Efficacy of human-simulated bronchopulmonary exposures of cefepime, zidebactam and the combination (WCK 5222) against MDR Pseudomonas aeruginosa in a neutropenic murine pneumonia model

被引:30
作者
Kidd, James M. [1 ]
Abdelraouf, Kamilia [1 ]
Nicolau, David P. [1 ]
机构
[1] Hartford Hosp, Ctr Antiinfect Res & Dev, Harford, CT 06106 USA
关键词
CEFTAZIDIME;
D O I
10.1093/jac/dkz414
中图分类号
R51 [传染病];
学科分类号
100401 ;
摘要
Objectives: WCK 5222 combines cefepime with zidebactam, alpha, B-lactam enhancer that binds PBP2 and inhibits doss A and C beta-lactamases. The efficacy of human-simulated bronchopuLmonary exposures of WCK 5222 against MDR Pseudomonas aeruginosa was investigated in a neutropenic murine pneumonia model. Methods: Nineteen MDR isoLates of P. aeruginosa (cefepime MICs >= 64 mg/L) were studied. MICs of zidebactam and WCK 5222 ranged from 4 to 512 mg/L and from 4 to 32 mg/L, respectiveLy. Dosing regimens of cefepime and zidebactam done and in combination that achieved epitheLiaL Lining fluid (ELF) exposures in mice approximating human ELF exposures after doses of 2 g of cefepime/1 g of zidebactam every 8 h (1 h infusion) were utilized; controls were vehicle-dosed. Lungs were intranasaLLy inoculated with 10(7) -10(8) cfu/mL bacteriaL suspensions. Mice were dosed subcutaneously 2 h after inoculation for 24 h, then Lungs were harvested. Results: In vitro MIC was predictive of in vivo response to WCK 5222 treatment. Mean +/- SD changes in bacteriaL density at 24 h compared with 0 h controls (6.72 +/- 0.50 Log(10) cfu/Lungs) for 13 isoLates with WCK 5222 MICs <= 16 mg/L were 1.17 +/- 1.00, -0.99 +/- 1.45 and -2.21 +/- 0.79 Log(10) cfu/lungs for cefepime, zidebactam and WCK 5222, respectiveLy. Against these isoLates, zidebactam yielded >1 Log(10) cfu/Lungs reductions in 8/13, while activity was enhanced with WCK 5222, producing >2 Log(10) cfu/Lungs reductions in 10/13 and >1 Log(10)cfu/Lungs reductions in 12/13. Among isoLates with WCK 5222 MICs of 32 mg/L, five out of six showed a bacteriostatic response. Conclusions: Human-simulated bronchopuLmonary exposure of WCK 5222 is effective against MDR P. aeruginosa at MIC <= 16 mg/L in a murine pneumonia modeL. These data support the clinical development of WCK 5222 for pseudomonaL Lung infections.
引用
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页码:149 / 155
页数:7
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共 26 条
  • [1] In Vivo Efficacy of Humanized WCK 5222 (Cefepime-Zidebactam) Exposures against Carbapenem-Resistant Acinetobacter baumannii in the Neutropenic Thigh Model
    Abuhussain, Safa S. Almarzoky
    Avery, Lindsay M.
    Abdelraouf, Kamilia
    Nicolau, David P.
    [J]. ANTIMICROBIAL AGENTS AND CHEMOTHERAPY, 2019, 63 (01)
  • [2] [Anonymous], WCK 5222 UNRAVELLING
  • [3] [Anonymous], 2017, ANTIMICROB AGENTS CH, DOI DOI 10.1128/AAC.02529-16
  • [4] Antibiotic resistance rates for Pseudomonas aeruginosa clinical respiratory and bloodstream isolates among the Veterans Affairs Healthcare System from 2009 to 2013
    Appaneal, Haley J.
    Caffrey, Aisling R.
    Jiang, Lan
    Dosa, David
    Mermel, Leonard A.
    LaPlante, Kerry L.
    [J]. DIAGNOSTIC MICROBIOLOGY AND INFECTIOUS DISEASE, 2018, 90 (04) : 311 - 315
  • [5] Avery LM, 2018, ANTIMICROB AGENTS CH, V62, DOI [10.1128/AAC.00948-18, 10.1128/aac.00948-18]
  • [6] CLSI, 2020, CLSI supplement M100, V30th
  • [7] Clinical Pharmacodynamics of Cefepime in Patients Infected with Pseudomonas aeruginosa
    Crandon, Jared L.
    Bulik, Catharine C.
    Kuti, Joseph L.
    Nicolau, David P.
    [J]. ANTIMICROBIAL AGENTS AND CHEMOTHERAPY, 2010, 54 (03) : 1111 - 1116
  • [8] Intensive care unit-acquired pneumonia due to Pseudomonas aeruginosa with and without multidrug resistance
    Fernandez-Barat, Laia
    Ferrer, Miquel
    De Rosa, Francesca
    Gabarrus, Albert
    Esperatti, Mariano
    Terraneo, Silvia
    Rinaudo, Mariano
    Li Bassi, Gianluigi
    Torres, Antoni
    [J]. JOURNAL OF INFECTION, 2017, 74 (02) : 142 - 152
  • [9] The final goal: penicillin-binding proteins and the target of cephalosporins
    Fontana, R
    Cornaglia, G
    Ligozzi, M
    Mazzariol, A
    [J]. CLINICAL MICROBIOLOGY AND INFECTION, 2000, 6 : 34 - 40
  • [10] Ceftolozane-Tazobactam for the Treatment of Multidrug-Resistant Pseudomonas aeruginosa Infections: Clinical Effectiveness and Evolution of Resistance
    Haidar, Ghady
    Philips, Nathan J.
    Shields, Ryan K.
    Snyder, Daniel
    Cheng, Shaoji
    Potoski, Brian A.
    Doi, Yohei
    Hao, Binghua
    Press, Ellen G.
    Cooper, Vaughn S.
    Clancy, Cornelius J.
    Hong Nguyen, M.
    [J]. CLINICAL INFECTIOUS DISEASES, 2017, 65 (01) : 110 - 120