化脓性链球菌                        
                
                                
                        
                            微生物学                        
                
                                
                        
                            红霉素                        
                
                                
                        
                            聚酮                        
                
                                
                        
                            生物                        
                
                                
                        
                            化学                        
                
                                
                        
                            金黄色葡萄球菌                        
                
                                
                        
                            抗生素                        
                
                                
                        
                            生物化学                        
                
                                
                        
                            细菌                        
                
                                
                        
                            基因                        
                
                                
                        
                            遗传学                        
                
                                
                        
                            生物合成                        
                
                        
                    
            作者
            
                Yuanfeng Yan,Ying Liu,Hangeri Liang,Le Cai,Xiao-Yan Yang,Tianpeng Yin            
         
                    
        
    
            
            标识
            
                                    DOI:10.1016/j.jprot.2023.105057
                                    
                                
                                 
         
        
                
            摘要
            
            The erythromycin polyketide compound TMC-154 is a secondary metabolite that is isolated from the rhizospheric fungus Clonostachys rogersoniana associated with Panax notoginseng, which possesses antibacterial activity. However, its antibacterial mechanism has not been investigated thus far. In this study, proteomics coupled with bioinformatics approaches was used to explore the antibacterial mechanism of TMC-154. KEGG pathway enrichment analysis indicated that eight signaling pathways were associated with TMC-154, including oxidative phosphorylation, cationic antimicrobial peptide (CAMP) resistance, benzoate degradation, heme acquisition systems, glycine/serine and threonine metabolism, beta-lactam resistance, ascorbate and aldarate metabolism, and phosphotransferase system (PTS). Cell biology experiments confirmed that TMC-154 could induce reactive oxygen species (ROS) generation in Streptococcus pyogenes; moreover, TMC-154-induced antibacterial effects could be blocked by the inhibition of ROS generation with the antioxidant N-acetyl L-cysteine. In addition, TMC-154 combined with ciprofloxacin or chloramphenicol had synergistic antibacterial effects. These findings indicate the potential of TMC-154 as a promising drug to treat S. pyogenes infections. Streptococcus pyogenes is a nearly ubiquitous human pathogen that causes a variety of diseases ranging from mild pharyngitis and skin infection to fatal sepsis and toxic heat shock syndrome. With the increasing incidence of known antibiotic resistance, there is an urgent need to find novel drugs with good antibacterial activity against S. pyogenes. In this study, we found that TMC-154, a secondary metabolite from the fungus Clonostachys rogersoniana, inhibited the growth of various bacteria, including Staphylococcus aureus, S. pyogenes, Streptococcus mutans, Pseudomonas aeruginosa and Vibrio parahemolyticus. Proteomic analysis combined with cell biology experiments revealed that TMC-154 stimulated ROS generation to exert antibacterial effects against S. pyogenes. This study provides potential options for the treatment of S. pyogenes infections in the future.
         
            
 
                 
                
                    
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