BMC Infectious Diseases (Apr 2010)

The development of a 16S rRNA gene based PCR for the identification of <it>Streptococcus pneumoniae </it>and comparison with four other species specific PCR assays

  • Deschaght Pieter,
  • Alkan Elife,
  • Saerens Bart,
  • De Baere Thierry,
  • Kaijalainen Tarja,
  • Emler Stefan,
  • El Aila Nabil,
  • Verhelst Rita,
  • Vaneechoutte Mario

DOI
https://doi.org/10.1186/1471-2334-10-104
Journal volume & issue
Vol. 10, no. 1
p. 104

Abstract

Read online

Abstract Background Streptococcus pneumoniae is one of the most frequently encountered pathogens in humans but its differentiation from closely related but less pathogenic streptococci remains a challenge. Methods This report describes a newly-developed PCR assay (Spne-PCR), amplifying a 217 bp product of the 16S rRNA gene of S. pneumoniae, and its performance compared to other genotypic and phenotypic tests. Results The new PCR assay designed in this study, proved to be specific at 57°C for S. pneumoniae, not amplifying S. pseudopneumoniae or any other streptococcal strain or any strains from other upper airway pathogenic species. PCR assays (psaA, LytA, ply, spn9802-PCR) were previously described for the specific amplification of S. pneumoniae, but psaA-PCR was the only one found not to cross-react with S. pseudopneumoniae. Conclusion Spne-PCR, developed for this study, and psaA-PCR were the only two assays which did not mis-identify S. pseudopneumoniae as S. pneumoniae. Four other PCR assays and the AccuProbe assay were unable to distinguish between these species.