Oral biofilm dysbiosis during experimental periodontitis.

IF 2.8 3区 医学 Q1 DENTISTRY, ORAL SURGERY & MEDICINE Molecular Oral Microbiology Pub Date : 2022-12-01 Epub Date: 2022-10-19 DOI:10.1111/omi.12389
Apoena Aguiar Ribeiro, Yizu Jiao, Mustafa Girnary, Tomaz Alves, Liang Chen, Anna Farrell, Di Wu, Flavia Teles, Naohiro Inohara, Karen V Swanson, Julie T Marchesan
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Abstract

Objectives: We have previously characterized the main osteoimmunological events that occur during ligature periodontitis. This study aims to determine the polymicrobial community shifts that occur during disease development.

Methods: Periodontitis was induced in C57BL/6 mice using the ligature-induced periodontitis model. Healthy oral mucosa swabs and ligatures were collected every 3 days from 0 to 18 days post-ligature placement. Biofilm samples were evaluated by 16SrRNA gene sequencing (Illumina MiSeq) and QIIME. Time-course changes were determined by relative abundance, diversity, and rank analyses (PERMANOVA, Bonferroni-adjusted).

Results: Microbial differences between health and periodontal inflammation were observed at all phylogenic levels. An evident microbial community shift occurred in 25 genera during the advancement of "gingivitis" (3-6 days) to periodontitis (9-18 days). From day 0 to 18, dramatic changes were identified in Streptococcus levels, with an overall decrease (54.04%-0.02%) as well an overall increase of Enterococcus and Lactobacillus (23.7%-73.1% and 10.1%-70.2%, respectively). Alpha-diversity decreased to its lowest at 3 days, followed by an increase in diversity as disease advancement. Beta-diversity increased after ligature placement, indicating that bone loss develops in response to a greater microbial variability (p = 0.001). Levels of facultative and strict anaerobic bacteria augmented over the course of disease progression, with a total of eight species significantly different during the 18-day period.

Conclusion: The data supports that murine gingival inflammation and alveolar bone loss develop in response to microbiome shifts. Bacterial diversity increased during progression to bone loss. These findings further support the utilization of the periodontitis ligature model for microbial shift analysis under different experimental conditions.

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实验性牙周炎期间的口腔生物膜菌群失调。
目的:我们曾描述过结扎性牙周炎期间发生的主要骨免疫学事件。本研究旨在确定疾病发展过程中发生的多微生物群落变化:方法:使用结扎诱导牙周炎模型诱导 C57BL/6 小鼠患牙周炎。从结扎后 0 到 18 天,每隔 3 天收集一次健康口腔黏膜拭子和结扎物。通过 16SrRNA 基因测序(Illumina MiSeq)和 QIIME 对生物膜样本进行评估。通过相对丰度、多样性和等级分析(PERMANOVA,Bonferroni-adjusted)确定时间变化:结果:在所有系统发生水平上都观察到了健康与牙周炎症之间的微生物差异。在从 "牙龈炎"(3-6 天)到牙周炎(9-18 天)的过程中,25 个属发生了明显的微生物群落变化。从第 0 天到第 18 天,链球菌的含量发生了巨大变化,总体下降(54.04%-0.02%),肠球菌和乳酸杆菌的含量总体上升(分别为 23.7%-73.1% 和 10.1%-70.2% )。α-多样性在 3 天时降至最低,随后随着病情的发展而增加。结扎后,β-多样性增加,表明骨质流失是对更大的微生物变异性的反应(p = 0.001)。随着疾病的发展,兼性厌氧菌和严格厌氧菌的数量也在增加,在 18 天的时间里,共有 8 个物种存在显著差异:结论:这些数据证实,小鼠牙龈炎症和牙槽骨缺失是随着微生物群的变化而发展的。细菌多样性在骨质流失过程中有所增加。这些发现进一步支持了利用牙周炎结扎模型在不同实验条件下进行微生物变迁分析。
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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.
期刊最新文献
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