Research Institute for Translational System Biomics, Chung-Ang University College of Medicine, 221 Heukseok-dong, Dongjak-gu, Seoul 156-756, Republic of Korea.
Department of Microbiology, Chung-Ang University College of Medicine, 221 Heukseok-dong, Dongjak-gu, Seoul 156-756, Republic of Korea.
J Med Microbiol. 2010 Oct;59(Pt 10):1146-1152. doi: 10.1099/jmm.0.017798-0. Epub 2010 Jul 8.
Streptococcus pneumoniae, the aetiological agent of pneumonia and non-gonococcal urethritis, shares a high degree of DNA sequence identity with the viridans group of streptococci, particularly Streptococcus mitis and Streptococcus oralis. Although their clinical and pathological manifestations are different, discrimination between S. pneumoniae and its close viridans cocci relatives is still quite difficult. Suppression subtractive hybridization was performed to identify the genomic differences between S. pneumoniae and S. mitis. Thirty-four resulting S. pneumoniae-specific clones were examined by sequence determination and comparative DNA sequence analysis using blast. S. pneumoniae-specific primers were subsequently designed from one of the clonal DNA sequences containing the cps gene (coding for capsular polysaccharide biosynthesis). The primer specificities were evaluated using 49 viridans streptococci including 26 S. pneumoniae, 54 other streptococci, 14 Lactococcus species, 14 Enterococcus species and three Vagococcus species, and compared with the specificities of previously described autolysin (lytA), pneumolysin (ply), Spn9802 and Spn9828 primers. The newly designed cpsA-specific primer set was highly specific to S. pneumoniae and was even better than the existing primers. These findings may help improve the rapid identification and differentiation of S. pneumoniae from closely related members of the viridans group streptococci.
肺炎链球菌是肺炎和非淋球菌性尿道炎的病原体,与草绿色链球菌群(尤其是缓症链球菌和口腔链球菌)具有高度的 DNA 序列同一性。尽管它们的临床表现和病理表现不同,但肺炎链球菌与其密切相关的草绿色链球菌属之间的鉴别仍然相当困难。采用抑制性消减杂交技术来鉴定肺炎链球菌和缓症链球菌之间的基因组差异。通过序列测定和使用 blast 进行比较 DNA 序列分析,对 34 个产生的肺炎链球菌特异性克隆进行了检查。随后,从包含 cps 基因(编码荚膜多糖生物合成)的一个克隆 DNA 序列中设计了肺炎链球菌特异性引物。使用包括 26 株肺炎链球菌、54 株其他链球菌、14 株乳球菌、14 株肠球菌和 3 株 Vagococcus 在内的 49 株草绿色链球菌对引物特异性进行了评估,并与先前描述的自溶素(lytA)、肺炎球菌溶血素(ply)、Spn9802 和 Spn9828 引物的特异性进行了比较。新设计的 cpsA 特异性引物组对肺炎链球菌具有高度特异性,甚至优于现有的引物。这些发现可能有助于提高从草绿色链球菌群中快速识别和区分肺炎链球菌。