| Literature DB >> 25229648 |
Sakura Ishida1, Le Hong Thuy Tien2, Ro Osawa3, Mari Tohya1, Ryohei Nomoto4, Yoshiaki Kawamura5, Tatsuhumi Takahashi6, Naoya Kikuchi6, Ken Kikuchi7, Tsutomu Sekizaki8.
Abstract
Thirty-five serotypes of Streptococcus suis (serotypes 1-34 and serotype 1/2) have so far been described on the basis of their polysaccharide capsular antigens. However, in the last decade, some serotype reference strains have been reexamined for their taxonomic status, and the reference strains of serotypes 20, 22, 26, 32, 33, and 34 may be different from taxon S. suis. In the present study, we developed a novel PCR method targeting the recombination/repair protein (recN) gene of S. suis, designated recN PCR, which corresponds to the current reclassification of this bacterium. We compared its specificity with other PCR methods for S. suis, and the results obtained confirmed its specificity. In addition, the detection limits of recN PCR were similar among all the reference strains of authentic S. suis, indicating that the recN PCR gave reliable results against bacterial strains and isolates used in this study. Therefore, recN PCR described in the present study will be a useful tool for the identification of authentic S. suis, and can also be used in epidemiological studies on this bacterium.Entities:
Keywords: Diagnosis; PCR assay; Reclassification; Streptococcus suis; recN gene
Mesh:
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Year: 2014 PMID: 25229648 DOI: 10.1016/j.mimet.2014.09.003
Source DB: PubMed Journal: J Microbiol Methods ISSN: 0167-7012 Impact factor: 2.363