利用变形链球菌双组分信号转导系统对龋齿治疗干预的调节作用。

IF 2.9 3区 医学 Q1 DENTISTRY, ORAL SURGERY & MEDICINE
Bingrun Qiu, Yalan Deng, Zhiheng Yi, Yingming Yang, Lei Lei, Tao Hu
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引用次数: 0

摘要

变形链球菌被认为是引起龋齿的主要病原体,具有很强的生物膜形成能力和对环境刺激的反应能力,这是其生存和致龋的必要条件。据报道,变形链球菌中有14个双组分信号转导系统(TCSs)调节广泛的生理过程,如细菌生物膜的形成、耐酸性、能力发展和有毒氧代谢物的抗性。这些系统通过协调对环境挑战的适应性反应共同促进变形链球菌的致病性。其中,VicRK系统是研究最广泛的系统之一,有流行病学证据表明,维克突变与儿童患龋风险增加有关。其他tcs,如ComDE、LiaRS、CiaRH和孤儿反应调节剂GcrR,也有助于致癌性调节。本文综述了tcs在变形链球菌毒力特性中的调控作用,重点介绍了tcs在生物膜形成中的调控作用,强调了它们作为通过生物膜抑制预防龋齿的治疗靶点的潜力。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Harnessing the Regulatory Effects of Streptococcus mutans Two-Component Signal Transduction Systems for Therapeutic Interventions Against Dental Caries.

Streptococcus mutans is considered the main pathogen causing dental caries and has a strong ability to establish biofilms and respond to environmental stimuli, which are essential for its survival and cariogenicity. Fourteen two-component signal transduction systems (TCSs) in S. mutans have been reported to regulate a broad range of physiological processes such as bacterial biofilm formation, acid resistance, competence development, and toxic oxygen metabolite resistance. These systems collectively contribute to the cariogenicity of S. mutans by coordinating adaptive responses to environmental challenges. Among them, the VicRK system has been one of the most extensively studied, with epidemiological evidence linking vicK mutations to increased caries risk in children. Other TCSs, such as ComDE, LiaRS, CiaRH, and the orphan response regulator GcrR, also contribute to cariogenicity regulation. The present review summarizes the regulatory roles of TCSs in virulence traits of S. mutans, with an emphasis on those involved in biofilm formation, which highlights their potential as therapeutic targets to prevent dental caries through biofilm inhibition.

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来源期刊
Molecular Oral Microbiology
Molecular Oral Microbiology DENTISTRY, ORAL SURGERY & MEDICINE-MICROBIOLOGY
CiteScore
6.50
自引率
5.40%
发文量
46
审稿时长
>12 weeks
期刊介绍: Molecular Oral Microbiology publishes high quality research papers and reviews on fundamental or applied molecular studies of microorganisms of the oral cavity and respiratory tract, host-microbe interactions, cellular microbiology, molecular ecology, and immunological studies of oral and respiratory tract infections. Papers describing work in virology, or in immunology unrelated to microbial colonization or infection, will not be acceptable. Studies of the prevalence of organisms or of antimicrobials agents also are not within the scope of the journal. The journal does not publish Short Communications or Letters to the Editor. Molecular Oral Microbiology is published bimonthly.
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