Biotin Limitation Attenuates Streptococcus mutans Cariogenicity by Disrupting Metabolic Flux and Virulence Pathways.

IF 2.6 2区 医学 Q1 DENTISTRY, ORAL SURGERY & MEDICINE
Caries Research Pub Date : 2025-10-06 DOI:10.1159/000548822
Zirui Qin, Zhenyu Yang, Yi Zhang, Linlong Qi, Yan Peng, Shuli Deng, Yuan Wang
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引用次数: 0

Abstract

Introduction: Our previous metagenomic analysis revealed higher frequencies of biotin-related genes (i.e., bioY, bioM, bccP) in caries-active children, indicating a potential role of biotin in caries pathogenesis. This study investigated a biotin limitation strategy against the primary cariogenic bacterium Streptococcus mutans (S. mutans), including its effects on cariogenic phenotypes, gene expression, and metabolomics.

Methods: S. mutans UA159 was cultured in biotin-free medium supplemented with different biotin concentrations. The cariogenic phenotypes of the strain, including growth kinetics, biofilm formation, exopolysaccharide (EPS) production, lactate synthesis, acid/oxidative tolerance, and membrane fluidity, were measured and compared across biotin concentrations. Biofilm architecture was visualized via confocal laser-scanning microscopy (CLSM) and scanning electron microscopy (SEM). Quantitative real-time polymerase chain reaction (RT-qPCR) was employed to analyze the expression of genes associated with virulence and biotin metabolism. Metabolomic analysis was performed to characterize metabolic perturbations induced by biotin limitation in S. mutans.

Results: Under biotin limitation, S. mutans exhibited significantly reduced cariogenic phenotypes, accompanied by cell elongation and reduced membrane fluidity. At the molecular level, biotin limitation suppressed the expression of key virulence-associated genes and induced a compensatory upregulation of genes involved in biotin uptake and biotin-dependent carboxylases. Metabolomic analysis under biotin-limited conditions in S. mutans revealed perturbed pathways in central carbon metabolism and nucleotide metabolism.

Conclusion: Biotin limitation significantly reduced the cariogenic potential of S. mutans by disrupting metabolic flux and virulence gene expression, highlighting biotin uptake and metabolism as potential targets for anti-caries therapies.

生物素限制通过破坏代谢通量和毒力途径减弱变形链球菌的致病性。
我们之前的宏基因组分析显示,生物素相关基因(即bioY, bioM, bccP)在龋齿活动性儿童中的频率更高,这表明生物素在龋齿发病中的潜在作用。本研究研究了针对原发性龋齿细菌变形链球菌(S. mutans)的生物素限制策略,包括其对龋齿表型、基因表达和代谢组学的影响。方法:在添加不同生物素浓度的无生物素培养基中培养变形链球菌UA159。研究人员测量了菌株的龋表型,包括生长动力学、生物膜形成、外多糖(EPS)产生、乳酸合成、酸/氧化耐受性和膜流动性,并对不同生物素浓度的菌株进行了比较。通过共聚焦激光扫描显微镜(CLSM)和扫描电镜(SEM)观察生物膜结构。采用实时定量聚合酶链反应(RT-qPCR)分析毒力和生物素代谢相关基因的表达。代谢组学分析表征了变形链球菌由生物素限制引起的代谢扰动。结果:在生物素限制下,变形链球菌表现出明显减少的龋齿表型,并伴有细胞伸长和膜流动性降低。在分子水平上,生物素限制抑制了关键毒力相关基因的表达,并诱导了参与生物素摄取和生物素依赖性羧化酶的基因的代偿性上调。在生物素限制条件下,变形链球菌的代谢组学分析揭示了中心碳代谢和核苷酸代谢的紊乱途径。结论:生物素限制通过破坏代谢通量和毒力基因表达显著降低变形链球菌的蛀牙潜力,强调生物素的摄取和代谢是抗蛀牙治疗的潜在靶点。
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来源期刊
Caries Research
Caries Research 医学-牙科与口腔外科
CiteScore
6.30
自引率
7.10%
发文量
34
审稿时长
6-12 weeks
期刊介绍: ''Caries Research'' publishes epidemiological, clinical and laboratory studies in dental caries, erosion and related dental diseases. Some studies build on the considerable advances already made in caries prevention, e.g. through fluoride application. Some aim to improve understanding of the increasingly important problem of dental erosion and the associated tooth wear process. Others monitor the changing pattern of caries in different populations, explore improved methods of diagnosis or evaluate methods of prevention or treatment. The broad coverage of current research has given the journal an international reputation as an indispensable source for both basic scientists and clinicians engaged in understanding, investigating and preventing dental disease.
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