AUTHOR=Yeh Jia-Yin , Lin Hwai-Jeng , Kuo Chia-Jung , Feng Chun-Lung , Chou Chia-Huei , Lin Chia-Der , Wu Hui-Yu , Li Chen-Yi , Chiu Cheng-Hsun , Lai Chih-Ho 

TITLE=Campylobacter jejuni Cytolethal Distending Toxin C Exploits Lipid Rafts to Mitigate Helicobacter pylori-Induced Pathogenesis

JOURNAL=Frontiers in Cell and Developmental Biology

VOLUME=8

YEAR=2021

URL=https://www.frontiersin.org/journals/cell-and-developmental-biology/articles/10.3389/fcell.2020.617419

DOI=10.3389/fcell.2020.617419

ISSN=2296-634X

ABSTRACT=<p><italic>Helicobacter pylori</italic> infection is associated with several gastrointestinal diseases, including gastritis, peptic ulcer, and gastrointestinal adenocarcinoma. Two major cytotoxins, vacuolating cytotoxin A (VacA) and cytotoxin-associated gene A (CagA), interact closely with lipid rafts, contributing to <italic>H. pylori</italic>-associated disease progression. The <italic>Campylobacter jejuni</italic> cytolethal distending toxin consists of three subunits: CdtA, CdtB, and CdtC. Among them, CdtA and CdtC bind to membrane lipid rafts, which is crucial for CdtB entry into cells. In this study, we employed recombinant CdtC (rCdtC) to antagonize the functions of <italic>H. pylori</italic> cytotoxin in cells. Our results showed that rCdtC alleviates cell vacuolation induced by <italic>H. pylori</italic> VacA. Furthermore, rCdtC reduces <italic>H. pylori</italic> CagA translocation, which decreases nuclear factor kappa-B activation and interleukin-8 production, resulting in the mitigation of gastric epithelial cell inflammation. These results reveal that CdtC hijacks cholesterol to compete for <italic>H. pylori</italic> cytotoxin actions <italic>via</italic> lipid rafts, ameliorating <italic>H. pylori</italic>-induced pathogenesis.</p>