Niclosamide as a Repurposing Drug against <i>Corynebacterium striatum</i> Multidrug-Resistant Infections
<i>Corynebacterium striatum</i> (<i>C. striatum</i>) is an emerging multidrug-resistant (MDR) pathogen associated with nosocomial infections. In this scenario, we screened the antimicrobial activity of the anthelmintic drugs doramectin, moxidectin, selamectin and niclosamide...
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Main Authors: | , , , , , , , , , , |
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Format: | Book |
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MDPI AG,
2022-05-01T00:00:00Z.
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Summary: | <i>Corynebacterium striatum</i> (<i>C. striatum</i>) is an emerging multidrug-resistant (MDR) pathogen associated with nosocomial infections. In this scenario, we screened the antimicrobial activity of the anthelmintic drugs doramectin, moxidectin, selamectin and niclosamide against 20 <i>C. striatum</i> MDR clinical isolates. Among these, niclosamide was the best performing drug against <i>C. striatum</i>. Niclosamide cytotoxicity was evaluated by a 3-(4,5-dimethylthiazol-2-yl)-2,5-diphenyl tetrazolium bromide (MTT) assay on immortalized human keratinocyte cells (HaCaT). After 20 h of treatment, the recorded 50% cytotoxic concentration (CC<sub>50</sub>) was 2.56 μg/mL. The antibacterial efficacy was determined via disc diffusion, broth microdilution method and time-killing. Against <i>C. striatum</i>, niclosamide induced a growth inhibitory area of 22 mm and the minimum inhibitory concentration that inhibits 90% of bacteria (MIC<sub>90</sub>) was 0.39 μg/mL, exhibiting bactericidal action. The biofilm biomass eradicating action was investigated through crystal violet (CV), MTT and confocal laser scanning microscopy (CLSM). Niclosamide affected the biofilm viability in a dose-dependent manner and degraded biomass by 55 and 49% at 0.39 μg/mL and 0.19 μg/mL. CLSM images confirmed the biofilm biomass degradation, showing a drastic reduction in cell viability. This study could promote the drug-repurposing of the anthelmintic FDA-approved niclosamide as a therapeutic agent to counteract the <i>C. striatum</i> MDR infections. |
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Item Description: | 10.3390/antibiotics11050651 2079-6382 |