et al., 1979;Macfarlane et al., 1985;Ferrer et al., 1995;Hsueh et al., 1995;Green et al., 2001; Yagcı et al., 2000), recent studies have indicated that they are also common inhabitants of soil and water and behave as low-grade opportunistic pathogens (Hugo et al., 2006). A novel bacterial strain, designated MY15 T , was isolated from a saliva sample obtained from an asymptomatic student during a teaching experiment at Weifang Medical University, China. A further attempt to isolate the bacterium from the same student a week later failed. The aim of the present study was to determine the exact taxonomic position of strain MY15T by using a polyphasic taxonomic approach.The saliva sample was diluted with sterile saline (0.9 % NaCl; w/v) and spread onto trypticase soy agar (TSA; Difco) plates that were incubated at 37 u C for 48 h. Strain MY15 T , which produced a yellow to brown diffusible pigment, was purified by streaking three times on TSA. Cultures were maintained on Luria-Bertani (LB) agar For 16S rRNA gene sequencing, cells grown in LB broth at 28 u C for 24 h were harvested by centrifugation. Extraction and purification of total genomic DNA from the cells and PCR amplification of the 16S rRNA gene were performed as described by Jin et al. (2010). The nearly complete 16S rRNA gene sequence (1356 nt) of strain MY15T was submitted to GenBank and EMBL to search for similar sequences using the BLAST algorithm. The identification of phylogenetic neighbours and the calculation of pairwise 16S rRNA gene sequence similarities were achieved using the EzTaxon server (http://www.eztaxon.org/; Chun et al., 2007). Multiple sequence alignment was performed by using CLUSTAL_X 1.8The GenBank/EMBL/DDBJ accession number for 16S rRNA gene sequence of Myroides phaeus sp. nov. MY15T is GU253339.A supplementary figure is available with the online version of this paper.