Genomic Characterization of NDM-1 Harboring Extensively-Drug Resistance Klebsiella pneumoniae Isolate From

Abolfazl Rafati Zomorodi1, Himen Salimizand2,3, Niloufar Mohseni4

  • 1Department of Bacteriology and Virology, School of Medicine, Shiraz University of Medical Sciences, Shiraz, Iran.

PubMed

Insights

Carbapenem-resistant Klebsiella pneumoniae (CR-KP) producing New Delhi metallo-beta-lactamase (NDM) is a global health threat. Genomic analysis identified an extensively drug-resistant NDM-1 CR-KP strain (ST15) from a COVID-19 patient, highlighting the need for local surveillance.

Area of Science:

  • Medical Microbiology
  • Genomics
  • Infectious Diseases

Background:

  • Carbapenem-resistant Klebsiella pneumoniae (CR-KP) strains, especially those producing New Delhi metallo-beta-lactamase (NDM), pose a significant global health risk.
  • The emergence of extensively drug-resistant (XDR) strains in intensive care units (ICUs) is a growing concern, particularly in patients with severe infections like COVID-19.

Purpose of the Study:

  • To perform a comprehensive genomic analysis of an NDM-1 producing CR-KP strain isolated from a COVID-19 patient in the ICU.
  • To characterize the antimicrobial resistance profile and genetic makeup of the identified CR-KP strain.

Main Methods:

  • Whole genome sequencing was employed for genomic analysis of the K. pneumoniae isolate.
  • Antimicrobial susceptibility testing was conducted using the VITEK 2 system to determine minimum inhibitory concentrations (MICs) for 15 antibiotics.
  • Multilocus sequence typing (MLST) was performed to identify the sequence type (ST) of the isolate.

Main Results:

  • The CRKP-51 strain, isolated from bronchoalveolar lavage fluid, was identified as XDR, resistant to all tested antibiotics except tigecycline.
  • The strain exhibited high resistance to sulfamethoxazole-trimethoprim (SXT), nitrofurantoin (NIT), and piperacillin-tazobactam (TZP).
  • Genomic analysis revealed the strain belongs to ST15 and harbors multiple resistance genes, including blaNDM-1, armA, msrE, mphE, and others, located on an IncHI1B plasmid.

Conclusions:

  • High-risk K. pneumoniae clones like ST15 are increasingly linked to antimicrobial resistance and XDR strain emergence in ICUs.
  • The study underscores the importance of monitoring local epidemiology for effective antimicrobial stewardship programs, given the global dissemination of NDM enzymes via various plasmid types.