Department of Animal Science, College of Animal Science and Technology, Northwest A&F University, Yangling, Shaanxi, 712100, China.
Mol Nutr Food Res. 2024 Jan;68(1):e2300236. doi: 10.1002/mnfr.202300236. Epub 2023 Oct 18.
Orosomucoid 2 (Orm2) is a hepatocyte-secreted protein that plays a crucial role in regulating obesity-type metabolic disease and immunity. The imbalance of gut microbiota is one of the causes of obesity, but the mechanism of the relationship between Orm2 and gut microbiota in obesity remains unclear.
Orm2-/- (Orm2 knockout) mice on a normal diet developed spontaneous obesity and metabolic disturbances at the 20th week. Through 16S rRNA gene sequencing, the study finds that the gut microbiota of Orm2-/- mice has a different microbial composition compared to wild type (WT) mice. Furthermore, a high-fat diet (HFD) for 16 weeks exacerbates obesity in Orm2-/- mice. Lack of Orm2 promotes dysregulation of gut microbiota under the HFD, especially a reduction of Clostridium spp. Supplementation with Clostridium butyricum alleviates obesity and alters the gut microbial composition in WT mice, but has minimal effects on Orm2-/- mice. In contrast, co-housing of Orm2-/- mice with WT mice rescues Orm2-/- obesity by reducing pathogenic bacteria and mitigating intestinal inflammation.
These findings suggest Orm2 deficiency exacerbates HFD-induced gut microbiota disturbance and intestinal inflammation, providing a novel insight into the complex bacterial flora but not a single probiotic administration in the therapeutic strategy of obesity.
血清类黏蛋白 2(Orm2)是一种由肝细胞分泌的蛋白质,在调节肥胖型代谢疾病和免疫方面发挥着关键作用。肠道微生物群失衡是肥胖的原因之一,但 Orm2 与肥胖症中肠道微生物群之间的关系机制尚不清楚。
正常饮食喂养的 Orm2-/-(Orm2 基因敲除)小鼠在第 20 周自发出现肥胖和代谢紊乱。通过 16S rRNA 基因测序,研究发现 Orm2-/- 小鼠的肠道微生物群与野生型(WT)小鼠的微生物组成不同。此外,高脂肪饮食(HFD)喂养 16 周会使 Orm2-/- 小鼠的肥胖加重。缺乏 Orm2 会促进 HFD 下肠道微生物群的失调,特别是梭菌属的减少。丁酸梭菌的补充可缓解 WT 小鼠的肥胖并改变其肠道微生物组成,但对 Orm2-/- 小鼠的影响较小。相比之下,将 Orm2-/- 小鼠与 WT 小鼠共饲养可通过减少病原菌和减轻肠道炎症来挽救 Orm2-/- 小鼠的肥胖。
这些发现表明,Orm2 缺乏会加剧 HFD 诱导的肠道微生物群失调和肠道炎症,为肥胖症的治疗策略提供了一个新的视角,即复杂的细菌菌群,而不仅仅是单一的益生菌治疗。