Inhibiting the Initiation of Clostridium difficile Spore Germination using Analogs of Chenodeoxycholic Acid, a Bile Acid

被引:268
作者
Sorg, Joseph A. [1 ]
Sonenshein, Abraham L. [1 ]
机构
[1] Tufts Univ, Dept Mol Biol & Microbiol, Sch Med, Boston, MA 02111 USA
基金
美国国家卫生研究院;
关键词
SP STRAIN VPI-12708; NUCLEAR RECEPTOR; CHANGING EPIDEMIOLOGY; VPI; 12708; DISEASE; DIARRHEA; IDENTIFICATION; RECOVERY; GENE; CARCINOGENESIS;
D O I
10.1128/JB.00610-10
中图分类号
Q93 [微生物学];
学科分类号
071005 ; 100705 ;
摘要
To cause disease, Clostridium difficile spores must germinate in the host gastrointestinal tract. Germination is initiated upon exposure to glycine and certain bile acids, e.g., taurocholate. Chenodeoxycholate, another bile acid, inhibits taurocholate-mediated germination. By applying Michaelis-Menten kinetic analysis to C. difficile spore germination, we found that chenodeoxycholate is a competitive inhibitor of taurocholate-mediated germination and appears to interact with the spores with greater apparent affinity than does taurocholate. We also report that several analogs of chenodeoxycholate are even more effective inhibitors. Some of these compounds resist 7 alpha-dehydroxylation by Clostridium scindens, a core member of the normal human colonic microbiota, suggesting that they are more stable than chenodeoxycholate in the colonic environment.
引用
收藏
页码:4983 / 4990
页数:8
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