Development, characterization, and evaluation of a simple polymicrobial colony biofilm model for testing of antimicrobial wound dressings

被引:2
|
作者
Robertson, Shaun N. [1 ]
Romero, Manuel [1 ,2 ,3 ]
Fenn, Samuel [1 ,4 ,5 ]
Riedi, Petra L. Kohler [6 ]
Camara, Miguel [1 ]
机构
[1] Univ Nottingham, Natl Biofilms Innovat Ctr, Biodiscovery Inst, Sch Life Sci, Univ Park, Nottingham NG7 2RD, England
[2] Univ Santiago De Compostela, Fac Biol CIBUS, Dept Microbiol & Parasitol, Santiago De Compostela 15782, Spain
[3] Univ Santiago De Compostela, Aquat One Hlth Res Ctr ARCUS, Santiago De Compostela 15782, Spain
[4] Univ Coll Cork, Sch Microbiol, APC Microbiome Ireland, Cork T12 TP07, Ireland
[5] Univ Coll Cork, Sch Med, APC Microbiome Ireland, Cork T12 TP07, Ireland
[6] 3 M Corp Res Mat Lab, St Paul, MN 55406 USA
基金
英国生物技术与生命科学研究理事会;
关键词
colony biofilm model; Pseudomonas aeruginosa; Staphylococcus aureus; Candida albicans; wound dressing testing; PSEUDOMONAS-AERUGINOSA; STAPHYLOCOCCUS-AUREUS; SILVER NANOPARTICLES; BACTERIAL-RESISTANCE; MANAGEMENT; IODINE; CYTOTOXICITY;
D O I
10.1093/jambio/lxae042
中图分类号
Q81 [生物工程学(生物技术)]; Q93 [微生物学];
学科分类号
071005 ; 0836 ; 090102 ; 100705 ;
摘要
Chronic wound infections are generally of polymicrobial nature with aerobic and anaerobic bacteria, as well as fungi frequently observed in them. Wound treatment involves a series of steps, including debridement of the wound, flushing, and often the use of multiple wound dressings many of which are antimicrobial. Yet, many wound dressings are tested versus single species of planktonic microbes, which fails to mirror the real-life presence of biofilms. Aims: Simple biofilm models are the first step to testing of any antimicrobial and wound dressing; therefore, the aim of this study was to develop and validate a simple polymicrobial colony biofilm wound model comprised of Pseudomonas aeruginosa, Staphylococcus aureus, and Candida albicans on RPMI-1640 agar. The model was then used to evaluate the topical disinfectant chlorohexidine and four commercially available wound dressings using the polymicrobial model. The model used was as a starting point to mimic debridement in clinical care of wounds and the effectiveness of wound dressings evaluated afterwards. Methods and Results: Planktonic assessment using AATCC100-2004 demonstrated that all antimicrobial wound dressings reduced the planktonic microbial burden below the limit of detection; however, when challenged with polymicrobial colony biofilms, silver wound dressings showed limited effectiveness (1-2 log CFU reductions). In contrast, a single iodine releasing wound dressing showed potent antibiofilm activity reducing all species CFUs below the limit of detection (>6-10 log) depending on the species. A disrupted biofilm model challenge was performed to represent the debridement of a wound and wound silver-based wound dressings were found to be marginally more effective than in whole colony biofilm challenges while the iodine containing wound dressing reduced microbial recovery below the limit of detection. Conclusions: In this model, silver dressings were ineffective versus the whole colony biofilms but showed some recovery of activity versus the disrupted colony biofilm. The iodine wound dressing reduced the viability of all species below the level of detection. This suggests that mode of action of wound dressing should be considered for the type of biofilm challenge as should the clinical use, e.g. debridement. Impact Statement These results demonstrate that biofilm management capabilities vary considerably among the wound dressings when tested in this in vitro model. The results from this study may have clinical implications for wound management.
引用
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页数:13
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