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预防生物材料上生物膜感染的策略:新型天然来源生物膜抑制剂对金黄色葡萄球菌和 SaOS-2 细胞在钛竞争定植模型中的作用

Strategies to Prevent Biofilm Infections on Biomaterials: Effect of Novel Naturally-Derived Biofilm Inhibitors on a Competitive Colonization Model of Titanium by and SaOS-2 Cells.

作者信息

Reigada Inés, Pérez-Tanoira Ramón, Patel Jayendra Z, Savijoki Kirsi, Yli-Kauhaluoma Jari, Kinnari Teemu J, Fallarero Adyary

机构信息

Drug Research Program, Division of Pharmaceutical Biosciences, Faculty of Pharmacy, University of Helsinki, Helsinki 00790, Finland.

Department of Otorhinolaryngology-Head and Neck Surgery, Helsinki University Hospital, University of Helsinki, Kasarmikatu 11-13, 00029 HUS, Helsinki 00130, Finland.

出版信息

Microorganisms. 2020 Feb 29;8(3):345. doi: 10.3390/microorganisms8030345.

Abstract

Biofilm-mediated infection is a major cause of bone prosthesis failure. The lack of molecules able to act in biofilms has driven research aimed at identifying new anti-biofilm agents via chemical screens. However, to be able to accommodate a large number of compounds, the testing conditions of these screenings end up being typically far from the clinical scenario. In this study, we assess the potential applicability of three previously discovered anti-biofilm compounds to be part of implanted medical devices by testing them on systems that more closely resemble the clinical scenario. To that end, we used a competition model based on the co-culture of SaOS-2 mammalian cells and (collection and clinical strains) on a titanium surface, as well as titanium pre-conditioned with high serum protein concentration. Additionally, we studied whether these compounds enhance the previously proven protective effect of pre-incubating titanium with SaOS-2 cells. Out of the three, DHA1 was the one with the highest potential, showing a preventive effect on bacterial adherence in all tested conditions, making it the most promising agent for incorporation into bone implants. This study emphasizes and demonstrates the importance of using meaningful experimental models, where potential antimicrobials ought to be tested for the protection of biomaterials in translational applications.

摘要

生物膜介导的感染是骨假体失效的主要原因。缺乏能够作用于生物膜的分子推动了旨在通过化学筛选鉴定新型抗生物膜药物的研究。然而,为了能够容纳大量化合物,这些筛选的测试条件最终通常与临床情况相差甚远。在本研究中,我们通过在更接近临床情况的系统上测试三种先前发现的抗生物膜化合物,评估它们作为植入式医疗器械一部分的潜在适用性。为此,我们使用了一种基于SaOS-2哺乳动物细胞与(收集菌株和临床菌株)在钛表面以及用高血清蛋白浓度预处理的钛上共培养的竞争模型。此外,我们研究了这些化合物是否增强了先前证明的用SaOS-2细胞预孵育钛的保护作用。在这三种化合物中,DHA1具有最高的潜力,在所有测试条件下均对细菌粘附显示出预防作用,使其成为最有希望纳入骨植入物的药物。本研究强调并证明了使用有意义的实验模型的重要性,在转化应用中,应在这些模型中测试潜在的抗菌剂对生物材料的保护作用。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/9dba/7143544/48190fe6486c/microorganisms-08-00345-g001.jpg

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