生物
微生物学
毒力因子
毒力
克莱德
受体
重组DNA
发病机制
地穴
遗传学
基因
免疫学
系统发育学
内分泌学
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
[Elsevier]
日期:2022-03-01
卷期号:185 (6): 980-994.e15
被引量:42
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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