人体肠道细菌通过改变它们的蛋白质折叠能力来对抗邻近细菌
Bentley Lim1, Jinghua Xu2, Igor H Wierzbicki3
1Department of Microbial Pathogenesis and Microbial Sciences Institute, Yale University School of Medicine, New Haven, CT 06536, USA.
Cell host & microbe
|February 5, 2025
概括
人的肠道微生物使用Bte1效应器来破坏邻近细胞中的蛋白质折叠,影响微生物社区的动态,并赋予健康优势. 这种相互作用凸显了肠道中的微生物军备竞赛.
科学领域:
- 微生物学 微生物学
- 分子生物学分子生物学
- 系统生物学 系统生物学
背景情况:
- 对抗性相互作用对微生物社区结构至关重要.
- 接触依赖的效应因子在人类肠道微生物群中广泛存在.
研究的目的:
- 研究人类肠道微生物中Bte1效应器的机制和功能.
- 了解Bte1如何影响微生物相互作用和社区动态.
主要方法:
- 对Bte1-PpiD-YfgM相互作用的结构,生化和遗传特征.
- 在哺乳动物肠道模型中使用Bacteroides的体内研究.
- 对Bte1基变异的肠道元基因组数据的分析.
主要成果:
- Bte1直接准并逆转PpiD-YfgM周等离子伴侣复合物的活性.
- Bte1促进受体细胞中的基质聚合和毒性,从而赋予体能优势.
- 表达Bte1的菌株利用炎症并与免疫编码菌株进行进化军备竞赛.
结论:
- 人的肠道微生物可以通过Bte1.1.这样的效应器操纵邻近细胞的蛋白质折叠能力.
- 这种相互作用改变了微生物社区的动态,并提出了微生物组操纵的新策略.
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