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Journal of Clinical Microbiology, 05 1995, 1215-1222, Vol 33, No. 5
K Kikuchi, T Enari, K Totsuka and K Shimizu
The rapid ID 32 Strep system (bioMerieux, Marcy l'Etoile, France) was
evaluated for its ability to identify 21 species of viridans group
streptococci; results were compared with DNA-DNA hybridization results and
results of conventional physiological tests. A total of 171 strains of the
21 species including 147 clinical strains was analyzed. Of the 156 strains
of species included in the database of this system, 136 strains (87%) were
correctly identified. Incorrect identification occurred for 13 strains
(8%), and no identification was given for 7 strains (5%). It was difficult
to differentiate S. mitis and S. oralis accurately with this system. Of the
17 strains identified as S. mitis by the rapid ID 32 Strep system, the
results of DNA-DNA hybridization were in agreement for only 3 strains. S.
crista and S. parasanguis, which are not included in the database, were
identified as S. mitis or S. sanguis or were not identified, but S.
parasanguis could probably be identified by using the rapid ID 32 Strep
system because the biochemical profile is well characterized for this
species. The rapid ID 32 Strep system can be used to differentiate most
species for which phenotypic characteristics have been described if the
database is revised according to recently reported amended criteria for the
identification of viridans group streptococci. However, identification of a
few species such as S. mitis and S. oralis is problematic with this system.
Copyright © 1995 by the American Society for Microbiology. All rights reserved.
Comparison of phenotypic characteristics, DNA-DNA hybridization results, and results with a commercial rapid biochemical and enzymatic reaction system for identification of viridans group streptococci
Department of Medicine, Tokyo Women's Medical College Hospital, Japan.
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