Sorenson Trent R, Zack Kira M, Joshi Suresh G
Center for Surgical Infections & Biofilm, School of Biomedical Engineering, Science & Health Systems, Drexel University, Philadelphia, PA 19104, USA.
Center for Surgical Infections & Biofilm, Department of Surgery, College of Medicine, Drexel University, Philadelphia, PA 19102, USA.
Microorganisms. 2025 Aug 4;13(8):1816. doi: 10.3390/microorganisms13081816.
Nosocomial infections caused by ESKAPE pathogens represent a significant burden to global health. These pathogens may exhibit multidrug resistance (MDR) mechanisms, of which mechanisms such as efflux pumps and biofilm formation are gaining significant importance. Multidrug resistance mechanisms in ESKAPE pathogens have led to an increase in the effective costs in health care and a higher risk of mortality in hospitalized patients. These pathogens utilize antimicrobial efflux pump mechanisms and bacterial biofilm-forming capabilities to escape the bactericidal action of antimicrobials. ESKAPE bacteria forming colonies demonstrate increased expression of efflux pump-encoding genes. Efflux pumps not only expel antimicrobial agents but also contribute to biofilm formation by bacteria through (1) transport of molecules and transcription factors involved in biofilm quorum sensing, (2) bacterial fimbriae structure transport for biofilm adhesion to surfaces, and (3) regulation of a transmembrane gradient to survive the difficult conditions of biofilm microenvironments. The synergistic role of these mechanisms complicates treatment outcomes. Given the mechanistic link between biofilms and efflux pumps, therapeutic strategies should focus on targeting anti-biofilm mechanisms alongside efflux pump inactivation with efflux pump inhibitors. This review explores the molecular interplay between efflux pumps and biofilm formation, emphasizing potential therapeutic strategies such as efflux pump inhibitors (EPIs) and biofilm-targeting agents.
由ESKAPE病原体引起的医院感染给全球健康带来了沉重负担。这些病原体可能表现出多重耐药(MDR)机制,其中诸如外排泵和生物膜形成等机制正变得越来越重要。ESKAPE病原体中的多重耐药机制导致了医疗保健有效成本的增加以及住院患者更高的死亡风险。这些病原体利用抗菌外排泵机制和细菌生物膜形成能力来逃避抗菌药物的杀菌作用。形成菌落的ESKAPE细菌表现出外排泵编码基因的表达增加。外排泵不仅能排出抗菌剂,还通过以下方式促进细菌生物膜的形成:(1)转运参与生物膜群体感应的分子和转录因子;(2)转运细菌菌毛结构以实现生物膜与表面的粘附;(3)调节跨膜梯度以在生物膜微环境的恶劣条件下存活。这些机制的协同作用使治疗结果变得复杂。鉴于生物膜和外排泵之间的机制联系,治疗策略应侧重于靶向抗生物膜机制,同时使用外排泵抑制剂使外排泵失活。本综述探讨了外排泵与生物膜形成之间的分子相互作用,强调了潜在的治疗策略,如外排泵抑制剂(EPI)和生物膜靶向剂。