Department of Microbiology and Molecular Genetics, Michigan State University, East Lansing, MI, USA.
BEACON Center for the Study of Evolution in Action, Michigan State University, East Lansing, MI, USA.
J Antimicrob Chemother. 2019 Apr 1;74(4):894-906. doi: 10.1093/jac/dky545.
To assess the ability of oxyclozanide to enhance tobramycin killing of Pseudomonas aeruginosa biofilms and elucidate its mechanism of action.
Twenty-four hour biofilms formed by the P. aeruginosa strain PAO1 and cystic fibrosis (CF) isolates were tested for susceptibility to oxyclozanide and tobramycin killing using BacTiter-Glo™ and cfu. Biofilm dispersal was measured using crystal violet staining. Membrane potential and permeabilization were quantified using DiOC2(3) and TO-PRO-3, respectively.
Here we show that the ionophore anthelmintic oxyclozanide, combined with tobramycin, significantly increased killing of P. aeruginosa biofilms over each treatment alone. This combination also significantly accelerated the killing of cells within biofilms and stationary phase cultures and it was effective against 4/6 CF clinical isolates tested, including a tobramycin-resistant strain. Oxyclozanide enhanced the ability of additional aminoglycosides and tetracycline to kill P. aeruginosa biofilms. Finally, oxyclozanide permeabilized cells within the biofilm, reduced the membrane potential and increased tobramycin accumulation within cells of mature P. aeruginosa biofilms.
Oxyclozanide enhances aminoglycoside and tetracycline activity against P. aeruginosa biofilms by reducing membrane potential, permeabilizing cells and enhancing tobramycin accumulation within biofilms. We propose that oxyclozanide counteracts the adaptive resistance response of P. aeruginosa to aminoglycosides, increasing both their maximum activity and rate of killing. As oxyclozanide is widely used in veterinary medicine for the treatment of parasitic worm infections, this combination could offer a new approach for the treatment of biofilm-based P. aeruginosa infections, repurposing oxyclozanide as an anti-biofilm agent.
评估奥硝哒唑增强妥布霉素对铜绿假单胞菌生物膜杀伤能力,并阐明其作用机制。
采用 BacTiter-Glo™ 和 cfu 检测法检测 24 小时铜绿假单胞菌 PAO1 株和囊性纤维化(CF)分离株形成的生物膜对奥硝哒唑和妥布霉素杀伤的敏感性。采用结晶紫染色法测量生物膜分散情况。分别采用 DiOC2(3)和 TO-PRO-3 定量测定膜电位和通透性。
本研究表明,驱虫离子载体奥硝哒唑与妥布霉素联合使用,可显著提高铜绿假单胞菌生物膜的杀伤作用,优于单独使用每种药物的效果。这种组合还显著加速了生物膜和静止期培养物中细胞的杀伤作用,对 6 株 CF 临床分离株中的 4 株(包括一株耐妥布霉素株)有效。奥硝哒唑增强了其他氨基糖苷类和四环素类药物对铜绿假单胞菌生物膜的杀伤作用。最后,奥硝哒唑使生物膜内的细胞通透性增加,降低了膜电位,并增加了妥布霉素在成熟铜绿假单胞菌生物膜内的积累。
奥硝哒唑通过降低膜电位、使细胞通透性增加并增强妥布霉素在生物膜内的积累,增强氨基糖苷类和四环素类药物对铜绿假单胞菌生物膜的活性。我们提出,奥硝哒唑对抗铜绿假单胞菌对氨基糖苷类药物的适应性耐药反应,增加了它们的最大活性和杀菌速度。由于奥硝哒唑在兽医临床上广泛用于治疗寄生虫感染,这种组合可能为治疗铜绿假单胞菌生物膜感染提供一种新方法,将奥硝哒唑重新用作抗生物膜剂。