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Updated: Jul 5, 2026

Non-Invasive Model of Neuropathogenic Escherichia coli Infection in the Neonatal Rat
Published on: October 29, 2014
Neonatal sepsis due to NDM-1 and VIM-2 co-producing Pseudomonas aeruginosa in Morocco
Dina Daaboul1,2, Marwan Osman3, Issmat I Kassem4
1Team ReSIST, UMR1184, INSERM, Université Paris-Saclay, CEA, School of Medicine, OI HEALTHI, Le Kremlin-Bicêtre, France.
Background:
Carbapenem-resistant Pseudomonas aeruginosa are being increasingly described worldwide. Here, we investigated the molecular mechanisms underlying carbapenem resistance in an extremely drug-resistant P. aeruginosa isolate from a neonatal intensive care unit in Morocco.
Materials And Methods:
P. aeruginosa strain O82J1 was identified using MALDI-TOF-MS. Carba NP, immunochromatographic assay NG Carba5 and antimicrobial susceptibility testing using disc diffusion and microbroth were performed. Whole-genome sequencing using the Illumina and MinION technologies and different software packages available at the Center of Genomic Epidemiology were used to predict the resistome, sequence type and plasmid types.
Results:
P. aeruginosa O82J1 co-expressed two metallo-β-lactamases, blaNDM-1 and blaVIM-2, and was susceptible to colistin and apramycin only. It belonged to ST773 that is frequently reported worldwide as a high-risk P. aeruginosa clone. The blaVIM-2 gene was integron-borne on a IncP-2 465-kb plasmid, whereas the blaNDM-1 gene was chromosomally encoded and embedded in an integrative conjugative element, probably at the origin of its acquisition. A total of 23 antimicrobial resistance genes were detected including a blaPER-1 ESBL gene, and an 16S-rRNA methyltransferase gene rmtB.
Conclusions:
The isolation of XDR P. aeruginosa isolates expressing several carbapenemases in a neonatal intensive care unit is of great concern due to the reduced treatment options, relying only on colistin, but not recommended in neonates, and apramycin, not yet approved for human therapy. Concerns were further elevated due to the resistance to cefiderocol and ATM/AVI, two novel and last-resort antibiotics recommended to treat infections caused by Gram-negative bacteria, particularly XDR P. aeruginosa in adults.
Insights
Extremely drug-resistant Pseudomonas aeruginosa in a Moroccan NICU co-expressed NDM-1 and VIM-2 carbapenemases. This high-risk clone (ST773) showed limited treatment options, highlighting urgent public health concerns.
Area of Science:
- Medical Microbiology
- Genomics
- Antimicrobial Resistance
Background:
- Increasing global prevalence of carbapenem-resistant Pseudomonas aeruginosa.
- Need to understand resistance mechanisms in extremely drug-resistant (XDR) isolates.
Purpose of the Study:
- Investigate molecular mechanisms of carbapenem resistance in an XDR P. aeruginosa isolate from a Moroccan neonatal intensive care unit (NICU).
Main Methods:
- Identification of P. aeruginosa strain O82J1 using MALDI-TOF-MS.
- Phenotypic antimicrobial susceptibility testing (Carba NP, NG-K5, disc diffusion, microbroth).
- Whole-genome sequencing (Illumina and MinION) to predict resistome, sequence type, and plasmid types.
Main Results:
- P. aeruginosa O82J1 co-expressed metallo-β-lactamases blaNDM-1 and blaVIM-2.
- Strain belonged to high-risk clone ST773; blaVIM-2 was plasmid-borne, blaNDM-1 was chromosomally encoded.
- 23 antimicrobial resistance genes detected, including blaPER-1 and rmtB, with susceptibility only to colistin and apramycin.
Conclusions:
- Isolation of XDR P. aeruginosa in NICUs poses significant treatment challenges due to limited effective antibiotics.
- Resistance to novel agents like cefiderocol and ATM/AVI is a major concern for managing Gram-negative infections.
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