微生物学
生物
假膜性结肠炎
艰难梭菌毒素A
造孔毒素
盲肠
腹泻
拉伤
艰难梭菌毒素B
毒素
体外
毒力
肠粘膜
上皮
下调和上调
肺
免疫学
转录组
寄生虫寄主
细胞培养
细胞生物学
寄主(生物学)
大肠
殖民地化
细菌
抗药性
结直肠癌
发病机制
作用机理
癌症研究
病毒学
毒力因子
抗生素
作者
Jazmín Meza‐Torres,Jean‐Yves Tinevez,Aline Crouzols,Héloïse Mary,Min-Hee Kim,Lise Hunault,Susan Chamorro-Rodriguez,Emilie Lejal,Pamela Altamirano-Silva,Déborah Groussard,Samy Gobaa,Johann Peltier,Benoît Chassaing,Bruno Dupuy
出处
期刊:Gut microbes
[Landes Bioscience]
日期:2024-12-24
卷期号:17 (1): 2444411-2444411
被引量:7
标识
DOI:10.1080/19490976.2024.2444411
摘要
Clinical symptoms of Clostridioides difficile infection (CDI) range from diarrhea to pseudomembranous colitis. A major challenge in managing CDI is the high rate of relapse. Several studies correlate the production of CDT binary toxin by clinical strains of C. difficile with higher relapse rates. Although the mechanism of action of CDT on host cells is known, its exact contribution to CDI is still unclear. To understand the physiological role of CDT during CDI, we established two hypoxic relevant intestinal models, Transwell and Microfluidic Intestine-on-Chip systems. Both were challenged with the epidemic strain UK1 CDT+ and its isogenic CDT- mutant. We report that CDT induces mucin-associated microcolonies that increase C. difficile colonization and display biofilm-like properties by enhancing C. difficile resistance to vancomycin. Importantly, biofilm-like microcolonies were also observed in the cecum and colon of infected mice. Hence, our study shows that CDT induces biofilm-like microcolonies, increasing C. difficile persistence and risk of relapse.
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