Center for Microbial Interface Biology, Departments of Microbial Infection and Immunity, Microbiology, Ohio State University, Columbus, OH, 43210, USA.
Department of Infectious Diseases, MedImmune, LLC, Gaithersburg, MD, 20878, USA.
Sci Rep. 2017 Nov 22;7(1):16065. doi: 10.1038/s41598-017-16215-6.
Bacterial biofilms are recalcitrant to antibiotic therapy and a major cause of persistent and recurrent infections. New antibody-based therapies may offer potential to target biofilm specific components for host-cell mediated bacterial clearance. For Pseudomonas aeruginosa, human monoclonal antibodies (mAbs) targeting the Psl biofilm exopolysaccharide exhibit protective activity against planktonic bacteria in acute infection models. However, anti-Psl mAb activity against P. aeruginosa biofilms is unknown. Here, we demonstrate that anti-Psl mAbs targeting three distinct Psl epitopes exhibit stratified binding in mature in vitro biofilms and bind Psl within the context of a chronic biofilm infection. These mAbs also exhibit differential abilities to inhibit early biofilm events and reduce biomass from mature biofilms in the presence of neutrophils. Importantly, a mAb mixture with neutrophils exhibited the greatest biomass reduction, which was further enhanced when combined with meropenem, a common anti-Pseudomonal carbapenem antibiotic. Moreover, neutrophil-mediated killing of biofilm bacteria correlated with the evident mAb epitope stratification within the biofilm. Overall, our results suggest that anti-Psl mAbs might be promising candidates for adjunctive use with antibiotics to inhibit/disrupt P. aeruginosa biofilms as a result of chronic infection.
细菌生物膜对抗生素治疗具有抗药性,是持续性和复发性感染的主要原因。新的基于抗体的疗法可能为针对生物膜特异性成分以实现宿主细胞介导的细菌清除提供了潜力。对于铜绿假单胞菌,针对 Psl 生物膜胞外多糖的人源单克隆抗体 (mAb) 在急性感染模型中显示出对浮游细菌的保护活性。然而,针对铜绿假单胞菌生物膜的抗 Psl mAb 活性尚不清楚。在这里,我们证明靶向三个不同 Psl 表位的抗 Psl mAb 在成熟的体外生物膜中表现出分层结合,并在慢性生物膜感染的背景下结合 Psl。这些 mAb 还表现出抑制早期生物膜事件和减少中性粒细胞存在时成熟生物膜生物量的不同能力。重要的是,含中性粒细胞的 mAb 混合物表现出最大的生物量减少,当与美罗培南(一种常见的抗假单胞菌碳青霉烯类抗生素)联合使用时,效果进一步增强。此外,中性粒细胞介导的生物膜细菌杀伤与生物膜内明显的 mAb 表位分层相关。总的来说,我们的结果表明,抗 Psl mAb 可能是与抗生素联合使用以抑制/破坏铜绿假单胞菌生物膜的有前途的候选物,因为它们是慢性感染的结果。