Molecular epidemiology of carbapenem-resistant Pseudomonas aeruginosa in an endemic area: comparison with global data

Theodoros Karampatakis1, Charalampos Antachopoulos1, Athanassios Tsakris2

  • 1Infectious Diseases Unit, 3rd Department of Pediatrics, Medical Faculty, School of Health Sciences, Hippokration General Hospital, Konstantinoupoleos 49, GR-546 42, Thessaloniki, Greece.

Insights

Carbapenem-resistant Pseudomonas aeruginosa (CRPA) is a significant issue in Greece, driven by metallo-β-lactamases (MBLs), particularly Verona integron-mediated (VIM) types. Understanding resistance mechanisms like Opr inactivation and efflux overexpression is crucial for future strategies.

Area of Science:

  • Medical Microbiology
  • Molecular Epidemiology
  • Antimicrobial Resistance

Background:

  • Carbapenem-resistant Pseudomonas aeruginosa (CRPA) emerged in Greece in the 1980s, coinciding with the introduction of carbapenem antibiotics.
  • Resistance mechanisms include outer membrane protein (Opr) inactivation (imipenem) and efflux overexpression (meropenem).
  • Metallo-β-lactamases (MBLs), especially Verona integron-mediated (VIM) types, are key drivers of CRPA in the region.

Purpose of the Study:

  • To review the molecular epidemiology of CRPA in Greece.
  • To compare local CRPA data with global trends.
  • To highlight emerging resistance mechanisms and subtypes.

Main Methods:

  • Literature review of molecular epidemiology studies on CRPA.
  • Analysis of carbapenemase types, particularly VIM subtypes.
  • Comparison of clonal complexes and resistance determinants.

Main Results:

  • VIM-2 and VIM-4 producing CRPA, associated with clonal complexes 111 and 235, are most frequent.
  • blaVIM-2 and blaVIM-4 are typically linked to class 1 integrons.
  • VIM-17 has been detected in Greece; other VIM subtypes and non-VIM MBLs remain absent but are anticipated.
  • A single KPC-producing CRPA isolate was reported.

Conclusions:

  • VIM-MBLs are the primary carbapenemases in Greek CRPA isolates.
  • Specific VIM subtypes and clonal complexes dominate the local epidemiology.
  • Further research into Opr deficiency and efflux mechanisms is needed.
  • Anticipation of new VIM subtypes and other MBLs necessitates ongoing surveillance.

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