| Literature DB >> 35303428 |
Jianhua Luo1, Qi Yang1, Xiaofeng Zhang2, Yuanyuan Zhang3, Li Wan2, Xiechao Zhan2, Yao Zhou1, Liuqing He1, Danyang Li1, Dazhi Jin4, Ying Zhen2, Jing Huang2, Yanyan Li5, Liang Tao6.
Abstract
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.Entities:
Keywords: CDI pathogenesis; CRISPR/Cas9 screen; Clostridioides difficile; TcdB; clade 2 C. difficile; colonic crypt; cryo-EM structure; receptor; tissue factor pathway inhibitor
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Year: 2022 PMID: 35303428 DOI: 10.1016/j.cell.2022.02.010
Source DB: PubMed Journal: Cell ISSN: 0092-8674 Impact factor: 41.582