首页> 外文期刊>Journal of Clinical Microbiology >rpoB Gene Sequence-Based Identification of Aerobic Gram-Positive Cocci of the Genera Streptococcus, Enterococcus, Gemella, Abiotrophia, and Granulicatella
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rpoB Gene Sequence-Based Identification of Aerobic Gram-Positive Cocci of the Genera Streptococcus, Enterococcus, Gemella, Abiotrophia, and Granulicatella

机译:基于rpoB基因序列的链球菌,肠球菌,双歧杆菌,生物富营养菌和颗粒菌属好氧革兰氏阳性球菌的鉴定

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We developed a new molecular tool based on rpoB gene (encoding the beta subunit of RNA polymerase) sequencing to identify streptococci. We first sequenced the complete rpoB gene for Streptococcus anginosus, S. equinus, and Abiotrophia defectiva. Sequences were aligned with these of S. pyogenes, S. agalactiae, and S. pneumoniae available in GenBank. Using an in-house analysis program (SVARAP), we identified a 740-bp variable region surrounded by conserved, 20-bp zones and, by using these conserved zones as PCR primer targets, we amplified and sequenced this variable region in an additional 30 Streptococcus, Enterococcus, Gemella, Granulicatella, and Abiotrophia species. This region exhibited 71.2 to 99.3% interspecies homology. We therefore applied our identification system by PCR amplification and sequencing to a collection of 102 streptococci and 60 bacterial isolates belonging to other genera. Amplicons were obtained in streptococci and Bacillus cereus, and sequencing allowed us to make a correct identification of streptococci. Molecular signatures were determined for the discrimination of closely related species within the S. pneumoniae-S. oralis-S. mitis group and the S. agalactiae-S. difficile group. These signatures allowed us to design a S. pneumoniae-specific PCR and sequencing primer pair.
机译:我们开发了一种基于 rpoB 基因(编码RNA聚合酶的β亚基)的新型分子工具,以鉴定链球菌。我们首先对链球菌Anginosus S的完整 rpoB 基因进行了测序。马科动物缺水牛营养菌。序列与 S的序列比对。化脓 S。无乳杆菌 S。 GenBank中有肺炎。使用内部分析程序(SVARAP),我们确定了一个740 bp可变区,周围有20 bp保守区,并将这些保守区用作PCR引物靶标,我们在另外30个扩增区对该序列进行了测序链球菌肠球菌吉姆拉格兰尼卡特菌厌氧菌。该区域表现出71.2%至99.3%的种间同源性。因此,我们通过PCR扩增和测序将鉴定系统应用于102个链球菌和60个属于其他属的细菌分离株。在链球菌和蜡状芽孢杆菌中获得了扩增子,测序结果使我们能够正确鉴定链球菌。确定分子标记以区分 S中的密切相关物种。肺炎- S。口服- S。 mitis 组和 S。无乳杆菌- S。困难组。这些签名使我们可以设计 S。肺炎链球菌特异性PCR和测序引物对。

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