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Unlabelled: The emergence of carbapenemase-producing represents a significant clinical challenge. Resistance mechanisms involve carbapenemase production, porin and efflux pump alterations, penicillin-binding protein (PBP) modifications, and biofilm formation. This study characterizes a KPC- and a concurrent isolate harboring the same resistance genes, with also exhibiting PBP3 mutations. Whole-genome sequencing and plasmid analysis identified an IncFII(K) plasmid carrying the gene. Both strains shared two resistance genes (, ). contained a single copy of on Tn, whereas carried two copies on separate Tn transposons. Plasmid reconstruction revealed high homology (99.85%) with plasmid pECAZ147_KPC and plasmid pKPC. This suggests that transposon-mediated transfer between the two strains may have occurred via the same plasmid. Moreover, harbored PBP3 mutations (A233T, I332V), which have been previously linked to increased ceftazidime MICs and two missense mutations in . Despite carrying two copies of the gene, along with and PBP3 mutations, our isolate did not exhibit a significant increase in ceftazidime/avibactam MIC. This phenomenon could be explained by avibactam’s ability to bind to PBP2, potentially compensating for the reduced binding of ceftazidime to the mutated PBP3.
Supplementary Information: The online version contains supplementary material available at 10.1038/s41598-025-07624-z.
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http://www.ncbi.nlm.nih.gov/pmc/articles/PMC12216380 | PMC |
http://dx.doi.org/10.1038/s41598-025-07624-z | DOI Listing |
Antibiotics (Basel)
August 2025
Center for Applied Biotechnology Studies, Department of Biological Science, College of Natural Sciences and Mathematics, California State University Fullerton, 800 N State College Blvd, Fullerton, CA 92831, USA.
Carbapenem-resistant (CRKP) is an urgent public health threat due to its rapid dissemination and resistance to last-line antibiotics. Cefiderocol (FDC), a novel siderophore cephalosporin, targets resistant Gram-negative pathogens by exploiting bacterial iron uptake mechanisms. However, resistance to FDC is emerging among carbapenemase (KPC)-producing strains.
View Article and Find Full Text PDFJAC Antimicrob Resist
August 2025
Dept. of Infectious Diseases, Medical Microbiology and Hygiene, Heidelberg University, Medical Faculty Heidelberg, Heidelberg, Germany.
Background: Ceftazidime/avibactam has been introduced as a promising treatment option against multidrug-resistant Gram-negative bacteria.
Objectives: To investigate the development of ceftazidime/avibactam resistance in a -carrying strain with YRIK insertion in penicillin-binding protein 3 (PBP3).
Methods: Eight clinical isolates were recovered from a single patient treated with ceftazidime/avibactam.
Emerg Microbes Infect
December 2025
Department of Laboratory Medicine, National University Hospital, Singapore.
A 60-year-old male with recurrent bacteremia associated with necrotizing pancreatitis was followed over 17 months, during which six clinical isolates of were obtained. The index isolate (R1) was susceptible to aztreonam-avibactam (MIC 4 mg/L), but resistance (MIC >64 mg/L) emerged with isolate B1, collected one month later, and persisted in subsequent isolates. To investigate the genomic and phenotypic evolution of six clinical isolates, focusing on mechanisms underlying the emergence of aztreonam-avibactam resistance.
View Article and Find Full Text PDFPathology
June 2025
Department of Laboratory Medicine, National University Hospital, Singapore.
Aztreonam-avibactam is a treatment option for metallo-β-lactamase carbapenemase-producing Enterobacterales (CPE). This study was performed to determine resistance rates of a collection of CPE against aztreonam-avibactam and characterise associated resistance mechanisms. Minimum inhibitory concentrations (MICs) of a collection of New Delhi metallo-β-lactamase (NDM)- and NDM/OXA-48-like dual-CPE isolates were determined using two methods, the MIC Test Strip (MTS) and broth microdilution (Sensititre).
View Article and Find Full Text PDFMicrobiol Spectr
August 2025
Antimicrobial Resistance Research Center, National Institute of Infectious Diseases, Japan Institute for Health Security, Higashimurayama, Tokyo, Japan.
The locus of gram-negative bacteria encodes penicillin-binding protein 3 (PBP3), a common target of β-lactam antibiotics. Recent genomic surveillance of carbapenem-resistant revealed that 17% of strains possessed nonsynonymous substitution in . However, the contribution of nonsynonymous substitution alone to the antimicrobial susceptibility of has not been formally evaluated.
View Article and Find Full Text PDF