Mishra Biswajit, Wang Guangshun
Department of Pathology and Microbiology, College of Medicine, University of Nebraska Medical Center, 986495 Nebraska Medical Center, Omaha, NE 68198-6495, USA.
Pharmaceuticals (Basel). 2017 Jun 25;10(3):58. doi: 10.3390/ph10030058.
is involved in a variety of difficult-to-treat infections frequently due to biofilm formation. To identify useful antibiofilm strategies, this article evaluated efficacy of two newly engineered cationic antimicrobial peptides (17BIPHE2 and DASamP2), traditional antibiotics, and their combinations against biofilms at different stages. 17BIPHE2 is designed based on the 3D structure of human cathelicidin LL-37 and DASamP2 is derived from database screening. While both peptides show effects on bacterial adhesion, biofilm formation, and preformed biofilms, select antibiotics only inhibit biofilm formation, probably due to direct bacterial killing. In addition, the time dependence of biofilm formation and treatment in a static in vitro biofilm model was also studied. The initial bacterial inoculum determines the peptide concentration needed to inhibit biofilm growth. When the bacterial growth time is less than 8 h, the biomass in the wells can be dispersed by either antibiotics alone or peptides alone. However, nearly complete biofilm disruption can be achieved when both the peptide and antibiotics are applied. Our results emphasize the importance of antibiofilm peptides, early treatment using monotherapy, and the combination therapy for already formed biofilms of .
由于生物膜的形成,它常常涉及多种难以治疗的感染。为了确定有用的抗生物膜策略,本文评估了两种新设计的阳离子抗菌肽(17BIPHE2和DASamP2)、传统抗生素及其组合在不同阶段对生物膜的疗效。17BIPHE2是基于人cathelicidin LL-37的三维结构设计的,DASamP2是通过数据库筛选获得的。虽然这两种肽都对细菌粘附、生物膜形成和已形成的生物膜有作用,但某些抗生素仅抑制生物膜形成,这可能是由于直接杀死细菌。此外,还研究了静态体外生物膜模型中生物膜形成和治疗的时间依赖性。初始细菌接种量决定了抑制生物膜生长所需的肽浓度。当细菌生长时间小于8小时时,孔中的生物量可以通过单独使用抗生素或单独使用肽来分散。然而,当同时应用肽和抗生素时,可以实现几乎完全的生物膜破坏。我们的结果强调了抗生物膜肽、早期单一疗法治疗以及对已形成生物膜的联合疗法的重要性。