首页> 外文期刊>Journal of Indian Society of Pedodontics and Preventive Dentistry >The significance of gtf genes in caries expression: A rapid identification of Streptococcus mutans from dental plaque of child patients
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The significance of gtf genes in caries expression: A rapid identification of Streptococcus mutans from dental plaque of child patients

机译:gtf基因在龋齿表达中的意义:从儿童患者牙菌斑中快速鉴定变形链球菌

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Aim: Rapid phylogenetic and functional gene (gtfB) identification of S. mutans from the dental plaque derived from children. Material and Methods: Dental plaque collected from fifteen patients of age group 7-12 underwent centrifugation followed by genomic DNA extraction for S. mutans. Genomic DNA was processed with S. mutans specific primers in suitable PCR condtions for phylogenetic and functional gene (gtfB) identification. The yield and results were confirmed by agarose gel electrophoresis. Results: 1% agarose gel electrophoresis depicts the positive PCR amplification at 1,485 bp when compared with standard 1 kbp indicating the presence of S. mutans in the test sample. Another PCR reaction was set using gtfB primers specific for S. mutans for functional gene identification. 1.2% agarose gel electrophoresis was done and a positive amplication was observed at 192 bp when compared to 100 bp standards. Conclusion: With the advancement in molecular biology techniques, PCR based identification and quantification of the bacterial load can be done within hours using species-specific primers and DNA probes. Thus, this technique may reduce the laboratory time spend in conventional culture methods, reduces the possibility of colony identification errors and is more sensitive to culture techniques.
机译:目的:从儿童牙菌斑中快速鉴定变形链球菌的系统发育和功能基因(gtfB)。材料和方法:收集15例7-12岁年龄组患者的牙菌斑,然后对其进行离心,然后从基因组DNA中提取变形链球菌。在适当的PCR条件下,用变形链球菌特异性引物处理基因组DNA,以鉴定系统发育和功能基因(gtfB)。琼脂糖凝胶电泳证实了产率和结果。结果:1%琼脂糖凝胶电泳显示与标准1 kbp相比,在1,485 bp处PCR阳性扩增,表明测试样品中存在变形链球菌。使用特异于变形链球菌的gtfB引物设置另一个PCR反应,以进行功能基因鉴定。进行了1.2%琼脂糖凝胶电泳,与100 bp标准液相比,在192 bp处观察到阳性扩增。结论:随着分子生物学技术的发展,可以使用物种特异性引物和DNA探针在数小时内完成基于PCR的细菌载量的鉴定和定量。因此,该技术可以减少传统培养方法中的实验室时间,减少菌落鉴定错误的可能性,并且对培养技术更加敏感。

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