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Published on: June 30, 2016
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.
Abstract:
Carbapenem-resistant Pseudomonas aeruginosa (CRPA) is an endemic problem in certain countries including Greece. CRPA and multidrug-resistant P. aeruginosa (MDRPA) firstly emerged in our region during the 80s, right after the launch of imipenem and meropenem as therapeutic agents against P. aeruginosa infections. The role of outer membrane protein (Opr) inactivation has been known to contribute to imipenem resistance since many years, while efflux overexpression systems have been mainly associated with meropenem resistance. Among carbapenemases, metallo-β-lactamases (MBL) and mostly Verona integron-mediated (VIM) MBL's have played the most crucial role in CRPA emergence. VIM-2 and VIM-4 producing CRPA, usually belonging to clonal complexes (CC) 111 and 235 respectively, have most frequently been isolated. BlaVIM-2 and blaVIM-4 are usually associated with a class 1 integron. VIM-17 also has appeared in Greece. On the other hand, other VIM subtypes detected in a global level, such as VIM-3, VIM-5, VIM-6, VIM-7, VIM-11, VIM-14, VIM-15, VIM-16 and VIM-18 have not yet emerged in Greece. However, new VIM subtypes will probably emerge in the future. In addition, MBL carbapenemases other than VIM, detected worldwide have not yet appeared. A single CRPA isolate producing KPC has emerged in our region several years ago. The study of the molecular basis of Opr deficiency and efflux overexpression remains a challenge for the future. In this article, we review the molecular epidemiology of CRPA in an endemic area, compared to global data.
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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