1. An outbreak of bla KPC-4 - and bla VIM-1 -producing Klebsiella pneumoniae and Klebsiella variicola at a single hospital in South Korea.
- Author
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Chu J, Choi J, Ji SK, Park C, Jung SH, Park SH, and Lee DG
- Subjects
- Humans, Republic of Korea epidemiology, Cross Infection microbiology, Cross Infection epidemiology, Bacterial Proteins genetics, Bacterial Proteins metabolism, Hospitals, Whole Genome Sequencing, Gene Transfer, Horizontal, Female, Anti-Bacterial Agents pharmacology, Male, beta-Lactamases genetics, beta-Lactamases metabolism, Disease Outbreaks, Klebsiella pneumoniae genetics, Klebsiella pneumoniae isolation & purification, Klebsiella Infections epidemiology, Klebsiella Infections microbiology, Klebsiella Infections transmission, Klebsiella genetics, Plasmids genetics
- Abstract
Background: The dissemination of Klebsiella spp. producing multiple carbapenemases has been increasingly recognized. Between July 2019 and August 2021, ten patients were found to carry Klebsiella spp. co-harboring bla
KPC-4 and blaVIM-1 across multiple wards at a Korean hospital, and one isolate was recovered from a hand-washing sink, more than a year after the outbreak. This study aimed to investigate the outbreak and conduct a genomic study of these isolates., Methods: Whole-genome sequencing, including long-read sequencing, was performed to analyze plasmid structures and mobile genetic elements (MGEs). Bioinformatics analyses were performed to trace clonal transmission chains and horizontal gene transfer., Results: The findings suggested that the inter-ward spread of Klebsiella spp. seemed to be facilitated by healthcare worker contact or patient movement. Of the nine isolates collected (eight clinical and one environmental), seven (including the environmental isolate) were identified as K. pneumoniae (ST3680) and two were K. variicola (single-locus variant of ST5252). These isolates showed high genetic relatedness within their species and harbored the IncHI5B plasmid carrying both blaKPC-4 and blaVIM-1 (pKPCVIM.1). On this plasmid, blaVIM-1 was located in the Class 1 integron associated with IS1326::IS1353 (In2), and Tn4401b carrying blaKPC-4 was inserted into IS1326::IS1353, creating a novel MGE construct (In2_blaVIM-1 -Tn4401b_blaKPC-4 )., Conclusion: The hospital-wide spread of blaKPC-4 and blaVIM-1 was facilitated by clonal spread and horizontal plasmid transfer. The persistence of this strain in the hospital sink suggests a potential reservoir of the strain. Understanding the transmission mechanisms of persistent pathogens is important for improving infection control strategies in hospitals., (© 2024. The Author(s).)- Published
- 2024
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