DOI: 10.1128/spectrum.02949-25 ISSN: 2165-0497
In vitro
activity of contezolid against gram-positive bacteria isolated from pediatric patients with invasive infections
Xinrong Li, Rubo Li, Suyun Qian, Quan Wang ABSTRACT
Contezolid, a novel oxazolidinone, exhibits potent activity against multidrug-resistant gram-positive pathogens, but data in pediatric populations remain limited. This study evaluated the
in vitro
activity of contezolid against
Streptococcus pneumoniae
(
n
= 53) and
Staphylococcus aureus
(
n
= 92) isolates recovered from sterile-site specimens of pediatric patients with invasive infections (2018–2023). MICs were determined by broth microdilution. For
S. pneumoniae
, contezolid MICs ranged from 0.125 to 1.000 µg/mL (MIC
50/90
, 0.250/0.500 µg/mL), with comparable activity against penicillin-susceptible and penicillin-nonsusceptible isolates. Contezolid exhibited low MIC values with a relatively narrow distribution across serotypes and specimen sources, without marked differences. For
S. aureus
, contezolid MICs ranged from 0.250 to 2.000 µg/mL (MIC
50/90
, 0.500/1.000 µg/mL), with equivalent activity against methicillin-susceptible
Staphylococcus aureu
s (MSSA) and methicillin-resistant
Staphylococcus aureus
(MRSA). All isolates were susceptible, with most MICs ≤ 0.500 µg/mL and a minority (
n
= 25) at 1–2 µg/mL, mostly involving isolates from blood. Contezolid exhibited potent and consistent
in vitro
activity against gram-positive pathogens isolated from invasive infections in pediatric patients, including MRSA and PNSP, with stable susceptibility profiles across major clonal lineages. These findings demonstrate favorable
in vitro
activity of contezolid against clinically significant isolates.
IMPORTANCE
This study provides an evaluation of the
in vitro
activity of contezolid against gram-positive bacterial isolates obtained exclusively from pediatric patients with invasive infections. By characterizing susceptibility patterns across resistance phenotypes and molecular backgrounds, our findings offer important baseline data to inform future clinical studies of contezolid in pediatric populations.