Department of Clinical Medical Research Center, The Second Clinical Medical College of Jinan University (Shenzhen People's Hospital), Shenzhen, China.
Biotree Institute of Health, Biotree, Shanghai, China.
Front Immunol. 2020 Jul 31;11:1703. doi: 10.3389/fimmu.2020.01703. eCollection 2020.
Systemic lupus erythematosus (SLE) is a systemic autoimmune disease that affects thousands of people worldwide. Recently, alterations in metabolism and gut microbiome have emerged as key regulators of SLE pathogenesis. However, it is not clear about the coordination of gut commensal bacteria and SLE metabolism. Here, by integrating 16S sequencing and metabolomics data, we characterized the gut microbiome and fecal and serum metabolome alterations in patients with SLE. Microbial diversity sequencing revealed gut microflora dysbiosis in SLE patients with significantly increased beta diversity. The metabolomics profiling identified 43 and 55 significantly changed metabolites in serum and feces samples in SLE patients. Notably, lipids accounted for about 65% altered metabolites in serum, highlighted the disruption of lipid metabolism. Integrated correlation analysis provided a link between the gut microbiome and lipid metabolism in patients with SLE, particularly according to regulate the conversion of primary bile acids to secondary bile acids. Overall, our results illustrate the perturbation of the gut microbiome and metabolome in SLE patients which may facilitate the development of new SLE interventions.
系统性红斑狼疮(SLE)是一种影响全球数千人的自身免疫性疾病。最近,代谢和肠道微生物组的改变已成为 SLE 发病机制的关键调节因子。然而,肠道共生细菌与 SLE 代谢之间的协调关系尚不清楚。在这里,我们通过整合 16S 测序和代谢组学数据,描述了 SLE 患者的肠道微生物组和粪便及血清代谢组的改变。微生物多样性测序显示 SLE 患者的肠道微生物群落失调,β多样性显著增加。代谢组学分析鉴定出 SLE 患者血清和粪便样本中有 43 种和 55 种明显改变的代谢物。值得注意的是,脂质约占血清中 65%改变的代谢物,突出了脂质代谢的紊乱。整合的相关分析提供了 SLE 患者肠道微生物组与脂质代谢之间的联系,特别是根据调节初级胆汁酸向次级胆汁酸的转化。总的来说,我们的研究结果说明了 SLE 患者肠道微生物组和代谢组的紊乱,这可能有助于开发新的 SLE 干预措施。