一个简单的硅胶弹性体定植模型突出了白色念珠菌和金黄色葡萄球菌在生物膜形成过程中相互作用的复杂性。

IF 2
Gail McConnell, Liam M Rooney, Mairi E Sandison, Paul A Hoskisson, Katherine J Baxter
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引用次数: 0

摘要

介绍。卫生保健相关感染(HAIs)是造成抗菌素耐药性负担的重要因素。HAIs的一个主要因素是由生物膜形成的机会性病原体如白色念珠菌和金黄色葡萄球菌在留置医疗器械中定植。这些生物经常共同感染,导致与增强的毒力和治疗耐药性的协同相互作用。假设/差距语句。白色念珠菌和金黄色葡萄球菌很容易在硅胶弹性体上形成双种生物膜,硅胶弹性体是一种常用的医疗器械材料,然而这些生物在这种表面上的定植表型仍然知之甚少。我们的目的是建立一个简单的,光学易于处理的模型来模拟留置医疗器械的定植,以研究白色念珠菌和金黄色葡萄球菌生物膜的形成。该系统利用嵌入琼脂中的硅弹性体盘,反映设备相关条件,并实现白色念珠菌和金黄色葡萄球菌共培养形成的生物膜的高分辨率成像。使用有机硅弹性体定植模型的初步结果显示强健的生物膜形成。这些生物膜在金黄色葡萄球菌与酵母或菌丝形式的白色念珠菌共同培养形成的双物种生物膜之间表现出形态差异,这表明在生物膜相关医疗器械定植过程中,不同的白色念珠菌细胞形态对硅胶弹性体的影响。结晶紫染色定量测定生物膜的形成,进一步验证了该体系的有效性。这些发现强调了开发更接近于感染微环境的生物膜研究工具的重要性,我们的工作详细介绍了这样一个系统,可以用于进一步研究,以改进针对设备相关HAIs的策略。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
A simple silicone elastomer colonization model highlights complexities of Candida albicans and Staphylococcus aureus interactions in biofilm formation.

Introduction. Healthcare-associated infections (HAIs) significantly contribute to the burden of antimicrobial resistance. A major factor in HAIs is the colonization of indwelling medical devices by biofilm-forming opportunistic pathogens such as Candida albicans and Staphylococcus aureus. These organisms frequently co-infect, resulting in synergistic interactions with enhanced virulence and resistance to treatment.Hypothesis/Gap statement. C. albicans and S. aureus readily form dual-species biofilms on silicone elastomers, a commonly used medical device material, yet the colonization phenotypes of these organisms on such surfaces remain poorly understood.Aim. We aimed to develop a simple, optically tractable model to mimic the colonization of indwelling medical devices to investigate C. albicans and S. aureus biofilm formation.Methodology. The system utilizes discs of a silicone elastomer embedded in agar, reflecting device-associated conditions and enabling high-resolution imaging of biofilms formed by C. albicans and S. aureus co-cultures.Results. Initial results using the silicone elastomer colonization model reveal robust biofilm formation. These biofilms exhibited morphological differences between dual-species biofilms formed by S. aureus co-cultures with either yeast- or hyphal-form C. albicans, indicating the impact of differing C. albicans cell morphotypes in biofilm-associated medical device colonization on silicone elastomers. Quantification of biofilm formation by crystal violet staining provided further validation of the system.Conclusion. These findings underscore the importance of developing tools for biofilm study which more closely resemble the infectious microenvironment, with our work detailing such a system which can be employed in further study to improve strategies against device-related HAIs.

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