Center for Microbial Pathogenesis, The Research Institute at Nationwide Children's Hospital, Columbus, OH, United States.
Mead Johnson Pediatric Nutrition Institute, Evansville, IN, United States.
Front Immunol. 2019 Jul 29;10:1774. doi: 10.3389/fimmu.2019.01774. eCollection 2019.
Exposure to stressful stimuli dysregulates inflammatory processes and alters the gut microbiota. Prebiotics, including long-chain fermentable fibers and milk oligosaccharides, have the potential to limit inflammation through modulation of the gut microbiota. To determine whether prebiotics attenuate stress-induced inflammation and microbiota perturbations, mice were fed either a control diet or a diet supplemented with galactooligosaccharides, polydextrose and sialyllactose (GOS+PDX+SL) or sialyllactose (SL) for 2 weeks prior to and during a 6-day exposure to a social disruption stressor. Spleens were collected for immunoreactivity assays. Colon contents were examined for stressor- and diet- induced changes in the gut microbiome and metabolome through 16S rRNA gene sequencing, shotgun metagenomic sequencing and UPLC-MS/MS. Stress increased circulating IL-6 and enhanced splenocyte immunoreactivity to an LPS challenge. Diets containing GOS+PDX+SL or SL alone attenuated these responses. Stress exposure resulted in large changes to the gut metabolome, including robust shifts in amino acids, peptides, nucleotides/nucleosides, tryptophan metabolites, and B vitamins. Multiple B vitamins were inversely associated with IL-6 and were augmented in mice fed either GOS+PDX+SL or SL diets. Stressed mice exhibited distinct microbial communities with lower abundances of spp. and higher abundances of spp. Diet supplementation with GOS+PDX+SL, but not SL alone, orthogonally altered the microbiome and enhanced the growth of spp. Metagenome-assembled genomes (MAGs) from mice fed the GOS+PDX+SL diet unveiled genes in a MAG for B vitamin synthesis. B vitamers directly attenuated the stressor-induced exacerbation of cytokine production in LPS-stimulated splenocytes. Overall, these data indicate that colonic metabolites, including B vitamins, are responsive to psychosocial stress. Dietary prebiotics reestablish colonic B vitamins and limit stress-induced inflammation.
暴露于应激刺激会扰乱炎症过程并改变肠道微生物群。益生元,包括长链可发酵纤维和乳寡糖,通过调节肠道微生物群有可能限制炎症。为了确定益生元是否可以减轻应激引起的炎症和微生物群扰动,在 6 天的社交破坏应激暴露之前和期间,将小鼠喂食对照饮食或补充半乳糖寡糖、聚右旋糖和唾液酸乳糖(GOS+PDX+SL)或唾液酸乳糖(SL)的饮食 2 周。收集脾脏进行免疫反应性测定。通过 16S rRNA 基因测序、鸟枪法宏基因组测序和 UPLC-MS/MS 检查结肠内容物,以检查应激和饮食引起的肠道微生物组和代谢组的变化。应激增加了循环中的 IL-6,并增强了 LPS 挑战后脾细胞的免疫反应性。含有 GOS+PDX+SL 或 SL 的饮食单独减轻了这些反应。应激暴露导致肠道代谢组发生了很大变化,包括氨基酸、肽、核苷酸/核苷、色氨酸代谢物和 B 族维生素的剧烈转移。多种 B 族维生素与 IL-6 呈负相关,并且在喂食 GOS+PDX+SL 或 SL 饮食的小鼠中增加。应激小鼠表现出独特的微生物群落,属的丰度较低,属的丰度较高。仅补充 GOS+PDX+SL 而不是 SL 会改变微生物群并促进属的生长。喂食 GOS+PDX+SL 饮食的小鼠的宏基因组组装基因组(MAG)揭示了用于 B 族维生素合成的 MAG 中的基因。B 维生素直接减弱了 LPS 刺激的脾细胞中应激源诱导的细胞因子产生的加剧。总体而言,这些数据表明,结肠代谢物,包括 B 族维生素,对心理社会应激有反应。膳食益生元重建结肠 B 族维生素并限制应激引起的炎症。