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

被引:40
作者
Park, Hee Kuk [1 ]
Lee, Hee Jung [1 ]
Kim, Wonyong [1 ]
机构
[1] Chung Ang Univ, Coll Med, Dept Microbiol & Res, Inst Translat Syst Bi, Seoul 156756, South Korea
关键词
Streptococcus; pneumonia; cpsA; qPCR; TaqMan; CAPSULAR POLYSACCHARIDE; PNEUMOCOCCAL PNEUMONIA; QUANTITATIVE DETECTION; CAMPYLOBACTER-JEJUNI; PANDEMIC INFLUENZA; IDENTIFICATION; GENES; DIAGNOSIS; FRAGMENT; MITIS;
D O I
10.1111/j.1574-6968.2010.02044.x
中图分类号
Q93 [微生物学];
学科分类号
071005 ; 100705 ;
摘要
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 C(T) 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.
引用
收藏
页码:48 / 53
页数:6
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