一种细菌硅糖苷酶介导先驱肠道共生菌的早期定殖

IF 20.6 1区 医学 Q1 MICROBIOLOGY Cell host & microbe Pub Date : 2024-01-15 DOI:10.1016/j.chom.2023.12.014
Ekaterina Buzun, Chia-Yun Hsu, Kristija Sejane, Renee E. Oles, Adriana Vasquez Ayala, Luke R. Loomis, Jiaqi Zhao, Leigh-Ana Rossitto, Dominic M. McGrosso, David J. Gonzalez, Lars Bode, Hiutung Chu
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引用次数: 0

摘要

胃肠道的早期微生物定植会对发育和健康产生长期影响。包括乳杆菌属在内的基石物种在生命早期非常突出,在维持肠道生态系统结构方面发挥着至关重要的作用。然而,人们对生命早期弹性群落的形成过程仍不甚了解。在这里,我们发现脆弱拟杆菌(Bacteroides fragilis)中的单个硅糖苷酶(NanH)能在生命早期稳定地占据肠粘膜,并调节共生定殖程序。这种程序是由包括母乳低聚糖和肠粘液中的糖在内的糖基化聚糖触发的。从母体到幼崽的垂直传播需要 NanH,它能促进脆弱拟杆菌在生命早期的优势地位。此外,在一个确定的微生物群落中,NanH 还能促进共生菌的恢复能力以及抗生素治疗后的恢复。总之,我们的研究揭示了宿主与微生物群之间通过宿主衍生的聚糖促进稳定定殖的共同进化机制。
本文章由计算机程序翻译,如有差异,请以英文原文为准。

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A bacterial sialidase mediates early-life colonization by a pioneering gut commensal

The early microbial colonization of the gastrointestinal tract can have long-term impacts on development and health. Keystone species, including Bacteroides spp., are prominent in early life and play crucial roles in maintaining the structure of the intestinal ecosystem. However, the process by which a resilient community is curated during early life remains inadequately understood. Here, we show that a single sialidase, NanH, in Bacteroides fragilis mediates stable occupancy of the intestinal mucosa in early life and regulates a commensal colonization program. This program is triggered by sialylated glycans, including those found in human milk oligosaccharides and intestinal mucus. NanH is required for vertical transmission from dams to pups and promotes B. fragilis dominance during early life. Furthermore, NanH facilitates commensal resilience and recovery after antibiotic treatment in a defined microbial community. Collectively, our study reveals a co-evolutionary mechanism between the host and microbiota mediated through host-derived glycans to promote stable colonization.

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来源期刊
Cell host & microbe
Cell host & microbe 生物-微生物学
CiteScore
45.10
自引率
1.70%
发文量
201
审稿时长
4-8 weeks
期刊介绍: Cell Host & Microbe is a scientific journal that was launched in March 2007. The journal aims to provide a platform for scientists to exchange ideas and concepts related to the study of microbes and their interaction with host organisms at a molecular, cellular, and immune level. It publishes novel findings on a wide range of microorganisms including bacteria, fungi, parasites, and viruses. The journal focuses on the interface between the microbe and its host, whether the host is a vertebrate, invertebrate, or plant, and whether the microbe is pathogenic, non-pathogenic, or commensal. The integrated study of microbes and their interactions with each other, their host, and the cellular environment they inhabit is a unifying theme of the journal. The published work in Cell Host & Microbe is expected to be of exceptional significance within its field and also of interest to researchers in other areas. In addition to primary research articles, the journal features expert analysis, commentary, and reviews on current topics of interest in the field.
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