Novel KPC-2 Plasmid in a Clinical Salmonella Rissen Selected by Antibiotic Pressure

María Aznar Fernández1,2, Ángel Rodríguez-Villodres1,2,3, María José Gómez-Gómez1

  • 1Clinical Unit of Infectious Diseases, Microbiology and Parasitology, University Hospital Virgen del Rocío, Seville, Spain.

PubMed

Insights

A novel IncN2 plasmid carrying the blaKPC-2 gene was found in Salmonella Rissen. This plasmid confers broad antimicrobial resistance, complicating treatment and highlighting plasmid-mediated gene spread.

Area of Science:

  • Microbiology
  • Genomics
  • Antimicrobial Resistance

Background:

  • The emergence of antibiotic-resistant bacteria poses a significant global health threat.
  • Carbapenemase-producing Enterobacterales (CPE) are a major concern, often carrying resistance genes on mobile genetic elements like plasmids.
  • Salmonella enterica serovar Rissen is an important foodborne pathogen.

Purpose of the Study:

  • To characterize the genomic features of a clinical Salmonella Rissen isolate.
  • To identify and analyze the novel IncN2 plasmid harboring the blaKPC-2 gene.
  • To understand the role of this plasmid in antimicrobial resistance.

Main Methods:

  • Whole-genome sequencing of the Salmonella Rissen isolate.
  • Plasmid identification and characterization using bioinformatic tools.
  • Antimicrobial susceptibility testing.

Main Results:

  • Genomic characterization revealed a novel IncN2 plasmid, designated pSEay-KPC.
  • The pSEay-KPC plasmid carried the blaKPC-2 gene, conferring resistance to carbapenems, along with blaACC-1, blaTEM-1, and qnrB genes.
  • The isolate exhibited broad-spectrum resistance, surviving ceftriaxone and ciprofloxacin treatments, but was susceptible to meropenem-vaborbactam.

Conclusions:

  • IncN2 plasmids are significant vectors for the dissemination of clinically important resistance genes, including blaKPC-2.
  • The presence of such plasmids in Salmonella Rissen complicates treatment strategies for infections.
  • Effective management of infections caused by MDR strains requires understanding plasmid-mediated resistance mechanisms and utilizing last-resort antibiotics.