In Vitro Susceptibility of Gram-negative Pathogens to Cefiderocol in Five Consecutive Annual Multinational SIDERO-WT Surveillance Studies (2014-2019)

Author:

Karlowsky James A.12,Hackel Meredith A.1ORCID,Takemura Miki3,Yamano Yoshinori4,Roger Echols5,Sahm Daniel F.1

Affiliation:

1. IHMA, Schaumburg, Illinois, USA

2. Department of Medical Microbiology and Infectious Diseases, Max Rady College of Medicine, University of Manitoba, Winnipeg, Manitoba, Canada

3. Laboratory for Drug Discovery and Disease Research, Shionogi & Co., Ltd., Osaka, Japan

4. Research Planning Department, Shionogi & Co., Ltd., Osaka, Japan

5. Infectious Disease Drug Development Consulting, LLC. Easton, Connecticut, USA

Abstract

We report in vitro susceptibility data from five consecutive annual SIDERO-WT surveillance studies (2014-2019) for cefiderocol and comparators tested against Gram-negative clinical isolates from North America and Europe. CLSI broth microdilution was used to determine MICs for Enterobacterales ( n =31,896), Pseudomonas aeruginosa ( n =7,700), Acinetobacter baumannii complex ( n =5,225), Stenotrophomonas maltophilia ( n =2,030), and Burkholderia cepacia complex ( n =425). MICs were interpreted by CLSI-approved clinical breakpoints (February 2021). Cefiderocol inhibited 99.8%, 96.7%, 91.6%, and 97.7% of all Enterobacterales , meropenem-nonsusceptible, ceftazidime-avibactam-nonsusceptible, and ceftolozane-tazobactam-nonsusceptible isolates, respectively, at ≤4 μg/ml (susceptible breakpoint). Cefiderocol inhibited 99.9%, 99.8%, 100%, and 99.8% of all P. aeruginosa , meropenem-nonsusceptible, ceftazidime-avibactam-nonsusceptible, and ceftolozane-tazobactam-nonsusceptible isolates, respectively, at ≤4 μg/ml (susceptible breakpoint). Cefiderocol inhibited 96.0% of all A. baumannii complex isolates and 94.2% of meropenem-nonsusceptible isolates at ≤4 μg/ml (susceptible breakpoint), and 98.6% of S. maltophilia isolates at ≤1 μg/ml (susceptible breakpoint). B. cepacia complex isolates tested with a MIC 50 of ≤0.03 μg/ml and MIC 90 of 0.5 μg/ml. Annual cefiderocol percent susceptible rates for Enterobacterales (North America, range 99.6-100%/year; Europe, range 99.3-99.9%/year) and P. aeruginosa (99.8-100%; 99.9-100%) were unchanged from 2014 to 2019. Annual percent susceptible rates for A. baumannii complex demonstrated sporadic, non-directional differences (97.5-100%; 90.4-97.5%); the wider range for Europe (∼7%) was due to isolates from Russia. Annual percent susceptible rates for S. maltophilia showed minor, non-directional differences (96.4-100%; 95.6-100%). We conclude that clinical isolates of Enterobacterales (99.8% susceptible), P. aeruginosa (99.9%), A. baumannii (96.0%), and S. maltophilia (98.6%) collected in North America and Europe from 2014 to 2019 were highly susceptible to cefiderocol.

Publisher

American Society for Microbiology

Subject

Infectious Diseases,Pharmacology (medical),Pharmacology

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