Kranjec Christian, Mathew Jills Puthiaparambil, Ovchinnikov Kirill, Fadayomi Idowu, Yang Ying, Kjos Morten, Li Wen-Wu
Laboratory of Microbial Gene Technology, Faculty of Chemistry, Biotechnology and Food Science. Norwegian University of Life Sciences, 1430, Ås, Norway.
School of Pharmacy and Bioengineering, Guy Hilton Research Centre, Keele University, Stoke-on-Trent, ST4 7QB, UK.
Biofilm. 2024 Jul 3;8:100211. doi: 10.1016/j.bioflm.2024.100211. eCollection 2024 Dec.
The ever-increasing use of exogenous materials as indwelling medical devices in modern medicine offers to pathogens new ways to gain access to human body and begin, in some cases, life threatening infections. Biofouling of such materials with bacteria or fungi is a major concern during surgeries, since this is often associated with biofilm formation and difficult to treat, recalcitrant infections. Intense research efforts have therefore developed several strategies to shield the medical devices' surface from colonization by pathogenic microorganisms. Here, we used dopamine as a coupling agent to coat four different materials of medical interest (plastic polyetheretherketone (PEEK), stainless steel, titanium and silicone catheter) with the bacteriocins, enterocin EJ97-short and the thiopeptide micrococcin P1. Water contact angle measurements and x-ray photoelectron spectroscopy were used to verify the effective coating of the materials. The effect of bacteriocins coated on these materials on the biofilm formation by a vancomycin resistant (VRE) strain was studied by biofilm-oriented antimicrobial test (BOAT) and electron scanning microscopy. The biocompatibility of bacteriocin-modified biomaterials was tested on cultured human cells. The results demonstrated that the binding of the bacteriocins to the implant surfaces is achieved, and the two bacteriocins in combination could inhibit biofilm formation by on all four materials. The modified implant showed no cytotoxicity to the human cells tested. Therefore, surface modification with the two bacteriocins may offer a novel and effective way to prevent biofilm formation on a wide range of implant materials.
在现代医学中,作为植入式医疗器械的外源材料的使用日益增加,这为病原体提供了新的途径进入人体,并在某些情况下引发危及生命的感染。在手术过程中,此类材料被细菌或真菌生物污染是一个主要问题,因为这通常与生物膜形成有关,且难以治疗,会导致顽固性感染。因此,大量的研究工作已经开发出了几种策略,以保护医疗器械表面不被病原微生物定植。在这里,我们使用多巴胺作为偶联剂,用细菌素、短肠球菌素EJ97和硫肽微球菌素P1包覆四种具有医学应用价值的不同材料(塑料聚醚醚酮(PEEK)、不锈钢、钛和硅胶导管)。通过测量水接触角和X射线光电子能谱来验证材料的有效包覆。通过生物膜导向抗菌试验(BOAT)和电子扫描显微镜研究了包覆在这些材料上的细菌素对耐万古霉素(VRE)菌株生物膜形成的影响。在培养的人类细胞上测试了细菌素修饰的生物材料的生物相容性。结果表明,细菌素与植入物表面实现了结合,两种细菌素联合使用可抑制所有四种材料上生物膜的形成。修饰后的植入物对所测试的人类细胞没有细胞毒性。因此,用这两种细菌素进行表面修饰可能为防止多种植入材料上生物膜的形成提供一种新颖有效的方法。