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Journal of Clinical Microbiology, October 2004, p. 4912-4913, Vol. 42, No. 10
0095-1137/04/$08.00+0 DOI: 10.1128/JCM.42.10.4912-4913.2004
Copyright © 2004, American Society for Microbiology. All Rights Reserved.
Novel Observations of Genotypic and Metabolic Characteristics of Three Subspecies of Streptococcus gallolyticus

LETTER
Streptococcus gallolyticus is often found as a normal member
of the gut microflora of various animals, while it has been
reported to cause mastitis in cattle, septicemia in pigeons,
and meningitis, sepsis, and endocarditis in humans (
2). The
species, which includes strains formerly identified as
Streptococcus bovis biotye I and
S. bovis biotype II/2, can be distinguished
from other related taxa or biotypes (i.e.,
Streptococcus equinus and
S. bovis biotype II/1) based on the results of DNA-DNA reassociation
experiments (
3). Recently, Schlegel et al. (
6) demonstrated
that
S. gallolyticus,
S. bovis biotype II/2,
Streptococcus macedonicus,
and
Streptococcus waius form a single DNA cluster and thus proposed
S. gallolyticus subsp.
gallolyticus subsp. nov.,
S. gallolyticus subsp.
macedonicus subsp. nov., and
S. gallolyticus subsp.
pasteurianus subsp. nov. within this species.
Meanwhile, Poyart et al. (4) demonstrated that a partial sequence of the manganese-dependent superoxide dismutase gene (sodA) provides a useful approach for species differentiation within the so-called S. bovis-Streptococcus equinus group. Consequently, Sasaki et al. (5) has developed a novel PCR-based assay targeting a partial sequence of S. gallolyticus specific sodA for species identification. We therefore performed this PCR assay on type or reference strains of the three subspecies of S. gallolyticus and closely related species, including S. equinus and Streptococcus infantarius. As shown in Table 1, the species-specific PCR product was only detected in the three subspecies, supporting the view of Schlegel et al. (6) that these subspecies forms a distinct single taxon at the species level.
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TABLE 1. Genotypic and metabolic characteristics of strains belonging to three subspecies of S. gallolyticus and its closely related species
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Most, if not all, of the strains belonging to
S. gallolyticus are able to decarboxylate gallate as well as produce tannase,
by which a hydrolyzable tannin (i.e., gallotannin) is hydrolyzed
to release gallic acid, which is subsequently decarboxylated
to pyrogallol (
3). Recently, Chamkha et al. (
1) demonstrated
that
S. gallolyticus ACM 3611
T also decarboxylated other aromatic
compounds, including protocatechuic acid,
p-coumaric acid, caffeic
acid, and ferulic acid. In this context, we examined the metabolism
of these phenolic acids by type strains of the three subspecies
of
S. gallolyticus, their respective reference strains, and
closely related species, including
S. equinus and
S. infantarius.
Tannase and gallate-decarboxylating activities of the strains
were determined by the methodology described previously (
3).
Metabolism of protocatechuic
, p-coumaric, caffeic, and ferulic
acids by the strains were detected spectrophotometrically, as
described by Chamkha et al. (
1). Our results showed that all
S. gallolyticus strains tested, inclusive of the three subspecies
strains, decarboxylated
p-coumaric acid and caffeic acid, while
the closely related species did not decarboxylate any of the
substrates (Table
1). It should also be noted that the strains
belonging to
S. gallolyticus subsp.
macedonicus did not decarboxylate
either protocatechuic acid or ferulic acid, which may prove
to be useful phenotypic characteristics for identification at
the subspecies level.

REFERENCES
1 - Chamkha, M., B. K. C. Patel, A. Traore, J. L. Garcia, and M. Labat. 2002. Isolation from a shea cake digester of a tannin-degrading Streptococcus gallolyticus strain that decarboxylates protocatechuic and hydroxycinnamic acids, and emendation of the species. Int. J. Syst. Evol. Microbiol. 52:939-944.[Abstract]
2 - Facklam, R. 2002. What happened to the streptococci: overview of taxonomic and nomenclature changes. Clin. Microbiol. Rev. 15:613-630.[Abstract/Free Full Text]
3 - Osawa, R., T. Fujisawa, and L. I. Sly. 1995. Streptococcus gallolyticus sp. nov.; gallate degrading organisms formerly assigned to Streptococcus bovis. Syst. Appl. Microbiol. 18:74-78.
4 - Poyart, C., G. Quesne, and P. Trieu-Cuot. 2002. Taxonomic dissection of the Streptococcus bovis group by analysis of manganese-dependent superoxide dismutase gene (sodA) sequences: reclassification of "Streptococcus infantarius subsp. coli" as Streptococcus lutetiensis sp. nov. and of Streptococcus bovis biotype 11.2 as Streptococcus pasteurianus sp. nov. Int. J. Syst. Evol. Microbiol. 52:1247-1255.[Abstract]
5 - Sasaki, E., R. Osawa, Y. Nishitani, and R. A. Whiley. 2004. Development of a diagnostic PCR assay targeting the Mn-dependent superoxide dismutase gene (sodA) for identification of Streptococcus gallolyticus. J. Clin. Microbiol. 42:1360-1362.[Abstract/Free Full Text]
6 - Schlegel, L., F. Grimont, E. Ageron, P. A. D. Grimont, and A. Bouvet. 2003. Reappraisal of the taxonomy of the Streptococcus bovis/Streptococcus equinus complex and related species: description of Streptococcus gallolyticus subsp. gallolyticus subsp. nov., S. gallolyticus subsp. macedonicus subsp. nov. and S. gallolyticus subsp. pasteurianus subsp. nov. Int. J. Syst. Evol. Microbiol. 53:631-645.[Abstract/Free Full Text]
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Ro Osawa* Eiki Sasaki
Department of Bioresource and Agrobiosciences Graduate School of Science and Technology Kobe University Rokko-dai 1-1, Nada-ku Kobe 657-8501 Japan
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* Phone and Fax: 81-78-803-5804, E-mail: osawa{at}ans.kobe-u.ac.jp. |
Journal of Clinical Microbiology, October 2004, p. 4912-4913, Vol. 42, No. 10
0095-1137/04/$08.00+0 DOI: 10.1128/JCM.42.10.4912-4913.2004
Copyright © 2004, American Society for Microbiology. All Rights Reserved.
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