Le Terrier Christophe, Bouvier Maxime, Kerbol Auriane, Dell'Acqua Chloé, Nordmann Patrice, Poirel Laurent
Medical and Molecular Microbiology Unit, Department of Medicine, Faculty of Science and Medicine, University of Fribourg, Chemin du Musée 18, Fribourg, CH-1700, Switzerland.
Division of Intensive Care Unit, University Hospitals of Geneva, Geneva, Switzerland.
Eur J Clin Microbiol Infect Dis. 2025 Mar;44(3):571-585. doi: 10.1007/s10096-024-04994-6. Epub 2024 Dec 20.
To evaluate the in-vitro activity of the novel commercially-available drugs, including meropenem-vaborbactam (MEV), ceftazidime-avibactam (CZA), ceftolozane-tazobactam (C/T), imipenem-relebactam (IPR) as well as cefiderocol (FDC), against carbapenem-resistant Pseudomonas spp. (CRP) isolates. All CRP isolates collected at the Swiss National Reference Laboratory (NARA) over the year 2022 (n = 170) have been included. Most of these isolates (n = 121) were non-carbapenemase producers. Among the 49 carbapenemase producers, 47 isolates produced metallo-β-lactamases (MBL) including NDM-1 (n = 11), VIM-like (n = 28), IMP-like (n = 7), and both NDM-1 and VIM-2 (n = 1) and two isolates produced the class A carbapenemase GES-5. Susceptibility testing was determined by broth microdilution method (BMD), or disk diffusion test, and results interpreted following EUCAST guidelines. The susceptibility rates for MEV, CZA, C/T and IPR were found to be 41%, 45%, 59% and 58%, respectively, for the whole set of isolates tested. Among non-carbapenemase producers, susceptibility rates for these β-lactam/β-lactamase inhibitors (BL/BLI) combinations were higher, determined at 55%, 61%, 83%, and 82%, respectively. The overall susceptibility of carbapenemase-producing Pseudomonas spp. to novel BL/BLI was relatively low, while 80% of these isolates demonstrated susceptibility to FDC, with a similar proportion (79%) observed among MBL producers. A total of 10 MBL-producing isolates (6%), mainly NDM-1, were found to exhibit resistance to all drugs tested, with the exception of colistin. FDC exhibited an excellent in-vitro activity against this collection of CRP recovered from Switzerland in 2022, including MBL producers. The new BL/BLI combinations displayed significant activity against non-carbapenemase CRP, with IPR and C/T showing the highest susceptibility rates.
评估新型市售药物,包括美罗培南-巴坦(MEV)、头孢他啶-阿维巴坦(CZA)、头孢洛扎-他唑巴坦(C/T)、亚胺培南-瑞来巴坦(IPR)以及头孢地尔(FDC),对耐碳青霉烯类假单胞菌属(CRP)分离株的体外活性。纳入了2022年在瑞士国家参考实验室(NARA)收集的所有CRP分离株(n = 170)。这些分离株中的大多数(n = 121)不产生碳青霉烯酶。在49株碳青霉烯酶产生菌中,47株分离株产生金属β-内酰胺酶(MBL),包括NDM-1(n = 11)、VIM样(n = 28)、IMP样(n = 7)以及NDM-1和VIM-2两者(n = 1),还有两株分离株产生A类碳青霉烯酶GES-5。药敏试验通过肉汤微量稀释法(BMD)或纸片扩散法测定,并按照欧盟CAST指南解释结果。对于整套测试分离株,发现MEV、CZA、C/T和IPR的药敏率分别为41%、45%、59%和58%。在非碳青霉烯酶产生菌中,这些β-内酰胺/β-内酰胺酶抑制剂(BL/BLI)组合的药敏率更高,分别测定为55%、61%、83%和82%。产碳青霉烯酶假单胞菌属对新型BL/BLI的总体药敏性相对较低,而这些分离株中有80%对FDC敏感,在MBL产生菌中观察到类似比例(79%)。总共发现10株产MBL的分离株(6%),主要是NDM-1,对所有测试药物均耐药,但对黏菌素除外。FDC对2022年从瑞士收集的这批CRP,包括MBL产生菌,表现出优异的体外活性。新型BL/BLI组合对非碳青霉烯酶CRP显示出显著活性,IPR和C/T的药敏率最高。