Institute for Molecular Infection Biology (IMIB), University of Würzburg, Würzburg, Germany.
Department of Tissue Engineering and Regenerative Medicine (TERM), University Hospital Würzburg, Würzburg, Germany.
Cell Microbiol. 2018 Feb;20(2). doi: 10.1111/cmi.12812. Epub 2017 Dec 5.
The human gastrointestinal tract is a complex ecosystem in which epithelial cells and microorganisms of the intestinal microbiota live in symbiosis. Certain members of the microbiota, in particular Escherichia coli strains of the B2 phylotype, carry the polyketide synthase-island encoding the genotoxin colibactin. Colibactin is a nonribosomal peptide or polyketide-nonribosomal peptide hybrid of still unsolved structure, which induces DNA double strand breaks (DSBs) in eukaryotic cells. However, direct contact between live bacteria and host cell is required in order to elicit these genotoxic effects. In this study, we used a variety of cell culture models, among them, a 3D cell culture approach based on decellularised small intestinal submucosa, to investigate whether the intestinal mucus layer has the potential to interfere with colibactin activity. We demonstrate that the expression of mucins and the formation of an adherent mucus layer significantly increased with increasing complexity of cell culture. Moreover, we show that the presence of an adherent mucus layer on epithelial cells attenuates the genotoxic activity of colibactin, by preventing the induction of DNA-DSBs. Removal of the adherent mucus layer restored the occurrence of DNA-DSBs.
人类胃肠道是一个复杂的生态系统,其中上皮细胞和肠道微生物菌群共生。某些微生物群成员,特别是 B2 型大肠杆菌菌株,携带编码遗传毒素大肠菌素的聚酮合酶岛。大肠菌素是一种尚未解决结构的非核糖体肽或聚酮-非核糖体肽杂合,它在真核细胞中诱导 DNA 双链断裂(DSB)。然而,为了引发这些遗传毒性作用,需要活细菌与宿主细胞之间的直接接触。在这项研究中,我们使用了多种细胞培养模型,其中包括基于脱细胞小肠黏膜下层的 3D 细胞培养方法,以研究肠道黏液层是否有可能干扰大肠菌素的活性。我们证明,随着细胞培养复杂性的增加,粘蛋白的表达和粘性黏液层的形成显著增加。此外,我们表明,上皮细胞上粘性黏液层的存在通过防止 DNA-DSB 的诱导,减弱了大肠菌素的遗传毒性活性。去除粘性黏液层恢复了 DNA-DSB 的发生。