牙周炎唾液微生物群通过肠道微生物群加剧结肠炎诱发的焦虑样行为

IF 7.8 1区 生物学 Q1 BIOTECHNOLOGY & APPLIED MICROBIOLOGY
Jun Qian, Jiangyue Lu, Shuyu Cheng, Xihong Zou, Qing Tao, Min Wang, Nannan Wang, Lichun Zheng, Wenzheng Liao, Yanfen Li, Fuhua Yan
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引用次数: 0

摘要

肠脑轴是肠道和中枢神经系统之间的双向交流系统。许多与宿主相关的因素都会影响肠道微生物群,包括口腔细菌,从而使大脑成为肠脑轴的易感目标。唾液中含有大量口腔细菌,而牙周炎这种常见的口腔疾病会改变唾液微生物群的组成。然而,牙周炎唾液微生物群(PSM)对肠道-大脑轴的作用和机制仍不清楚。在此,我们利用葡聚糖硫酸钠盐(DSS)诱导的小鼠焦虑样行为研究了这种关系的性质和机制。与健康的唾液微生物群相比,PSM 会加重焦虑样行为;它会显著减少 DSS 小鼠正常神经元的数量并激活小胶质细胞。抗生素治疗消除了 PSM 对焦虑样行为的影响,而移植 PSM 灌胃小鼠的粪便微生物群则加剧了焦虑样行为。这些观察结果表明,PSM 的焦虑加剧效应依赖于肠道微生物群。此外,PSM 对焦虑样行为的影响在非 DSS 小鼠中并不存在,这表明 DSS 处理是 PSM 加剧焦虑的前提条件。从机理上讲,PSM 改变了组氨酸在肠道和大脑代谢组学中的代谢。补充组氨酸相关代谢物与PSM具有相似的焦虑加剧效应,表明组氨酸代谢可能是这一过程中的关键途径。我们的研究结果表明,PSM可通过直接影响宿主肠道微生物群而加剧结肠炎诱发的焦虑样行为,这强调了口腔疾病在肠道-大脑轴中的重要性。
本文章由计算机程序翻译,如有差异,请以英文原文为准。

Periodontitis salivary microbiota exacerbates colitis-induced anxiety-like behavior via gut microbiota

Periodontitis salivary microbiota exacerbates colitis-induced anxiety-like behavior via gut microbiota

The gut–brain axis is a bidirectional communication system between the gut and central nervous system. Many host-related factors can affect gut microbiota, including oral bacteria, making the brain a vulnerable target via the gut–brain axis. Saliva contains a large number of oral bacteria, and periodontitis, a common oral disease, can change the composition of salivary microbiota. However, the role and mechanism of periodontitis salivary microbiota (PSM) on the gut–brain axis remain unclear. Herein, we investigated the nature and mechanisms of this relationship using the mice with dextran sulfate sodium salt (DSS)-induced anxiety-like behavior. Compared with healthy salivary microbiota, PSM worsened anxiety-like behavior; it significantly reduced the number of normal neurons and activated microglia in DSS mice. Antibiotic treatment eliminated the effect of PSM on anxiety-like behavior, and transplantation of fecal microbiota from PSM-gavaged mice exacerbated anxiety-like behavior. These observations indicated that the anxiety-exacerbating effect of PSM was dependent on the gut microbiota. Moreover, the PSM effect on anxiety-like behavior was not present in non-DSS mice, indicating that DSS treatment was a prerequisite for PSM to exacerbate anxiety. Mechanistically, PSM altered the histidine metabolism in both gut and brain metabolomics. Supplementation of histidine-related metabolites had a similar anxiety-exacerbating effect as that of PSM, suggesting that histidine metabolism may be a critical pathway in this process. Our results demonstrate that PSM can exacerbate colitis-induced anxiety-like behavior by directly affecting the host gut microbiota, emphasizing the importance of oral diseases in the gut–brain axis.

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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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