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环二鸟苷酸(3′-5′-环化二鸟苷酸)对变形链球菌生物膜形成和黏附的影响。

The effect of c-di-GMP (3'-5'-cyclic diguanylic acid) on the biofilm formation and adherence of Streptococcus mutans.

机构信息

Department of Operative Dentistry and Endodontics, School of Stomatology, Fourth Military Medical University, Xi'an 710032, PR China.

出版信息

Microbiol Res. 2010 Feb 28;165(2):87-96. doi: 10.1016/j.micres.2008.10.001. Epub 2009 Jan 30.

Abstract

Depending on a biofilm lifestyle, Streptococcus mutans (S. mutans) is thought to be one of the primary causative agents of dental caries. Biofilm formation and adhesion are crucial physiological functions and virulence factors for S. mutans. Thus, attempts to control the development of dental caries only by inhibiting one of the several virulence factors are not effective. Cyclic diguanylate (c-di-GMP) [bis(3',5')-cyclic diguanylic acid] is a prokaryotic cyclic dinucleotide second messenger that has been implicated in determining the timing and amplitude of complex biological processes from biofilm formation and virulence to photosynthesis. Here, we demonstrate that this signaling molecule also plays a role in the ability of S. mutans to initiate biofilm formation and adhere to tooth surfaces. To test this hypothesis, S. mutans UA159 and its gcp gene knockout mutant were assayed for their ability to initiate biofilm formation and adherence. The spatial distribution and architecture of the biofilms were examined by scanning electron microscopy. These results show that inactivation of the gcp gene resulted in the formation of an abnormal biofilm. We confirmed that c-di-GMP was effective in preventing biofilm formation of S. mutans UA159. We also found that extracellular c-di-GMP inhibited the adherence of S. mutans to tooth surfaces and reduced (>50%) biofilm formation compared to the untreated control. These results indicate that c-di-GMP attenuates the caries-inducing virulence factors of S. mutans. This suggests that c-di-GMP may be used alone or in combination with other antimicrobial agents, and that such a treatment could be developed into a novel method to prevent tooth decay.

摘要

依赖生物膜生活方式,变形链球菌(S. mutans)被认为是龋齿的主要致病因子之一。生物膜形成和黏附是 S. mutans 的关键生理功能和毒力因子。因此,仅通过抑制几种毒力因子之一来尝试控制龋齿的发展是无效的。环二鸟苷酸(c-di-GMP)[双(3',5')-环二鸟苷酸]是一种原核环二核苷酸第二信使,它参与调节从生物膜形成和毒力到光合作用等复杂生物过程的时间和幅度。在这里,我们证明这种信号分子也在 S. mutans 启动生物膜形成和黏附到牙齿表面的能力中发挥作用。为了验证这一假设,我们检测了 S. mutans UA159 及其 gcp 基因敲除突变体启动生物膜形成和黏附的能力。通过扫描电子显微镜检查生物膜的空间分布和结构。这些结果表明,gcp 基因的失活导致了异常生物膜的形成。我们证实 c-di-GMP 可有效阻止 S. mutans UA159 的生物膜形成。我们还发现细胞外 c-di-GMP 抑制了 S. mutans 对牙齿表面的黏附,并与未处理的对照相比,减少了(>50%)生物膜形成。这些结果表明 c-di-GMP 减弱了 S. mutans 的致龋毒力因子。这表明 c-di-GMP 可单独使用或与其他抗菌剂联合使用,并且这种治疗方法可以开发成一种预防龋齿的新方法。

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