Alginate oligosaccharides enhance the antifungal activity of nystatin against candidal biofilms

被引:14
作者
Powell, Lydia C. C. [1 ,2 ]
Adams, Jennifer Y. M. [1 ]
Quoraishi, Sadik [3 ]
Py, Charlene [1 ,4 ]
Oger, Anais [1 ,4 ]
Gazze, Salvatore A. A. [5 ]
Francis, Lewis W. W. [5 ]
von Ruhland, Christopher [6 ]
Owens, David [7 ]
Rye, Philip D. D. [8 ]
Hill, Katja E. E. [1 ]
Pritchard, Manon F. F. [1 ]
Thomas, David W. W. [1 ]
机构
[1] Cardiff Univ, Adv Therapies Grp, Sch Dent, Cardiff, Wales
[2] Swansea Univ, Microbiol & Infect Dis Grp, Med Sch, Swansea, Wales
[3] New Cross Hosp, Otolaryngol Dept, Wolverhampton, England
[4] Univ Angers, Sch Engn, Angers, France
[5] Swansea Univ, Ctr Nanohlth, Med Sch, Swansea, Wales
[6] Cardiff Univ, Cent Biotechnol Serv, Sch Med, Cardiff, Wales
[7] Univ Hosp Wales, Head & Neck Directorate, Cardiff, Wales
[8] AlgiPharma, Sandvika, Norway
来源
FRONTIERS IN CELLULAR AND INFECTION MICROBIOLOGY | 2023年 / 13卷
基金
欧洲研究理事会;
关键词
antifungal; alginate oligosaccharide; nystatin; Candida spp; biofilm; IN-VITRO MODEL; ALBICANS BIOFILMS; FLUCONAZOLE RESISTANCE; DRUG-RESISTANCE; EFFLUX PUMPS; CALCIUM; CANDIDIASIS; BINDING; QUANTIFICATION; INHIBITION;
D O I
10.3389/fcimb.2023.1122340
中图分类号
R392 [医学免疫学]; Q939.91 [免疫学];
学科分类号
100102 ;
摘要
BackgroundThe increasing prevalence of invasive fungal infections in immuno-compromised patients is a considerable cause of morbidity and mortality. With the rapid emergence of antifungal resistance and an inadequate pipeline of new therapies, novel treatment strategies are now urgently required. MethodsThe antifungal activity of the alginate oligosaccharide OligoG in conjunction with nystatin was tested against a range of Candida spp. (C. albicans, C. glabrata, C. parapsilosis, C. auris, C. tropicalis and C. dubliniensis), in both planktonic and biofilm assays, to determine its potential clinical utility to enhance the treatment of candidal infections. The effect of OligoG (0-6%) +/- nystatin on Candida spp. was examined in minimum inhibitory concentration (MIC) and growth curve assays. Antifungal effects of OligoG and nystatin treatment on biofilm formation and disruption were characterized using confocal laser scanning microscopy (CLSM), scanning electron microscopy (SEM) and ATP cellular viability assays. Effects on the cell membrane were determined using permeability assays and transmission electron microscopy (TEM). ResultsMIC and growth curve assays demonstrated the synergistic effects of OligoG (0-6%) with nystatin, resulting in an up to 32-fold reduction in MIC, and a significant reduction in the growth of C. parapsilosis and C. auris (minimum significant difference = 0.2 and 0.12 respectively). CLSM and SEM imaging demonstrated that the combination treatment of OligoG (4%) with nystatin (1 mu g/ml) resulted in significant inhibition of candidal biofilm formation on glass and clinical grade silicone surfaces (p < 0.001), with increased cell death (p < 0.0001). The ATP biofilm disruption assay demonstrated a significant reduction in cell viability with OligoG (4%) alone and the combined OligoG/nystatin (MIC value) treatment (p < 0.04) for all Candida strains tested. TEM studies revealed the combined OligoG/nystatin treatment induced structural reorganization of the Candida cell membrane, with increased permeability when compared to the untreated control (p < 0.001). ConclusionsAntimicrobial synergy between OligoG and nystatin against Candida spp. highlights the potential utility of this combination therapy in the prevention and topical treatment of candidal biofilm infections, to overcome the inherent tolerance of biofilm structures to antifungal agents.
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页数:11
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