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肠道微生物群紊乱和血浆代谢谱可能与淋巴结结核有关。

Disorders of Gut Microbiota and Plasma Metabolic Profiles May Be Associated with Lymph Node Tuberculosis.

作者信息

Long Yun, Huang Jiamin, Zheng Shasha, Bai Shimeng, Liu Zhe, Li Xue, Gao Wenying, Ke Xue, Tang Yunyan, Yang Liang, Wang Haijiang, Li Guobao

机构信息

Shenzhen Third People's Hospital, National Clinical Research Centre for Infectious Disease, The Second Affiliated Hospital of Southern University of Science and Technology, Shenzhen 518112, China.

Department of Pharmacology, Joint Laboratory of Guangdong-Hong Kong Universities for Vascular Homeostasis and Diseases, SUSTech Homeostatic Medicine Institute, School of Medicine, Southern University of Science and Technology, Shenzhen 518055, China.

出版信息

Microorganisms. 2025 Jun 23;13(7):1456. doi: 10.3390/microorganisms13071456.

Abstract

The association of gut microbiota with lymph node tuberculosis (LNTB) remains unexplored. This study employed metagenomic sequencing and plasma metabolomics analyses to investigate the role of gut microbiota in LNTB patients. Significant alterations in gut microbial diversity were observed in LNTB patients, characterized by a notable reduction in bacterial taxa involved in short-chain fatty acid (SCFA) synthesis, including , , , and , compared to healthy individuals. KEGG pathway analysis further revealed that gut dysbiosis could negatively impact SCFA biosynthesis and metabolism. Plasma metabolomics demonstrated disruptions in metabolites associated with SCFA synthesis and inflammation pathways in the LNTB group. Integrated analysis indicated significant correlations between specific gut microbiota (, , , , , ) and plasma metabolites, including α-benzylbutyric acid, acetic acid, and succinic acid. Our findings demonstrate that gut microbiota dysbiosis and related metabolic dysfunction significantly reduce SCFA production in LNTB patients, potentially identifying novel therapeutic targets for LNTB management.

摘要

肠道微生物群与淋巴结结核(LNTB)之间的关联尚未得到探索。本研究采用宏基因组测序和血浆代谢组学分析来研究肠道微生物群在LNTB患者中的作用。与健康个体相比,LNTB患者的肠道微生物多样性发生了显著变化,其特征是参与短链脂肪酸(SCFA)合成的细菌类群显著减少,包括 、 、 和 。KEGG通路分析进一步表明,肠道生态失调会对SCFA的生物合成和代谢产生负面影响。血浆代谢组学显示,LNTB组中与SCFA合成和炎症通路相关的代谢物出现紊乱。综合分析表明,特定的肠道微生物群( 、 、 、 、 、 )与血浆代谢物之间存在显著相关性,这些代谢物包括α-苄基丁酸、乙酸和琥珀酸。我们的研究结果表明,肠道微生物群失调和相关的代谢功能障碍显著降低了LNTB患者的SCFA产生,这可能为LNTB的管理确定新的治疗靶点。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/5ff6/12298930/3264363c9342/microorganisms-13-01456-g001.jpg

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