Suzuki Nao, Seki Mitsuko, Nakano Yoshio, Kiyoura Yusuke, Maeno Masao, Yamashita Yoshihisa
Department of Oral Medical Science, School of Dentistry, Tomitamachi, Koriyama, Japan.
J Clin Microbiol. 2005 Sep;43(9):4528-34. doi: 10.1128/JCM.43.9.4528-4534.2005.
Two oligonucleotide primer sets for the discrimination of Streptococcus pneumoniae from "pneumococcus-like" oral streptococcal isolates by PCR were developed. Genomic subtractive hybridization was performed to search for differences between Streptococcus pneumoniae strain WU2 and the most closely related oral streptococcus, Streptococcus mitis strain 903. We identified 19 clones that contained S. pneumoniae-specific nucleotide fragments that were absent from the chromosomal DNA of typical laboratory strains of S. mitis and other oral bacteria. Subsequently, oligonucleotide PCR primers for the detection of S. pneumoniae were designed from the sequences of the subtracted DNA fragments, and the specificities of the 19 primer sets were evaluated by PCR using chromosomal DNAs extracted from four S. pneumoniae clinical isolates and from 20 atypical organisms classified as S. mitis or S. oralis, which harbored genes encoding the pneumococcal virulence factors autolysin (lytA) or pneumolysin (ply), as templates. Of the 19 primer sets, two (Spn9802 and Spn9828) did not amplify PCR products from any of the pneumococcus-like streptococcal strains that we examined. The genes containing the Spn9802 and Spn9828 sequences encoded proteins of unknown function that did not correspond to any previously described proteins in other bacteria. These new oligonucleotide primers may be very useful for early and correct diagnosis of S. pneumoniae infections.
开发了两套寡核苷酸引物组,用于通过聚合酶链反应(PCR)从“肺炎球菌样”口腔链球菌分离株中鉴别肺炎链球菌。进行了基因组消减杂交,以寻找肺炎链球菌WU2菌株与最密切相关的口腔链球菌——缓症链球菌903菌株之间的差异。我们鉴定出19个克隆,其包含肺炎链球菌特异性核苷酸片段,而典型的缓症链球菌实验室菌株和其他口腔细菌的染色体DNA中不存在这些片段。随后,根据消减DNA片段的序列设计了用于检测肺炎链球菌的寡核苷酸PCR引物,并使用从4株肺炎链球菌临床分离株以及20株被分类为缓症链球菌或口腔链球菌的非典型菌株中提取的染色体DNA作为模板,通过PCR评估了这19套引物组的特异性,这些非典型菌株含有编码肺炎球菌毒力因子自溶素(lytA)或肺炎溶血素(ply)的基因。在这19套引物组中,两套(Spn9802和Spn9828)未从我们检测的任何肺炎球菌样链球菌菌株中扩增出PCR产物。含有Spn9802和Spn9828序列的基因编码功能未知的蛋白质,这些蛋白质与其他细菌中任何先前描述的蛋白质均不对应。这些新的寡核苷酸引物可能对肺炎链球菌感染的早期和正确诊断非常有用。