口腔链球菌
轻度链球菌
多重聚合酶链反应
生物
微生物学
肺炎链球菌
多路复用
聚合酶链反应
链球菌
基因
细菌
遗传学
抗生素
作者
Wonyong Kim,Hee Kuk Park,Woo-Jin Hwang,Hyoung‐Shik Shin
摘要
ABSTRACT A multiplex PCR (mPCR) protocol was developed for simultaneous detection of the gyrB gene in Streptococcus pneumoniae , Streptococcus mitis , and Streptococcus oralis , and the specificity was evaluated using 141 coccus strains. Genomic DNAs purified from S. pneumoniae , S. mitis , and S. oralis strains were efficiently detected with size differences, whereas no PCR products were amplified from any of the reference strains tested. A pilot study of 47 human oral swab specimens was conducted in parallel, and the mPCR assay identified S. pneumoniae in 1 sample, S. mitis in 8 samples, and S. oralis in 2 samples, providing a powerful means for characterization at the level of species compared with traditional culture analysis. Our results suggest that the mPCR protocol presented here is a sensitive and promising tool for the rapid detection and discrimination of S. pneumoniae , S. mitis , and S. oralis from clinical specimens.
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