延伸因子 Tu 通过介导细菌粘附促进牙周炎的发生。

IF 7.8 1区 生物学 Q1 BIOTECHNOLOGY & APPLIED MICROBIOLOGY
Leyi Xiao, Yingying Pu, Yu Cui, Chen Chen, Qi Xiao, Yulan Wang, Yan Wei, Mengge Feng, Tiange Zhang, Shanyi Yang, Jingxuan Zhou, Yueqi Ni, Jinglun Zhang, Hebin Liao, Jingwen Wu, Yufeng Zhang
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引用次数: 0

摘要

牙周炎是成人牙齿脱落的主要原因,与各种全身性疾病有关,是由龈下菌斑生物膜促进的,链球菌是负责表面粘附的早期定植菌。目前关于链球菌黏附的研究主要集中在细菌表面黏附蛋白与牙齿表面获得的蛋白质膜上,但没有关于牙龈下菌斑整体早期黏附的关键蛋白的报道。在这里,我们发现链球菌EF-Tu的“桶状粘附结构域”促进细胞表面附着,促进生物膜的形成,并有助于牙周炎的发展。在贴壁状态下,EF-Tu通过膜泡从细胞质转运到细胞表面。此外,我们首次发现fda批准的药物simeprevir与EF-Tu的“桶状粘附结构域”结合,并有效抑制蛋白质的表面粘附和分泌途径。西莫普韦显示出抑制牙菌斑形成的能力,并提供预防和治疗牙周炎。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Elongation factor Tu promotes the onset of periodontitis through mediating bacteria adhesion.

Periodontitis, a leading cause of adult tooth loss and linked to various systemic diseases, is promoted by subgingival plaque biofilms, with Streptococci as early colonizers responsible for surface adhesion. Current studies of Streptococci adhesion have focused on bacteria surface adhesins with acquired protein membranes on the tooth surface, yet no critical proteins with implications for the overall early adhesion of subgingival plaque have been reported. Here, we identified that the "Barrel-like adhesion domain" of streptococcal EF-Tu facilitates cell-surface attachment, promotes biofilm formation, and contributes to the development of periodontitis. In the adherent state, EF-Tu is transported from the cytoplasm to the cell surface through membrane vesicles. Furthermore, we first found that simeprevir, an FDA-approved drug, binds to the "Barrel-like adhesion domain" of EF-Tu and effectively inhibits the protein's surface adhesion and secretory pathways. Simeprevir showed the ability to inhibit dental plaque formation and provided prevention and treatments for periodontitis.

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来源期刊
npj Biofilms and Microbiomes
npj Biofilms and Microbiomes Immunology and Microbiology-Microbiology
CiteScore
12.10
自引率
3.30%
发文量
91
审稿时长
9 weeks
期刊介绍: npj Biofilms and Microbiomes is a comprehensive platform that promotes research on biofilms and microbiomes across various scientific disciplines. The journal facilitates cross-disciplinary discussions to enhance our understanding of the biology, ecology, and communal functions of biofilms, populations, and communities. It also focuses on applications in the medical, environmental, and engineering domains. The scope of the journal encompasses all aspects of the field, ranging from cell-cell communication and single cell interactions to the microbiomes of humans, animals, plants, and natural and built environments. The journal also welcomes research on the virome, phageome, mycome, and fungome. It publishes both applied science and theoretical work. As an open access and interdisciplinary journal, its primary goal is to publish significant scientific advancements in microbial biofilms and microbiomes. The journal enables discussions that span multiple disciplines and contributes to our understanding of the social behavior of microbial biofilm populations and communities, and their impact on life, human health, and the environment.
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