School of Pharmacy, Shenzhen University Medical School, Shenzhen University, Shenzhen, 518055, Guangdong, China.
Department of Infectious Diseases and Shenzhen Key Laboratory for Endogenous Infections, Huazhong University of Science and Technology Union Shenzhen Hospital, No. 89 Taoyuan Road, Nanshan District, Shenzhen, 518052, China.
Curr Microbiol. 2024 Nov 25;82(1):8. doi: 10.1007/s00284-024-04001-3.
Infections and antimicrobial resistance are becoming serious global public health crises. Multidrug-resistant Staphylococcus aureus (S. aureus) infections necessitate novel antimicrobial development. In this study, we demonstrated TAK-285, a novel dual HER2/EGFR inhibitor, exerted antibacterial activity against 17 clinical methicillin-resistant S. aureus (MRSA) and 15 methicillin sensitive S. aureus (MSSA) isolates in vitro, with a minimum inhibitory concentration (MIC) of 13.7 μg/mL. At 1 × MIC, TAK-285 completely inhibited the growth of S. aureus bacterial planktonic cells, and at 2 × MIC, it exhibited a superior inhibitory effect on intracellular S. aureus SA113-GFP compared to linezolid. Moreover, TAK-285 effectively inhibited biofilm formation at sub-MIC, eradicated mature biofilm and eliminated bacteria within biofilms, as confirmed by CLSM. Furthermore, the disruption of cell membrane permeability and potential was found by TAK-285 on S. aureus, suggesting its targeting of cell membrane integrity. Global proteomic analysis demonstrated that TAK-285 disturbed the metabolic processes of S. aureus, interfered with biofilm-related gene expression, and disrupted membrane-associated proteins. Conclusively, we repurposed TAK-285 as an antimicrobial with anti-biofilm properties against S. aureus by targeting cell membrane. This study provided strong evidence for the potential of TAK-285 as a promising antimicrobial agent against S. aureus.
感染和抗微生物药物耐药性正成为严重的全球公共卫生危机。耐多药金黄色葡萄球菌(S. aureus)感染需要新的抗菌药物开发。在这项研究中,我们证明了新型双重 HER2/EGFR 抑制剂 TAK-285 在体外对 17 株临床耐甲氧西林金黄色葡萄球菌(MRSA)和 15 株甲氧西林敏感金黄色葡萄球菌(MSSA)分离株具有抗菌活性,最低抑菌浓度(MIC)为 13.7μg/mL。在 1×MIC 时,TAK-285 完全抑制了金黄色葡萄球菌浮游细胞的生长,在 2×MIC 时,它对细胞内金黄色葡萄球菌 SA113-GFP 的抑制作用优于利奈唑胺。此外,TAK-285 在亚 MIC 时有效抑制生物膜形成,根除成熟生物膜并消除生物膜内的细菌,这一点通过 CLSM 得到了证实。此外,TAK-285 对金黄色葡萄球菌的细胞膜通透性和电位有破坏作用,表明其针对细胞膜完整性。全蛋白质组分析表明,TAK-285 扰乱了金黄色葡萄球菌的代谢过程,干扰了生物膜相关基因的表达,并破坏了膜相关蛋白。总之,我们通过靶向细胞膜将 TAK-285 重新用作具有抗生物膜特性的抗金黄色葡萄球菌药物。这项研究为 TAK-285 作为一种有前途的抗金黄色葡萄球菌药物提供了有力证据。