Ruiz Joaquim
Grupo de Investigación en Dinámicas y Epidemiología de la Resistencia a Antimicrobianos-"One Health", Universidad Científica del Sur, Lima 15067, Peru.
Life (Basel). 2024 Mar 14;14(3):383. doi: 10.3390/life14030383.
Quinolone resistance has been largely related to the presence of specific point mutations in chromosomal targets, with an accessory role of impaired uptake and enhanced pump-out. Meanwhile the relevance of transferable mechanisms of resistance able to protect the target of pump-out or inactivate quinolones has been increasingly reported since 1998. Nevertheless, bacteria have other strategies and mechanisms allowing them to survive and even proliferate in the presence of quinolones, which might be qualified as resistance or resilience mechanisms. These include decreasing levels of quinolone target production, transient amoeba protection, benthonic lifestyle, nutrient-independent slow growth, activation of stringent response, inactivation or degradation of quinolones as well as apparently unrelated or forgotten chromosomal mutations. These mechanisms have been largely overlooked, either because of the use of classical approaches to antibiotic resistance determination or due to the low increase in final minimum inhibitory concentration levels. This article is devoted to a review of a series of these mechanisms.
喹诺酮耐药性在很大程度上与染色体靶点中的特定点突变有关,摄取受损和泵出增强起辅助作用。与此同时,自1998年以来,能够保护泵出靶点或使喹诺酮失活的可转移耐药机制的相关性越来越多地被报道。然而,细菌还有其他策略和机制使其能够在喹诺酮存在的情况下存活甚至增殖,这些策略和机制可被视为耐药或适应机制。这些机制包括降低喹诺酮靶点的产生水平、短暂的变形虫保护、底栖生活方式、营养物非依赖型缓慢生长、严格反应的激活、喹诺酮的失活或降解以及明显不相关或被遗忘的染色体突变。这些机制在很大程度上被忽视了,要么是因为使用了经典的抗生素耐药性测定方法,要么是因为最终最低抑菌浓度水平的增加幅度较小。本文致力于对一系列这些机制进行综述。