In-vitro activity of the novel β-lactam/β-lactamase inhibitor combinations and cefiderocol against carbapenem-resistant Pseudomonas spp. clinical isolates collected in Switzerland in 2022

被引:0
|
作者
Le Terrier, Christophe [1 ,3 ,4 ]
Bouvier, Maxime [1 ,2 ]
Kerbol, Auriane [1 ,2 ]
Dell'Acqua, Chloe [1 ]
NARA Network, Patrice
Nordmann, Patrice [1 ,2 ]
Poirel, Laurent [1 ,2 ]
机构
[1] Univ Fribourg, Fac Sci & Med, Dept Med, Med & Mol Microbiol Unit, Chemin Musee 18, CH-1700 Fribourg, Switzerland
[2] Univ Fribourg, Swiss Natl Reference Ctr Emerging Antibiot Resista, Fribourg, Switzerland
[3] Univ Hosp Geneva, Div Intens Care Unit, Geneva, Switzerland
[4] Fribourg Hosp, Emergency Dept, Fribourg, Switzerland
关键词
Cefiderocol; Ceftolozane; Imipenem; Meropenem; Avibactam; Relebactam; Vaborbactam; Beta-lactamase; Carbapenemase; CEFTOLOZANE-TAZOBACTAM; AERUGINOSA;
D O I
10.1007/s10096-024-04994-6
中图分类号
R51 [传染病];
学科分类号
100401 ;
摘要
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-beta-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 beta-lactam/beta-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.
引用
收藏
页码:571 / 585
页数:15
相关论文
共 50 条
  • [21] In vitro activity of tigecycline against carbapenem-susceptible and -resistant isolates of Klebsiella spp. and Enterobacter spp.
    Woodford, Neil
    Hill, Robert L. R.
    Livermore, David M.
    JOURNAL OF ANTIMICROBIAL CHEMOTHERAPY, 2007, 59 (03) : 582 - 583
  • [22] In-Vitro Activity of Dimercaptosuccinic Acid in Combination with Carbapenems Against Carbapenem-Resistant Pseudomonas aeruginosa
    Bouvier, Maxime
    Freire, Samanta
    Findlay, Jacqueline
    Nordmann, Patrice
    MICROBIAL DRUG RESISTANCE, 2025, 31 (01) : 16 - 20
  • [23] In vitro activity of cefiderocol against a global collection of carbapenem-resistant Pseudomonas aeruginosa with a high level of carbapenemase diversity
    Gill, Christian M.
    Santini, Debora
    Nicolau, David P.
    ERACE PA Global Study Grp
    JOURNAL OF ANTIMICROBIAL CHEMOTHERAPY, 2024, 79 (02) : 412 - 416
  • [24] In vitro potency of xeruborbactam in combination with multiple β-lactam antibiotics in comparison with other β-lactam/β-lactamase inhibitor (BLI) combinations against carbapenem-resistant and extended-spectrum β-lactamase-producing Enterobacterales
    Lomovskaya, Olga
    Castanheira, Mariana
    Lindley, Jill
    Rubio-Aparicio, Debora
    Nelson, Kirk
    Tsivkovski, Ruslan
    Sun, Dongxu
    Totrov, Maxim
    Loutit, Jeffery
    Dudley, Michael
    ANTIMICROBIAL AGENTS AND CHEMOTHERAPY, 2023, 67 (11)
  • [25] IN-VITRO ACTIVITY OF CEFIDEROCOL AGAINST CARBAPENEM-RESISTANT GRAM-NEGATIVE BACILLI: FIRST STUDY FROM INDIA
    Didwania, A.
    Mohapatra, S.
    Kocher, D.
    Sharma, P.
    Kaur, P.
    Gautam, H.
    Kumar, A.
    Soneja, M.
    Vikram, N.
    Sood, S.
    Dhawan, B.
    Das, B.
    Wig, N.
    Chaudhry, R.
    Kapil, A.
    INTERNATIONAL JOURNAL OF INFECTIOUS DISEASES, 2023, 130 : S14 - S14
  • [26] Activities of aztreonam in combination with several novel β-lactam-β-lactamase inhibitor combinations against carbapenem-resistant Klebsiella pneumoniae strains coproducing KPC and NDM
    Li, Xinhui
    Zhang, Jisheng
    Wang, Jianmin
    Long, Wenzhang
    Liang, Xushan
    Yang, Yang
    Gong, Xue
    Li, Jie
    Liu, Longjin
    Zhang, Xiaoli
    FRONTIERS IN MICROBIOLOGY, 2024, 15
  • [27] Comparing the activity of novel antibiotic agents against carbapenem-resistant Enterobacterales clinical isolates
    Tamma, Pranita D.
    Bergman, Yehudit
    Jacobs, Emily B.
    Lee, Jae Hyoung
    Lewis, Shawna
    Cosgrove, Sara E.
    Simner, Patricia J.
    INFECTION CONTROL & HOSPITAL EPIDEMIOLOGY, 2023, 44 (05) : 762 - 767
  • [28] Impact of chromosomally encoded resistance mechanisms and transferable β-lactamases on the activity of cefiderocol and innovative β-lactam/β-lactamase inhibitor combinations against Pseudomonas aeruginosa
    Gonzalez-Pinto, Lucia
    Alonso-Garcia, Isaac
    Blanco-Martin, Tania
    Camacho-Zamora, Pablo
    Fraile-Ribot, Pablo Arturo
    Outeda-Garcia, Michelle
    Lasarte-Monterrubio, Cristina
    Guijarro-Sanchez, Paula
    Maceiras, Romina
    Moya, Bartolome
    Juan, Carlos
    Vazquez-Ucha, Juan Carlos
    Beceiro, Alejandro
    Oliver, Antonio
    Bou, German
    Arca-Suarez, Jorge
    JOURNAL OF ANTIMICROBIAL CHEMOTHERAPY, 2024, 79 (10) : 2591 - 2597
  • [29] Carbapenem-resistant Gram-negative pathogens in a German university medical center: Prevalence, clinical implications and the role of novel β-lactam/β-lactamase inhibitor combinations
    Katchanov, Juri
    Asar, Lucia
    Klupp, Eva-Maria
    Both, Anna
    Rothe, Camilla
    Koenig, Christina
    Rohde, Holger
    Kluge, Stefan
    Maurer, Florian P.
    PLOS ONE, 2018, 13 (04):
  • [30] Discovery of a Novel Metallo-β-Lactamase Inhibitor That Potentiates Meropenem Activity against Carbapenem-Resistant Enterobacteriaceae
    Everett, Martin
    Sprynski, Nicolas
    Coelho, Alicia
    Castandet, Jerome
    Bayet, Maelle
    Bougnon, Juliette
    Lozano, Clarisse
    Davies, David T.
    Leiris, Simon
    Zalacain, Magdalena
    Morrissey, Ian
    Magnet, Sophie
    Holden, Kirsty
    Warn, Peter
    De Luca, Filomena
    Docquier, Jean-Denis
    Lemonnier, Marc
    ANTIMICROBIAL AGENTS AND CHEMOTHERAPY, 2018, 62 (05)