Yang Sydney, Stern Alexa, Duncan Gregg
Fischell Department of Bioengineering, University of Maryland, College Park, MD 20742, USA.
bioRxiv. 2024 Aug 10:2024.08.09.607383. doi: 10.1101/2024.08.09.607383.
Bacterial biofilms are often highly resistant to antimicrobials causing persistent infections which when not effectively managed can significantly worsen clinical outcomes. As such, alternatives to standard antibiotic therapies have been highly sought after to address difficult-to-treat biofilm-associated infections. We hypothesized a biomaterial-based approach using the innate functions of mucins to modulate bacterial surface attachment and virulence could provide a new therapeutic strategy against biofilms. Based on our testing in biofilms, we found synthetic mucus biomaterials can inhibit biofilm formation and significantly reduce the thickness of mature biofilms. In addition, we evaluated if synthetic mucus biomaterials could work synergistically with DNase and/or α-amylase for enhanced biofilm dispersal. Combination treatment with these antibiofilm agents and synthetic mucus biomaterials resulted in up to 3 log reductions in viability of mature biofilms. Overall, this work provides a new bio-inspired, combinatorial approach to address biofilms and antibiotic-resistant bacterial infections.
细菌生物膜通常对抗菌药物具有高度抗性,从而导致持续性感染,如果不能得到有效控制,可能会显著恶化临床结果。因此,人们一直在大力寻求标准抗生素疗法的替代方案,以应对难以治疗的生物膜相关感染。我们推测,基于生物材料的方法利用粘蛋白的固有功能来调节细菌表面附着和毒力,可能会提供一种针对生物膜的新治疗策略。基于我们在生物膜中的测试,我们发现合成粘液生物材料可以抑制生物膜形成,并显著降低成熟生物膜的厚度。此外,我们评估了合成粘液生物材料是否可以与脱氧核糖核酸酶和/或α-淀粉酶协同作用,以增强生物膜的分散。这些抗生物膜剂与合成粘液生物材料联合治疗可使成熟生物膜的活力降低多达3个对数。总体而言,这项工作提供了一种新的受生物启发的组合方法,以应对生物膜和抗生素耐药细菌感染。