Belanger Corrie R, Mansour Sarah C, Pletzer Daniel, Hancock Robert E W
Centre for Microbial Diseases and Immunity Research, Department of Microbiology and Immunology, University of British Columbia, Vancouver, British Columbia, Canada.
Emerg Top Life Sci. 2017 Apr 21;1(1):41-53. doi: 10.1042/ETLS20160020.
Biofilms represent an adaptive lifestyle where microbes grow as structured aggregates in many different environments, e.g. on body surfaces and medical devices. They are a profound threat in medical (and industrial) settings and cause two-thirds of all infections. Biofilm bacteria are especially recalcitrant to common antibiotic treatments, demonstrating adaptive multidrug resistance. For this reason, novel methods to eradicate or prevent biofilm infections are greatly needed. Recent advances have been made in exploring alternative strategies that affect biofilm lifestyle, inhibit biofilm formation, degrade biofilm components and/or cause dispersal. As such, naturally derived compounds, molecules that interfere with bacterial signaling systems, anti-biofilm peptides and phages show great promise. Their implementation as either stand-alone drugs or complementary therapies has the potential to eradicate resilient biofilm infections. Additionally, altering the surface properties of indwelling medical devices through bioengineering approaches has been examined as a method for preventing biofilm formation. There is also a need for improving current biofilm detection methods since in vitro methods often do not accurately measure live bacteria in biofilms or mimic in vivo conditions. We propose that the design and development of novel compounds will be enabled by the improvement and use of appropriate in vitro and in vivo models.
生物膜代表了一种适应性生存方式,微生物在许多不同环境中以结构化聚集体的形式生长,例如在体表和医疗设备上。它们在医疗(和工业)环境中构成了严重威胁,导致了三分之二的感染。生物膜细菌对常见的抗生素治疗尤其顽固,表现出适应性多药耐药性。因此,迫切需要根除或预防生物膜感染的新方法。在探索影响生物膜生存方式、抑制生物膜形成、降解生物膜成分和/或导致生物膜分散的替代策略方面已经取得了进展。因此,天然衍生化合物、干扰细菌信号系统的分子、抗生物膜肽和噬菌体显示出巨大的潜力。将它们用作单独药物或辅助疗法有可能根除顽固的生物膜感染。此外,通过生物工程方法改变植入式医疗设备的表面特性已被作为一种预防生物膜形成的方法进行了研究。由于体外方法往往不能准确测量生物膜中的活菌或模拟体内条件,因此也需要改进当前的生物膜检测方法。我们认为,新型化合物的设计和开发将通过改进和使用合适的体外和体内模型来实现。