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Global dissemination of conjugative virulence plasmids coharboring hypervirulence and multidrug resistance genes in Klebsiella pneumoniae

Research output: Journal Publications and ReviewsRGC 21 - Publication in refereed journalpeer-review

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Abstract

Carbapenem-resistant hypervirulent Klebsiella pneumoniae (CR-hvKp) has led to a high mortality rate in the clinical setting and garnered significant attention in the clinical and scientific communities. It is still not clear which major mechanisms mediate the rapid evolution of hvKp in clinical settings since the plasmid-encoding hypervirulence phenotype is considered non-conjugative. In this study, we revealed a conjugative plasmid, p16HN200-Vir, encoding virulence-associated iuc operon (iucABCDiutA) and resulting in a hypervirulent phenotype. In silico analysis of Kp strains from NCBI predicted a total of 94 p16HN200-Vir-like conjugative virulence plasmids. These sequences were identified in 19 sequence types (STs) of the host with significant geographical variations in distribution across countries and continents. Notably, ST11 was predominant in China, while ST147 and ST395 were prominent in the United Kingdom and Russia, respectively. These plasmids could be categorized into seven lineages, some of which formed distinct geographical clusters in China and the UK, while others exhibited a hybrid population. Importantly, most of the plasmids carried different carbapenemases, including blaNDM-1/5 (lineage 6 and 7), and blaOXA-48/232 (lineage 2 and 5). Specifically, plasmids recovered from the United Kingdom and Russia were lineage-specific, with blaNDM-1 present in lineage 6 and blaNDM-5 in lineage 7. Our data suggest that this type of conjugative plasmids has spread around the world and contributed significantly to the current rapid evolution of CR-hvKp in clinical settings. Further surveillance of these types of conjugative plasmids in clinical Kp is warranted. Copyright © 2025 Xu et al.
Original languageEnglish
Article numbere01675-24
JournalmSystems
Volume10
Issue number4
Online published25 Mar 2025
DOIs
Publication statusPublished - 22 Apr 2025

Funding

This study was funded by the Theme-Based Research Scheme (T11-104/22-R) and the Research Impact Fund (R1011-23) from the Research Grant Council of the Government of Hong Kong SAR. Research Grants Council, University Grants Committee T11-104/22-R Sheng Chen Research Grants Council, University Grants Committee R1011-23 Sheng Chen

UN SDGs

This output contributes to the following UN Sustainable Development Goals (SDGs)

  1. SDG 3 - Good Health and Well-being
    SDG 3 Good Health and Well-being

Research Keywords

  • conjugative
  • hypervirulence
  • Klebsiella pneumoniae
  • multidrug resistance
  • pVir-MDR

Publisher's Copyright Statement

  • This full text is made available under CC-BY 4.0. https://creativecommons.org/licenses/by/4.0/

RGC Funding Information

  • RGC-funded

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