新型变形链球菌生物膜的两阶段扩展支持以eps为目标的早期儿童龋齿预防策略。

IF 7.8 1区 生物学 Q1 BIOTECHNOLOGY & APPLIED MICROBIOLOGY
Jeongmi Moon, Kyoungjin Seo, Jae-Sung Kwon
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引用次数: 0

摘要

幼儿龋病(ECC)影响了全世界近一半的学龄前儿童,其特点是在多颗牙齿上迅速发展。虽然变形链球菌(S. mutans)是龋齿的关键物种,但其快速生物膜扩张的过程尚不清楚。利用模拟口腔环境的气固界面模型,我们发现了变形链球菌生物膜的一种新的扩展。我们的研究结果表明,变形链球菌采用了一种独特的两步扩张策略。通过渗透压,细胞外聚合物质(EPS)传播和运输细菌簇到新的位置。随后,羟基磷灰石表面形成新的菌落。羟基磷灰石的酸中和特性对细菌的生长和定植至关重要。尽管EPS成功扩散,但没有羟基磷灰石的环境无法支持新菌落的形成。这些结果揭示了ECC在富糖环境中快速发展的独特模式,并确立了EPS作为一个有希望的治疗靶点,促进了对龋齿生物膜行为和ECC预防策略的理解。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Novel two-stage expansion of Streptococcus mutans biofilm supports EPS-targeted prevention strategies for early childhood caries.

Early childhood caries (ECC) affects nearly half of preschool children worldwide and characterized by rapid progression across multiple teeth. While Streptococcus mutans (S. mutans) is a keystone species in dental caries, its process for rapid biofilm expansion remains unclear. Using an air-solid interface model simulating the oral environment, we uncovered a novel expansion for S. mutans biofilms. Our findings reveal that S. mutans employs a distinct two-step expansion strategy. Through osmotic pressure, extracellular polymeric substances (EPS) spread and transport bacterial clusters to new sites. Subsequently, the hydroxyapatite surface enables new colony formation. Hydroxyapatite's acid-neutralization properties appear critical for bacterial growth and colonization. Despite successful EPS spreading, environments without hydroxyapatite failed to support new colony formation. These results reveal the unique pattern of rapid ECC progression in sugar-rich environments and establish EPS as a promising therapeutic target, advancing understanding of cariogenic biofilm behavior and preventative strategies for ECC prevention.

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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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