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RecA-based PCR assay for accurate differentiation of Streptococcus pneumoniae from other viridans streptococci.


ABSTRACT: Proper identification of Streptococcus pneumoniae by conventional methods remains problematic. The discriminatory power of the 16S rRNA gene, which can be considered the "gold standard" for molecular identification, is too low to differentiate S. pneumoniae from closely related species such as Streptococcus pseudopneumoniae, Streptococcus mitis, and Streptococcus oralis in the routine clinical laboratory. A 313-bp part of recA was selected on the basis of variability within the S. mitis group, showing <95.8% interspecies homology. In addition, 6 signature nucleotides specific for S. pneumoniae were identified within the 313-bp recA fragment. We show that recA analysis is a useful tool for proper identification to species level within the S. mitis group, in particular, for pneumococci.

SUBMITTER: Zbinden A 

PROVIDER: S-EPMC3043496 | biostudies-literature | 2011 Feb

REPOSITORIES: biostudies-literature

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recA-based PCR assay for accurate differentiation of Streptococcus pneumoniae from other viridans streptococci.

Zbinden A A   Köhler N N   Bloemberg G V GV  

Journal of clinical microbiology 20101208 2


Proper identification of Streptococcus pneumoniae by conventional methods remains problematic. The discriminatory power of the 16S rRNA gene, which can be considered the "gold standard" for molecular identification, is too low to differentiate S. pneumoniae from closely related species such as Streptococcus pseudopneumoniae, Streptococcus mitis, and Streptococcus oralis in the routine clinical laboratory. A 313-bp part of recA was selected on the basis of variability within the S. mitis group, s  ...[more]

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