Department of Chemistry and Biochemistry, University of South Carolina, Columbia, SC, 29208, USA.
Department of Chemistry, University of South Florida, Tampa, FL, 33620, USA.
Adv Healthc Mater. 2023 Dec;12(31):e2301764. doi: 10.1002/adhm.202301764. Epub 2023 Aug 30.
Among multiple approaches to combating antimicrobial resistance, a combination therapy of existing antibiotics with bacterial membrane-perturbing agents is promising. A viable platform of metallopolymers as adjuvants in combination with traditional antibiotics is reported in this work to combat both planktonic and stationary cells of Gram-negative superbugs and their biofilms. Antibacterial efficacy, toxicity, antibiofilm activity, bacterial resistance propensity, and mechanisms of action of metallopolymer-antibiotic combinations are investigated. These metallopolymers exhibit 4-16-fold potentiation of antibiotics against Gram-negative bacteria with negligible toxicity toward mammalian cells. More importantly, the lead combinations (polymer-ceftazidime and polymer-rifampicin) eradicate preformed biofilms of MDR E. coli and P. aeruginosa, respectively. Further, β-lactamase inhibition, outer membrane permeabilization, and membrane depolarization demonstrate synergy of these adjuvants with different antibiotics. Moreover, the membrane-active metallopolymers enable the antibiotics to circumvent bacterial resistance development. Altogether, the results indicate that such non-antibiotic adjuvants bear the promise to revitalize the efficacy of existing antibiotics to tackle Gram-negative bacterial infections.
在对抗抗微生物药物耐药性的多种方法中,用现有的抗生素与破坏细菌膜的药物联合进行治疗具有很大的前景。本工作报道了将金属聚合物作为佐剂与传统抗生素联合使用的可行平台,以对抗革兰氏阴性超级细菌及其生物膜的浮游细胞和静止细胞。研究了金属聚合物-抗生素组合的抗菌功效、毒性、抗生物膜活性、细菌耐药倾向和作用机制。这些金属聚合物对革兰氏阴性细菌的抗生素增效作用达到 4-16 倍,对哺乳动物细胞的毒性可忽略不计。更重要的是,这些组合(聚合物-头孢他啶和聚合物-利福平)分别消除了多药耐药大肠杆菌和铜绿假单胞菌的已形成生物膜。此外,β-内酰胺酶抑制、外膜通透性和膜去极化表明这些佐剂与不同抗生素具有协同作用。此外,这些具有膜活性的金属聚合物使抗生素能够避免细菌耐药性的发展。总之,这些结果表明,这种非抗生素佐剂具有重振现有抗生素疗效的潜力,以应对革兰氏阴性细菌感染。