与重度氟斑牙相关的牙生物膜宏基因组和代谢组特征

IF 5.5 2区 医学 Q2 MICROBIOLOGY
Journal of Oral Microbiology Pub Date : 2025-09-23 eCollection Date: 2025-01-01 DOI:10.1080/20002297.2025.2560591
Penpitcha Ajrithirong, Annop Krasaesin, Wannakorn Sriarj, Patcharaporn Gavila, Wanna Chetruengchai, Kanokwan Sriwattanapong, Chawan Manaspon, Lakshman Samaranayake, Thantrira Porntaveetus
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引用次数: 0

摘要

目的:探讨重度氟牙症(SF)牙菌斑生物膜微生物组,并描述其宏基因组和代谢组。方法:从8名6- 15岁的泰国SF儿童和8名年龄匹配的无龋儿童和对照组中收集16个菌斑生物膜样本。生物膜分析采用散弹枪宏基因组测序,然后进行生物信息学评价。结果:对SF和对照的生物膜进行分类分析,鉴定出12门354种。α多样性组间差异不大,而β多样性组间差异较大(P = 0.0010)。LEfSe强调了关键的区分分类群:5种与健康相关的物种(牙齿放线菌,Tannerella sp. HOT 286, Candidatus Nanosynbacter sp,缺氧硒单胞菌和密螺旋体sp. OMZ 804)在对照组中富集,而以氟敏感酯酶生产而著称的镰刀奈瑟菌在SF中显著升高。功能上,8条代谢途径发生改变;其中三个(磷脂酰胆碱酰基编辑,无水多肽回收II,泛醇-7生物合成),假设支持镰刀菌活性,在SF组上调。结论:SF与生物膜微生物群的显著变化有关,其特征是镰刀菌的富集和与健康相关的分类群的减少。支持镰孢霉的代谢途径的改变为其作为氟中毒候选生物标志物的作用提供了机制见解,值得进一步研究。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
The metagenome and metabolome signatures of dental biofilms associated with severe dental fluorosis.

Objective: To explore the plaque biofilm microbiome associated with severe dental fluorosis (SF), and to describe its metagenome and metabolome.

Methods: Sixteen plaque biofilm samples were collected from eight 6- to 15-year-old Thai children with SF and eight age-matched, caries-free and controls. Biofilms were analyzed using shotgun metagenomic sequencing, followed by bioinformatics evaluation.

Results: Taxonomic profiling of biofilms from SF and controls identified a total of 12 phyla and 354 species. While alpha diversity was similar between the groups, beta diversity analysis (P = 0.0010) indicated distinct microbial community structures. LEfSe highlighted key discriminatory taxa: five health-associated species (Actinomyces dentalis, Tannerella sp. HOT 286, Candidatus Nanosynbacter sp, Selenomonas noxia and Treponema sp OMZ 804 ) were enriched in controls, while Neisseria sicca, known for fluoride-sensitive esterase production, was significantly elevated in SF. Functionally, eight metabolic pathways were altered; three of these (phosphatidylcholine acyl editing, anhydromuropeptides recycling II, ubiquinol-7 biosynthesis), hypothesized to support N. sicca activity, were upregulated in the SF group.

Conclusion: SF is associated with a significant shift in the biofilm microbiota, characterized by enrichment of N. sicca and a reduction in health-associated taxa. Altered metabolic pathways supporting N. sicca provide mechanistic insights into its role as a candidate biomarker for fluorosis, warranting further investigation.

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来源期刊
CiteScore
8.00
自引率
4.40%
发文量
52
审稿时长
12 weeks
期刊介绍: As the first Open Access journal in its field, the Journal of Oral Microbiology aims to be an influential source of knowledge on the aetiological agents behind oral infectious diseases. The journal is an international forum for original research on all aspects of ''oral health''. Articles which seek to understand ''oral health'' through exploration of the pathogenesis, virulence, host-parasite interactions, and immunology of oral infections are of particular interest. However, the journal also welcomes work that addresses the global agenda of oral infectious diseases and articles that present new strategies for treatment and prevention or improvements to existing strategies. Topics: ''oral health'', microbiome, genomics, host-pathogen interactions, oral infections, aetiologic agents, pathogenesis, molecular microbiology systemic diseases, ecology/environmental microbiology, treatment, diagnostics, epidemiology, basic oral microbiology, and taxonomy/systematics. Article types: original articles, notes, review articles, mini-reviews and commentaries
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