Carbapenemase-producing Enterobacterales in solid organ transplantation: Tip of the iceberg?

Kyle C Molina1,2,3, Valida Bajrovic3, Robert A Bonomo4,5,6,7

  • 1Department of Pharmacy Services, University of Colorado Hospital, Aurora, Colorado, USA.

Insights

A liver transplant patient developed a urinary tract infection with dual carbapenemase-producing bacteria. Silent plasmid transmission between these organisms poses an emergent threat to infection prevention and antimicrobial stewardship.

Area of Science:

  • Microbiology
  • Infectious Diseases
  • Genomics

Background:

  • A liver transplant recipient experienced a urinary tract infection (UTI) caused by Citrobacter freundii complex and Klebsiella aerogenes.
  • Both bacterial species were found to produce dual carbapenemases, specifically KPC-3 and NDM-1, conferring resistance to a broad spectrum of antibiotics.

Discussion:

  • Whole-genome sequencing revealed evidence of plasmid transfer between Citrobacter freundii and Klebsiella aerogenes within the patient.
  • This horizontal gene transfer facilitated the dissemination of carbapenemase genes, contributing to the multidrug-resistant nature of the infection.
  • The findings underscore the potential for silent plasmid transmission to drive the emergence and spread of carbapenem-resistant Enterobacteriaceae (CRE) in clinical settings.

Key Insights:

  • Dual carbapenemase production (KPC-3/NDM-1) in common UTI pathogens like C. freundii and K. aerogenes presents a significant clinical challenge.
  • Whole-genome sequencing is a powerful tool for elucidating the mechanisms of antimicrobial resistance gene dissemination, such as plasmid transfer.
  • The study highlights the critical need for enhanced surveillance and infection control strategies to mitigate the threat of CRE.

Outlook:

  • Implications for infection prevention protocols in immunocompromised patients, including liver transplant recipients.
  • Recommendations for targeted screening strategies to detect carriers of carbapenemase-producing organisms.
  • Emphasis on the importance of robust antimicrobial stewardship programs to preserve the efficacy of last-resort antibiotics.

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