Authors
Mariana Castanheira, John H Kimbrough, Maura Karr, Helio S Sader
Published in
Antimicrobial agents and chemotherapy. Pages e0012926. Sep 09, 2026. Epub Sep 09, 2026.
Abstract
We evaluated the presence and phenotypic impact of PBP3 insertions YRIN (n = 44) and YRIK (n = 18) among 124 Escherichia coli isolates belonging to high-risk lineages selected from 1,471 isolates displaying resistance to β-lactams. PBP3 insertions were detected among 62 isolates. YRIN insertions were detected among isolates belonging to ST167 (n = 23), ST361 (n = 7), ST410 (n = 10), ST617 (n = 1), and ST648 (n = 3), while YRIK insertions were observed in ST405 (n = 9), ST410 (n = 5), and ST617 (n = 4). Aztreonam-avibactam inhibited 90.3% of all isolates from high-risk clones and 80.6% of the isolates harboring PBP3 insertions when applying the EUCAST breakpoints. Aztreonam-avibactam inhibited 66.7% of the YRIK-harboring isolates (MIC50/90, 2/16 mg/L) and 86.4% of the ones harboring YRIN insertions (MIC50/90, 1/8 mg/L); however, the susceptibilities to other β-lactams were lower among YRIN isolates (25.6%-60.5%) compared to YRIK (55.6%-88.9%). Overall, ST617 was more resistant to all agents when compared to other STs, regardless of PBP3 insertions or the presence of other examined resistance mechanisms. Acquired β-lactamase genes and OmpC deleterious alterations were present in all isolates. CMY-42, CMY-141, and CMY-145 that have been associated with elevated aztreonam-avibactam MICs were detected among 13 isolates, and 4 (30.8%) were susceptible to this combination. All isolates harboring blaNDM-5 (n = 37) possessed PBP3 insertions. Aztreonam-avibactam inhibited 83.8% of these isolates. Resistance to aztreonam-avibactam is multifactorial, and singular resistance mechanisms are unable to elevate MIC values to resistant categories. Additionally, lineage-specific contributions to resistance play an important role in the overall development of β-lactam resistance, although these mechanisms appear to function outside the known repertoire of resistance-conferring mutations and warrant further study.
PMID:
42714383
Bibliographic data and abstract were imported from PubMed on 09 Sep 2026.
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