Characterization of Enterobacterales growing on selective CPE screening plates with a focus on non-carbapenemase-producing strains

  • 0National Institute for Antibiotic Resistance and Infection Control, Israel Ministry of Health, Tel Aviv, Israel.

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Summary

This summary is machine-generated.

Most bacteria growing on Carbapenemase-producing Enterobacterales (CPE) screening plates are not CPE but are multidrug-resistant (MDR). Reporting these MDR non-CPE isolates could aid treatment and infection control efforts.

Area Of Science

  • Clinical Microbiology
  • Infectious Diseases
  • Antimicrobial Resistance

Background

  • Selective screening plates are crucial for detecting Carbapenemase-producing Enterobacterales (CPE) carriers to prevent healthcare-associated infections.
  • These plates are designed to isolate CPE, but non-CPE bacteria can also grow, and their characterization is often overlooked.
  • Understanding the prevalence and characteristics of non-CPE isolates on CPE selective media is essential for comprehensive infection control.

Purpose Of The Study

  • To characterize the non-carbapenemase-producing Enterobacterales (non-CPE) that grow on selective CPE screening plates.
  • To determine the antibiotic susceptibility profiles and resistance mechanisms of these non-CPE isolates.
  • To assess the clinical relevance of reporting non-CPE isolates detected during routine CPE screening.

Main Methods

  • Isolates were collected from two Israeli medical institutions over a six-month period.
  • Species identification and antibiotic susceptibility testing were performed using VITEK systems, with meropenem MICs determined by E-test.
  • Fourier-transform infrared spectroscopy (FTIR) and whole genome sequencing were employed for phenotypic and genotypic characterization of key isolates.

Main Results

  • 60.4% of isolates growing on CPE selective plates were non-CPE, predominantly Klebsiella pneumoniae and Escherichia coli.
  • A significant proportion (78.2%) of non-CP K. pneumoniae and E. coli were susceptible to meropenem, but all were multidrug-resistant (MDR).
  • Sequenced non-CPE isolates exhibited multiple resistance mechanisms, including various beta-lactamases, penicillin-binding protein modifications, and porin mutations.

Conclusions

  • The majority of isolates recovered from CPE selective screening plates are non-CPE but possess multidrug resistance.
  • These MDR non-CPE isolates, though not the primary target, represent a significant bacterial population with potential clinical implications.
  • Laboratory reporting of MDR non-CPE isolates could enhance treatment guidance, prophylaxis strategies, and overall infection control measures.