早产婴儿的克洛斯特里迪亚会代谢母乳的寡糖类,抑制病原生物,调节有机体中的肠功能
Jonathan A Chapman1, Andrea C Masi1, Lauren C Beck1
1Translational and Clinical Research Institute, Newcastle University, Newcastle upon Tyne, UK.
Nature microbiology
|March 17, 2026
概括
某些Clostridium物种,特别是那些缺乏PfoA毒素的物种,可以代谢母乳寡糖化物 (HMO). 这些微生物产生有益的化合物,可以通过抑制有害细菌和减少炎症来支持健康的婴儿肠道发育.
科学领域:
- 微生物学 微生物学
- 婴儿营养 婴儿营养
- 肠道微生物组研究研究
背景情况:
- 婴儿肠道微生物组的发展受到母乳和人乳寡糖化物 (HMO) 的影响.
- HMO代谢主要研究在Bifidobacteria中,但其他能够利用HMO的物种在很大程度上是未知的.
- 结核性肠球炎是早产婴儿的病理,可以受到肠道微生物组合的影响.
研究的目的:
- 调查HMO利用的微生物物种范围,超出早产婴儿肠道中的Bifidobacteria.
- 描述Clostridium物种对婴儿肠道环境的代谢潜力和功能影响.
- 探索特定的Clostridium菌株在促进健康的肠道微生物群和减轻病理方面的潜力.
主要方法:
- 用基因组,蛋白质组和代谢组分析来识别和描述HMO代谢细菌.
- 进行了体外培养实验,以评估代谢物生产和微生物相互作用.
- 使用结肠细胞系和早产的肠道器官的实验进行,以评估Clostridium物种及其超级生物的功能作用.
主要成果:
- 克洛斯特里物种,包括缺乏perfringolysin O (PfoA) 的Clostridium perfringens菌株,被确定为HMO代谢器.
- 与Bifidobacterium物种相比,这些Clostridium物种产生了更多的有益代谢物,例如短链脂肪酸和托催化剂.
- 来自缺乏PfoA的C. perfringens的无细胞超级生物抑制了病原生物的生长,促进了开始性Bifidobacteria的生长,抑制了有机体的炎症,对结肠细胞无毒.
结论:
- 这项研究扩大了已知的HMO代谢微生物的范围,包括某些Clostridium物种.
- 缺乏PfoA的Clostridium perfringens菌株表现出有益的特性,包括产生促进健康的代谢物和调节肠道环境.
- 这些发现表明,特定的C. perfringens菌株可能在支持健康的婴儿肠道发育方面发挥作用,并且可能是未来治疗干预的候选人.
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