Emergence of Carbapenem-Hydrolyzing Oxacillinases in Acinetobacter baumannii in Children from Croatia
Introduction: Carbapenem resistance in Acinetobacter baumannii can be mediated by carbapenemases of class A, class B metallo-β-lactamases (MBLs), and class D carbapenem-hydrolyzing oxacillinases (CHDL). The aim of the study was to investigate the antimicrobial susceptibility and β-lactamase producti...
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creator | Lukić-Grlić, Amarela Kos, Matea Žižek, Marta Luxner, Josefa Grisold, Andrea Zarfel, Gernot Bedenić, Branka |
description | Introduction: Carbapenem resistance in Acinetobacter baumannii can be mediated by carbapenemases of class A, class B metallo-β-lactamases (MBLs), and class D carbapenem-hydrolyzing oxacillinases (CHDL). The aim of the study was to investigate the antimicrobial susceptibility and β-lactamase production of carbapenem-resistant A. baumannii isolates (CRAB) from the Children’s Hospital Zagreb, Croatia. Methods: A total of 12 A. baumannii isolates collected between August 2016 and March 2018 were analyzed. Antibiotic susceptibility was determined by the broth microdilution method. The presence of MBLs was explored by combined disk test with EDTA. The presence of carbapenemases of class A, B, and D was explored by PCR. The occurrence of the ISAba1 upstream of the bla OXA-51-like or bla OXA-23-like was determined by PCR mapping. Epidemiological typing was performed by determination of sequence groups (SG). Genotyping was performed by SG determination, rep-PCR, and MLST. Results: All CRAB were resistant to piperacillin/tazobactam, ceftazidime, cefotaxime, ceftriaxone, cefepime, imipenem, meropenem, gentamicin, and ciprofloxacin. Moderate resistance rates were observed for ampicillin/sulbactam (67%) and tigecycline (42%). The isolates were uniformly susceptible to colistin. PCR revealed the presence of genes encoding OXA-24-like CHDL in nine and OXA-23-like CHDL in three isolates. bla OXA-51 genes were preceded by ISAba1. PCR for the common MBLs in Acinetobacter was negative. All isolates belonged to SG 1 corresponding to ICL (International Clonal Lineage) II. Rep-PCR identified four major clones. Conclusions: The study found OXA-24-like β-lactamase to be the dominant CHDL among children’sCRAB. The predominant spread of OXA-24-like is in contrast with the recent global dissemination of OXA-23 reported all over the world. In contrast to the previous studies in which emergency of OXA-24-like positive isolates was monoclonal, we found considerable genetic diversity of the isolates. |
doi_str_mv | 10.1159/000503746 |
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The aim of the study was to investigate the antimicrobial susceptibility and β-lactamase production of carbapenem-resistant A. baumannii isolates (CRAB) from the Children’s Hospital Zagreb, Croatia. Methods: A total of 12 A. baumannii isolates collected between August 2016 and March 2018 were analyzed. Antibiotic susceptibility was determined by the broth microdilution method. The presence of MBLs was explored by combined disk test with EDTA. The presence of carbapenemases of class A, B, and D was explored by PCR. The occurrence of the ISAba1 upstream of the bla OXA-51-like or bla OXA-23-like was determined by PCR mapping. Epidemiological typing was performed by determination of sequence groups (SG). Genotyping was performed by SG determination, rep-PCR, and MLST. Results: All CRAB were resistant to piperacillin/tazobactam, ceftazidime, cefotaxime, ceftriaxone, cefepime, imipenem, meropenem, gentamicin, and ciprofloxacin. Moderate resistance rates were observed for ampicillin/sulbactam (67%) and tigecycline (42%). The isolates were uniformly susceptible to colistin. PCR revealed the presence of genes encoding OXA-24-like CHDL in nine and OXA-23-like CHDL in three isolates. bla OXA-51 genes were preceded by ISAba1. PCR for the common MBLs in Acinetobacter was negative. All isolates belonged to SG 1 corresponding to ICL (International Clonal Lineage) II. Rep-PCR identified four major clones. Conclusions: The study found OXA-24-like β-lactamase to be the dominant CHDL among children’sCRAB. The predominant spread of OXA-24-like is in contrast with the recent global dissemination of OXA-23 reported all over the world. In contrast to the previous studies in which emergency of OXA-24-like positive isolates was monoclonal, we found considerable genetic diversity of the isolates.</description><identifier>ISSN: 0009-3157</identifier><identifier>EISSN: 1421-9794</identifier><identifier>DOI: 10.1159/000503746</identifier><identifier>PMID: 31707391</identifier><language>eng</language><publisher>Basel, Switzerland: Karger</publisher><subject>Acinetobacter baumannii - drug effects ; Acinetobacter baumannii - enzymology ; Acinetobacter baumannii - isolation & purification ; Acinetobacter Infections - diagnosis ; Acinetobacter Infections - microbiology ; Anti-Bacterial Agents - pharmacology ; Antimicrobial Section / Original Paper ; Bacterial Proteins - genetics ; Bacterial Proteins - metabolism ; beta-Lactamases - genetics ; beta-Lactamases - metabolism ; Carbapenems - metabolism ; Child ; Croatia ; Drug Resistance, Multiple, Bacterial - drug effects ; Drug Resistance, Multiple, Bacterial - genetics ; Genotype ; Humans ; Hydrolysis ; Life Sciences & Biomedicine ; Microbial Sensitivity Tests ; Multilocus Sequence Typing ; Oncology ; Pharmacology & Pharmacy ; Science & Technology</subject><ispartof>Chemotherapy (Basel), 2020-03, Vol.64 (4), p.167-172</ispartof><rights>2019 S. Karger AG, Basel</rights><rights>2019 S. Karger AG, Basel.</rights><lds50>peer_reviewed</lds50><woscitedreferencessubscribed>true</woscitedreferencessubscribed><woscitedreferencescount>5</woscitedreferencescount><woscitedreferencesoriginalsourcerecordid>wos000521046600001</woscitedreferencesoriginalsourcerecordid><citedby>FETCH-LOGICAL-c334t-a6d9a35398d119f6e32ef7fd217a75310d7f886e1196fa36a4f57822776a267b3</citedby><cites>FETCH-LOGICAL-c334t-a6d9a35398d119f6e32ef7fd217a75310d7f886e1196fa36a4f57822776a267b3</cites><orcidid>0000-0002-6937-521X ; 0000-0001-5673-4511</orcidid></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><link.rule.ids>315,782,786,2433,27933,27934,28257</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/31707391$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Lukić-Grlić, Amarela</creatorcontrib><creatorcontrib>Kos, Matea</creatorcontrib><creatorcontrib>Žižek, Marta</creatorcontrib><creatorcontrib>Luxner, Josefa</creatorcontrib><creatorcontrib>Grisold, Andrea</creatorcontrib><creatorcontrib>Zarfel, Gernot</creatorcontrib><creatorcontrib>Bedenić, Branka</creatorcontrib><title>Emergence of Carbapenem-Hydrolyzing Oxacillinases in Acinetobacter baumannii in Children from Croatia</title><title>Chemotherapy (Basel)</title><addtitle>CHEMOTHERAPY</addtitle><addtitle>Chemotherapy</addtitle><description>Introduction: Carbapenem resistance in Acinetobacter baumannii can be mediated by carbapenemases of class A, class B metallo-β-lactamases (MBLs), and class D carbapenem-hydrolyzing oxacillinases (CHDL). The aim of the study was to investigate the antimicrobial susceptibility and β-lactamase production of carbapenem-resistant A. baumannii isolates (CRAB) from the Children’s Hospital Zagreb, Croatia. Methods: A total of 12 A. baumannii isolates collected between August 2016 and March 2018 were analyzed. Antibiotic susceptibility was determined by the broth microdilution method. The presence of MBLs was explored by combined disk test with EDTA. The presence of carbapenemases of class A, B, and D was explored by PCR. The occurrence of the ISAba1 upstream of the bla OXA-51-like or bla OXA-23-like was determined by PCR mapping. Epidemiological typing was performed by determination of sequence groups (SG). Genotyping was performed by SG determination, rep-PCR, and MLST. Results: All CRAB were resistant to piperacillin/tazobactam, ceftazidime, cefotaxime, ceftriaxone, cefepime, imipenem, meropenem, gentamicin, and ciprofloxacin. Moderate resistance rates were observed for ampicillin/sulbactam (67%) and tigecycline (42%). The isolates were uniformly susceptible to colistin. PCR revealed the presence of genes encoding OXA-24-like CHDL in nine and OXA-23-like CHDL in three isolates. bla OXA-51 genes were preceded by ISAba1. PCR for the common MBLs in Acinetobacter was negative. All isolates belonged to SG 1 corresponding to ICL (International Clonal Lineage) II. Rep-PCR identified four major clones. Conclusions: The study found OXA-24-like β-lactamase to be the dominant CHDL among children’sCRAB. The predominant spread of OXA-24-like is in contrast with the recent global dissemination of OXA-23 reported all over the world. In contrast to the previous studies in which emergency of OXA-24-like positive isolates was monoclonal, we found considerable genetic diversity of the isolates.</description><subject>Acinetobacter baumannii - drug effects</subject><subject>Acinetobacter baumannii - enzymology</subject><subject>Acinetobacter baumannii - isolation & purification</subject><subject>Acinetobacter Infections - diagnosis</subject><subject>Acinetobacter Infections - microbiology</subject><subject>Anti-Bacterial Agents - pharmacology</subject><subject>Antimicrobial Section / Original Paper</subject><subject>Bacterial Proteins - genetics</subject><subject>Bacterial Proteins - metabolism</subject><subject>beta-Lactamases - genetics</subject><subject>beta-Lactamases - metabolism</subject><subject>Carbapenems - metabolism</subject><subject>Child</subject><subject>Croatia</subject><subject>Drug Resistance, Multiple, Bacterial - drug effects</subject><subject>Drug Resistance, Multiple, Bacterial - genetics</subject><subject>Genotype</subject><subject>Humans</subject><subject>Hydrolysis</subject><subject>Life Sciences & Biomedicine</subject><subject>Microbial Sensitivity Tests</subject><subject>Multilocus Sequence Typing</subject><subject>Oncology</subject><subject>Pharmacology & Pharmacy</subject><subject>Science & Technology</subject><issn>0009-3157</issn><issn>1421-9794</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2020</creationdate><recordtype>article</recordtype><sourceid>AOWDO</sourceid><sourceid>EIF</sourceid><recordid>eNqN0c1LwzAUAPAgipvTg3eRgieRatK0SXscZTphsIuey2v7MqNtMtIOnX-9GZ07efCUj_d7j7wXQi4ZvWcsyR4opQnlMhZHZMziiIWZzOJjMvb3WchZIkfkrOve_ZELzk7JiDNJJc_YmOCsRbdCU2FgVZCDK2GNBttwvq2dbbbf2qyC5RdUumm0gQ67QJtgWmmDvS2h6tEFJWxaMEbrXSh_003t0ATK2TbInYVewzk5UdB0eLFfJ-T1cfaSz8PF8uk5ny7CivO4D0HUGfCEZ2nNWKYE8giVVHXEJMiEM1pLlaYCfVAo4AJilcg0iqQUEAlZ8gm5HepWznadQ1WsnW7BbQtGi92oisOovL0e7HpTtlgf5O9sPEgH8ImlVV2ld1M6sF2hiNFYCL-jLNe9b9Sa3G5M71Pv_p_q9c2gP8B_hTu4fD4b3lqsa-XV1Z9q384PfaiZVA</recordid><startdate>20200301</startdate><enddate>20200301</enddate><creator>Lukić-Grlić, Amarela</creator><creator>Kos, Matea</creator><creator>Žižek, Marta</creator><creator>Luxner, Josefa</creator><creator>Grisold, Andrea</creator><creator>Zarfel, Gernot</creator><creator>Bedenić, Branka</creator><general>Karger</general><scope>AOWDO</scope><scope>BLEPL</scope><scope>DTL</scope><scope>CGR</scope><scope>CUY</scope><scope>CVF</scope><scope>ECM</scope><scope>EIF</scope><scope>NPM</scope><scope>AAYXX</scope><scope>CITATION</scope><orcidid>https://orcid.org/0000-0002-6937-521X</orcidid><orcidid>https://orcid.org/0000-0001-5673-4511</orcidid></search><sort><creationdate>20200301</creationdate><title>Emergence of Carbapenem-Hydrolyzing Oxacillinases in Acinetobacter baumannii in Children from Croatia</title><author>Lukić-Grlić, Amarela ; Kos, Matea ; Žižek, Marta ; Luxner, Josefa ; Grisold, Andrea ; Zarfel, Gernot ; Bedenić, Branka</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c334t-a6d9a35398d119f6e32ef7fd217a75310d7f886e1196fa36a4f57822776a267b3</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2020</creationdate><topic>Acinetobacter baumannii - drug effects</topic><topic>Acinetobacter baumannii - enzymology</topic><topic>Acinetobacter baumannii - isolation & purification</topic><topic>Acinetobacter Infections - diagnosis</topic><topic>Acinetobacter Infections - microbiology</topic><topic>Anti-Bacterial Agents - pharmacology</topic><topic>Antimicrobial Section / Original Paper</topic><topic>Bacterial Proteins - genetics</topic><topic>Bacterial Proteins - metabolism</topic><topic>beta-Lactamases - genetics</topic><topic>beta-Lactamases - metabolism</topic><topic>Carbapenems - metabolism</topic><topic>Child</topic><topic>Croatia</topic><topic>Drug Resistance, Multiple, Bacterial - drug effects</topic><topic>Drug Resistance, Multiple, Bacterial - genetics</topic><topic>Genotype</topic><topic>Humans</topic><topic>Hydrolysis</topic><topic>Life Sciences & Biomedicine</topic><topic>Microbial Sensitivity Tests</topic><topic>Multilocus Sequence Typing</topic><topic>Oncology</topic><topic>Pharmacology & Pharmacy</topic><topic>Science & Technology</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Lukić-Grlić, Amarela</creatorcontrib><creatorcontrib>Kos, Matea</creatorcontrib><creatorcontrib>Žižek, Marta</creatorcontrib><creatorcontrib>Luxner, Josefa</creatorcontrib><creatorcontrib>Grisold, Andrea</creatorcontrib><creatorcontrib>Zarfel, Gernot</creatorcontrib><creatorcontrib>Bedenić, Branka</creatorcontrib><collection>Web of Science - Science Citation Index Expanded - 2020</collection><collection>Web of Science Core Collection</collection><collection>Science Citation Index Expanded</collection><collection>Medline</collection><collection>MEDLINE</collection><collection>MEDLINE (Ovid)</collection><collection>MEDLINE</collection><collection>MEDLINE</collection><collection>PubMed</collection><collection>CrossRef</collection><jtitle>Chemotherapy (Basel)</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Lukić-Grlić, Amarela</au><au>Kos, Matea</au><au>Žižek, Marta</au><au>Luxner, Josefa</au><au>Grisold, Andrea</au><au>Zarfel, Gernot</au><au>Bedenić, Branka</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Emergence of Carbapenem-Hydrolyzing Oxacillinases in Acinetobacter baumannii in Children from Croatia</atitle><jtitle>Chemotherapy (Basel)</jtitle><stitle>CHEMOTHERAPY</stitle><addtitle>Chemotherapy</addtitle><date>2020-03-01</date><risdate>2020</risdate><volume>64</volume><issue>4</issue><spage>167</spage><epage>172</epage><pages>167-172</pages><issn>0009-3157</issn><eissn>1421-9794</eissn><abstract>Introduction: Carbapenem resistance in Acinetobacter baumannii can be mediated by carbapenemases of class A, class B metallo-β-lactamases (MBLs), and class D carbapenem-hydrolyzing oxacillinases (CHDL). The aim of the study was to investigate the antimicrobial susceptibility and β-lactamase production of carbapenem-resistant A. baumannii isolates (CRAB) from the Children’s Hospital Zagreb, Croatia. Methods: A total of 12 A. baumannii isolates collected between August 2016 and March 2018 were analyzed. Antibiotic susceptibility was determined by the broth microdilution method. The presence of MBLs was explored by combined disk test with EDTA. The presence of carbapenemases of class A, B, and D was explored by PCR. The occurrence of the ISAba1 upstream of the bla OXA-51-like or bla OXA-23-like was determined by PCR mapping. Epidemiological typing was performed by determination of sequence groups (SG). Genotyping was performed by SG determination, rep-PCR, and MLST. Results: All CRAB were resistant to piperacillin/tazobactam, ceftazidime, cefotaxime, ceftriaxone, cefepime, imipenem, meropenem, gentamicin, and ciprofloxacin. Moderate resistance rates were observed for ampicillin/sulbactam (67%) and tigecycline (42%). The isolates were uniformly susceptible to colistin. PCR revealed the presence of genes encoding OXA-24-like CHDL in nine and OXA-23-like CHDL in three isolates. bla OXA-51 genes were preceded by ISAba1. PCR for the common MBLs in Acinetobacter was negative. All isolates belonged to SG 1 corresponding to ICL (International Clonal Lineage) II. Rep-PCR identified four major clones. Conclusions: The study found OXA-24-like β-lactamase to be the dominant CHDL among children’sCRAB. The predominant spread of OXA-24-like is in contrast with the recent global dissemination of OXA-23 reported all over the world. In contrast to the previous studies in which emergency of OXA-24-like positive isolates was monoclonal, we found considerable genetic diversity of the isolates.</abstract><cop>Basel, Switzerland</cop><pub>Karger</pub><pmid>31707391</pmid><doi>10.1159/000503746</doi><tpages>6</tpages><orcidid>https://orcid.org/0000-0002-6937-521X</orcidid><orcidid>https://orcid.org/0000-0001-5673-4511</orcidid></addata></record> |
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subjects | Acinetobacter baumannii - drug effects Acinetobacter baumannii - enzymology Acinetobacter baumannii - isolation & purification Acinetobacter Infections - diagnosis Acinetobacter Infections - microbiology Anti-Bacterial Agents - pharmacology Antimicrobial Section / Original Paper Bacterial Proteins - genetics Bacterial Proteins - metabolism beta-Lactamases - genetics beta-Lactamases - metabolism Carbapenems - metabolism Child Croatia Drug Resistance, Multiple, Bacterial - drug effects Drug Resistance, Multiple, Bacterial - genetics Genotype Humans Hydrolysis Life Sciences & Biomedicine Microbial Sensitivity Tests Multilocus Sequence Typing Oncology Pharmacology & Pharmacy Science & Technology |
title | Emergence of Carbapenem-Hydrolyzing Oxacillinases in Acinetobacter baumannii in Children from Croatia |
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