# P-1294. Epidemiology of Carbapenem-resistance Mechanisms and the Utility of Newly Introduced Beta-lactams/beta-lactam Inhibitors in Patients with Pseudomonas aeruginosa Bacteremia

**Authors:** Young Kyung Yoon, Yoon Hyun Sung, Jeong Yeon Kim, Jang Wook Sohn

PMC · DOI: 10.1093/ofid/ofaf695.1482 · Open Forum Infectious Diseases · 2026-01-11

## TL;DR

This study examines the resistance patterns of Pseudomonas aeruginosa to various new antibiotics in South Korea and finds that aztreonam-avibactam is most effective.

## Contribution

The study provides new insights into the molecular mechanisms and antibiotic susceptibility patterns of CRPA in South Korea.

## Key findings

- CRPA isolates showed the highest susceptibility to aztreonam-avibactam (90.2%) compared to other beta-lactam combinations.
- The most common carbapenemase gene was blaNDM, found in 82.6% of isolates producing carbapenemase.
- Porin loss was confirmed in 80.4% of isolates, contributing to resistance mechanisms.

## Abstract

The aim of this study was to analyze the molecular epidemiology of carbapenem-resistance in blood isolates of carbapenem-resistant Pseudomonas aeruginosa (CRPA) and the cross-resistance to new beta-lactams/beta-lactam inhibitors.

In a prospective observational study, CRPA isolates were collected from patients diagnosed with CRPA bacteremia in a university-affiliated hospital of the Republic of Korea (ROK) from May 2020 to February 2025. CRPA isolates were tested for antibiotic susceptibility to ceftolozane-tazobactam (C/T), ceftazidime-avibactam (CZA), imipenem-relebactam (I/R), meropenem-vaborbactam (MVB), and aztreonam-avibactam (AZA) using the broth microdilution method. Molecular mechanisms of carbapenem-resistance were determined by polymerase chain reaction (PCR) for six resistance genes (blaVIM, blaIMP, blaNDM, blaGES, blaKPC, and blaOXA-48). Real-time reverse transcription PCR analysis was performed to confirm reduced expression of oprD or overexpression of mexB, mexD, mexF, mexY, and ampC.

A total of 51 patients with CRPA bacteremia were included in our analysis. In-hospital mortality rate was 52.9%. The MIC50/MIC90 of the CRPA isolates of C/T, CZA, I/R, MVB, and AZA were 4/ >256 mg/L, 16/ >256 mg/L, 8/ >256 mg/L, 32/ >256 mg/L, and 8/16 mg/L, respectively. AZA showed the highest susceptibility (90.20%), followed by C/T (50.98%), CZA (41.18%), I/R (23.53%), and MVB (19.61%). The proportion of isolates producing carbapenememase was 45.1%. Among them, blaNDM was the most common at 82.6%, followed by blaIMP (26.1%) and blaGES (17.4%). Among all isolates, porin loss and efflux pump overexpression were confirmed in 80.4% and 27.5%, respectively. Isolates non-susceptible to C/T showed 4.0% and 92.0% susceptibility to CZA and AZA, respectively, and resistance to both I/R and MVB. On the other hand, isolates non-susceptible to CZA showed 20.0% and 93.3% susceptibility to C/T and AZA, respectively, and resistance to both I/R and MVB.

In the ROK, CRPA isolates showed high resistance rates to C/T and CZA at 45.1% and 58.8%, respectively. Meanwhile, they showed the highest susceptibility at 90.2% to AZA. Therefore, the introduction of new antibiotics such as AZA is required to overcome the carbapenem-resistance of CRPA isolates in the ROK.

All Authors: No reported disclosures

## Linked entities

- **Genes:** OPRD1 (opioid receptor delta 1) [NCBI Gene 4985], mexB (multidrug resistance protein MexB) [NCBI Gene 877852], mexD (resistance-nodulation-cell division (RND) multidrug efflux transporter MexD) [NCBI Gene 881071], mexF (resistance-nodulation-cell division (RND) multidrug efflux transporter MexF) [NCBI Gene 882884], mexY (multidrug efflux RND transporter permease subunit MexY) [NCBI Gene 77221396], ampC (beta-lactamase) [NCBI Gene 878149]
- **Chemicals:** ceftolozane-tazobactam (PubChem CID 86291594), ceftazidime-avibactam (PubChem CID 90643431), meropenem-vaborbactam (PubChem CID 86298703)
- **Diseases:** bacteremia (MONDO:0005229)
- **Species:** Pseudomonas aeruginosa (taxon 287)

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Source: https://tomesphere.com/paper/PMC12791415