Locke Landon W, Shankaran Kothandaraman, Gong Li, Stoodley Paul, Vozar Samuel L, Cole Sara L, Tweedle Michael F, Wozniak Daniel J
National Centre for Advanced Tribology at Southampton (nCATS) and National Biofilm Innovation Centre (NBIC), Mechanical Engineering, University of Southampton, Southampton SO17 1BJ, United Kingdom.
ACS Infect Dis. 2020 Aug 14;6(8):2086-2098. doi: 10.1021/acsinfecdis.0c00125. Epub 2020 Jul 14.
The clinical management of bacterial biofilm infections represents an enormous challenge in today's healthcare setting. The NIH estimates that 65% of bacterial infections are biofilm-related, and therapeutic outcomes are positively correlated with early intervention. Currently, there is no reliable imaging technique to detect biofilm infections , and current clinical protocols for accurate and direct biofilm identification are nonexistent. In orthopedic implant-associated biofilm infections, for example, current detection methods are based on nonspecific X-ray or radiolabeled white blood cell imaging, coupled with peri-prosthetic tissue or fluid samples taken invasively, and must be cultured. This approach is time-consuming and often fails to detect biofilm bacteria due to sampling errors and a lack of sensitivity. The ability to quantify bacterial biofilms by real-time noninvasive imaging is an urgent unmet clinical need that would revolutionize the management and treatment of these devastating types of infections. In the present study, we assembled a collection of fluorescently labeled peptide candidates to specifically explore their biofilm targeting properties. We evaluated these fluorescently labeled peptides using various assays for their ability to specifically and nondestructively target biofilms produced by model bacterial pathogen . The lead candidate that emerged, 4Iphf-HN17, demonstrated rapid biofilm labeling kinetics, a lack of bactericidal activity, and biofilm targeting specificity in human cell infection models. fluorescently labeled 4Iphf-HN17 showed enhanced accumulation in biofilm-infected wounds, thus warranting further study.
在当今的医疗环境中,细菌生物膜感染的临床管理是一项巨大的挑战。美国国立卫生研究院估计,65%的细菌感染与生物膜有关,治疗结果与早期干预呈正相关。目前,尚无可靠的成像技术来检测生物膜感染,也不存在用于准确直接鉴定生物膜的现行临床方案。例如,在骨科植入物相关的生物膜感染中,目前的检测方法基于非特异性X射线或放射性标记白细胞成像,再加上通过侵入性方式采集的假体周围组织或液体样本,且必须进行培养。这种方法耗时且由于采样误差和缺乏敏感性,常常无法检测到生物膜细菌。通过实时无创成像对细菌生物膜进行定量的能力是一项迫切未满足的临床需求,这将彻底改变这些毁灭性感染类型的管理和治疗方式。在本研究中,我们收集了一系列荧光标记的肽候选物,以专门探究它们的生物膜靶向特性。我们使用各种检测方法评估这些荧光标记的肽,以确定它们特异性且无损地靶向由模型细菌病原体产生的生物膜的能力。筛选出的主要候选物4Iphf-HN17在人类细胞感染模型中表现出快速的生物膜标记动力学、缺乏杀菌活性以及生物膜靶向特异性。荧光标记的4Iphf-HN17在生物膜感染的伤口中显示出增强的聚集,因此值得进一步研究。