Douchant Katya, He Shu-Mei, Noordhof Curtis, Greenlaw Jill, Vancuren Sarah, Schroeter Kathleen, Allen-Vercoe Emma, Sjaarda Calvin, Vanner Stephen J, Petrof Elaine O, Sheth Prameet M, Guzman Mabel
The Gastrointestinal Disease Research Unit (GIDRU), Kingston Health Sciences Center, Kingston, K7L2V7, ON, Canada.
Department of Biomedical and Molecular Sciences, Queen's University, Kingston, K7L3N6, ON, Canada.
Commun Biol. 2024 Jan 27;7(1):135. doi: 10.1038/s42003-024-05778-6.
Clostridioides difficile is the leading cause of antibiotic-associated infectious diarrhea. The development of C.difficile infection is tied to perturbations of the bacterial community in the gastrointestinal tract, called the gastrointestinal microbiota. Repairing the gastrointestinal microbiota by introducing lab-designed bacterial communities, or defined microbial communities, has recently shown promise as therapeutics against C.difficile infection, however, the mechanisms of action of defined microbial communities remain unclear. Using an antibiotic- C.difficile mouse model, we report the ability of an 18-member community and a refined 4-member community to protect mice from two ribotypes of C.difficile (CD027, CD078; p < 0.05). Furthermore, bacteria-free supernatant delivered orally to mice from the 4-member community proteolyzed C.difficile toxins in vitro and protected mice from C.difficile infection in vivo (p < 0.05). This study demonstrates that bacteria-free supernatant is sufficient to protect mice from C.difficile; and could be further explored as a therapeutic strategy against C.difficile infection.
艰难梭菌是抗生素相关性感染性腹泻的主要病因。艰难梭菌感染的发生与胃肠道中细菌群落(即胃肠道微生物群)的扰动有关。通过引入实验室设计的细菌群落或特定微生物群落来修复胃肠道微生物群,最近已显示出作为治疗艰难梭菌感染的潜力,然而,特定微生物群落的作用机制仍不清楚。利用抗生素-艰难梭菌小鼠模型,我们报告了一个由18个成员组成的群落和一个经过优化的由4个成员组成的群落保护小鼠免受两种艰难梭菌核糖型(CD027、CD078;p<0.05)感染的能力。此外,从4个成员组成的群落口服给小鼠的无菌上清液在体外可降解艰难梭菌毒素,并在体内保护小鼠免受艰难梭菌感染(p<0.05)。这项研究表明,无菌上清液足以保护小鼠免受艰难梭菌感染;并且可以作为一种治疗艰难梭菌感染的策略进行进一步探索。