Pl. Shewmaker et al., DNA relatedness, phenotypic characteristics, and antimicrobial susceptibilities of Globicatella sanguinis strains, J CLIN MICR, 39(11), 2001, pp. 4052-4057
DNA-DNA reassociation was performed on 15 strains of Globicatella sanguinis
to compare their taxonomic status with phenotypic characterization. All 15
strains selected for DNA-DNA reassociation readily met the criteria for sp
ecies relatedness. The relative binding ratio was 81% or greater at the opt
imal temperature and 76% or greater at the stringent temperature, and the d
ivergence was less than 3% for all strains hybridized with the type strain.
These strains included nine strains from the Centers for Disease Control S
treptococcus Laboratory culture collection that were previously included in
comparative 16S rRNA gene sequencing studies as well as six additional phe
notypically variant isolates. DNA-DNA relatedness was less than 18% at the
optimal reassociation temperature to Aerococcus viridans, Enterococcus aviu
m, and Streptococcus uberis, which are phenotypically similar to G. sanguin
is. This study confirms these Globicatella strains were previously misident
ified as S. uberis or S. uberis-like strains based on biochemical character
istics. The biochemical data from 28 strains was compiled to further define
the phenotypic criteria for identification of this species. A revised desc
ription of the species should be variable reaction for pyrrolidonylarylamid
ase production (75% positive), positive reaction for the bile esculin test
(100%), growth at 45 C (96%), variable reaction for acid production from ar
abinose (45% positive), and negative starch hydrolysis (0% positive). We al
so evaluated four rapid identification systems, the Biomerieux rapid ID32 S
TREP (ID32), the Crystal rapid gram-positive identification (Cry4), the BBL
Crystal gram-positive identification (Cry24), and the Remel IDS RapID STR
(IDS) systems for their ability to identify these strains.