Identification and Evaluation of Besifloxacin as Repurposed Antifungal Drug in Combination With Fluconazole Against Candida albicans

IF 3.3 4区 医学 Q2 BIOCHEMISTRY & MOLECULAR BIOLOGY
Shuvechha Chakraborty, Ameya Pawaskar, Siddhanath Metkari, Taruna Madan, Susan Idicula-Thomas
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引用次数: 0

Abstract

Emergence of life-threatening fungal infections like systemic candidiasis concurrently with bacterial infections and limitations of current antifungal therapies warrant the discovery of novel inhibitors. We identified besifloxacin (BS), an FDA-approved antibacterial, as a potent antifungal inhibitor. A combination of besifloxacin with fluconazole showed a positive synergy (δ = 29.58) resulting in 80% inhibition of microbial growth. BS was able to reduce the MIC of FLC from 2 mg/L to 0.5 mg/L when used in combination. Additionally, in murine systemic Candida infection, BS reduced fungal load by 83% in mice kidneys at a dose of 100 mg/kg/day. The findings demonstrated the antifungal potential of BS, proposing its use in combination therapy with fluconazole to combat resistance through alternative mechanisms.

Abstract Image

贝西沙星与氟康唑联合应用抗白色念珠菌的鉴定与评价
危及生命的真菌感染,如全身性念珠菌病,与细菌感染同时出现,以及当前抗真菌治疗的局限性,需要发现新的抑制剂。我们发现贝西沙星(BS)是一种fda批准的抗菌药物,是一种有效的抗真菌抑制剂。贝西沙星与氟康唑联合使用对微生物的抑制率为80%,具有正协同效应(δ = 29.58)。BS可将FLC的MIC从2 mg/L降至0.5 mg/L。此外,在小鼠全身念珠菌感染中,100 mg/kg/天剂量的BS使小鼠肾脏的真菌负荷降低了83%。研究结果证明了BS的抗真菌潜力,建议将其与氟康唑联合治疗,通过其他机制对抗耐药性。
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来源期刊
Chemical Biology & Drug Design
Chemical Biology & Drug Design 医学-生化与分子生物学
CiteScore
5.10
自引率
3.30%
发文量
164
审稿时长
4.4 months
期刊介绍: Chemical Biology & Drug Design is a peer-reviewed scientific journal that is dedicated to the advancement of innovative science, technology and medicine with a focus on the multidisciplinary fields of chemical biology and drug design. It is the aim of Chemical Biology & Drug Design to capture significant research and drug discovery that highlights new concepts, insight and new findings within the scope of chemical biology and drug design.
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