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仿生调节剂打破致病菌的生态位,调节结肠炎失调的微生物组。

Bionic Regulators Break the Ecological Niche of Pathogenic Bacteria for Modulating Dysregulated Microbiome in Colitis.

机构信息

School of Pharmaceutical Sciences, Zhengzhou University, Zhengzhou, 450001, China.

Key Laboratory of Targeting Therapy and Diagnosis for Critical Diseases, Zhengzhou University, Zhengzhou, 450001, China.

出版信息

Adv Mater. 2022 Sep;34(39):e2204650. doi: 10.1002/adma.202204650. Epub 2022 Aug 26.

DOI:10.1002/adma.202204650
PMID:35924734
Abstract

Therapeutic approaches that reprogram the gut microbiome are promising strategies to alleviate and cure inflammatory bowel disease (IBD). However, abnormal expansion of Escherichia coli during inflammation can promote pathogenic bacteria occupying ecological niches to resist reprogramming of the microbiome. Herein, a bionic regulator (CaWO @YCW) is developed to efficiently and precisely regulate the gut microbiome by specifically suppressing the abnormal expansion of E. coli during colitis and boosting probiotic growth. Inspired by the binding of E. coli strains to the mannose-rich yeast cell wall (YCW), YCW is chosen as the bionic shell to encapsulate CaWO . It is demonstrated that the YCW shell endows CaWO with superior resistance to the harsh environment of the gastrointestinal tract and adheres to the abnormally expanded E. coli in colitis, specifically as a positioner. Notably, the high expression of calprotectin at the colitis site triggers the release of tungsten ions through calcium deprivation in CaWO , thus inhibiting E. coli growth by replacing molybdenum in the molybdopterin cofactor. Moreover, YCW functions as a prebiotic and promotes probiotic growth. Consequently, CaWO @YCW can efficiently and precisely reprogram the gut microbiome by eliminating pathogenic bacteria and providing prebiotics, resulting in an extraordinary therapeutic advantage for DSS-induced colitis.

摘要

通过重编程肠道微生物组来治疗的方法是缓解和治疗炎症性肠病(IBD)的有前景的策略。然而,在炎症期间大肠杆菌的异常扩张会促进占据生态位的病原菌抵抗微生物组的重编程。在此,开发了一种仿生调节剂(CaWO@YCW),通过在结肠炎期间特异性抑制大肠杆菌的异常扩张并促进益生菌的生长,来有效地、精确地调控肠道微生物组。受大肠杆菌菌株与富含甘露糖的酵母细胞壁(YCW)结合的启发,选择 YCW 作为仿生外壳来包裹 CaWO。结果表明,YCW 外壳赋予了 CaWO 优越的胃肠道恶劣环境的抗性,并在结肠炎中黏附于异常扩张的大肠杆菌,特别作为定位器。值得注意的是,在结肠炎部位高表达的钙卫蛋白通过剥夺 CaWO 中的钙触发钨离子的释放,从而通过取代钼喋呤辅酶中的钼来抑制大肠杆菌的生长。此外,YCW 作为一种益生元,促进益生菌的生长。因此,CaWO@YCW 可以通过消除病原菌和提供益生元来有效地、精确地重编程肠道微生物组,从而为 DSS 诱导的结肠炎提供卓越的治疗优势。

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