Kratochvil Michael J, Yang Tian, Blackwell Helen E, Lynn David M
Department of Chemistry, University of Wisconsin-Madison , 1101 University Avenue, Madison, Wisconsin 53706, United States.
Department of Chemical and Biological Engineering, University of Wisconsin-Madison , 1415 Engineering Drive, Madison, Wisconsin 53706, United States.
ACS Infect Dis. 2017 Apr 14;3(4):271-280. doi: 10.1021/acsinfecdis.6b00173. Epub 2017 Feb 20.
We report the fabrication and biological evaluation of nonwoven polymer nanofiber coatings that inhibit quorum sensing (QS) and virulence in the human pathogen Staphylococcus aureus. Our results demonstrate that macrocyclic peptide 1, a potent and synthetic nonbactericidal quorum sensing inhibitor (QSI) in S. aureus, can be loaded into degradable polymer nanofibers by electrospinning and that this approach can deposit QSI-loaded nanofiber coatings onto model nonwoven mesh substrates. The QSI was released over ∼3 weeks when these materials were incubated in physiological buffer, retained its biological activity, and strongly inhibited agr-based QS in a GFP reporter strain of S. aureus for at least 14 days without promoting cell death. These materials also inhibited production of hemolysins, a QS-controlled virulence phenotype, and reduced the lysis of erythrocytes when placed in contact with wild-type S. aureus growing on surfaces. This approach is modular and can be used with many different polymers, active agents, and processing parameters to fabricate nanofiber coatings on surfaces important in healthcare contexts. S. aureus is one of the most common causative agents of bacterial infections in humans, and strains of this pathogen have developed significant resistance to conventional antibiotics. The QSI-based strategies reported here thus provide springboards for the development of new anti-infective materials and novel treatment strategies that target virulence as opposed to growth in S. aureus. This approach also provides porous scaffolds for cell culture that could prove useful in future studies on the influence of QS modulation on the development and structure of bacterial communities.
我们报告了可抑制人类病原体金黄色葡萄球菌群体感应(QS)和毒力的非织造聚合物纳米纤维涂层的制备及生物学评估。我们的结果表明,大环肽1是一种有效的金黄色葡萄球菌合成非杀菌群体感应抑制剂(QSI),可通过静电纺丝加载到可降解聚合物纳米纤维中,并且这种方法可将负载QSI的纳米纤维涂层沉积到模型非织造网片基材上。当这些材料在生理缓冲液中孵育时,QSI在约3周内释放,保留其生物活性,并在金黄色葡萄球菌的绿色荧光蛋白报告菌株中强烈抑制基于agr的群体感应至少14天,而不促进细胞死亡。这些材料还抑制了溶血素的产生,溶血素是一种群体感应控制的毒力表型,并且当与在表面生长的野生型金黄色葡萄球菌接触时减少了红细胞的裂解。这种方法具有模块化,可与许多不同的聚合物、活性剂和加工参数一起使用,以在医疗保健环境中重要的表面上制备纳米纤维涂层。金黄色葡萄球菌是人类细菌感染最常见的病原体之一,并且该病原体的菌株已对传统抗生素产生了显著抗性。因此,这里报道的基于QSI的策略为开发新的抗感染材料和针对金黄色葡萄球菌毒力而非生长的新型治疗策略提供了跳板。这种方法还为细胞培养提供了多孔支架,这在未来关于群体感应调节对细菌群落发育和结构影响的研究中可能会证明是有用的。