生物
微生物学
毒力因子
毒力
克莱德
受体
遗传学
基因
系统发育学
作者
Jianhua Luo,Qi Yang,Xiaofeng Zhang,Yuanyuan Zhang,Li Wan,Xiechao Zhan,Yao Zhou,Liuqing He,Danyang Li,Dazhi Jin,Ying Zhen,Jing Huang,Yanyan Li,Liang Tao
出处
期刊:Cell
[Cell Press]
日期:2022-03-01
卷期号:185 (6): 980-994.e15
被引量:51
标识
DOI:10.1016/j.cell.2022.02.010
摘要
The emergence of hypervirulent clade 2 Clostridioides difficile is associated with severe symptoms and accounts for >20% of global infections. TcdB is a dominant virulence factor of C. difficile, and clade 2 strains exclusively express two TcdB variants (TcdB2 and TcdB4) that use unknown receptors distinct from the classic TcdB. Here, we performed CRISPR/Cas9 screens for TcdB4 and identified tissue factor pathway inhibitor (TFPI) as its receptor. Using cryo-EM, we determined a complex structure of the full-length TcdB4 with TFPI, defining a common receptor-binding region for TcdB. Residue variations within this region divide major TcdB variants into 2 classes: one recognizes Frizzled (FZD), and the other recognizes TFPI. TFPI is highly expressed in the intestinal glands, and recombinant TFPI protects the colonic epithelium from TcdB2/4. These findings establish TFPI as a colonic crypt receptor for TcdB from clade 2 C. difficile and reveal new mechanisms for CDI pathogenesis.
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