代谢组                        
                
                                
                        
                            甘油磷脂                        
                
                                
                        
                            肠道菌群                        
                
                                
                        
                            代谢组学                        
                
                                
                        
                            生物                        
                
                                
                        
                            厚壁菌                        
                
                                
                        
                            代谢途径                        
                
                                
                        
                            微生物群                        
                
                                
                        
                            脂质代谢                        
                
                                
                        
                            蛋白质细菌                        
                
                                
                        
                            新陈代谢                        
                
                                
                        
                            脂肪酸代谢                        
                
                                
                        
                            亚油酸                        
                
                                
                        
                            生物化学                        
                
                                
                        
                            微生物学                        
                
                                
                        
                            脂肪酸                        
                
                                
                        
                            生物信息学                        
                
                                
                        
                            磷脂                        
                
                                
                        
                            膜                        
                
                                
                        
                            16S核糖体RNA                        
                
                                
                        
                            基因                        
                
                        
                    
            作者
            
                Yannan Zhang,Mengyao Li,Zhiyu Pu,Xi Chi,Jianjun Yang            
         
                    
        
    
            
            标识
            
                                    DOI:10.1016/j.ecoenv.2023.115182
                                    
                                
                                 
         
        
                
            摘要
            
            The relationships between fine particulate matter (PM2.5) exposure and health effects are complex and incompletely understood. Evidence suggests that PM2.5 exposure alters gut microbiota composition and metabolites, but the connections between these changes remain unclear. The aim of our study was to investigate how gut microbiota are involved in the systemic metabolic changes following PM2.5 gastrointestinal exposure. We used multi-omics approaches, including 16S rRNA sequencing and serum metabolomics, to identify alterations in gut microbes and metabolites of PM2.5-exposed rats. We then explored correlations between perturbed gut microbiota and metabolic changes, and conducted pathway analyses to determine critical metabolic pathways impacted by PM2.5 exposure. To verify links between gut microbiome and metabolome disruptions, we performed fecal microbiota transplantation (FMT) experiment. A total of 30 differential gut microbe taxa were identified between PM2.5 and control groups, primarily in Firmicutes, Acidobacteria, and Proteobacteria phyla. We also identified 30 differential metabolites, including glycerophospholipids, fatty acyls, amino acids and others. Pathway analysis revealed disruptions in glycerophospholipid metabolism, steroid hormone biosynthesis, and linoleic acid metabolism. Through FMT, we confirmed PM2.5 altered phosphatidylcholine and linoleic acid metabolism by changing specific gut bacteria. Our results suggest that PM2.5 gastrointestinal exposure triggers systemic metabolic changes by disrupting the gut microbiome, especially glycerophospholipid and linoleic acid metabolism pathways.
         
            
 
                 
                
                    
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