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 |
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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] |
doi_str_mv | 10.1159/000316332 |
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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. Karger AG, Basel</rights><lds50>peer_reviewed</lds50><woscitedreferencessubscribed>false</woscitedreferencessubscribed></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><link.rule.ids>314,780,784,27924,27925</link.rule.ids></links><search><creatorcontrib>Sardelic, Sanda</creatorcontrib><creatorcontrib>Bedenic, Branka</creatorcontrib><creatorcontrib>Sijak, Dubravko</creatorcontrib><creatorcontrib>Colinon, Celine</creatorcontrib><creatorcontrib>Kalenic, Smilja</creatorcontrib><title>Emergence of Proteus mirabilis Isolates Producing TEM-52 Extended-Spectrum [beta]-Lactamases in Croatia</title><title>Chemotherapy (Basel)</title><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]</description><subject>Antibiotics</subject><subject>Bacteria</subject><subject>Drug resistance</subject><subject>Microbiology</subject><subject>Molecular biology</subject><subject>Nosocomial infections</subject><issn>0009-3157</issn><issn>1421-9794</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2010</creationdate><recordtype>article</recordtype><sourceid>8G5</sourceid><sourceid>ABUWG</sourceid><sourceid>AFKRA</sourceid><sourceid>AZQEC</sourceid><sourceid>BENPR</sourceid><sourceid>CCPQU</sourceid><sourceid>DWQXO</sourceid><sourceid>GNUQQ</sourceid><sourceid>GUQSH</sourceid><sourceid>M2O</sourceid><recordid>eNqNi81KxDAURoMoWH8WvkFwH81tmg5ZDxUFBcHZiQx32jslQ5uMuQn4-HbAB3D1wTnnE-IO9AOAdY9aawOtMfWZqKCpQbmVa85FtXCnDNjVpbhiPpyy1kAlxm6mNFLoSca9fE8xU2E5-4Q7P3mWLxwnzMQnNZTeh1Fuujdla9n9ZAoDDerjSH1OZZafO8r4pV6xzzgjLycf5DpFzB5vxMUeJ6bbv70W90_dZv2sjil-F-K8PcSSwqK2bWMbZ0GD-Vf0C2uMSu0</recordid><startdate>20100601</startdate><enddate>20100601</enddate><creator>Sardelic, Sanda</creator><creator>Bedenic, Branka</creator><creator>Sijak, Dubravko</creator><creator>Colinon, Celine</creator><creator>Kalenic, Smilja</creator><general>S. Karger AG</general><scope>3V.</scope><scope>7X7</scope><scope>7XB</scope><scope>88E</scope><scope>8AO</scope><scope>8FI</scope><scope>8FJ</scope><scope>8FK</scope><scope>8G5</scope><scope>ABUWG</scope><scope>AFKRA</scope><scope>AZQEC</scope><scope>BENPR</scope><scope>CCPQU</scope><scope>DWQXO</scope><scope>FYUFA</scope><scope>GHDGH</scope><scope>GNUQQ</scope><scope>GUQSH</scope><scope>K9.</scope><scope>M0S</scope><scope>M1P</scope><scope>M2O</scope><scope>MBDVC</scope><scope>PQEST</scope><scope>PQQKQ</scope><scope>PQUKI</scope><scope>PRINS</scope><scope>Q9U</scope></search><sort><creationdate>20100601</creationdate><title>Emergence of Proteus mirabilis Isolates Producing TEM-52 Extended-Spectrum [beta]-Lactamases in Croatia</title><author>Sardelic, Sanda ; Bedenic, Branka ; Sijak, Dubravko ; Colinon, Celine ; Kalenic, Smilja</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-proquest_journals_6454951013</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2010</creationdate><topic>Antibiotics</topic><topic>Bacteria</topic><topic>Drug resistance</topic><topic>Microbiology</topic><topic>Molecular biology</topic><topic>Nosocomial infections</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Sardelic, Sanda</creatorcontrib><creatorcontrib>Bedenic, Branka</creatorcontrib><creatorcontrib>Sijak, Dubravko</creatorcontrib><creatorcontrib>Colinon, Celine</creatorcontrib><creatorcontrib>Kalenic, Smilja</creatorcontrib><collection>ProQuest Central (Corporate)</collection><collection>Health & Medical Collection</collection><collection>ProQuest Central (purchase pre-March 2016)</collection><collection>Medical Database (Alumni Edition)</collection><collection>ProQuest Pharma Collection</collection><collection>Hospital Premium Collection</collection><collection>Hospital Premium Collection (Alumni Edition)</collection><collection>ProQuest Central (Alumni) (purchase pre-March 2016)</collection><collection>Research Library (Alumni Edition)</collection><collection>ProQuest Central (Alumni Edition)</collection><collection>ProQuest Central UK/Ireland</collection><collection>ProQuest Central Essentials</collection><collection>ProQuest Central</collection><collection>ProQuest One Community College</collection><collection>ProQuest Central Korea</collection><collection>Health Research Premium Collection</collection><collection>Health Research Premium Collection (Alumni)</collection><collection>ProQuest Central Student</collection><collection>Research Library Prep</collection><collection>ProQuest Health & Medical Complete (Alumni)</collection><collection>Health & Medical Collection (Alumni Edition)</collection><collection>Medical Database</collection><collection>Research Library</collection><collection>Research Library (Corporate)</collection><collection>ProQuest One Academic Eastern Edition (DO NOT USE)</collection><collection>ProQuest One Academic</collection><collection>ProQuest One Academic UKI Edition</collection><collection>ProQuest Central China</collection><collection>ProQuest Central Basic</collection><jtitle>Chemotherapy (Basel)</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Sardelic, Sanda</au><au>Bedenic, Branka</au><au>Sijak, Dubravko</au><au>Colinon, Celine</au><au>Kalenic, Smilja</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Emergence of Proteus mirabilis Isolates Producing TEM-52 Extended-Spectrum [beta]-Lactamases in Croatia</atitle><jtitle>Chemotherapy (Basel)</jtitle><date>2010-06-01</date><risdate>2010</risdate><volume>56</volume><issue>3</issue><spage>208</spage><pages>208-</pages><issn>0009-3157</issn><eissn>1421-9794</eissn><abstract>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]</abstract><cop>Basel</cop><pub>S. Karger AG</pub><doi>10.1159/000316332</doi></addata></record> |
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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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