Enterohemorrhagic Escherichia coli O157 outer membrane vesicles induce interleukin 8 production in human intestinal epithelial cells by signaling via Toll-like receptors TLR4 and TLR5 and activation of the nuclear factor NF-κB
Language English Country Germany Media print-electronic
Document type Journal Article
PubMed
29934223
DOI
10.1016/j.ijmm.2018.06.004
PII: S1438-4221(18)30224-8
Knihovny.cz E-resources
- Keywords
- Enterohemorrhagic Escherichia coli O157, Flagellin, Immunomodulation, Lipopolysaccharide, Outer membrane vesicles, Proinflammatory cytokines,
- MeSH
- Cell Membrane metabolism MeSH
- HT29 Cells MeSH
- Caco-2 Cells MeSH
- Epithelial Cells metabolism MeSH
- Escherichia coli O157 pathogenicity MeSH
- Virulence Factors metabolism MeSH
- Flagellin metabolism MeSH
- Escherichia coli Infections microbiology pathology MeSH
- Interleukin-8 biosynthesis MeSH
- Humans MeSH
- Cell Line, Tumor MeSH
- NF-kappa B metabolism MeSH
- Bacterial Outer Membrane Proteins metabolism MeSH
- Escherichia coli Proteins metabolism MeSH
- Signal Transduction MeSH
- Intestinal Mucosa cytology microbiology pathology MeSH
- Toll-Like Receptor 4 metabolism MeSH
- Toll-Like Receptor 5 metabolism MeSH
- Check Tag
- Humans MeSH
- Publication type
- Journal Article MeSH
- Names of Substances
- CXCL8 protein, human MeSH Browser
- Virulence Factors MeSH
- Flagellin MeSH
- Interleukin-8 MeSH
- NF-kappa B MeSH
- Bacterial Outer Membrane Proteins MeSH
- Escherichia coli Proteins MeSH
- TLR4 protein, human MeSH Browser
- TLR5 protein, human MeSH Browser
- Toll-Like Receptor 4 MeSH
- Toll-Like Receptor 5 MeSH
Proinflammatory cytokines play important roles in the pathogenesis of diseases caused by enterohemorrhagic Escherichia coli (EHEC) O157, but the spectrum of bacterial components involved in the proinflammatory responses is not fully understood. Here, we investigated the abilities of outer membrane vesicles (OMVs), nanoparticles released by EHEC O157 during growth, to induce production of proinflammatory cytokines in human intestinal epithelial cells. OMVs from both EHEC O157:H7 and sorbitol-fermenting (SF) EHEC O157:H- induced production of interleukin-8 (IL-8) in Caco-2, HCT-8, and HT-29 intestinal epithelial cell lines. H7 flagellin was the key IL-8-inducing component of EHEC O157:H7 OMVs, whereas cytolethal distending toxin V and O157 lipopolysaccharide (LPS) largely contributed to IL-8 production elicited by flagellin-lacking OMVs from SF EHEC O157:H-. The H7 flagellin-mediated signaling via Toll-like receptor (TLR) 5, and O157 LPS-mediated signaling via TLR4/MD-2 complex, which were followed by activation of the nuclear factor NF-κB were major pathways underlying IL-8 production induced by EHEC O157 OMVs. The proinflammatory and immunomodulatory capacities of EHEC O157 OMVs have pathogenetic implications and support the OMVs as suitable vaccine candidates.
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