Service de microbiologie clinique et dosage des anti-infectieux, Groupe Hospitalier Paris Saint Joseph, 75014 Paris, France; EA4043 Unité Bactéries Pathogènes et Santé, Université Paris-Sud Saclay, Chatenay-Malabry, France.
Laboratoire Bactériologie-Virologie-Hygiène, Hôpital Avicenne, Université Paris 13, 93000 Bobigny, France.
Int J Antimicrob Agents. 2020 Feb;55(2):105834. doi: 10.1016/j.ijantimicag.2019.10.015. Epub 2019 Nov 1.
The burden of antibiotic-resistant infections among Gram-negative bacteria is increasing. Resistance to third-generation cephalosporins (3GCs) in Enterobacteriaceae is mainly conferred by the acquisition of β-lactamases or by deregulation of natural genetically-encoded β-lactamase enzymes. Enterobacteriaceae such as Enterobacter spp., Serratia marcescens, Citrobacter freundii, Providencia spp. and Morganella morganii (ESCPM group) possess chromosomally-encoded inducible AmpC β-lactamases. AmpC can be overproduced as a response to β-lactam antibiotic exposure or by constitutive dysfunction of the AmpC regulation system. This overproduction can lead to the inactivation of 3GCs. Based on small clinical studies, international guidelines and expert recommendations suggest that 3GCs should be avoided as definitive therapy for infections caused by ESCPM group organisms. In this narrative review, we discuss the published literature and evaluate the risk related to 3GC use in the case of documented ESCPM infection.
革兰氏阴性菌的抗生素耐药性感染负担正在增加。肠杆菌科对第三代头孢菌素(3GCs)的耐药性主要是通过获得β-内酰胺酶或通过天然基因编码β-内酰胺酶的调节失活来实现的。肠杆菌科如肠杆菌属、粘质沙雷氏菌、弗氏柠檬酸杆菌、普罗维登斯菌属和摩根摩根菌(ESCPM 组)拥有染色体编码的诱导型 AmpC β-内酰胺酶。AmpC 可以作为对β-内酰胺类抗生素暴露的反应或 AmpC 调节系统的组成性功能障碍而过度产生。这种过度产生会导致 3GCs 的失活。基于小型临床研究、国际指南和专家建议,对于由 ESCPM 组生物体引起的感染,应避免将 3GCs 作为明确的治疗药物。在这篇叙述性综述中,我们讨论了已发表的文献,并评估了在有记录的 ESCPM 感染情况下使用 3GC 的风险。