Shi Xiaoyi, Zarkan Ashraf
Cambridge Centre for International Research, Cambridge CB4 0PZ, UK.
Department of Genetics, University of Cambridge, Cambridge CB2 3EH, UK.
Microbiology (Reading). 2022 Dec;168(12). doi: 10.1099/mic.0.001266.
Bacteria withstand antibiotic onslaughts by employing a variety of strategies, one of which is persistence. Persistence occurs in a bacterial population where a subpopulation of cells (persisters) survives antibiotic treatment and can regrow in a drug-free environment. Persisters may cause the recalcitrance of infectious diseases and can be a stepping stone to antibiotic resistance, so understanding persistence mechanisms is critical for therapeutic applications. However, current understanding of persistence is pervaded by paradoxes that stymie research progress, and many aspects of this cellular state remain elusive. In this review, we summarize the putative persister mechanisms, including toxin-antitoxin modules, quorum sensing, indole signalling and epigenetics, as well as the reasons behind the inconsistent body of evidence. We highlight present limitations in the field and underscore a clinical context that is frequently neglected, in the hope of supporting future researchers in examining clinically important persister mechanisms.
细菌通过采用多种策略来抵御抗生素的攻击,其中之一是形成持留菌。持留菌出现在细菌群体中,即有一部分细胞(持留菌)在抗生素治疗后存活下来,并能在无药环境中重新生长。持留菌可能导致传染病难以治愈,并且可能成为抗生素耐药性的一个跳板,因此了解持留菌机制对于治疗应用至关重要。然而,目前对持留菌的理解充满了阻碍研究进展的悖论,这种细胞状态的许多方面仍然难以捉摸。在这篇综述中,我们总结了假定的持留菌机制,包括毒素-抗毒素模块、群体感应、吲哚信号传导和表观遗传学,以及证据不一致背后的原因。我们强调了该领域目前的局限性,并强调了一个经常被忽视的临床背景,希望能支持未来的研究人员研究临床上重要的持留菌机制。