Carbapenem-hydrolysing -lactamase KPC-2 in Klebsiella pneumoniae isolated in Rio de Janeiro, Brazil
Objectives The aim of this study was to characterize the KPC-type carbapenem-hydrolysing β-lactamase, extended-spectrum β-lactamases (ESBLs) and class 1 integrons among nosocomial Klebsiella pneumoniae isolated in Rio de Janeiro, Brazil. Methods MICs were determined and isolates were screened for ES...
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Veröffentlicht in: | Journal of antimicrobial chemotherapy 2009-02, Vol.63 (2), p.265-268 |
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creator | Peirano, G. Seki, L. M. Val Passos, V. L. Pinto, M. C. F. G. Guerra, L. R. Asensi, M. D. |
description | Objectives The aim of this study was to characterize the KPC-type carbapenem-hydrolysing β-lactamase, extended-spectrum β-lactamases (ESBLs) and class 1 integrons among nosocomial Klebsiella pneumoniae isolated in Rio de Janeiro, Brazil. Methods MICs were determined and isolates were screened for ESBLs, metallo-β-lactamases (MBLs) and class A carbapenemase-producing phenotypes. The main β-lactamases resistance genes (blaTEM , blaSHV , blaCTX-M , blaKPC , blaIMP and blaVIM ) and class 1 integrons were detected by PCR followed by DNA sequencing. The genetic relatedness of isolates was determined by PFGE. Results All K . pneumoniae isolates were positive for ESBL and class A carbapenemase production and negative for MBL production. All isolates were resistant to all β-lactam antibiotics, ciprofloxacin and gentamicin, being susceptible only to tigecycline and polymyxin B. The blaKPC-2 , blaCTX-M-1 , blaCTX-M-2 , blaCTX-M-8 and blaSHV-11 genes were detected. PFGE analysis revealed two clonal types among KPC-producing isolates, both identified in the same hospital. Conclusions Our findings should alert medical authorities to implement stringent methods for the detection and spread control of emerging KPC-2 carbapenemases in the hospital setting in Brazil. [PUBLICATION ABSTRACT] |
doi_str_mv | 10.1093/jac/dkn484 |
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M. ; Val Passos, V. L. ; Pinto, M. C. F. G. ; Guerra, L. R. ; Asensi, M. D.</creator><creatorcontrib>Peirano, G. ; Seki, L. M. ; Val Passos, V. L. ; Pinto, M. C. F. G. ; Guerra, L. R. ; Asensi, M. D.</creatorcontrib><description>Objectives The aim of this study was to characterize the KPC-type carbapenem-hydrolysing β-lactamase, extended-spectrum β-lactamases (ESBLs) and class 1 integrons among nosocomial Klebsiella pneumoniae isolated in Rio de Janeiro, Brazil. Methods MICs were determined and isolates were screened for ESBLs, metallo-β-lactamases (MBLs) and class A carbapenemase-producing phenotypes. The main β-lactamases resistance genes (blaTEM , blaSHV , blaCTX-M , blaKPC , blaIMP and blaVIM ) and class 1 integrons were detected by PCR followed by DNA sequencing. The genetic relatedness of isolates was determined by PFGE. Results All K . pneumoniae isolates were positive for ESBL and class A carbapenemase production and negative for MBL production. All isolates were resistant to all β-lactam antibiotics, ciprofloxacin and gentamicin, being susceptible only to tigecycline and polymyxin B. The blaKPC-2 , blaCTX-M-1 , blaCTX-M-2 , blaCTX-M-8 and blaSHV-11 genes were detected. PFGE analysis revealed two clonal types among KPC-producing isolates, both identified in the same hospital. Conclusions Our findings should alert medical authorities to implement stringent methods for the detection and spread control of emerging KPC-2 carbapenemases in the hospital setting in Brazil. [PUBLICATION ABSTRACT]</description><identifier>ISSN: 0305-7453</identifier><identifier>EISSN: 1460-2091</identifier><identifier>DOI: 10.1093/jac/dkn484</identifier><language>eng</language><publisher>Oxford: Oxford Publishing Limited (England)</publisher><subject>Antibiotics ; Antimicrobial agents ; Drug resistance ; Nosocomial infections ; Pneumonia</subject><ispartof>Journal of antimicrobial chemotherapy, 2009-02, Vol.63 (2), p.265-268</ispartof><rights>The Author 2008. Published by Oxford University Press on behalf of the British Society for Antimicrobial Chemotherapy. All rights reserved. For Permissions, please e-mail: journals.permissions@oxfordjournals.org</rights><lds50>peer_reviewed</lds50><oa>free_for_read</oa><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c1394-8c7ead23e1b03e3d0893920a1742aecb3f1aa539df05df678f262fc1d6dc6c383</citedby><cites>FETCH-LOGICAL-c1394-8c7ead23e1b03e3d0893920a1742aecb3f1aa539df05df678f262fc1d6dc6c383</cites></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><link.rule.ids>315,781,785,27929,27930</link.rule.ids></links><search><creatorcontrib>Peirano, G.</creatorcontrib><creatorcontrib>Seki, L. M.</creatorcontrib><creatorcontrib>Val Passos, V. L.</creatorcontrib><creatorcontrib>Pinto, M. C. F. G.</creatorcontrib><creatorcontrib>Guerra, L. R.</creatorcontrib><creatorcontrib>Asensi, M. D.</creatorcontrib><title>Carbapenem-hydrolysing -lactamase KPC-2 in Klebsiella pneumoniae isolated in Rio de Janeiro, Brazil</title><title>Journal of antimicrobial chemotherapy</title><description>Objectives The aim of this study was to characterize the KPC-type carbapenem-hydrolysing β-lactamase, extended-spectrum β-lactamases (ESBLs) and class 1 integrons among nosocomial Klebsiella pneumoniae isolated in Rio de Janeiro, Brazil. Methods MICs were determined and isolates were screened for ESBLs, metallo-β-lactamases (MBLs) and class A carbapenemase-producing phenotypes. The main β-lactamases resistance genes (blaTEM , blaSHV , blaCTX-M , blaKPC , blaIMP and blaVIM ) and class 1 integrons were detected by PCR followed by DNA sequencing. The genetic relatedness of isolates was determined by PFGE. Results All K . pneumoniae isolates were positive for ESBL and class A carbapenemase production and negative for MBL production. All isolates were resistant to all β-lactam antibiotics, ciprofloxacin and gentamicin, being susceptible only to tigecycline and polymyxin B. The blaKPC-2 , blaCTX-M-1 , blaCTX-M-2 , blaCTX-M-8 and blaSHV-11 genes were detected. PFGE analysis revealed two clonal types among KPC-producing isolates, both identified in the same hospital. Conclusions Our findings should alert medical authorities to implement stringent methods for the detection and spread control of emerging KPC-2 carbapenemases in the hospital setting in Brazil. [PUBLICATION ABSTRACT]</description><subject>Antibiotics</subject><subject>Antimicrobial agents</subject><subject>Drug resistance</subject><subject>Nosocomial infections</subject><subject>Pneumonia</subject><issn>0305-7453</issn><issn>1460-2091</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2009</creationdate><recordtype>article</recordtype><recordid>eNotkEtOwzAURS0EEqUwYQUWQ4SpP_k4Q6j4thIIwTh6sV_AxXGC3Q7KalgLK6NVGd3J0T3SIeRU8EvBKzVZgJnYz5DpbI-MRFZwJnkl9smIK56zMsvVITlKacE5L_JCjwhOITYwYMCOfaxt7P06ufBOf3-YB7OEDhLS2fOUSeoCnXlskkPvgQ4BV10fHCB1qfewRLslXlxPLdJHCOhif0GvI3w7f0wOWvAJT_53TN5ub16n92z-dPcwvZozI1SVMW1KBCsVioYrVJbrSlWSgygzCWga1QqAXFW25blti1K3spCtEbawpjBKqzE52_0Osf9aYVrWi34Vw0ZZS1EWWueab6DzHWRin1LEth6i6yCua8HrbcV6U7HeVVR_x89m0g</recordid><startdate>20090201</startdate><enddate>20090201</enddate><creator>Peirano, G.</creator><creator>Seki, L. M.</creator><creator>Val Passos, V. L.</creator><creator>Pinto, M. C. F. G.</creator><creator>Guerra, L. R.</creator><creator>Asensi, M. D.</creator><general>Oxford Publishing Limited (England)</general><scope>AAYXX</scope><scope>CITATION</scope><scope>7QL</scope><scope>7QO</scope><scope>7T7</scope><scope>7U7</scope><scope>7U9</scope><scope>8FD</scope><scope>C1K</scope><scope>FR3</scope><scope>H94</scope><scope>K9.</scope><scope>M7N</scope><scope>NAPCQ</scope><scope>P64</scope></search><sort><creationdate>20090201</creationdate><title>Carbapenem-hydrolysing -lactamase KPC-2 in Klebsiella pneumoniae isolated in Rio de Janeiro, Brazil</title><author>Peirano, G. ; Seki, L. M. ; Val Passos, V. L. ; Pinto, M. C. F. G. ; Guerra, L. R. ; Asensi, M. D.</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c1394-8c7ead23e1b03e3d0893920a1742aecb3f1aa539df05df678f262fc1d6dc6c383</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2009</creationdate><topic>Antibiotics</topic><topic>Antimicrobial agents</topic><topic>Drug resistance</topic><topic>Nosocomial infections</topic><topic>Pneumonia</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Peirano, G.</creatorcontrib><creatorcontrib>Seki, L. M.</creatorcontrib><creatorcontrib>Val Passos, V. L.</creatorcontrib><creatorcontrib>Pinto, M. C. F. G.</creatorcontrib><creatorcontrib>Guerra, L. R.</creatorcontrib><creatorcontrib>Asensi, M. D.</creatorcontrib><collection>CrossRef</collection><collection>Bacteriology Abstracts (Microbiology B)</collection><collection>Biotechnology Research Abstracts</collection><collection>Industrial and Applied Microbiology Abstracts (Microbiology A)</collection><collection>Toxicology Abstracts</collection><collection>Virology and AIDS Abstracts</collection><collection>Technology Research Database</collection><collection>Environmental Sciences and Pollution Management</collection><collection>Engineering Research Database</collection><collection>AIDS and Cancer Research Abstracts</collection><collection>ProQuest Health & Medical Complete (Alumni)</collection><collection>Algology Mycology and Protozoology Abstracts (Microbiology C)</collection><collection>Nursing & Allied Health Premium</collection><collection>Biotechnology and BioEngineering Abstracts</collection><jtitle>Journal of antimicrobial chemotherapy</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Peirano, G.</au><au>Seki, L. M.</au><au>Val Passos, V. L.</au><au>Pinto, M. C. F. G.</au><au>Guerra, L. R.</au><au>Asensi, M. D.</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Carbapenem-hydrolysing -lactamase KPC-2 in Klebsiella pneumoniae isolated in Rio de Janeiro, Brazil</atitle><jtitle>Journal of antimicrobial chemotherapy</jtitle><date>2009-02-01</date><risdate>2009</risdate><volume>63</volume><issue>2</issue><spage>265</spage><epage>268</epage><pages>265-268</pages><issn>0305-7453</issn><eissn>1460-2091</eissn><abstract>Objectives The aim of this study was to characterize the KPC-type carbapenem-hydrolysing β-lactamase, extended-spectrum β-lactamases (ESBLs) and class 1 integrons among nosocomial Klebsiella pneumoniae isolated in Rio de Janeiro, Brazil. Methods MICs were determined and isolates were screened for ESBLs, metallo-β-lactamases (MBLs) and class A carbapenemase-producing phenotypes. The main β-lactamases resistance genes (blaTEM , blaSHV , blaCTX-M , blaKPC , blaIMP and blaVIM ) and class 1 integrons were detected by PCR followed by DNA sequencing. The genetic relatedness of isolates was determined by PFGE. Results All K . pneumoniae isolates were positive for ESBL and class A carbapenemase production and negative for MBL production. All isolates were resistant to all β-lactam antibiotics, ciprofloxacin and gentamicin, being susceptible only to tigecycline and polymyxin B. The blaKPC-2 , blaCTX-M-1 , blaCTX-M-2 , blaCTX-M-8 and blaSHV-11 genes were detected. PFGE analysis revealed two clonal types among KPC-producing isolates, both identified in the same hospital. Conclusions Our findings should alert medical authorities to implement stringent methods for the detection and spread control of emerging KPC-2 carbapenemases in the hospital setting in Brazil. 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subjects | Antibiotics Antimicrobial agents Drug resistance Nosocomial infections Pneumonia |
title | Carbapenem-hydrolysing -lactamase KPC-2 in Klebsiella pneumoniae isolated in Rio de Janeiro, Brazil |
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