ABSTRACT:
The
in vitro
activity of two novel antibiotics with different modes of action, (i) siderophore cefiderocol and (ii) β-lactam-enhancer mechanism-based cefepime/zidebactam, was tested against New Delhi Metallo-β-lactamase (NDM)-producing Enterobacterales and
Pseudomonas aeruginosa
collected in India. Minimum inhibitory concentrations of antibiotics against multicentric NDM-producing
Escherichia coli
(
n
= 117),
Klebsiella pneumoniae
(
n
= 103), and
P. aeruginosa
(
n
= 72) were determined by the reference broth microdilution method. Among
E. coli
, 111 isolates were NDM-alone, and six were NDM + OXA-48-like producers. Among
K. pneumoniae
, 47 and 56 isolates were NDM-alone and NDM + OXA-48-like producers, respectively. All
E. coli
isolates harbored four amino acid inserts in their penicillin-binding protein 3. Using the highest susceptible breakpoint among CLSI, FDA, and EUCAST interpretive criteria, cefiderocol susceptibility was 39.3%, ≤80%, and 57%, for NDM ± OXA-48-like-producing
E. coli
, NDM ± OXA-48-like-producing
K. pneumoniae,
and NDM-producing
P. aeruginosa
, respectively. At a cefepime break point of ≤8 mg/L, 100% of Enterobacterales and ≥90% of
P. aeruginosa
isolates were cefepime/zidebactam-susceptible. NDM being a dominant carbapenemase among Enterobacterales and
P. aeruginosa
in India, the variable activity of cefiderocol against NDM producers is a concern. Post approval, cefepime/zidebactam could offer a promising treatment option against NDM producers.
IMPORTANCE:
Metallo-β-lactamases are therapeutically challenging due to the limited treatment options. Against such isolates, currently approved newer β-lactam/β-lactamase inhibitor combinations are ineffective. In this study, we tested siderophore cephalosporin, cefiderocol, which utilizes an unconventional iron uptake pathway for efficient cellular penetration, and cefepime/zidebactam that utilizes novel β-lactam enhancer mechanisms for overcoming diverse carbapenemases. Cefiderocol showed limited activity against
Escherichia coli
isolates co-harboring New Delhi metallo-β-lactamase (NDM) with PBP3 insert, dual carbapenemase (NDM with OXA-48 like)-producing
Klebsiella pneumoniae
, and NDM-producing
Pseudomonas aeruginosa
isolates, while cefepime/zidebactam potently inhibited NDM-producing Enterobacterales and
P. aeruginosa
isolates. NDM being a dominant carbapenemase among Enterobacterales and
P. aeruginosa
in India, the variable activity of cefiderocol against NDM producers is a concern. Post approval, cefepime/zidebactam could offer a promising treatment option against NDM producers.