Park Soon-Nang, Lim Yun Kyong, Kook Joong-Ki
Korean Collection for Oral Microbiology and Department of Oral Biochemistry, School of Dentistry, Chosun University, 309 Pilmun-daero, Dong-gu, Gwangju, 501-759, Republic of Korea.
Arch Microbiol. 2014 Sep;196(9):661-6. doi: 10.1007/s00203-014-1007-x. Epub 2014 Jun 19.
In this study, we introduced species-specific quantitative real-time PCR (qPCR) primers designed based on a DNA-dependent RNA polymerase beta-subunit gene for detecting anginosus group streptococci (AGS), Streptococcus anginosus, S. constellatus, and S. intermedius. The specificity of the qPCR primers was confirmed by conventional PCR with the genomic DNAs of 76 strains regarding 44 bacterial species including the type strain for the target species. The standard curves revealed the lower detection limits of these species-specific qPCR primers was 40 fg at below a cycle threshold (CT) value of 35. These results suggest that AGS species-specific qPCR primers are suitable for applications in epidemiological studies associated with infectious diseases related to AGS.
在本研究中,我们引入了基于DNA依赖性RNA聚合酶β亚基基因设计的种特异性定量实时PCR(qPCR)引物,用于检测咽峡炎链球菌群(AGS)、咽峡炎链球菌、星座链球菌和中间链球菌。通过常规PCR,用包括目标菌种模式菌株在内的44种细菌的76株菌株的基因组DNA,证实了qPCR引物的特异性。标准曲线显示,这些种特异性qPCR引物在低于35的循环阈值(CT)值时的最低检测限为40 fg。这些结果表明,AGS种特异性qPCR引物适用于与AGS相关传染病的流行病学研究。