Cushnie T P Tim, O'Driscoll Noëlle H, Lamb Andrew J
Faculty of Medicine, Mahasarakham University, Khamriang, Kantarawichai, Maha Sarakham, 44150, Thailand.
School of Pharmacy and Life Sciences, Robert Gordon University, Sir Ian Wood Building, Garthdee Road, Aberdeen, AB10 7GJ, UK.
Cell Mol Life Sci. 2016 Dec;73(23):4471-4492. doi: 10.1007/s00018-016-2302-2. Epub 2016 Jul 8.
Efforts to reduce the global burden of bacterial disease and contend with escalating bacterial resistance are spurring innovation in antibacterial drug and biocide development and related technologies such as photodynamic therapy and photochemical disinfection. Elucidation of the mechanism of action of these new agents and processes can greatly facilitate their development, but it is a complex endeavour. One strategy that has been popular for many years, and which is garnering increasing interest due to recent technological advances in microscopy and a deeper understanding of the molecular events involved, is the examination of treated bacteria for changes to their morphology and ultrastructure. In this review, we take a critical look at this approach. Variables affecting antibacterial-induced alterations are discussed first. These include characteristics of the test organism (e.g. cell wall structure) and incubation conditions (e.g. growth medium osmolarity). The main body of the review then describes the different alterations that can occur. Micrographs depicting these alterations are presented, together with information on agents that induce the change, and the sequence of molecular events that lead to the change. We close by highlighting those morphological and ultrastructural changes which are consistently induced by agents sharing the same mechanism (e.g. spheroplast formation by peptidoglycan synthesis inhibitors) and explaining how changes that are induced by multiple antibacterial classes (e.g. filamentation by DNA synthesis inhibitors, FtsZ disruptors, and other types of agent) can still yield useful mechanistic information. Lastly, recommendations are made regarding future study design and execution.
为减轻细菌性疾病的全球负担并应对不断升级的细菌耐药性,抗菌药物和杀菌剂研发以及光动力疗法和光化学消毒等相关技术正在不断创新。阐明这些新药物和新方法的作用机制能够极大地推动其研发进程,但这是一项复杂的工作。多年来一直流行的一种策略,由于显微镜技术的最新进展以及对相关分子事件的更深入理解而受到越来越多的关注,即检查经处理的细菌的形态和超微结构变化。在本综述中,我们对这种方法进行了批判性审视。首先讨论影响抗菌诱导变化的变量。这些变量包括受试生物体的特征(如细胞壁结构)和培养条件(如生长培养基渗透压)。综述的主体部分随后描述了可能发生的不同变化。展示了描绘这些变化的显微照片,以及诱导变化的药物信息和导致变化的分子事件序列。我们通过强调由具有相同作用机制的药物一致诱导的那些形态和超微结构变化(如肽聚糖合成抑制剂诱导的原生质球形成),并解释由多种抗菌类别诱导的变化(如DNA合成抑制剂、FtsZ破坏剂和其他类型药物诱导的丝状化)如何仍能产生有用的作用机制信息来结束本文。最后,针对未来的研究设计和实施提出了建议。