Institute of Translational Immunology, Univ. Medical Center, Johannes Gutenberg University Mainz, Germany; Research Center for Immunotherapy, Univ. Medical Center, Johannes Gutenberg University Mainz, Germany.
Department of Medicine 1, Friedrich-Alexander-University, Erlangen, Germany.
Gastroenterology. 2020 Jul;159(1):257-272.e17. doi: 10.1053/j.gastro.2020.03.064. Epub 2020 Apr 3.
BACKGROUND & AIMS: Wheat has become the world's major staple and its consumption correlates with prevalence of noncommunicable disorders such as inflammatory bowel diseases. Amylase trypsin inhibitors (ATIs), a component of wheat, activate the intestine's innate immune response via toll-like receptor 4 (TLR4). We investigated the effects of wheat and ATIs on severity of colitis and fecal microbiota in mice.
C57BL/6 wild-type and Tlr4 mice were fed wheat- or ATI-containing diets or a wheat-free (control) diet and then given dextran sodium sulfate to induce colitis; we also studied Il10 mice, which develop spontaneous colitis. Changes in fecal bacteria were assessed by taxa-specific quantitative polymerase chain reaction and 16S ribosomal RNA metagenomic sequencing. Feces were collected from mice on wheat-containing, ATI-containing, control diets and transplanted to intestines of mice with and without colitis on control or on ATI-containing diets. Intestinal tissues were collected and analyzed by histology, immunohistochemistry, and flow cytometry. Bacteria with reported immunomodulatory effects were incubated with ATIs and analyzed in radial diffusion assays.
The wheat- or ATI-containing diets equally increased inflammation in intestinal tissues of C57BL/6 mice with colitis, compared with mice on control diets. The ATI-containing diet promoted expansion of taxa associated with development of colitis comparable to the wheat-containing diet. ATIs inhibited proliferation of specific human commensal bacteria in radial diffusion assays. Transplantation of microbiota from feces of mice fed the wheat- or ATI-containing diets to intestines of mice on control diets increased the severity of colitis in these mice. The ATI-containing diet did not increase the severity of colitis in Tlr4 mice.
Consumption of wheat or wheat ATIs increases intestinal inflammation in mice with colitis, via TLR4, and alters their fecal microbiota. Wheat-based, ATI-containing diets therefore activate TLR4 signaling and promote intestinal dysbiosis.
小麦已成为世界上的主要主食,其消费与非传染性疾病(如炎症性肠病)的流行密切相关。麦类中的淀粉酶抑制剂(ATIs)通过 Toll 样受体 4(TLR4)激活肠道固有免疫反应。我们研究了小麦和 ATIs 对小鼠结肠炎严重程度和粪便微生物群的影响。
用含小麦或 ATI 的饮食或无小麦(对照)饮食喂养 C57BL/6 野生型和 Tlr4 小鼠,然后给予葡聚糖硫酸钠诱导结肠炎;我们还研究了自发性结肠炎的 Il10 小鼠。通过分类特异性定量聚合酶链反应和 16S 核糖体 RNA 宏基因组测序评估粪便细菌的变化。收集含小麦、含 ATI、对照饮食的小鼠粪便,并移植到对照或含 ATI 饮食的有或无结肠炎的小鼠肠道中。收集肠组织,通过组织学、免疫组织化学和流式细胞术进行分析。用 ATIs 孵育具有报道的免疫调节作用的细菌,并在放射扩散试验中进行分析。
与对照饮食组相比,含小麦或 ATI 的饮食同样增加了 C57BL/6 结肠炎小鼠肠道组织的炎症,而含 ATI 的饮食促进了与结肠炎发展相关的分类群的扩张,与含小麦的饮食相当。ATIs 在放射扩散试验中抑制了特定人类共生菌的增殖。将来自饲喂含小麦或 ATI 饮食的小鼠粪便的微生物群移植到对照饮食的小鼠肠道中,增加了这些小鼠结肠炎的严重程度。含 ATI 的饮食并没有增加 Tlr4 小鼠结肠炎的严重程度。
小麦或小麦 ATIs 通过 TLR4 增加了结肠炎小鼠的肠道炎症,并改变了它们的粪便微生物群。基于小麦的 ATI 饮食因此激活了 TLR4 信号通路,并促进了肠道菌群失调。