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出 处:《中华微生物学和免疫学杂志》2010年第3期205-208,共4页Chinese Journal of Microbiology and Immunology
基 金:基金项目:广东省医学科研基金项目(A2008488)
摘 要:目的观察不同浓度蔗糖环境对变形链球菌葡聚糖结合蛋白c编码基因gbpc表达的影响。方法变形链球菌分别在0.5%、1.0%、5.0%蔗糖条件下培养,提取总RNA,逆转录成eDNA,利用TaqMan实时荧光定量PCR技术检测不同环境条件下变形链球菌gbpC基因的表达。结果当蔗糖浓度从0.5%升高至1.0%时变形链球菌gbpc基因表达明显上调(P〈0.05),而5.0%蔗糖较1.0%蔗糖条件下gbpc表达无明显改变(P〉0.05);黏附较强菌株其gbpc基因表达高于黏附较弱菌株,特别是在0.5%和1.0%蔗糖环境中差异具统计学意义(P〈0.05)。结论蔗糖量从0.5%增至1.0%可促进变形链球菌gbpc基因表达,这可能是蔗糖促进变形链球菌黏附的机制之一;gbpC基因的表达量可能与变形链球菌黏附力相关。Objective To assess the influence of concentrations of sucrose on Streptococcus mutans (S. mutans) gbpC expression. Methods Total RNA was extracted from S. mutaus after cultured in 0.5%, 1.0%, 5.0% sucrose and then reversely transcripted to cDNA. By TaqMan RT-RCR technique, we checked gbpC expression. Results Compared with 0.5% sucrose, 1.0% sucrose significantly upregulated gbpC expression(P 〈0. 05 ) ; gbpC expression of more-adherent S. mutans strains was higher than that of less-adherent strains. Conclusion The upregulation of gbpC expression by sucrose may be one of the mechanisms underlying the increased adherence; There might be some correlation between gbpC expression and S. mutaus adherence.
关 键 词:变形链球菌 葡聚糖结合蛋白C 黏附 TaqMan实时荧光定量PCR
分 类 号:R378[医药卫生—病原生物学]
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