National Reference Laboratory for Antibiotics, Centre for Epidemiology and Microbiology, National Institute of Public Health, Prague, Czech Republic.
Department of Microbiology, 3rd Faculty of Medicine, Kralovske Vinohrady University Hospital and National Institute of Public Health, Charles University, Prague, Czech Republic.
Microb Drug Resist. 2023 Oct;29(10):485-491. doi: 10.1089/mdr.2023.0090. Epub 2023 Aug 22.
The objective of this study was to assess the susceptibility of cefiderocol against multidrug-resistant carbapenemase-producing and nonproducing bacteria. The panel comprised 182 isolates of the order , and 40 strains of . Antimicrobial susceptibility testing has been performed using broth microdilution method according to the European Committee on Antimicrobial Susceptibility Testing recommendations. Mass spectrometry matrix-assisted laser desorption/ionization-time of flight mass spectrometry and carbapenemase-producing test were used to verify the presence of carbapenemases in clinical isolates. The genetic expression of single carbapenemases (, , , , , ) was determined by real-time polymerase chain reaction. Cefiderocol exhibited a good activity against the majority of strains tested in this study. Altogether, growth of 81.9% ( = 149) strains of the order and 77.5% ( = 31) of isolates were inhibited at minimal inhibitory concentration (MIC) ≤2 mg/L. Values MIC/MIC were 0.5/8 mg/L for enterobacteria, and 1/8 mg/L for . One isolate () harboring two carbapenemases (, ) had cefiderocol MIC 0.5 mg/L. In enterobacteria resistant to cefiderocol, carbapenemase prevailed (43.3%, = 29), followed by (31.3%, = 21) and (4.5%, = 3). ( = 8) and a ( = 1) metallo-β-lactamases dominated in cefiderocol-resistant ( = 9) isolates. Very good susceptibility (100%) to this drug showed -positive strains of ( = 8) and isolates resistant to meropenem without confirmed carbapenemase gene ( = 10). In this study, cefiderocol demonstrated potent activity against important nosocomial pathogens, therefore, therapeutic options of this drug against multidrug-resistant bacteria should be considered.
这项研究的目的是评估头孢地尔在多药耐药碳青霉烯酶产生菌和非产酶菌中的敏感性。该研究包含 182 株菌,40 株菌。根据欧洲抗菌药物敏感性试验委员会的建议,采用肉汤微量稀释法进行药敏试验。基质辅助激光解吸电离飞行时间质谱和产碳青霉烯酶试验用于验证临床分离株中碳青霉烯酶的存在。通过实时聚合酶链反应确定单碳青霉烯酶(、、、、、)的基因表达。头孢地尔对本研究中检测到的大多数菌株表现出良好的活性。总的来说,在最小抑菌浓度(MIC)≤2mg/L 时,81.9%(149/182)的菌株和 77.5%(31/40)的菌株生长受到抑制。肠杆菌的 MIC/MIC 值为 0.5/8mg/L,而的 MIC/MIC 值为 1/8mg/L。一株同时携带两种碳青霉烯酶(和)的菌株()的头孢地尔 MIC 为 0.5mg/L。对头孢地尔耐药的肠杆菌中,主要是碳青霉烯酶(43.3%,29/67),其次是(31.3%,21/67)和(4.5%,3/67)。头孢地尔耐药的(9/11)株菌中,主要是(8/11)和金属β-内酰胺酶(1/11)。对这种药物具有很好的敏感性(100%)的菌株有 8/8 株和对美罗培南耐药但未确认碳青霉烯酶基因的菌株 10/10 株。在这项研究中,头孢地尔对重要的医院获得性病原体表现出强大的活性,因此,应该考虑将这种药物作为治疗多药耐药菌的选择。