稀聚维酮碘对多重耐药细菌生物膜、真菌生物膜和真菌孢子的抑制作用

Kara Capriotti, J. Pelletier, S. Barone, J. Capriotti
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引用次数: 26

摘要

目的:研究新型低剂量聚维碘定制剂对已建立的多重耐药金黄色葡萄球菌、肺炎克雷伯菌、铜绿假单胞菌和白色念珠菌生物膜的体外抑菌效果,并测定其对金黄色念珠菌、毛癣菌、犬小孢子菌、白色念珠菌和烟曲霉的最小抑菌浓度。方法:采用卡尔加里生物膜装置板在固体表面制备多重耐药金黄色葡萄球菌、肺炎克雷伯菌、铜绿假单胞菌和白色念珠菌的生物膜。然后确定每种试验药物以及已知抗菌剂环丙沙星和伊曲康唑的对照样品的最小生物膜根除浓度。在Sabouraud’s Dextrose琼脂平板上培养耳念珠菌、墨农毛菌、犬小孢子菌、白色念珠菌和烟曲霉等质量控制真菌菌株进行抗真菌敏感性试验。结果:低剂量聚维酮碘制剂完全消除了试验系统中所有细菌和真菌物种的生物膜。环丙沙星只有在浓度大于0.25 ug/mL时才能够根除一个细菌生物膜。氟康唑对白色念珠菌、烟曲霉和耳念珠菌无效。两性霉素B对真菌具有良好的抗真菌活性。结论:这些新型稀释PVP-I制剂是有效的体外抗生物膜和抗真菌/杀孢剂。有必要在活体模型中进行进一步的评估。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Efficacy of Dilute Povidone-Iodine against Multi- Drug Resistant Bacterial Biofilms, Fungal Biofilms and Fungal Spores
Objective: To study the in vitro effect of novel low-dose povidoneiodine formulations against established biofilms of multi-drug resistant Staphylococcus aureus, Klebsiella pneumoniae, Pseudomonas aeruginosa and Candida albicans and to test the Minimal Inhibitory Concentration of the same formulations against Candida auris, Trichophton mentagrophytes, Microsporum canis, Candida albicans and Aspergillus fumigatus. Methods: Biofilms of multi-drug resistant Staphylococcus aureus, Klebsiella pneumoniae, Pseudomonas aeruginosa and Candida albicans were developed on solid surfaces using the Calgary Biofilm Device plate. Minimum biofilm eradication concentration was then determined for each test drug and for control samples of known antimicrobials, ciprofloxacin and itraconazole. Quality control fungal strains of Candida auris, Trichophton mentagrophytes, Microsporum canis, Candida albicans and Aspergillus fumigatus were grown on Sabouraud’s Dextrose Agar plates as the growth medium for the anti-fungal susceptibility. Minimal Inhibitory Concentration was then determined for each test drug and for control samples of know antifungals, fluconazole and amphotericin B. Results: The low-dose povidone-iodine formulations completely eliminated all biofilms of bacterial and fungal species in the test systems. Ciprofloxacin was able to eradicate one bacterial biofilm only at concentrations greater than 0.25 ug/mL. Fluconazole was ineffective against C. albicans, A. fumigatus and C. auris. Amphotericin B had good anti-fungal activity against fungal strains. Conclusions: These novel dilute PVP-I formulations are effective anti-biofilm and anti-fungal /sporicidal agents in vitro. Further evaluation in living models is warranted.
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