Shi Yanmin, Yang Jianya, Tian Tao, Li Suyun, Xie Yang
National Regional Traditional Chinese Medicine (Lung Disease) Diagnosis and Treatment Center, The First Affiliated Hospital of Henan University of Chinese Medicine, Zhengzhou, China.
Collaborative Innovation Center for Chinese Medicine and Respiratory Diseases Co-Construction by Henan Province and Education Ministry of P.R. China, Henan University of Chinese Medicine, Zhengzhou, China.
Front Microbiol. 2024 Oct 16;15:1487393. doi: 10.3389/fmicb.2024.1487393. eCollection 2024.
The acute exacerbation of chronic obstructive pulmonary disease seriously affects the respiratory system function and quality of life of patients. This study employed 16S rRNA sequencing and metabolomics techniques to analyze the respiratory microbiota and serum metabolites of COPD and AECOPD patients. The results showed that the microbial diversity in the respiratory tract of AECOPD patients was significantly lower than that of COPD patients, and the relative abundance of Bacteroidetes, and in the respiratory tract of AECOPD patients was significantly lower than that of COPD patients. However, the relative abundance of , and , in AECOPD patients was significantly higher than that of COPD patients, and the ability of respiratory microbiota in AECOPD patients to participate in alanine metabolism was significantly lower than that of COPD patients. Metabolome results further revealed that the serum alanine levels in AECOPD patients were significantly lower than those in COPD patients, and these differential metabolites were mainly involved in linoleic acid metabolism, protein digestion and absorption and regulation of lipolysis in adipocytes. In summary, the structural characteristics of respiratory microbiota in COPD and AECOPD patients are different from those in healthy populations, and their microbiota diversity decreases and microbial community structure and function will also undergo changes when acute exacerbations occur. In addition, the predicted microbial community function and metabolomics results indicate that the onset of AECOPD is mainly related to energy and amino acid metabolism disorders, especially alanine metabolism.
慢性阻塞性肺疾病急性加重严重影响患者呼吸系统功能及生活质量。本研究采用16S rRNA测序和代谢组学技术分析慢性阻塞性肺疾病(COPD)和慢性阻塞性肺疾病急性加重(AECOPD)患者的呼吸道微生物群和血清代谢产物。结果显示,AECOPD患者呼吸道微生物多样性显著低于COPD患者,且AECOPD患者呼吸道中拟杆菌门、 和 的相对丰度显著低于COPD患者。然而,AECOPD患者中 、 和 的相对丰度显著高于COPD患者,且AECOPD患者呼吸道微生物群参与丙氨酸代谢的能力显著低于COPD患者。代谢组学结果进一步显示,AECOPD患者血清丙氨酸水平显著低于COPD患者,这些差异代谢产物主要参与亚油酸代谢、蛋白质消化吸收及脂肪细胞中脂解的调节。综上所述,COPD和AECOPD患者呼吸道微生物群的结构特征与健康人群不同,急性加重时其微生物群多样性降低,微生物群落结构和功能也会发生变化。此外,预测的微生物群落功能和代谢组学结果表明,AECOPD的发病主要与能量和氨基酸代谢紊乱有关,尤其是丙氨酸代谢。