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Niclosamide as a repurposing drug against Gram-positive bacterial infections

氯硝柳胺 金黄色葡萄球菌 微生物学 体内 抗菌剂 革兰氏阳性菌 抗菌活性 药理学 化学 细菌 生物 生态学 遗传学 生物技术
作者
Wei Zhang,Jinxin Ran,Lu Shang,Lifang Zhang,Mi Wang,Chenzhong Fei,Chan Chen,Feng Gu,Yingchun Liu
出处
期刊:Journal of Antimicrobial Chemotherapy [Oxford University Press]
卷期号:77 (12): 3312-3320 被引量:7
标识
DOI:10.1093/jac/dkac319
摘要

Niclosamide is commonly used as an antiparasitic drug in veterinary clinics. The objectives of this study were to evaluate the efficacy of niclosamide against resistant Gram-positive bacteria in vitro and in an in vivo experimental model of topical bacterial infection. Moreover, to study the antibacterial mechanism of niclosamide to Staphylococcus aureus.A mouse topical infection model was established to detect the antibacterial activity of niclosamide in vivo. The antimicrobial mechanism was probed by visualizing the bacterial morphologies using scanning electron microscopy and transmission electron microscopy. Moreover, the haemolytic assay and western blotting analysis were performed to evaluate whether niclosamide could inhibit the secretion of alpha-haemolysin (α-HL) from S. aureus.The MICs of niclosamide were below 0.5 mg/L for Gram-positive bacteria, showing excellent antibacterial activity in vitro. The in vivo antibacterial activity results indicated that niclosamide treatment at 10 mg/kg of body weight caused a significant reduction in the abscess area and the number of S. aureus cells. Moreover, the antibacterial mechanism of niclosamide showed that the surface morphology of S. aureus displayed noticeable shrinkage, with an increasing number of small vacuole-like structures observed as the drug concentration increased. Intracellular ATP levels were found to decrease in a niclosamide dose-dependent manner. Haemolysis and western blotting analyses revealed that niclosamide inhibited the haemolytic activity of S. aureus by inhibiting α-HL expression under subinhibitory concentration conditions.Niclosamide has significant potential for development into drugs that prevent and treat diseases caused by Gram-positive bacteria such as Staphylococcus and Streptococcus.
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