Department of Microbiology and Immunology, Indiana University School of Medicine, South Bend, IN, USA.
Department of Biology, University of Notre Dame, South Bend, IN, USA.
Gut Microbes. 2022 Jan-Dec;14(1):2123677. doi: 10.1080/19490976.2022.2123677.
Changes in the spatial organization, or biogeography, of colonic microbes have been observed in human inflammatory bowel disease (IBD) and mouse models of IBD. We have developed a mouse model of IBD that occurs spontaneously and consistently in the absence of adaptive immunity. Mice expressing tumor necrosis factor-induced protein 3 (TNFAIP3) in intestinal epithelial cells (villin-TNFAIP3) develop colitis when interbred with Recombination Activating 1-deficient mice (RAG1<sup>-/-</sup>). The colitis in villin-TNFAIP3 × RAG1<sup>-/-</sup> (TRAG) mice is prevented by antibiotics, indicating a role for microbes in this innate colitis. We therefore explored the biogeography of microbes and responses to antibiotics in TRAG colitis. Laser capture microdissection and 16S rRNA sequencing revealed altered microbial populations across the transverse axis of the colon as the inner mucus layer of TRAG, but not RAG1<sup>-/-</sup>, mice was infiltrated by microbes, which included increased abundance of the classes Gammaproteobacteria and Actinobacteria. Along the longitudinal axis differences in the efficacy of antibiotics to prevent colitis were evident. Neomycin was most effective for prevention of inflammation in the cecum, while ampicillin was most effective in the proximal and distal colon. RAG1<sup>-/-</sup>, but not TRAG, mice exhibited a structured pattern of bacterial abundance with decreased Firmicutes and Proteobacteria but increased Bacteroidetes along the proximal to distal axis of the gut. TRAG mice exhibited increased relative abundance of potential pathobionts including <i>Bifidobacterium animalis</i> along the longitudinal axis of the gut whereas others, like <i>Helicobacter hepaticus</i> were increased only in the cecum. Potential beneficial organisms including <i>Roseburia</i> were decreased in the proximal regions of the TRAG colon, while <i>Bifidobacterium pseudolongulum</i> was decreased in the TRAG distal colon. Thus, the innate immune system maintains a structured, spatially organized, gut microbiome along the transverse and longitudinal axis of the gut, and disruption of this biogeography is a feature of innate immune colitis.
在人类炎症性肠病 (IBD) 和 IBD 的小鼠模型中,已经观察到结肠微生物的空间组织或生物地理学发生变化。我们开发了一种自发性且一致发生的 IBD 小鼠模型,在没有适应性免疫的情况下发生。在肠上皮细胞中表达肿瘤坏死因子诱导蛋白 3 (TNFAIP3) 的小鼠 (villin-TNFAIP3) 与重组激活 1 缺陷型小鼠 (RAG1<sup>-/-</sup>) 杂交后会发生结肠炎。在 villin-TNFAIP3×RAG1<sup>-/-</sup> (TRAG) 小鼠中,抗生素可预防结肠炎,表明微生物在这种先天结肠炎中起作用。因此,我们探讨了 TRAG 结肠炎中微生物的生物地理学和对抗生素的反应。激光捕获显微切割和 16S rRNA 测序显示,随着 TRAG 小鼠的内层黏液层被微生物浸润,结肠的横向轴上微生物种群发生了改变,而 RAG1<sup>-/-</sup> 小鼠则没有。这些微生物包括γ变形菌纲和放线菌纲的丰度增加。沿纵向轴,抗生素预防结肠炎的效果存在差异。新霉素对盲肠炎症的预防最有效,而氨苄西林对近端和远端结肠最有效。RAG1<sup>-/-</sup> 而不是 TRAG 小鼠表现出细菌丰度的结构化模式,随着从近端到远端肠道的轴,厚壁菌门和变形菌门减少,但拟杆菌门增加。TRAG 小鼠沿肠道的纵向轴显示出潜在的条件致病菌(包括<i>双歧杆菌动物亚种</i>)相对丰度增加,而其他细菌(如<i>嗜肝螺杆菌</i>)仅在盲肠中增加。TRAG 结肠近端的有益菌(如<i>罗斯伯里氏菌</i>)减少,而 TRAG 远端结肠的<i>假长双歧杆菌</i>减少。因此,先天免疫系统维持着肠道的横向和纵向轴的结构化、空间组织的肠道微生物组,而这种生物地理学的破坏是先天免疫性结肠炎的一个特征。