色氨酸-吲哚代谢途径在牙周炎牙龈卟啉单胞菌毒力和菌群失调中的调节。

IF 7.8 1区 生物学 Q1 BIOTECHNOLOGY & APPLIED MICROBIOLOGY
Jing Ding, Lingping Tan, Lingzhi Wu, Jinyu Li, Yong Zhang, Zongshan Shen, Chi Zhang, Chuanjiang Zhao, Li Gao
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引用次数: 0

摘要

牙周炎的发病机制以菌群失调和宿主反应紊乱为特征。牙龈卟啉单胞菌是牙周炎的重要病原菌,表达多种重要的毒力因子。本研究旨在阐明牙龈假单胞菌色氨酸-吲哚代谢途径在牙周炎发病中的作用及机制。本研究表明牙周炎患者表现出色氨酸代谢升高和唾液病原体丰富。色氨酸酶基因缺乏改变了牙龈假单胞菌的蛋白质组和代谢组,抑制了牙龈假单胞菌毒力因子的表达、生物膜的生长、血红素的利用、细胞粘附/侵袭和促炎症能力。牙龈假单胞菌色氨酸-吲哚途径刺激牙周炎生物膜形成,诱导口腔微生物群失调。在牙周炎小鼠中,牙龈假单胞菌的这一途径加重了牙槽骨丢失和牙龈组织破坏,导致口腔和肠道微生物群失调。本研究表明,色氨酸-吲哚途径是牙龈卟啉卟啉毒力和口腔微生物群失调的重要调节因子,这也与肠道失调有关。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Regulation of tryptophan-indole metabolic pathway in Porphyromonas gingivalis virulence and microbiota dysbiosis in periodontitis.

Pathogenesis of periodontitis is marked by microbiota dysbiosis and disrupted host responses. Porphyromonas gingivalis is a keystone pathogen of periodontitis which expresses various crucial virulence factors. This study aimed to clarify the role and mechanisms of P. gingivalis tryptophan-indole metabolic pathway in the pathogenesis of periodontitis. This study showed that periodontitis patients exhibited elevated tryptophan metabolism and salivary pathogen abundance. Tryptophanase gene-deficiency altered proteome and metabolome of P. gingivalis, inhibited P. gingivalis virulent factors expression, biofilm growth, hemin utilization, cell adhesion/invasion and pro-inflammation ability. Tryptophan-indole pathway of P. gingivalis stimulated periodontitis biofilm formation and induced oral microbiota dysbiosis. In periodontitis mice, this pathway of P. gingivalis aggravated alveolar bone loss and gingival tissue destruction, causing oral and gut microbiota dysbiosis. This study indicates that the tryptophan-indole pathway serves as a significant regulator of P. gingivalis virulence and oral microbiota dysbiosis, which is also associated with gut dysbiosis.

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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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