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Emergence of Multidrug-Resistant NDM-5-Producing ST307 Klebsiella pneumoniae in Uruguay, 2023
Carmen Magallanes1, Eliana Eugster1, Felipe Clavijo2
1Laboratorio de Microbiología Clínica, Departamento de Bioquímica Clínica, Facultad de Química, Universidad de la República, Montevideo, Uruguay.
Abstract:
Carbapenem and colistin-resistant Klebsiella pneumoniae pose a significant threat to public health, particularly in intensive care units, due to high morbidity and mortality rates. This study aimed to analyze five NDM carbapenemase-producing multidrug-resistant K. pneumoniae isolates from different hospitals. Antimicrobial susceptibility testing, hypermucoviscosity analysis, biofilm production assessment, MLST, PCR, and whole-genome sequencing were conducted. All isolates harbored NDM-5 metallo-β-lactamase, belonging to MLST 307, were biofilm producers and exhibited a stop codon (Q30) along MgrB. Genomic analysis revealed multiple-replicon plasmids carrying resistance genes, notably blaNDM-5, blaCTX-M-15, rmtB, and qnrB1, with complex genetic structures encoding several mobile genetic elements, including the Tn3 family and IS26. All isolates harbored wzi173 (capsule-locus KL102), iutA (a siderophore-associated gene), and the type 3 fimbriae mrkABCDFHIJ operon. The core genome single nucleotide polymorphisms (SNPs) analysis suggests the circulation of two strains of ST307 clone (SNPs range differences 4-77). These findings highlight the potential plasticity of the high-risk ST307 clone and the urgent need for surveillance and intervention strategies to combat antimicrobial resistance. To our knowledge, this is the first report of K. pneumoniae ST307 carrying blaNDM-5 and the first description of ST307 in Uruguay. The presence of blaNDM-5 and pan-aminoglycoside resistance rmtB genes are identified for the first time in Uruguay.
Insights
Multidrug-resistant Klebsiella pneumoniae isolates in Uruguay carry NDM-5 carbapenemase and rmtB, conferring resistance to critical antibiotics. This highlights the urgent need for enhanced surveillance and control strategies against these high-risk bacterial strains.
Area of Science:
- Microbiology and Infectious Diseases
- Genomics and Molecular Biology
- Public Health and Epidemiology
Background:
- Carbapenem and colistin-resistant Klebsiella pneumoniae are critical threats, causing high mortality in intensive care units.
- The emergence of NDM carbapenemase-producing strains necessitates detailed characterization to understand resistance mechanisms and epidemiology.
Purpose of the Study:
- To analyze five NDM carbapenemase-producing multidrug-resistant Klebsiella pneumoniae isolates from Uruguayan hospitals.
- To investigate antimicrobial resistance profiles, genetic relatedness, and virulence factors, including biofilm production and specific gene carriage.
Main Methods:
- Antimicrobial susceptibility testing, hypermucoviscosity analysis, and biofilm production assays were performed.
- Multilocus Sequence Typing (MLST), Polymerase Chain Reaction (PCR), and whole-genome sequencing (WGS) were employed for genetic analysis.
- Core genome single nucleotide polymorphism (SNP) analysis was used to assess strain relatedness.
Main Results:
- All isolates harbored the blaNDM-5 gene, belonged to ST307, were biofilm producers, and had a MgrB stop codon (Q30).
- Genomic analysis identified plasmids carrying blaNDM-5, blaCTX-M-15, rmtB, and qnrB1, alongside mobile genetic elements.
- Isolates possessed capsule locus KL102, iutA, and the type 3 fimbriae mrk operon; SNP analysis indicated two circulating ST307 strains.
Conclusions:
- This study reports the first Klebsiella pneumoniae ST307 isolates carrying blaNDM-5 in Uruguay, demonstrating significant antimicrobial resistance.
- The findings reveal the genetic plasticity of the high-risk ST307 clone and the presence of critical resistance genes (blaNDM-5, rmtB) for the first time in Uruguay.
- Urgent surveillance and intervention strategies are needed to combat the spread of these multidrug-resistant pathogens.
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