Characterization of KPC-encoding plasmids from two endemic settings, Greece and Italy
Language English Country Great Britain, England Media print-electronic
Document type Journal Article
PubMed
27334661
DOI
10.1093/jac/dkw227
PII: dkw227
Knihovny.cz E-resources
- MeSH
- Drug Resistance, Bacterial genetics MeSH
- Bacterial Proteins genetics MeSH
- beta-Lactamases genetics MeSH
- Endemic Diseases MeSH
- Epidemics MeSH
- Escherichia coli genetics MeSH
- Klebsiella Infections epidemiology microbiology MeSH
- Carbapenems pharmacology MeSH
- Klebsiella pneumoniae drug effects enzymology genetics MeSH
- Humans MeSH
- Microbial Sensitivity Tests MeSH
- Multilocus Sequence Typing methods MeSH
- Plasmids genetics MeSH
- Polymorphism, Restriction Fragment Length MeSH
- Electrophoresis, Gel, Pulsed-Field MeSH
- Sequence Analysis, DNA MeSH
- Check Tag
- Humans MeSH
- Publication type
- Journal Article MeSH
- Geographicals
- Italy epidemiology MeSH
- Greece epidemiology MeSH
- Names of Substances
- Bacterial Proteins MeSH
- beta-Lactamases MeSH
- carbapenemase MeSH Browser
- Carbapenems MeSH
OBJECTIVES: Global dissemination of KPC-type carbapenemases is mainly associated with the spread of high-risk clones of Klebsiella pneumoniae and of KPC-encoding plasmids. In this study, we explored the population structure of KPC-encoding plasmids from the recent epidemics of KPC-producing K. pneumoniae (KPC-Kp) in Greece and Italy, the two major European endemic settings. METHODS: Thirty-four non-replicate clinical strains of KPC-Kp representative of the early phases (2008-11) of the Greek (n = 22) and Italian (n = 12) epidemics were studied. Isolates were typed by MLST, and blaKPC-carrying plasmids were characterized by S1 profiling, PCR-based replicon typing and RFLP. Transfer experiments by conjugation or transformation were carried out with Escherichia coli recipients. Eleven plasmids, representative of all different restriction profiles, were completely sequenced. RESULTS: The representative Greek strains belonged to 14 sequence types (STs), with a predominance of ST258. The representative Italian strains belonged to three STs, with a predominance of clonal complex 258 (ST258, ST512). The 34 strains carried plasmids of variable size (78-166 kb), either with blaKPC-2 or blaKPC-3 gene embedded in a Tn4401a transposon. Plasmids from Greek strains were mostly of a single RFLP type (A) and resembled the archetypal pKpQIL KPC-encoding plasmid, while plasmids from Italian strains belonged to a more heterogeneous population, showing five RFLP profiles (A, C-F). Types A and C resembled pKpQIL or deletion derivatives thereof, while types D-F included plasmids with hybrid structures between pKpQIL, pKPN3 and pKPN101-IT. CONCLUSIONS: pKpQIL-like plasmids played a major role in the dissemination of blaKPC in Greece and Italy, but evolved with different dynamics in these endemic settings.
Department of Medical Biotechnologies University of Siena Siena Italy
Department of Microbiology National School of Public Health Athens Greece
Laboratory of Bacteriology Hellenic Pasteur Institute Athens Greece
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