Real-time PCR assays for the detection and quantification of Streptococcus pneumoniae

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Abstract

Streptococcus pneumoniae is the main etiologic agent of pneumonia worldwide. Because the members of the viridans group streptococci share a high degree of DNA sequence homologies, phenotypic and genotypic discriminations of S. pneumoniae from the viridans group are difficult. A quantitative real-time PCR assay targeting the capsular polysaccharide biosynthesis gene (cpsA) was developed as a species-specific detection tool for S. pneumoniae. The specificity was evaluated using genomic DNAs extracted from 135 oral cocci strains. Twenty-seven S. pneumoniae strains tested positive, whereas 108 other strains including Streptococcus pseudopneumoniae, Streptococcus mitis, and Streptococcus oralis did not show a specific signal. The linear regression of standard curves indicated high correlations between the log numbers of S. pneumoniae cells and the CT values (R2=0.99). The minimal limit of detection was 32 fg of purified genomic DNA, equivalent to 14 genomes of S. pneumoniae. This new real-time PCR method may be very useful as a rapid and specific tool for detecting and quantifying S. pneumoniae. © 2010 Federation of European Microbiological Societies Published by Blackwell Publishing Ltd. All rights reserved.

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APA

Park, H. K., Lee, H. J., & Kim, W. (2010). Real-time PCR assays for the detection and quantification of Streptococcus pneumoniae. FEMS Microbiology Letters, 310(1), 48–53. https://doi.org/10.1111/j.1574-6968.2010.02044.x

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