Preparing a Dual-Species In Vitro Biofilm Model for Testing Antibiofilm Efficacy.

IF 4.5 2区 医学 Q2 MEDICINE, RESEARCH & EXPERIMENTAL
Kelli Randmäe, Kairi Lorenz, Marta Putrinš, Tanel Tenson, Karin Kogermann
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Abstract

All wounds are contaminated, and there is a risk of developing an infection. Furthermore, most wounds contain biofilm and are contaminated by two bacteria, termed dual-species, or more bacteria, termed polybacterial biofilms. New antibacterial and antibiofilm wound care products are constantly being developed to combat this problem. There is a need to develop more biorelevant and reproducible models to test the efficacy of these wound care products. We used an electrospun (ES) gelatin-glucose matrix (Gel-Gluc) as an artificial skin substrate for dual-species biofilm formation using wound pathogens Staphylococcus aureus, Escherichia coli, and Pseudomonas aeruginosa, combining them in pairs. When analyzing the biofilms, selective agars were used to differentiate various bacteria from one another while counting. The developed method supported the growth of dual-species biofilm that contained both bacteria up to 108 CFU/Gel-Gluc after 24 h. Over 48 h, there was a decrease in the number of S. aureus in the biofilms. Confocal microscopy imaging allowed monitoring of the location of bacteria in the Gel-Gluc and proved that different species were located closely together. ES polycaprolactone (PCL) fibrous wound dressings containing chloramphenicol (CAM) or ciprofloxacin (CIP), or their pristine analogs, were used to test the model. Both ES fibrous wound dressings were effective in preventing dual-species biofilm formation. PCL-CIP fibrous dressing was also effective in treating biofilms. The efficacy of treatment of E. coli varied in different dual-species combinations of E. coli. The developed dual-species biofilm model on artificial skin (Gel-Gluc) supported the successful growth of different bacterial combinations and proved to be suitable for testing the efficacy of ES fibrous wound dressings in preventing and treating biofilms.

制备双菌种体外生物膜模型检测抗生物膜效果。
所有的伤口都被污染了,有发生感染的风险。此外,大多数伤口含有生物膜,并被两种细菌(称为双种细菌)或更多细菌(称为多细菌生物膜)污染。新的抗菌和抗生物膜伤口护理产品不断被开发来解决这个问题。有必要开发更多的生物相关和可重复的模型来测试这些伤口护理产品的功效。我们使用电纺丝(ES)明胶-葡萄糖基质(Gel-Gluc)作为人工皮肤基质,将伤口病原菌金黄色葡萄球菌、大肠杆菌和铜绿假单胞菌成对结合,形成双种生物膜。在分析生物膜时,在计数时使用选择性琼脂来区分各种细菌。所建立的方法支持双菌种生物膜的生长,24 h后两种细菌的含量高达108 CFU/Gel-Gluc。超过48 h,生物膜中的金黄色葡萄球菌数量减少。共聚焦显微镜成像可以监测凝胶- gluc中细菌的位置,并证明不同的物种被紧密地定位在一起。使用含有氯霉素(CAM)或环丙沙星(CIP)或其原始类似物的ES聚己内酯(PCL)纤维伤口敷料来测试模型。两种ES纤维创面敷料均能有效防止双种生物膜的形成。PCL-CIP纤维敷料对生物膜也有较好的处理效果。不同双种大肠杆菌组合对大肠杆菌的治疗效果不同。所建立的人工皮肤双菌种生物膜模型(Gel-Gluc)支持不同细菌组合的成功生长,适用于ES纤维创面敷料预防和治疗生物膜的效果测试。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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来源期刊
Molecular Pharmaceutics
Molecular Pharmaceutics 医学-药学
CiteScore
8.00
自引率
6.10%
发文量
391
审稿时长
2 months
期刊介绍: Molecular Pharmaceutics publishes the results of original research that contributes significantly to the molecular mechanistic understanding of drug delivery and drug delivery systems. The journal encourages contributions describing research at the interface of drug discovery and drug development. Scientific areas within the scope of the journal include physical and pharmaceutical chemistry, biochemistry and biophysics, molecular and cellular biology, and polymer and materials science as they relate to drug and drug delivery system efficacy. Mechanistic Drug Delivery and Drug Targeting research on modulating activity and efficacy of a drug or drug product is within the scope of Molecular Pharmaceutics. Theoretical and experimental peer-reviewed research articles, communications, reviews, and perspectives are welcomed.
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