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