ArticleThe Journal of infectious diseases2025
An Omics-Guided Investigation of a Hospital Outbreak Caused by blaNDM-1-Producing Pseudocitrobacter faecalis.
Article in The Journal of infectious diseases, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 1 paper.
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The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.
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1 citing paper in PubMed.
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11 authors.
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Abstract
Carbapenemase-producing Enterobacterales (CPE) pose a major healthcare challenge. We report the first hospital outbreak of Pseudocitrobacter faecalis carrying blaNDM-1 using an omics-based approach. Short- and long-read sequencing enabled genomic epidemiological investigation to track its spread, characterize its resistome, and analyze the genomic context of blaNDM-1. Additionally, we developed and implemented a matrix-assisted laser desorption/ionization-time of flight mass spectrometry (MALDI-TOF MS)-based method for rapid outbreak isolate typing using protein biomarkers. Our investigation identified 2 independent blaNDM-1-producing clonal clusters of multidrug- and carbapenem-resistant P faecalis circulating for over 3 years, carrying blaNDM-1 either chromosomally or on a plasmid. MALDI-TOF MS spectra analysis revealed candidate protein markers corresponding to genomic clusters, with 1 predicted biomarker applicable for rapid typing. Pseudocitrobacter faecalis is an emerging CPE taxon requiring hospital surveillance. Early whole genome sequencing unexpectedly revealed 2 intertwined clones with independent carbapenemase acquisition routes. Cluster-specific markers enabled rapid typing, serving as proof of concept for validating proteomics in future surveillance.
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