Emergence of Proteus mirabilis Isolates Producing TEM-52 Extended-Spectrum [beta]-Lactamases in Croatia

Background: An increased frequency of extended-spectrum β-lactamase (ESBL)-positive Proteus mirabilis isolates was observed recently in the Clinical Hospital Center Split in Croatia. The aim of this study was the molecular characterization of ESBLs in P. mirabilis isolates from this hospital. Materi...

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Veröffentlicht in:Chemotherapy (Basel) 2010-06, Vol.56 (3), p.208
Hauptverfasser: Sardelic, Sanda, Bedenic, Branka, Sijak, Dubravko, Colinon, Celine, Kalenic, Smilja
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container_start_page 208
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creator Sardelic, Sanda
Bedenic, Branka
Sijak, Dubravko
Colinon, Celine
Kalenic, Smilja
description Background: An increased frequency of extended-spectrum β-lactamase (ESBL)-positive Proteus mirabilis isolates was observed recently in the Clinical Hospital Center Split in Croatia. The aim of this study was the molecular characterization of ESBLs in P. mirabilis isolates from this hospital. Material and Methods: Seven strains showing reduced susceptibility to ceftazidime were investigated. Antimicrobial susceptibility was determined using the broth microdilution method. ESBLs were characterized by PCR and sequencing of blaESBL genes. Quinolone resistance determinants (qnr genes) were characterized by PCR. Genotyping of strains was performed by pulsed-field gel electrophoresis (PFGE). Results: The presence of an ESBL was confirmed in all strains by a double-disk synergy test. All strains were resistant to amoxicillin, piperacillin, gentamicin, ciprofloxacin, chloramphenicol, sulfamethoxazole and trimethoprim, but susceptible to ceftazidime/clavulanic acid, piperacillin/tazobactam, cefoxitin, imipenem and meropenem; PCR sequencing using primers targeting blaESBL genes revealed TEM-52 β-lactamase. PFGE genotyping demonstrated the clonal relatedness of TEM-52-producing P. mirabilis strains isolated from different clinical samples and wards within the hospital. BlaTEM-52 in 3 isolates was carried by a 70-kb conjugative plasmid. Conclusions: Our findings indicate the emergence of the TEM-52 enzyme among P. mirabilis in Croatia.[PUBLICATION ABSTRACT]
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The aim of this study was the molecular characterization of ESBLs in P. mirabilis isolates from this hospital. Material and Methods: Seven strains showing reduced susceptibility to ceftazidime were investigated. Antimicrobial susceptibility was determined using the broth microdilution method. ESBLs were characterized by PCR and sequencing of blaESBL genes. Quinolone resistance determinants (qnr genes) were characterized by PCR. Genotyping of strains was performed by pulsed-field gel electrophoresis (PFGE). Results: The presence of an ESBL was confirmed in all strains by a double-disk synergy test. All strains were resistant to amoxicillin, piperacillin, gentamicin, ciprofloxacin, chloramphenicol, sulfamethoxazole and trimethoprim, but susceptible to ceftazidime/clavulanic acid, piperacillin/tazobactam, cefoxitin, imipenem and meropenem; PCR sequencing using primers targeting blaESBL genes revealed TEM-52 β-lactamase. PFGE genotyping demonstrated the clonal relatedness of TEM-52-producing P. mirabilis strains isolated from different clinical samples and wards within the hospital. BlaTEM-52 in 3 isolates was carried by a 70-kb conjugative plasmid. Conclusions: Our findings indicate the emergence of the TEM-52 enzyme among P. mirabilis in Croatia.[PUBLICATION ABSTRACT]</description><identifier>ISSN: 0009-3157</identifier><identifier>EISSN: 1421-9794</identifier><identifier>DOI: 10.1159/000316332</identifier><language>eng</language><publisher>Basel: S. Karger AG</publisher><subject>Antibiotics ; Bacteria ; Drug resistance ; Microbiology ; Molecular biology ; Nosocomial infections</subject><ispartof>Chemotherapy (Basel), 2010-06, Vol.56 (3), p.208</ispartof><rights>Copyright (c) 2010 S. 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The aim of this study was the molecular characterization of ESBLs in P. mirabilis isolates from this hospital. Material and Methods: Seven strains showing reduced susceptibility to ceftazidime were investigated. Antimicrobial susceptibility was determined using the broth microdilution method. ESBLs were characterized by PCR and sequencing of blaESBL genes. Quinolone resistance determinants (qnr genes) were characterized by PCR. Genotyping of strains was performed by pulsed-field gel electrophoresis (PFGE). Results: The presence of an ESBL was confirmed in all strains by a double-disk synergy test. All strains were resistant to amoxicillin, piperacillin, gentamicin, ciprofloxacin, chloramphenicol, sulfamethoxazole and trimethoprim, but susceptible to ceftazidime/clavulanic acid, piperacillin/tazobactam, cefoxitin, imipenem and meropenem; PCR sequencing using primers targeting blaESBL genes revealed TEM-52 β-lactamase. PFGE genotyping demonstrated the clonal relatedness of TEM-52-producing P. mirabilis strains isolated from different clinical samples and wards within the hospital. BlaTEM-52 in 3 isolates was carried by a 70-kb conjugative plasmid. 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subjects Antibiotics
Bacteria
Drug resistance
Microbiology
Molecular biology
Nosocomial infections
title Emergence of Proteus mirabilis Isolates Producing TEM-52 Extended-Spectrum [beta]-Lactamases in Croatia
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