Stedtfeld Robert D, Chai Benli, Crawford Robert B, Stedtfeld Tiffany M, Williams Maggie R, Xiangwen Shao, Kuwahara Tomomi, Cole James R, Kaminski Norbert E, Tiedje James M, Hashsham Syed A
Department of Civil and Environmental Engineering, East LansingMI, United States.
Center for Microbial Ecology, Michigan State University, East LansingMI, United States.
Front Microbiol. 2017 Sep 7;8:1708. doi: 10.3389/fmicb.2017.01708. eCollection 2017.
Environmental toxicants such as 2,3,7,8-tetrachlorodibenzo--dioxin (TCDD), an aryl hydrocarbon receptor (AhR), are known to induce host toxicity and structural shifts in the gut microbiota. Key bacterial populations with similar or opposing functional responses to AhR ligand exposure may potentially help regulate expression of genes associated with immune dysfunction. To examine this question and the mechanisms for AhR ligand-induced bacterial shifts, C57BL/6 gnotobiotic mice were colonized with and without segmented filamentous bacteria (SFB) - an immune activator. Mice were also colonized with polysaccharide A producing - an immune suppressor to serve as a commensal background. Following colonization, mice were administered TCDD (30 μg/kg) every 4 days for 28 days by oral gavage. Quantified with the nCounter mouse immunology panel, opposing responses in ileal gene expression (e.g., genes associated with T-cell differentiation via the class II major histocompatibility complex) as a result of TCDD dosing and SFB colonization were observed. Genes that responded to TCDD in the presence of SFB did not show a significant response in the absence of SFB, and vice versa. Regulatory T-cells examined in the mesenteric lymph-nodes, spleen, and blood were also less impacted by TCDD in mice colonized with SFB. TCDD-induced shifts in abundance of SFB and compared with previous studies in mice with a traditional gut microbiome. With regard to the mouse model colonized with individual populations, results indicate that TCDD-induced host response was significantly modulated by the presence of SFB in the gut microbiome, providing insight into therapeutic potential between AhR ligands and key commensals.
环境毒素,如2,3,7,8-四氯二苯并 - 对二恶英(TCDD)这种芳烃受体(AhR),已知会诱导宿主毒性并导致肠道微生物群的结构变化。对AhR配体暴露具有相似或相反功能反应的关键细菌种群可能有助于调节与免疫功能障碍相关基因的表达。为了研究这个问题以及AhR配体诱导细菌变化的机制,将有无分节丝状细菌(SFB,一种免疫激活剂)定殖于C57BL / 6无菌小鼠体内。小鼠还定殖有产生多糖A的细菌(一种免疫抑制剂)作为共生背景。定殖后,通过口服灌胃每4天给小鼠施用TCDD(30μg / kg),持续28天。用nCounter小鼠免疫学检测板进行定量分析,观察到由于TCDD给药和SFB定殖导致的回肠基因表达的相反反应(例如,通过II类主要组织相容性复合体与T细胞分化相关的基因)。在有SFB存在的情况下对TCDD有反应的基因在没有SFB的情况下未显示出显著反应,反之亦然。在肠系膜淋巴结、脾脏和血液中检测的调节性T细胞在定殖有SFB的小鼠中也受TCDD的影响较小。与先前对具有传统肠道微生物群的小鼠的研究相比,TCDD诱导的SFB丰度变化。关于定殖有单个种群的小鼠模型,结果表明肠道微生物群中SFB的存在显著调节了TCDD诱导的宿主反应,为AhR配体与关键共生菌之间的治疗潜力提供了见解。