In Vitro Activity of Cefiderocol Against a Broad Range of Clinically Important Gram-negative Bacteria

被引:154
作者
Yamano, Yoshinori [1 ]
机构
[1] Shionogi & Co Ltd, Pharmaceut Res Div, 3-1-1 Futaba Cho, Toyonaka, Osaka 5610825, Japan
关键词
carbapenem-resistant Acinetobacter; carbapenem-resistant Enterobacteriaceae; carbapenem-resistant Pseudomonas; cefiderocol; Stenotrophomonas maltophilia; SIDEROPHORE CEPHALOSPORIN CEFIDEROCOL; STENOTROPHOMONAS-MALTOPHILIA; ANTIBIOTICS; INFECTIONS; S-649266;
D O I
10.1093/cid/ciz827
中图分类号
R392 [医学免疫学]; Q939.91 [免疫学];
学科分类号
100102 ;
摘要
Carbapenem-resistant gram-negative bacteria including Enterobacteriaceae as well as nonfermenters, such as Pseudomonas aeruginosa and Acinetobacter baumannii, have emerged as significant global clinical threats. Although new agents have recently been approved, none are active across the entire range of resistance mechanisms presented by carbapenem-resistant gram-negative bacteria. Cefiderocol, a novel siderophore cephalosporin, has been shown in large surveillance programs and independent in vitro studies to be highly active against all key gram-negative causative pathogens isolated from patients with hospital-acquired or ventilator-associated pneumonia, bloodstream infections, or complicated urinary tract infections. The improved structure, the novel mode of entry into bacteria, and its stability against carbapenemases enables cefiderocol to exhibit high potency against isolates that produce carbapenemases of all classes or are resistant due to porin channel mutations and/or efflux pump overexpression. Resistance to cefiderocol is uncommon and appears to be multifactorial.
引用
收藏
页码:544 / 551
页数:8
相关论文
共 48 条
[1]   Stenotrophomonas maltophilia: an Emerging Global Opportunistic Pathogen [J].
Brooke, Joanna S. .
CLINICAL MICROBIOLOGY REVIEWS, 2012, 25 (01) :2-41
[2]   Update on infections caused by Stenotrophomonas maltophilia with particular attention to resistance mechanisms and therapeutic options [J].
Chang, Ya-Ting ;
Lin, Chun-Yu ;
Chen, Yen-Hsu ;
Hsueh, Po-Ren .
FRONTIERS IN MICROBIOLOGY, 2015, 6
[3]  
Clinical and Laboratory Standards Institute, 2019, M100 Performance Standars for Antimicrobial Susceptibility Testing
[4]   Activity of the novel siderophore cephalosporin cefiderocol against multidrug-resistant Gram-negative pathogens [J].
Dobias, J. ;
Denervaud-Tendon, V. ;
Poirel, L. ;
Nordmann, P. .
EUROPEAN JOURNAL OF CLINICAL MICROBIOLOGY & INFECTIOUS DISEASES, 2017, 36 (12) :2319-2327
[6]   Design of Data Management for Multi SPMD Workflow Programming Model [J].
Dufaud, Thomas ;
Tsuji, Miwako ;
Sato, Mitsuhisa .
PROCEEDINGS OF 2018 IEEE/ACM 4TH INTERNATIONAL WORKSHOP ON EXTREME SCALE PROGRAMMING MODELS AND MIDDLEWARE (ESPM2 2018), 2018, :9-18
[7]   Activity of cefiderocol (S-649266) against carbapenem-resistant Gram-negative bacteria collected from inpatients in Greek hospitals [J].
Falagas, Matthew E. ;
Skalidis, Tilemachos ;
Vardakas, Konstantinos Z. ;
Legakis, Nicholas J. .
JOURNAL OF ANTIMICROBIAL CHEMOTHERAPY, 2017, 72 (06) :1704-1708
[8]   Humanized Exposures of Cefiderocol, a Siderophore Cephalosporin, Display Sustained in vivo Activity against Siderophore-Resistant Pseudomonas aeruginosa [J].
Ghazi, Islam M. ;
Monogue, Marguerite L. ;
Tsuji, Masakatsu ;
Nicolau, David P. .
PHARMACOLOGY, 2018, 101 (5-6) :278-284
[9]   Cation Concentration Variability of Four Distinct Mueller-Hinton Agar Brands Influences Polymyxin B Susceptibility Results [J].
Girardello, Raquel ;
Bispo, Paulo J. M. ;
Yamanaka, Tiago M. ;
Gales, Ana C. .
JOURNAL OF CLINICAL MICROBIOLOGY, 2012, 50 (07) :2414-2418
[10]  
Hackel M, 2016, IDWEEK 2016 NEW ORL