Lin Qiong, Hao Wu-Juan, Zhou Ren-Min, Huang Cui-Lan, Wang Xu-Yang, Liu Yan-Shan, Li Xiao-Zhong
Nephrology and Immunology Department, Children's Hospital of Soochow University, Suzhou, Jiangsu, China.
Department of Digestive, Affiliated Children's Hospital of Jiangnan University, Wuxi, Jiangsu, China.
Front Microbiol. 2023 Jun 6;14:1211259. doi: 10.3389/fmicb.2023.1211259. eCollection 2023.
Inflammatory bowel disease (IBD) is a chronic lifelong inflammatory disease. Probiotics such as are considered to be beneficial to the recovery of intestinal inflammation by interaction with gut microbiota. Our goals were to define the effect of the exclusive use of BAA2573 on dextran sulfate sodium (DSS)-induced colitis, including improvement of symptoms, alleviation of histopathological damage, and modulation of gut microbiota.
In the present study, we pretreated C57BL/6J mice with BAA2573, one of the main components in an over-the-counter (OTC) probiotic mixture BIFOTO capsule, before modeling with DSS. 16S rDNA sequencing and liquid chromatography-tandem mass spectrometry (LC-MS/MS)-based non-targeted metabolomic profiling were performed with the collected feces.
We found that pretreatment of BAA2573 given by gavage significantly improved symptoms and histopathological damage in DSS-induced colitis mice. After the BAA2573 intervention, 57 genera and 39 metabolites were significantly altered. Pathway enrichment analysis demonstrated that starch and sucrose metabolism, vitamin B6 metabolism, and sphingolipid metabolism may contribute to ameliorating colitis. Moreover, we revealed that the gut microbiome and metabolites were interrelated in the BAA2573 intervention group, while Alistipes was the core genus.
Our study demonstrates the impact of BAA2573 on the gut microbiota and reveals a possible novel adjuvant therapy for IBD patients.
炎症性肠病(IBD)是一种慢性终身炎症性疾病。诸如[具体益生菌名称未给出]等益生菌被认为通过与肠道微生物群相互作用,对肠道炎症的恢复有益。我们的目标是确定单独使用BAA2573对葡聚糖硫酸钠(DSS)诱导的结肠炎的影响,包括症状改善、组织病理学损伤减轻以及肠道微生物群的调节。
在本研究中,我们在用DSS建模之前,用非处方(OTC)益生菌混合物BIFOTO胶囊中的主要成分之一BAA2573对C57BL/6J小鼠进行预处理。对收集的粪便进行16S rDNA测序和基于液相色谱 - 串联质谱(LC - MS/MS)的非靶向代谢组学分析。
我们发现通过灌胃给予BAA2573预处理可显著改善DSS诱导的结肠炎小鼠的症状和组织病理学损伤。BAA2573干预后,57个属和39种代谢物发生了显著变化。通路富集分析表明,淀粉和蔗糖代谢、维生素B6代谢以及鞘脂代谢可能有助于改善结肠炎。此外,我们发现BAA2573干预组中肠道微生物群和代谢物相互关联,而Alistipes是核心属。
我们的研究证明了BAA2573对肠道微生物群的影响,并揭示了一种可能用于IBD患者的新型辅助治疗方法。