Periodontitis aggravates bone loss through gut microbiota alterations in ovariectomized mice.

IF 11.4 1区 生物学 Q1 BIOTECHNOLOGY & APPLIED MICROBIOLOGY
Hua Nie, Nannan Wang, Haowei Mao, Yuan Wei, Jun Qian, Rixin Chen, Qiao Yuan, Yin Xiao, Li Zhang, Fuhua Yan
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Abstract

Epidemiological evidence suggests a bidirectional relationship between periodontitis and osteoporosis, yet the underlying mechanisms remain unclear. In this study, using a mouse model combining ovariectomy-induced osteoporosis and ligature-induced periodontitis, we demonstrated that periodontitis significantly aggravated both alveolar and femoral bone loss, impaired intestinal barrier integrity, and elevated systemic inflammation. Gut microbiota and metabolomic analyses revealed that periodontitis induced distinct alterations in gut microbial composition and intestinal metabolic profiles, potentially contributing to systemic inflammation and bone metabolic dysregulation. Furthermore, fecal microbiota transplantation demonstrated that gut microbiota from periodontitis donors aggravated bone loss and inflammation in recipient mice, whereas microbiota from donors that received periodontal treatment partially alleviated inflammatory responses and skeletal deterioration. Collectively, these findings suggest that periodontitis may aggravate osteoporosis via gut microbiota-mediated mechanisms, highlighting the importance of maintaining oral health to mitigate the adverse impact of periodontitis on systemic bone metabolism.

在去卵巢小鼠中,牙周炎通过肠道菌群改变加重骨质流失。
流行病学证据表明牙周炎和骨质疏松症之间存在双向关系,但潜在的机制尚不清楚。在这项研究中,我们使用了一个结合卵巢切除引起的骨质疏松症和结扎引起的牙周炎的小鼠模型,我们证明牙周炎显著加重了牙槽骨和股骨骨丢失、肠道屏障完整性受损和全身炎症升高。肠道微生物群和代谢组学分析显示,牙周炎引起肠道微生物组成和肠道代谢谱的明显改变,可能导致全身性炎症和骨代谢失调。此外,粪便微生物群移植表明,来自牙周炎供体的肠道微生物群加重了受体小鼠的骨质流失和炎症,而来自接受牙周治疗的供体的微生物群部分减轻了炎症反应和骨骼恶化。总之,这些发现表明牙周炎可能通过肠道微生物介导的机制加重骨质疏松症,强调了维持口腔健康以减轻牙周炎对全身骨代谢的不利影响的重要性。
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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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