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Biofilm Assays on Fibrinogen-coated Silicone Catheters and 96-well Polystyrene Plates

生物膜 微生物学 粪肠球菌 细菌 导管 抗生素 生物 化学 金黄色葡萄球菌 医学 外科 遗传学
作者
Cristina Colomer‐Winter,José A. Lemos,Ana L. Flores‐Mireles
出处
期刊:Bio-protocol [American Academy of Arts and Sciences]
卷期号:9 (6) 被引量:25
标识
DOI:10.21769/bioprotoc.3196
摘要

Biofilm formation is a well-known bacterial strategy that protects cells from hostile environments. During infection, bacteria found in a biofilm community are less sensitive to antibiotics and to the immune response, often allowing them to colonize and persist in the host niche. Not surprisingly, biofilm formation on medical devices, such as urinary catheters, is a major problem in hospital settings. To be able to eliminate such biofilms, it is important to understand the key bacterial factors that contribute to their formation. A common practice in the lab setting is to study biofilms grown in laboratory media. However, these media do not fully reflect the host environment conditions, potentially masking relevant biological determinants. This is the case during urinary catheterization, where a key element for Enterococcus faecalis and Staphylococcus aureus colonization and biofilm formation is the release of fibrinogen (Fg) into the bladder and its deposition on the urinary catheter. To recapitulate bladder conditions during catheter-associated urinary tract infection (CAUTI), we have developed a fibrinogen-coated catheter and 96-well plate biofilm assay in urine. Notably, enterococcal biofilm factors identified in these in vitro assays proved to be important for biofilm formation in vivo in a mouse model of CAUTI. Thus, the method described herein can be used to uncover biofilm-promoting factors that are uniquely relevant in the host environment, and that can be exploited to develop new antibacterial therapies.

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