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Vancomycin and daptomycin minimum inhibitory concentration distribution and occurrence of heteroresistance among methicillin-resistant Staphylococcus aureus blood isolates in Turkey
The aim of this study was to determine the distribution of vancomycin and daptomycin MICs among methicillin-resistant Staphylococcus aureus (MRSA) blood isolates, the prevalence of heterogeneous vancomycin-intermediate S. aureus (hVISA) and the relationship between hVISA and vancomycin MIC values. A...
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Published in: | BMC infectious diseases 2013-12, Vol.13 (1), p.583-583, Article 583 |
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creator | Sancak, Banu Yagci, Server Gür, Deniz Gülay, Zeynep Ogunc, Dilara Söyletir, Güner Yalcin, Ata Nevzat Dündar, Devrim Oztürk Topçu, Ayşe Willke Aksit, Filiz Usluer, Gaye Ozakin, Cüneyt Akalin, Halis Hayran, Mutlu Korten, Volkan |
description | The aim of this study was to determine the distribution of vancomycin and daptomycin MICs among methicillin-resistant Staphylococcus aureus (MRSA) blood isolates, the prevalence of heterogeneous vancomycin-intermediate S. aureus (hVISA) and the relationship between hVISA and vancomycin MIC values.
A total of 175 MRSA blood isolates were collected from seven university hospitals in Turkey. All isolates were tested for susceptibility to vancomycin and daptomycin by reference broth microdilution (BMD) and by standard Etest method. BMD test was performed according to CLSI guidelines and Etest was performed according to the instructions of the manufacturer. All isolates were screened for the presence of the hVISA by using macro Etest (MET) and population analysis profile-area under the curve (PAP-AUC) methods.
The vancomycin MIC50, MIC90 and MIC ranges were 1, 2, and 0.5-2 μg/ml, respectively, by both of BMD and Etest. The daptomycin MIC50, MIC90 and MIC ranges were 0.5, 1 and 0.125 -1 μg/ml by BMD and 0.25, 0.5 and 0.06-1 μg/ml by Etest, respectively. The vancomycin MIC for 40.6% (71/175) of the MRSA isolates tested was >1 μg/ml by BMD. No vancomycin and daptomycin resistance was found among MRSA isolates. Percent agreement of Etest MICs with BMD MICs within ±1 doubling dilution was 100% and 73.1% for vancomycin and daptomycin, respectively. The prevalence of hVISA among MRSA blood isolates was 13.7% (24/175) by PAP-AUC method. MET identified only 14 of the hVISA strains (sensitivity, 58.3%), and there were 12 strains identified as hVISA that were not subsequently confirmed by PAP-AUC (specificity, 92.1%).
Agreement between BMD and Etest MICs is high both for vancomycin and daptomycin. Daptomycin was found to be highly active against MRSA isolates including hVISA. A considerable number of isolates are determined as hVISA among blood isolates. As it is impractical to use the reference method (PAP-AUC) for large numbers of isolates, laboratory methods for rapid and accurate identification of hVISA need to be developed. |
doi_str_mv | 10.1186/1471-2334-13-583 |
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A total of 175 MRSA blood isolates were collected from seven university hospitals in Turkey. All isolates were tested for susceptibility to vancomycin and daptomycin by reference broth microdilution (BMD) and by standard Etest method. BMD test was performed according to CLSI guidelines and Etest was performed according to the instructions of the manufacturer. All isolates were screened for the presence of the hVISA by using macro Etest (MET) and population analysis profile-area under the curve (PAP-AUC) methods.
The vancomycin MIC50, MIC90 and MIC ranges were 1, 2, and 0.5-2 μg/ml, respectively, by both of BMD and Etest. The daptomycin MIC50, MIC90 and MIC ranges were 0.5, 1 and 0.125 -1 μg/ml by BMD and 0.25, 0.5 and 0.06-1 μg/ml by Etest, respectively. The vancomycin MIC for 40.6% (71/175) of the MRSA isolates tested was >1 μg/ml by BMD. No vancomycin and daptomycin resistance was found among MRSA isolates. Percent agreement of Etest MICs with BMD MICs within ±1 doubling dilution was 100% and 73.1% for vancomycin and daptomycin, respectively. The prevalence of hVISA among MRSA blood isolates was 13.7% (24/175) by PAP-AUC method. MET identified only 14 of the hVISA strains (sensitivity, 58.3%), and there were 12 strains identified as hVISA that were not subsequently confirmed by PAP-AUC (specificity, 92.1%).
Agreement between BMD and Etest MICs is high both for vancomycin and daptomycin. Daptomycin was found to be highly active against MRSA isolates including hVISA. A considerable number of isolates are determined as hVISA among blood isolates. As it is impractical to use the reference method (PAP-AUC) for large numbers of isolates, laboratory methods for rapid and accurate identification of hVISA need to be developed.</description><identifier>ISSN: 1471-2334</identifier><identifier>EISSN: 1471-2334</identifier><identifier>DOI: 10.1186/1471-2334-13-583</identifier><identifier>PMID: 24325260</identifier><language>eng</language><publisher>England: BioMed Central Ltd</publisher><subject>Agreements ; Anti-Bacterial Agents - pharmacology ; Area Under Curve ; Bacteremia - microbiology ; Blood ; College students ; Daptomycin - pharmacology ; Drug resistance in microorganisms ; Drug therapy ; Genotype & phenotype ; Health aspects ; Hospitals ; Humans ; Medical schools ; Methicillin-Resistant Staphylococcus aureus - drug effects ; Methicillin-Resistant Staphylococcus aureus - genetics ; Methicillin-Resistant Staphylococcus aureus - isolation & purification ; Methods ; Microbial Sensitivity Tests ; Microbiology ; Prevalence ; Staphylococcal Infections - blood ; Staphylococcal Infections - epidemiology ; Staphylococcal Infections - microbiology ; Staphylococcus aureus ; Staphylococcus aureus infections ; Staphylococcus infections ; Studies ; Turkey ; Turkey - epidemiology ; Vancomycin ; Vancomycin - pharmacology ; Vancomycin Resistance - drug effects</subject><ispartof>BMC infectious diseases, 2013-12, Vol.13 (1), p.583-583, Article 583</ispartof><rights>COPYRIGHT 2013 BioMed Central Ltd.</rights><rights>2013 Sancak et al.; licensee BioMed Central Ltd. This is an open access article distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/2.0), which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited.</rights><rights>Copyright © 2013 Sancak et al.; licensee BioMed Central Ltd. 2013 Sancak et al.; licensee BioMed Central Ltd.</rights><lds50>peer_reviewed</lds50><oa>free_for_read</oa><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-b718t-a78e714f0aa30c670f79d88776ff2d88b81fb85d8158680d2c86901fe585e8723</citedby><cites>FETCH-LOGICAL-b718t-a78e714f0aa30c670f79d88776ff2d88b81fb85d8158680d2c86901fe585e8723</cites></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><linktopdf>$$Uhttps://www.ncbi.nlm.nih.gov/pmc/articles/PMC3866574/pdf/$$EPDF$$P50$$Gpubmedcentral$$Hfree_for_read</linktopdf><linktohtml>$$Uhttps://www.proquest.com/docview/1469714754?pq-origsite=primo$$EHTML$$P50$$Gproquest$$Hfree_for_read</linktohtml><link.rule.ids>230,314,727,780,784,885,25753,27924,27925,37012,37013,44590,53791,53793</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/24325260$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Sancak, Banu</creatorcontrib><creatorcontrib>Yagci, Server</creatorcontrib><creatorcontrib>Gür, Deniz</creatorcontrib><creatorcontrib>Gülay, Zeynep</creatorcontrib><creatorcontrib>Ogunc, Dilara</creatorcontrib><creatorcontrib>Söyletir, Güner</creatorcontrib><creatorcontrib>Yalcin, Ata Nevzat</creatorcontrib><creatorcontrib>Dündar, Devrim Oztürk</creatorcontrib><creatorcontrib>Topçu, Ayşe Willke</creatorcontrib><creatorcontrib>Aksit, Filiz</creatorcontrib><creatorcontrib>Usluer, Gaye</creatorcontrib><creatorcontrib>Ozakin, Cüneyt</creatorcontrib><creatorcontrib>Akalin, Halis</creatorcontrib><creatorcontrib>Hayran, Mutlu</creatorcontrib><creatorcontrib>Korten, Volkan</creatorcontrib><title>Vancomycin and daptomycin minimum inhibitory concentration distribution and occurrence of heteroresistance among methicillin-resistant Staphylococcus aureus blood isolates in Turkey</title><title>BMC infectious diseases</title><addtitle>BMC Infect Dis</addtitle><description>The aim of this study was to determine the distribution of vancomycin and daptomycin MICs among methicillin-resistant Staphylococcus aureus (MRSA) blood isolates, the prevalence of heterogeneous vancomycin-intermediate S. aureus (hVISA) and the relationship between hVISA and vancomycin MIC values.
A total of 175 MRSA blood isolates were collected from seven university hospitals in Turkey. All isolates were tested for susceptibility to vancomycin and daptomycin by reference broth microdilution (BMD) and by standard Etest method. BMD test was performed according to CLSI guidelines and Etest was performed according to the instructions of the manufacturer. All isolates were screened for the presence of the hVISA by using macro Etest (MET) and population analysis profile-area under the curve (PAP-AUC) methods.
The vancomycin MIC50, MIC90 and MIC ranges were 1, 2, and 0.5-2 μg/ml, respectively, by both of BMD and Etest. The daptomycin MIC50, MIC90 and MIC ranges were 0.5, 1 and 0.125 -1 μg/ml by BMD and 0.25, 0.5 and 0.06-1 μg/ml by Etest, respectively. The vancomycin MIC for 40.6% (71/175) of the MRSA isolates tested was >1 μg/ml by BMD. No vancomycin and daptomycin resistance was found among MRSA isolates. Percent agreement of Etest MICs with BMD MICs within ±1 doubling dilution was 100% and 73.1% for vancomycin and daptomycin, respectively. The prevalence of hVISA among MRSA blood isolates was 13.7% (24/175) by PAP-AUC method. MET identified only 14 of the hVISA strains (sensitivity, 58.3%), and there were 12 strains identified as hVISA that were not subsequently confirmed by PAP-AUC (specificity, 92.1%).
Agreement between BMD and Etest MICs is high both for vancomycin and daptomycin. Daptomycin was found to be highly active against MRSA isolates including hVISA. A considerable number of isolates are determined as hVISA among blood isolates. As it is impractical to use the reference method (PAP-AUC) for large numbers of isolates, laboratory methods for rapid and accurate identification of hVISA need to be developed.</description><subject>Agreements</subject><subject>Anti-Bacterial Agents - pharmacology</subject><subject>Area Under Curve</subject><subject>Bacteremia - microbiology</subject><subject>Blood</subject><subject>College students</subject><subject>Daptomycin - pharmacology</subject><subject>Drug resistance in microorganisms</subject><subject>Drug therapy</subject><subject>Genotype & phenotype</subject><subject>Health aspects</subject><subject>Hospitals</subject><subject>Humans</subject><subject>Medical schools</subject><subject>Methicillin-Resistant Staphylococcus aureus - drug effects</subject><subject>Methicillin-Resistant Staphylococcus aureus - genetics</subject><subject>Methicillin-Resistant Staphylococcus aureus - isolation & purification</subject><subject>Methods</subject><subject>Microbial Sensitivity Tests</subject><subject>Microbiology</subject><subject>Prevalence</subject><subject>Staphylococcal Infections - blood</subject><subject>Staphylococcal Infections - epidemiology</subject><subject>Staphylococcal Infections - microbiology</subject><subject>Staphylococcus aureus</subject><subject>Staphylococcus aureus infections</subject><subject>Staphylococcus infections</subject><subject>Studies</subject><subject>Turkey</subject><subject>Turkey - epidemiology</subject><subject>Vancomycin</subject><subject>Vancomycin - pharmacology</subject><subject>Vancomycin Resistance - drug effects</subject><issn>1471-2334</issn><issn>1471-2334</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2013</creationdate><recordtype>article</recordtype><sourceid>PIMPY</sourceid><recordid>eNqNk8Fu1DAQhiMEoqVw54QscSmHFDtOYu8FqVoVqFSpEi29Wo4z3nVJ7MV2EHmwvh8Ou10aVCTkg-2Zb_7Y8ztZ9prgE0J4_Z6UjOQFpWVOaF5x-iQ73IeePlgfZC9CuMWYMF4snmcHRUmLqqjxYXZ3I61y_aiMRdK2qJWbuNv2xpp-6JGxa9OY6PyIlLMKbPQyGmdRa0L0phl-b6Zip9TgPSQGOY3WEME7DyFhcorJ3tkV6iGujTJdZ2x-n4zoKsrNeuycmjQCkoOHNDWdcy0ywXUyQkgnQdeD_wbjy-yZll2AV7v5KPv68ex6-Tm_uPx0vjy9yBtGeMwl48BIqbGUFKuaYc0WLeeM1VoXadFwohtetZxUvOa4LRSvF5hoqHgFnBX0KPuw1d0MTQ_t9u6d2HjTSz8KJ42YZ6xZi5X7ISiv64qVSWC5FWiM-4fAPJO8EJNtYrJNECqSq0nleHcM774PEKLoTVDQddKCG0IqWCQzeVHghL79C711g7epSYmqF6kbrCr_UCvZgTBWu_RxNYmK04qWNWac8USdPEKl0UJv0lMAbVJ8VvBuVpCYCD_jSg4hiPOrL__PXt7MWbxllXcheND7BhIsph_hsZa9eejcvuD-5dNfA5YHSg</recordid><startdate>20131210</startdate><enddate>20131210</enddate><creator>Sancak, Banu</creator><creator>Yagci, Server</creator><creator>Gür, Deniz</creator><creator>Gülay, Zeynep</creator><creator>Ogunc, Dilara</creator><creator>Söyletir, Güner</creator><creator>Yalcin, Ata Nevzat</creator><creator>Dündar, Devrim Oztürk</creator><creator>Topçu, Ayşe Willke</creator><creator>Aksit, Filiz</creator><creator>Usluer, Gaye</creator><creator>Ozakin, Cüneyt</creator><creator>Akalin, Halis</creator><creator>Hayran, Mutlu</creator><creator>Korten, Volkan</creator><general>BioMed Central Ltd</general><general>BioMed Central</general><scope>CGR</scope><scope>CUY</scope><scope>CVF</scope><scope>ECM</scope><scope>EIF</scope><scope>NPM</scope><scope>AAYXX</scope><scope>CITATION</scope><scope>IOV</scope><scope>ISR</scope><scope>3V.</scope><scope>7QL</scope><scope>7T2</scope><scope>7U9</scope><scope>7X7</scope><scope>7XB</scope><scope>88E</scope><scope>8C1</scope><scope>8FI</scope><scope>8FJ</scope><scope>8FK</scope><scope>ABUWG</scope><scope>AFKRA</scope><scope>AZQEC</scope><scope>BENPR</scope><scope>C1K</scope><scope>CCPQU</scope><scope>DWQXO</scope><scope>FYUFA</scope><scope>GHDGH</scope><scope>H94</scope><scope>K9.</scope><scope>M0S</scope><scope>M1P</scope><scope>M7N</scope><scope>PIMPY</scope><scope>PQEST</scope><scope>PQQKQ</scope><scope>PQUKI</scope><scope>5PM</scope></search><sort><creationdate>20131210</creationdate><title>Vancomycin and daptomycin minimum inhibitory concentration distribution and occurrence of heteroresistance among methicillin-resistant Staphylococcus aureus blood isolates in Turkey</title><author>Sancak, Banu ; Yagci, Server ; Gür, Deniz ; Gülay, Zeynep ; Ogunc, Dilara ; Söyletir, Güner ; Yalcin, Ata Nevzat ; Dündar, Devrim Oztürk ; Topçu, Ayşe Willke ; Aksit, Filiz ; Usluer, Gaye ; Ozakin, Cüneyt ; Akalin, Halis ; Hayran, Mutlu ; Korten, Volkan</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-b718t-a78e714f0aa30c670f79d88776ff2d88b81fb85d8158680d2c86901fe585e8723</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2013</creationdate><topic>Agreements</topic><topic>Anti-Bacterial Agents - 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A total of 175 MRSA blood isolates were collected from seven university hospitals in Turkey. All isolates were tested for susceptibility to vancomycin and daptomycin by reference broth microdilution (BMD) and by standard Etest method. BMD test was performed according to CLSI guidelines and Etest was performed according to the instructions of the manufacturer. All isolates were screened for the presence of the hVISA by using macro Etest (MET) and population analysis profile-area under the curve (PAP-AUC) methods.
The vancomycin MIC50, MIC90 and MIC ranges were 1, 2, and 0.5-2 μg/ml, respectively, by both of BMD and Etest. The daptomycin MIC50, MIC90 and MIC ranges were 0.5, 1 and 0.125 -1 μg/ml by BMD and 0.25, 0.5 and 0.06-1 μg/ml by Etest, respectively. The vancomycin MIC for 40.6% (71/175) of the MRSA isolates tested was >1 μg/ml by BMD. No vancomycin and daptomycin resistance was found among MRSA isolates. Percent agreement of Etest MICs with BMD MICs within ±1 doubling dilution was 100% and 73.1% for vancomycin and daptomycin, respectively. The prevalence of hVISA among MRSA blood isolates was 13.7% (24/175) by PAP-AUC method. MET identified only 14 of the hVISA strains (sensitivity, 58.3%), and there were 12 strains identified as hVISA that were not subsequently confirmed by PAP-AUC (specificity, 92.1%).
Agreement between BMD and Etest MICs is high both for vancomycin and daptomycin. Daptomycin was found to be highly active against MRSA isolates including hVISA. A considerable number of isolates are determined as hVISA among blood isolates. As it is impractical to use the reference method (PAP-AUC) for large numbers of isolates, laboratory methods for rapid and accurate identification of hVISA need to be developed.</abstract><cop>England</cop><pub>BioMed Central Ltd</pub><pmid>24325260</pmid><doi>10.1186/1471-2334-13-583</doi><tpages>1</tpages><oa>free_for_read</oa></addata></record> |
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source | Publicly Available Content Database; PubMed Central |
subjects | Agreements Anti-Bacterial Agents - pharmacology Area Under Curve Bacteremia - microbiology Blood College students Daptomycin - pharmacology Drug resistance in microorganisms Drug therapy Genotype & phenotype Health aspects Hospitals Humans Medical schools Methicillin-Resistant Staphylococcus aureus - drug effects Methicillin-Resistant Staphylococcus aureus - genetics Methicillin-Resistant Staphylococcus aureus - isolation & purification Methods Microbial Sensitivity Tests Microbiology Prevalence Staphylococcal Infections - blood Staphylococcal Infections - epidemiology Staphylococcal Infections - microbiology Staphylococcus aureus Staphylococcus aureus infections Staphylococcus infections Studies Turkey Turkey - epidemiology Vancomycin Vancomycin - pharmacology Vancomycin Resistance - drug effects |
title | Vancomycin and daptomycin minimum inhibitory concentration distribution and occurrence of heteroresistance among methicillin-resistant Staphylococcus aureus blood isolates in Turkey |
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