华西口腔医学杂志

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不同基因型变异链球菌临床分离株的分离和鉴定

王成龙1  苏东华1  刘佼佼2  储冰峰1  李少华3  夏伟3  罗燕萍4  杨继勇4  丁红梅3  赵强3  邓斌1  席庆1  徐娟1  邵宁生3   

  1. 1.中国人民解放军总医院  口腔科, 北京 100853;2.沈阳军区总医院 口腔科, 沈阳 110840;3.军事医学科学院 基础医学研究所, 北京 100850;4.中国人民解放军总医院 微生物科, 北京 100853
  • 出版日期:2013-02-01 发布日期:2013-02-01
  • 通讯作者: 王成龙,Tel:010-66937964
  • 作者简介:王成龙(1966—),男,安徽人,副教授,博士
  • 基金资助:

    国家自然科学基金资助项目(30772426,81041028)

Isolation and identification of Streptococcus mutans strains with different genotype from clinical samples

Wang Chenglong1, Su Donghua1, Liu Jiaojiao2, Chu Bingfeng1, Li Shaohua3, Xia Wei3, Luo Yanping4, Yang Jiyong4, Ding Hongmei3, Zhao Qiang3, Deng Bin1, Xi Qing1, Xu Juan1, Shao Ningsheng3   

  1. 1. Dept. of Stomatology, Chinese PLA General Hospital, Beijing 100853, China; 2. Dept. of Stomatology, Chinese PLA Shenyang General Hospital, Shenyang 110840, China; 3. Institute of Basic Medical Sciences, Academy of Military Medical Sciences, Beijing 100850, China; 4. Dept. of Microbiology, Chinese PLA General Hospital, Beijing 100853, China
  • Online:2013-02-01 Published:2013-02-01

摘要:

目的 分离鉴定变异链球菌临床分离株。方法  收集高龋患者和无龋健康人口腔中牙菌斑标本进行厌氧培养,通过细菌形态学观察、生物化学鉴定、自动微生物分析系统分析、聚合酶链反应(PCR)扩增变异链球菌基因的特异性片段表面蛋白抗原Ⅰ/Ⅱ(spaP)、葡糖基转移酶B(gtfB)和葡聚糖酶(dexA)以及基因分型等方法对获得的变异 链球菌临床分离株进行鉴定。结果 从32例临床受试者口腔中分离获得46株变异链球菌临床分离株,经生物化学, 自动微生物分析系统,变异链球菌的特异性基因spaP、gtfB和dexA的PCR扩增均鉴定为变异链球菌,基因分型发现 其中5株临床分离株的基因型与其他菌株相同。结论 获得41株不同基因型变异链球菌临床分离株。

关键词: 变异链球菌, 基因型, 分离, 鉴定

Abstract:

Objective  To identify Streptococcus mutans(S. mutans) strains from clinical samples. Methods  Plaque samples from caries-active and caries-free sites on enamel surfaces were obtained and cultivated for S. mutans isolation. Morphology, biochemistry, automatic microorganism analysis system and polymerase chain reaction using primers homo- logous to surface protein antigen Ⅰ/Ⅱ(spaP), glucosyltransferase B(gtfB) and dextranase(dexA) were used to identify S. mutans. Genotype of isolated S. mutans was determined by arbitrarily primed polymerase chain reaction. Results  Forty-six strains of S. mutans were obtained from the 32 subjects and were identified as S. mutans by biochemistry, automatic microorganism analysis system and polymerase chain reaction. Five identical genotypes were found by arbitrarily primed polymerase chain reaction. Conclusion  Forty -one strains of S. mutans with different genotype were obtained from clinical samples.

Key words: Streptococcus mutans, genotype, isolation, identification