Division of Biomedical Sciences, University of California Riverside School of Medicine, Riverside, California, USA
Division of Biomedical Sciences, University of California Riverside School of Medicine, Riverside, California, USA.
Infect Immun. 2020 Apr 20;88(5). doi: 10.1128/IAI.00859-19.
Implanted medical device-associated infections pose significant health risks, as they are often the result of bacterial biofilm formation. is a leading cause of biofilm-associated infections which persist due to mechanisms of device surface adhesion, biofilm accumulation, and reprogramming of host innate immune responses. We found that the fibronectin binding protein A (FnBPA) is required for normal biofilm development in mammalian serum and that the SaeRS two-component system is required for functional FnBPA activity in serum. Furthermore, serum-developed biofilms deficient in FnBPA were more susceptible to macrophage invasion, and in a model of biofilm-associated implant infection, we found that FnBPA is crucial for the establishment of infection. Together, these findings show that FnBPA plays an important role in physical biofilm development and represents a potential therapeutic target for the prevention and treatment of device-associated infections.
植入式医疗器械相关感染会带来严重的健康风险,因为它们通常是细菌生物膜形成的结果。 是生物膜相关感染的主要原因,这些感染持续存在是因为器械表面黏附、生物膜积聚和宿主固有免疫反应重编程的机制。我们发现纤连蛋白结合蛋白 A(FnBPA)在哺乳动物血清中正常生物膜发育是必需的,而 SaeRS 双组分系统是血清中功能性 FnBPA 活性所必需的。此外,缺乏 FnBPA 的血清生物膜更易被巨噬细胞入侵,在生物膜相关植入物感染模型中,我们发现 FnBPA 对感染的建立至关重要。总之,这些发现表明 FnBPA 在物理生物膜发育中发挥重要作用,是预防和治疗器械相关感染的潜在治疗靶点。