Lai Hsin-Chih, Lin Tzu-Lung, Chen Ting-Wen, Kuo Yu-Lun, Chang Chih-Jung, Wu Tsung-Ru, Shu Ching-Chung, Tsai Ying-Huang, Swift Simon, Lu Chia-Chen
Department of Medical Biotechnology and Laboratory Science, College of Medicine, Chang Gung University, Taoyuan, Taiwan.
Microbiota Research Center and Emerging Viral Infections Research Center, Chang Gung University, Taoyuan, Taiwan.
Gut. 2022 Feb;71(2):309-321. doi: 10.1136/gutjnl-2020-322599. Epub 2021 Mar 9.
Chronic obstructive pulmonary disease (COPD) is a global disease characterised by chronic obstruction of lung airflow interfering with normal breathing. Although the microbiota of respiratory tract is established to be associated with COPD, the causality of gut microbiota in COPD development is not yet established. We aimed to address the connection between gut microbiota composition and lung COPD development, and characterise bacteria and their derived active components for COPD amelioration.
A murine cigarette smoking (CS)-based model of COPD and strategies evaluating causal effects of microbiota were performed. Gut microbiota structure was analysed, followed by isolation of target bacterium. Single cell RNA sequencing, together with sera metabolomics analyses were performed to identify host responsive molecules. Bacteria derived active component was isolated, followed by functional assays.
Gut microbiota composition significantly affects CS-induced COPD development, and faecal microbiota transplantation restores COPD pathogenesis. A commensal bacterium was isolated and shown to ameliorate COPD. Reduction of intestinal inflammation and enhancement of cellular mitochondrial and ribosomal activities in colon, systematic restoration of aberrant host amino acids metabolism in sera, and inhibition of lung inflammations act as the important COPD ameliorative mechanisms. Besides, the lipopolysaccharide derived from is anti-inflammatory, and significantly ameliorates COPD by acting as an antagonist of toll-like receptor 4 signalling pathway.
The gut microbiota-lung COPD axis was connected. A potentially benefial bacterial strain and its functional component may be developed and used as alternative agents for COPD prevention or treatment.
慢性阻塞性肺疾病(COPD)是一种全球性疾病,其特征为肺气流长期受阻,影响正常呼吸。尽管呼吸道微生物群已被证实与COPD有关,但肠道微生物群在COPD发展中的因果关系尚未明确。我们旨在探讨肠道微生物群组成与肺部COPD发展之间的联系,并鉴定可改善COPD的细菌及其衍生的活性成分。
采用基于小鼠吸烟(CS)的COPD模型以及评估微生物群因果效应的策略。分析肠道微生物群结构,随后分离目标细菌。进行单细胞RNA测序以及血清代谢组学分析,以鉴定宿主反应性分子。分离细菌衍生的活性成分,随后进行功能测定。
肠道微生物群组成显著影响CS诱导的COPD发展,粪便微生物群移植可恢复COPD发病机制。分离出一种共生细菌,其可改善COPD。减轻肠道炎症、增强结肠细胞线粒体和核糖体活性、系统性恢复血清中异常的宿主氨基酸代谢以及抑制肺部炎症是重要的COPD改善机制。此外,源自该细菌的脂多糖具有抗炎作用,通过作为Toll样受体4信号通路的拮抗剂显著改善COPD。
肠道微生物群与肺部COPD轴相联系。一种潜在有益的菌株及其功能成分可能被开发并用作COPD预防或治疗的替代药物。