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ORIGINAL RESEARCH article

Front. Microbiol.

Sec. Antimicrobials, Resistance and Chemotherapy

Volume 16 - 2025 | doi: 10.3389/fmicb.2025.1543509

This article is part of the Research Topic Opportunistic pathogens: pathogenesis and multi-drug resistance mechanisms View all 9 articles

High Prevalence of Carbapenem-Resistant Pseudomonas aeruginosa and identification of a novel VIM-type metallo-β-lactamase, VIM-92, in Clinical Isolates from Northern China

Provisionally accepted
Linbo Zhao Linbo Zhao 1Jiekun Pu Jiekun Pu 1Yunning Liu Yunning Liu 1*Heng Cai Heng Cai 2*Meijuan Han Meijuan Han 3*Yunsong Yu Yunsong Yu 2*Jianhua Tang Jianhua Tang 1*
  • 1 First Affiliated Hospital of Hebei North University, Zhangjiakou, China
  • 2 Department of Infectious Diseases, Sir Run Run Shaw Hospital, Hangzhou, Jiangsu Province, China
  • 3 Department of Pharmacy, Cangzhou Central Hospital, Cangzhou, China

The final, formatted version of the article will be published soon.

    Carbapenem-Resistant Pseudomonas Aeruginosa (CRPA) has become a serious global health concern due to the limited treatment options. The primary resistance mechanism in CRPA involves the production of metallo-β-lactamases (MBLs), making MBL-producing P. aeruginosa a significant component of CRPA cases. To understand the prevalence of CRPA in hospitals in northern China, we conducted a preliminary screening and identification of CRPA in 143 clinical isolates of P. aeruginosa collected from various departments of a tertiary hospital between 2021 and 2023, analyzing CRPA resistance trends in certain regions of northern China during this period. We identified 71 CRPA isolates that exhibited high carbapenem resistance and phylogenetic tree analysis revealed that ST244 CRPA isolates had widely spread across various departments of the same hospital over three consecutive years. We also identified two VIM-producing isolates, PJK40 and PJK43, both of which carried the same novel VIM-type metallo-β-lactamase, VIM-92, encoded by a newly identified gene, blaVIM-92, closely related to blaVIM-24. blaVIM-92 was embedded in class 1 integrons within the Tn1403 transposon. The blaVIM-92-carrying plasmid, pPJK40, was found to resemble the pJB37 megaplasmid. The expression of VIM-92 and VIM-24 in DH5α and PAO1 revealed similar effects of the MICs of β-lactams, except for aztreonam. The high prevalence of CRPA in clinical settings, and the identification of VIM-92, highlights the urgent need for ongoing surveillance of CRPA and emerging MBL variants in P. aeruginosa.

    Keywords: Pseudomonas aeruginosa, Epidemiological investigation, metallo-β-lactamase, VIM-92, Plasmid

    Received: 11 Dec 2024; Accepted: 13 Feb 2025.

    Copyright: © 2025 Zhao, Pu, Liu, Cai, Han, Yu and Tang. This is an open-access article distributed under the terms of the Creative Commons Attribution License (CC BY). The use, distribution or reproduction in other forums is permitted, provided the original author(s) or licensor are credited and that the original publication in this journal is cited, in accordance with accepted academic practice. No use, distribution or reproduction is permitted which does not comply with these terms.

    * Correspondence:
    Yunning Liu, First Affiliated Hospital of Hebei North University, Zhangjiakou, China
    Heng Cai, Department of Infectious Diseases, Sir Run Run Shaw Hospital, Hangzhou, 310016, Jiangsu Province, China
    Meijuan Han, Department of Pharmacy, Cangzhou Central Hospital, Cangzhou, 061001, China
    Yunsong Yu, Department of Infectious Diseases, Sir Run Run Shaw Hospital, Hangzhou, 310016, Jiangsu Province, China
    Jianhua Tang, First Affiliated Hospital of Hebei North University, Zhangjiakou, China

    Disclaimer: All claims expressed in this article are solely those of the authors and do not necessarily represent those of their affiliated organizations, or those of the publisher, the editors and the reviewers. Any product that may be evaluated in this article or claim that may be made by its manufacturer is not guaranteed or endorsed by the publisher.

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