Roder Christine, Athan Eugene
School of Medicine, Deakin University, Geelong, VIC, Australia.
Department of Infectious Diseases, Barwon Health, Geelong, VIC, Australia.
Drugs R D. 2020 Sep;20(3):209-216. doi: 10.1007/s40268-020-00306-3.
Clostridium difficile infection is the leading cause of hospital-acquired gastrointestinal infection and incidence rates continue to rise. Clostridium difficile infection is becoming increasingly complex to treat owing to the rise in treatment failures and recurrent infections. There is a clear need for new therapeutic options for the management of this disease.
This study aimed to assess auranofin, a drug approved for the treatment of arthritis, as a treatment for C. difficile infection. Previous investigations have demonstrated potential antimicrobial activity of auranofin against C. difficile and other organisms.
The activity of auranofin was assessed by in vitro investigations of its effect on C. difficile M7404 growth, vegetative cell viability, and spore viability. Activity of auranofin was also compared to that of the current treatments, metronidazole and vancomycin.
Auranofin showed bactericidal activity at concentrations as low as 4.07 µg/mL, effectively reducing bacterial cell density by 50-70% and the viable vegetative cell and spore yields by 100%. The activity of auranofin was shown to be non-inferior to that of metronidazole and vancomycin.
Auranofin is highly efficacious against C. difficile M7404 in vitro and has the potential to be an ideal therapeutic option for the treatment of C. difficile infection.
艰难梭菌感染是医院获得性胃肠道感染的主要原因,且发病率持续上升。由于治疗失败和反复感染的增加,艰难梭菌感染的治疗变得越来越复杂。显然需要新的治疗选择来管理这种疾病。
本研究旨在评估已被批准用于治疗关节炎的药物金诺芬作为艰难梭菌感染的治疗方法。先前的研究已证明金诺芬对艰难梭菌和其他微生物具有潜在的抗菌活性。
通过体外研究金诺芬对艰难梭菌M7404生长、营养细胞活力和孢子活力的影响来评估其活性。还将金诺芬的活性与当前治疗药物甲硝唑和万古霉素的活性进行比较。
金诺芬在低至4.07μg/mL的浓度下显示出杀菌活性,有效降低细菌细胞密度50%-70%,并使存活的营养细胞和孢子产量降低100%。金诺芬的活性被证明不低于甲硝唑和万古霉素。
金诺芬在体外对艰难梭菌M7404高度有效,有潜力成为治疗艰难梭菌感染的理想治疗选择。