilus sister-relationship and the concomitant early divergence of S. salivarius at the base of the salivarius clade, which is in agreement with previous 16S rDNA/sodA-based phylogenetic inferences [2, 14]. One of the main reasons for conducting the present study was the paucity of phylogenetic studies involving all three species making up the salivarius group. Although IWR-1 a number of studies that included S. salivarius and S. vestibularis have been published, S. thermophilus has been omitted more often than not since it is not retrieved from human clinical isolates.

Since the complete genome sequences of three S. thermophilus strains are now available, it would be interesting to revisit phylogenetic studies that involve different phylogenetic markers and S. salivarius/S. vestibularis but not S. thermophilus to verify whether the addition of S. thermophilus would result in a similar branching order among salivarius streptococci. Methods Source organisms Streptococcus salivarius strains ATCC 7073 and 25975 and Streptococcus vestibularis strain ATCC 49124 were obtained

from the American Type Culture Collection (Manassas, VA, USA). Protein tyrosine phosphatase Streptococcus salivarius strain K12 was obtained from BLIS Technologies Ltd. (Dunedin, New Zealand). Streptococcus salivarius strains CCUG 32452 and 25922 and Streptococcus vestibularis strains CCUG 7215 and 27306 (renamed S. salivarius strains CCUG 7215 and 27306 herein) were obtained from the University of Göteborg Culture Collection (Göteborg, Sweden). Streptococcus salivarius clinical isolates CCRI 17344 and CCRI 17393 and Streptococcus vestibularis clinical isolate CCRI 17387 were obtained from the Centre de Recherche en Infectiologie of the Centre Hospitalier Universitaire de Québec (CHUQ), CHUL Pavilion (Quebec City, QC, Canada). The identity of the S. vestibularis strains was confirmed by comparative growth on TYE medium containing either raffinose or glucose as the sole carbon source. DNA isolation and sequencing Streptococcal strains were grown in TYE-glucose liquid medium as described in Lévesque et al. [23] or on sheep-blood agar medium overnight at 35°C in a 5% CO2 atmosphere.