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Sequetyping: Serotyping Streptococcus pneumoniae by a Single PCR Sequencing Strategy

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DOI

Author(s)

Marcus Leung, Kevin Bryson, Kathrin Freystatter, Bruno Pichon, Giles Edwards, Bambos Charalambous, Stephen Henry Gillespie

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Abstract

The introduction of pneumococcal conjugate vaccines necessitates continued monitoring of circulating strains to assess vaccine efficacy and replacement serotypes. Conventional serological methods are costly, labor-intensive, and prone to misidentification, while current DNA-based methods have limited serotype coverage requiring multiple PCR primers. In this study, a computer algorithm was developed to interrogate the capsulation locus (cps) of vaccine serotypes to locate primer pairs in conserved regions that border variable regions and could differentiate between serotypes. In silico analysis of cps from 92 serotypes indicated that a primer pair spanning the regulatory gene cpsB could putatively amplify 84 serotypes and differentiate 46. This primer set was specific to Streptococcus pneumoniae, with no amplification observed for other species, including S. mitis, S. oralis, and S. pseudopneumoniae. One hundred thirty-eight pneumococcal strains covering 48 serotypes were tested. Of 23 vaccine serotypes included in the study, most (19/22, 86%) were identified correctly at least to the serogroup level, including all of the 13-valent conjugate vaccine and other replacement serotypes. Reproducibility was demonstrated by the correct sequetyping of different strains of a serotype. This novel sequence-based method employing a single PCR primer pair is cost-effective and simple. Furthermore, it has the potential to identify new serotypes that may evolve in the future.
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Details

Original languageEnglish
Pages (from-to)2419-2427
Number of pages9
JournalJournal of Clinical Microbiology
Volume50
Issue number7
DOIs
Publication statusPublished - 2012

    Research areas

  • Diagnosis, serotyping , Streptococcus pneumoniae, MOLECULAR

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