Sanofi Pasteur, Cambridge, Massachusetts, USA.
Sanofi Pasteur, Cambridge, Massachusetts, USA
Infect Immun. 2014 Sep;82(9):3764-74. doi: 10.1128/IAI.02168-14. Epub 2014 Jun 23.
Biofilm formation on central lines or peripheral catheters is a serious threat to patient well-being. Contaminated vascular devices can act as a nidus for bloodstream infection and systemic pathogen dissemination. Staphylococcal biofilms are the most common cause of central-line-associated bloodstream infections, and antibiotic resistance makes them difficult to treat. As an alternative to antibiotic intervention, we sought to identify anti-staphylococcal biofilm targets for the development of a vaccine or antibody prophylactic. A screening strategy was devised using a microfluidic system to test antibody-mediated biofilm inhibition under biologically relevant conditions of shear flow. Affinity-purified polyclonal antibodies to target antigen PhnD inhibited both Staphylococcus epidermidis and S. aureus biofilms. PhnD-specific antibodies blocked biofilm development at the initial attachment and aggregation stages, and deletion of phnD inhibited normal biofilm formation. We further adapted our microfluidic biofilm system to monitor the interaction of human neutrophils with staphylococcal biofilms and demonstrated that PhnD-specific antibodies also serve as opsonins to enhance neutrophil binding, motility, and biofilm engulfment. These data support the identification of PhnD as a lead target for biofilm intervention strategies performed either by vaccination or through passive administration of antibodies.
生物膜在中心静脉导管或外周导管上的形成是威胁患者健康的严重问题。污染的血管装置可以作为血流感染和全身病原体传播的根源。葡萄球菌生物膜是中心静脉相关血流感染的最常见原因,而抗生素耐药性使它们难以治疗。作为抗生素干预的替代方法,我们试图确定抗葡萄球菌生物膜的靶点,以开发疫苗或抗体预防剂。我们设计了一种筛选策略,使用微流控系统在生物相关的切变流条件下测试抗体介导的生物膜抑制作用。针对靶抗原 PhnD 的亲和纯化多克隆抗体抑制了表皮葡萄球菌和金黄色葡萄球菌生物膜的形成。PhnD 特异性抗体在初始附着和聚集阶段阻止生物膜的形成,并且 phnD 的缺失抑制了正常的生物膜形成。我们进一步调整了我们的微流控生物膜系统来监测人嗜中性粒细胞与葡萄球菌生物膜的相互作用,并证明 PhnD 特异性抗体也作为调理素增强嗜中性粒细胞的结合、迁移和生物膜吞噬作用。这些数据支持将 PhnD 鉴定为生物膜干预策略的潜在靶点,这些策略可以通过疫苗接种或通过被动给予抗体来实现。