Department of Medical Biochemistry and Cell Biology, Institute of Biomedicine, University of Gothenburg, Gothenburg, Sweden.
Department of Molecular and Clinical Medicine, Institute of Medicine, University of Gothenburg, Gothenburg, Sweden.
Gut Microbes. 2024 Jan-Dec;16(1):2409247. doi: 10.1080/19490976.2024.2409247. Epub 2024 Sep 30.
The anaerobic spirochete causes intestinal spirochetosis, characterized by the intimate attachment of bacterial cells to the colonic mucosa, potentially leading to symptoms such as diarrhea, abdominal pain, and weight loss. Despite the clinical significance of infections, the mechanism of the interaction between and the colon epithelium is not known. We characterized the molecular mechanism of the -epithelium interaction and its impact on the epithelial barrier during infection. Through a proteomics approach, we identified BPP43_05035 as a candidate surface protein that mediates bacterial attachment to cultured human colonic epithelial cells. The crystal structure of BPP43_05035 revealed a globular lipoprotein with a six-bladed beta-propeller domain. Blocking the native BPP43_05035 on , either with a specific antibody or via competitive inhibition, abrogated its binding to epithelial cells, which required cell surface-exposed -glycans. Proximity labeling and interaction assays revealed that BPP43_05035 bound to tight junctions, thereby increasing the permeability of the epithelial monolayer. Extending our investigation to humans, we discovered a downregulation of tight junction and brush border genes in -infected patients carrying detectable levels of epithelium-bound BPP43_05035. Collectively, our findings identify BPP43_05035 as a adhesin that weakens the colonic epithelial barrier during infection.
产甲烷螺旋菌导致肠道螺旋体病,其特征为细菌细胞与结肠黏膜紧密附着,可能导致腹泻、腹痛和体重减轻等症状。尽管 感染具有临床意义,但 与结肠上皮相互作用的机制尚不清楚。我们描述了 与上皮相互作用的分子机制及其在感染过程中对上皮屏障的影响。通过蛋白质组学方法,我们鉴定出 BPP43_05035 是一种候选的 表面蛋白,介导细菌与培养的人结肠上皮细胞的附着。BPP43_05035 的晶体结构揭示了一种具有六叶β-螺旋桨结构域的球形脂蛋白。用特异性抗体或竞争性抑制来阻断 上的天然 BPP43_05035,均可消除其与上皮细胞的结合,而这种结合需要细胞表面暴露的 -聚糖。接近标记和相互作用试验表明,BPP43_05035 与紧密连接结合,从而增加了上皮单层的通透性。将我们的研究扩展到人类,我们发现,在感染 且上皮结合的 BPP43_05035 可检测到的患者中,紧密连接和刷状缘基因下调。总之,我们的研究结果确定 BPP43_05035 是一种 黏附素,它在感染过程中削弱结肠上皮屏障。