首页|期刊导航|食品与发酵工业|联合宏基因组学及代谢组学探讨长双歧杆菌长亚种HSBL001后生元缓解结肠炎作用机制

联合宏基因组学及代谢组学探讨长双歧杆菌长亚种HSBL001后生元缓解结肠炎作用机制OA

Mechanism of the effect of postbiotic from Bifidobacterium longum subsp. longum HSBL001 on colitis based on integrated metagenomics and metabolomics

中文摘要英文摘要

后生元是指对宿主健康有益的灭活微生物或包括其代谢产物,相比活的益生菌,其具有更高的安全性、稳定性及更广泛的作用靶点,在缓解炎性肠病方面具有显著优势.研究以葡聚糖硫酸钠诱导的溃疡性结肠炎小鼠为模型,评价长双歧杆菌长亚种HSBL001后生元(HSBL001)对溃疡性结肠炎症状的改善作用,并结合宏基因组学及代谢组学探讨其潜在机制.结果显示,HSBL001干预可显著缓解结肠炎系列症状,表现为降低疾病活动指数、增加结肠长度、改善组织病理学损伤、缓解炎症(提高IL-10抗炎因子分泌,降低IL-6和TNF-α促炎因子分泌)和脾脏肿大.宏基因组数据分析表明,HSBLO01能够调节肠道菌群的组成和丰度,维持肠道菌群稳态.HS-BL001 显著提高了 Duncaniella dubosii、Faecalibaculum rodentium 和 Bacteroides thetaiotaomicron 等有益菌的丰度,降低了 Mucispirillum schaedleri、Pumilib acter muris等的丰度.代谢组学分析表明,相比于模型组,HSBL001显著上调了 95种代谢物,包括S-亚硝基谷胱甘肽、α-亚麻酸和7α-羟基-3-氧代胆甾-4-烯-27-酸等,且显著下调了 3-羟基异戊酸和N-乙酰葡糖胺醇等80种代谢物水平.对差异代谢物通路富集分析表明,HSBL001主要调节初级胆汁酸生物合成和α-亚麻酸代谢等通路.综上所述,补充长双歧杆菌长亚种HSBL001后生元可以缓解溃疡性结肠炎小鼠症状,其潜在机制与调节肠道菌群组成相关,还可提高D.dubosii和F.rodentium等丰度,同时可调节初级胆汁酸生物合成和α-亚麻酸代谢,该研究为缓解结肠炎症状提供新的干预方法和研究思路,也为后生元的产业化应用提供理论依据.

Postbiotics are inactivated microorganisms or included their metabolites that benefit host health.Compared with probiotics,they have higher safety,stronger stability,and a broader range of action targets,thus showing significant advantages in alleviating inflam-matory bowel disease.This study evaluated the ameliorative effect of the postbiotic from Bifidobacterium longum subsp.longum HSBLOO1 on dextran sulfate sodium-induced ulcerative colitis mouse model,and explored the potential mechanism of this effect via metagenomics and metabolomics.Results indicate that HSBL001 significantly alleviates colitis-related symptoms,including reducing the disease activity index,increasing colon length,improving histopathological damage,regulating inflammatory cytokine secretion(increasing IL-10 while decreasing IL-6 and TNF-α),and alleviating splenomegaly.Metagenomic analysis showed that HSBL001 significantly increased the abun-dance of beneficial bacteria such as Duncaniella dubosii,Faecalibacterium rodentium,and Bacteroides thetaiotaomicron,while reducing the abundance of bacteria like Mucispirillum schaedleri and Pumilibacter muris.Metabolomic analysis revealed that HSBLO01 significant-ly upregulated 95 metabolites compared to the model group,including S-nitrosoglutathione,α-linolenic acid,and 7α-hydroxy-3-oxochol-est-4-en-27-oic acid,while significantly downregulating 80 metabolites including 3-hydroxyisovaleric acid and N-Acetyl-D-glucosaminitol.Pathway enrichment analysis of these differential metabolites shows that the postbiotic alleviates colitis mainly by regulating pathways such as primary bile acid biosynthesis and α-linolenic acid metabolism.In conclusion,supplementation with the HSBL001 effectively alleviates ulcerative colitis symptoms in mice.Its potential mechanisms are closely linked to regulating gut microbiota composition,increasing the a-bundance of bacteria such as D.dubosii and F.rodentium,as well as modulating primary bile acid biosynthesis and α-linolenic acid metab-olism.This study provides a new intervention method and research insights for alleviating colitis,and a theoretical basis for the industrial application of postbiotics.

刘建兵;程浩;熊艳霞;陈会军;殷丽丽;梅丽亚;张妍;谢有发;张阳

江中药业股份有限公司,江西 南昌,330077江中药业股份有限公司,江西 南昌,330077江中药业股份有限公司,江西 南昌,330077晋城海斯制药有限公司,山西 晋城,048006晋城海斯制药有限公司,山西 晋城,048006江中药业股份有限公司,江西 南昌,330077江中药业股份有限公司,江西 南昌,330077江中药业股份有限公司,江西 南昌,330077江中药业股份有限公司,江西 南昌,330077

葡聚糖硫酸钠炎症因子胆汁酸代谢溃疡性结肠炎乳基后生元

dextran sodium sulfateinflammatory factorsbile acid metabolismulcerative colitismilk-based postbiotic elements

《食品与发酵工业》 2026 (5)

121-131,11

江西省高价值专利培育项目(微生态大健康产品关键技术及产业化研究)

10.13995/j.cnki.11-1802/ts.044477

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