Silva Kalinga Pavan T, Khare Anupama
Laboratory of Molecular Biology, National Cancer Institute, National Institutes of Health, Bethesda, MD, 20892, USA.
NPJ Antimicrob Resist. 2024 Nov 6;2(1):35. doi: 10.1038/s44259-024-00052-5.
Apart from horizontal gene transfer and sequence-altering mutational events, antibiotic resistance can emerge due to the formation of tandem repeats of genomic regions. This phenomenon, also known as gene amplification, has been implicated in antibiotic resistance in both laboratory and clinical scenarios, where the evolution of resistance via amplifications can affect treatment efficacy. Antibiotic resistance mediated by gene amplifications is unstable and consequently can be difficult to detect, due to amplification loss in the absence of the selective pressure of the antibiotic. Further, due to variable copy numbers in a population, amplifications result in heteroresistance, where only a subpopulation is resistant to an antibiotic. While gene amplifications typically lead to resistance by increasing the expression of resistance determinants due to the higher copy number, the underlying mechanisms of resistance are diverse. In this review article, we describe the various pathways by which gene amplifications cause antibiotic resistance, from efflux and modification of the antibiotic, to target modification and bypass. We also discuss how gene amplifications can engender resistance by alternate mutational outcomes such as altered regulation and protein structure, in addition to just an increase in copy number and expression. Understanding how amplifications contribute to bacterial survival following antibiotic exposure is critical to counter their role in the rise of antimicrobial resistance.
除了水平基因转移和改变序列的突变事件外,抗生素耐药性还可能由于基因组区域串联重复的形成而出现。这种现象,也称为基因扩增,在实验室和临床情况下都与抗生素耐药性有关,通过扩增产生耐药性的进化会影响治疗效果。由基因扩增介导的抗生素耐药性不稳定,因此由于在没有抗生素选择压力的情况下扩增丢失,可能难以检测。此外,由于群体中拷贝数可变,扩增会导致异质性耐药,即只有亚群对抗生素耐药。虽然基因扩增通常通过增加耐药决定因素的表达导致耐药,因为拷贝数较高,但耐药的潜在机制多种多样。在这篇综述文章中,我们描述了基因扩增导致抗生素耐药性的各种途径,从抗生素的外排和修饰,到靶点修饰和旁路。我们还讨论了基因扩增如何通过改变调控和蛋白质结构等替代突变结果产生耐药性,而不仅仅是拷贝数和表达的增加。了解扩增如何在抗生素暴露后促进细菌存活对于对抗它们在抗菌药物耐药性上升中的作用至关重要。