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Molecular Epidemiology of a Vancomycin-Intermediate Heteroresistant Staphylococcus epidermidis Outbreak in a Neonatal Intensive Care Unit
Coagulase-negative staphylococci (CoNS) have become the leading cause of bloodstream infections (BSIs) in intensive care units (ICUs), particularly in premature neonates. Vancomycin-intermediate heteroresistant CoNS (hVICoNS) have been identified as sources of BSIs worldwide, and their potential to...
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Published in: | Antimicrobial agents and chemotherapy 2016-10, Vol.60 (10), p.5673-5681 |
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description | Coagulase-negative staphylococci (CoNS) have become the leading cause of bloodstream infections (BSIs) in intensive care units (ICUs), particularly in premature neonates. Vancomycin-intermediate heteroresistant CoNS (hVICoNS) have been identified as sources of BSIs worldwide, and their potential to emerge as significant pathogens in the neonatal ICU (NICU) remains uncertain. This study describes the molecular epidemiology of an outbreak of vancomycin-heteroresistant (hV) Staphylococcus epidermidis central-line-associated BSI (CLABSI) in a single tertiary care NICU and compares it to a second tertiary care NICU that had not been associated with an outbreak. Between November 2009 and April 2014, 119 S. epidermidis CLABSIs were identified in two tertiary care NICUs in Quebec, Canada. Decreased vancomycin susceptibility was identified in about 88% of all collected strains using Etest methods. However, discrepancies were found according to the Etest and population analysis profiling-area under the concentration-time curve (PAP-AUC) methods used. All strains were susceptible to linezolid, and a few isolates were nonsusceptible to daptomycin. Great genetic diversity was observed within the collection, with 31 pulsed-field gel electrophoresis (PFGE) patterns identified. The outbreak strains were all determined to be heteroresistant to vancomycin and were polyclonal. The study identified two major clones, PFGE patterns E and G, which were found in both NICUs across the 5-year study period. This suggests the persistence of highly successful clones that are well adapted to the hospital environment. hV S. epidermidis seems more common than currently realized in the NICU, and certain hV S. epidermidis clones can become endemic to the NICU. The reservoirs for these clones remain unknown at this time, and identification of the reservoirs is needed to better understand the impact of hV S. epidermidis in the NICU and to inform infection prevention strategies. In addition, there is a need to investigate and validate hV determination protocols for different species of CoNS. |
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Vancomycin-intermediate heteroresistant CoNS (hVICoNS) have been identified as sources of BSIs worldwide, and their potential to emerge as significant pathogens in the neonatal ICU (NICU) remains uncertain. This study describes the molecular epidemiology of an outbreak of vancomycin-heteroresistant (hV) Staphylococcus epidermidis central-line-associated BSI (CLABSI) in a single tertiary care NICU and compares it to a second tertiary care NICU that had not been associated with an outbreak. Between November 2009 and April 2014, 119 S. epidermidis CLABSIs were identified in two tertiary care NICUs in Quebec, Canada. Decreased vancomycin susceptibility was identified in about 88% of all collected strains using Etest methods. However, discrepancies were found according to the Etest and population analysis profiling-area under the concentration-time curve (PAP-AUC) methods used. All strains were susceptible to linezolid, and a few isolates were nonsusceptible to daptomycin. Great genetic diversity was observed within the collection, with 31 pulsed-field gel electrophoresis (PFGE) patterns identified. The outbreak strains were all determined to be heteroresistant to vancomycin and were polyclonal. The study identified two major clones, PFGE patterns E and G, which were found in both NICUs across the 5-year study period. This suggests the persistence of highly successful clones that are well adapted to the hospital environment. hV S. epidermidis seems more common than currently realized in the NICU, and certain hV S. epidermidis clones can become endemic to the NICU. The reservoirs for these clones remain unknown at this time, and identification of the reservoirs is needed to better understand the impact of hV S. epidermidis in the NICU and to inform infection prevention strategies. In addition, there is a need to investigate and validate hV determination protocols for different species of CoNS.</description><identifier>ISSN: 0066-4804</identifier><identifier>EISSN: 1098-6596</identifier><identifier>DOI: 10.1128/AAC.00726-16</identifier><identifier>PMID: 27401579</identifier><language>eng</language><publisher>United States: American Society for Microbiology</publisher><subject>Bacteremia - epidemiology ; Bacteremia - microbiology ; Disease Outbreaks ; Drug Resistance, Bacterial ; Drug Resistance, Bacterial - drug effects ; Electrophoresis, Gel, Pulsed-Field ; Epidemiology and Surveillance ; Female ; Humans ; Infant ; Infant, Newborn ; Intensive Care Units, Neonatal ; Male ; Microbial Sensitivity Tests ; Molecular Epidemiology ; Multilocus Sequence Typing ; Quebec - epidemiology ; Staphylococcal Infections ; Staphylococcal Infections - drug therapy ; Staphylococcal Infections - epidemiology ; Staphylococcal Infections - microbiology ; Staphylococcal Infections - mortality ; Staphylococcus epidermidis ; Staphylococcus epidermidis - drug effects ; Staphylococcus epidermidis - isolation & purification ; Staphylococcus epidermidis - pathogenicity ; Vancomycin ; Vancomycin - pharmacology</subject><ispartof>Antimicrobial agents and chemotherapy, 2016-10, Vol.60 (10), p.5673-5681</ispartof><rights>Copyright © 2016, American Society for Microbiology. All Rights Reserved.</rights><rights>Copyright © 2016, American Society for Microbiology. All Rights Reserved. 2016 American Society for Microbiology</rights><lds50>peer_reviewed</lds50><oa>free_for_read</oa><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-a451t-7d75548d865da09fcc766a03fd4c756660dafaf58d3cc3872f45b7610fd9e6803</citedby><cites>FETCH-LOGICAL-a451t-7d75548d865da09fcc766a03fd4c756660dafaf58d3cc3872f45b7610fd9e6803</cites></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><linktopdf>$$Uhttps://journals.asm.org/doi/pdf/10.1128/AAC.00726-16$$EPDF$$P50$$Gasm2$$H</linktopdf><linktohtml>$$Uhttps://journals.asm.org/doi/full/10.1128/AAC.00726-16$$EHTML$$P50$$Gasm2$$H</linktohtml><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/27401579$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Chong, Jasmine</creatorcontrib><creatorcontrib>Quach, Caroline</creatorcontrib><creatorcontrib>Blanchard, Ana C</creatorcontrib><creatorcontrib>Poliquin, Philippe Guillaume</creatorcontrib><creatorcontrib>Golding, George R</creatorcontrib><creatorcontrib>Laferrière, Céline</creatorcontrib><creatorcontrib>Lévesque, Simon</creatorcontrib><title>Molecular Epidemiology of a Vancomycin-Intermediate Heteroresistant Staphylococcus epidermidis Outbreak in a Neonatal Intensive Care Unit</title><title>Antimicrobial agents and chemotherapy</title><addtitle>Antimicrob Agents Chemother</addtitle><addtitle>Antimicrob Agents Chemother</addtitle><description>Coagulase-negative staphylococci (CoNS) have become the leading cause of bloodstream infections (BSIs) in intensive care units (ICUs), particularly in premature neonates. Vancomycin-intermediate heteroresistant CoNS (hVICoNS) have been identified as sources of BSIs worldwide, and their potential to emerge as significant pathogens in the neonatal ICU (NICU) remains uncertain. This study describes the molecular epidemiology of an outbreak of vancomycin-heteroresistant (hV) Staphylococcus epidermidis central-line-associated BSI (CLABSI) in a single tertiary care NICU and compares it to a second tertiary care NICU that had not been associated with an outbreak. Between November 2009 and April 2014, 119 S. epidermidis CLABSIs were identified in two tertiary care NICUs in Quebec, Canada. Decreased vancomycin susceptibility was identified in about 88% of all collected strains using Etest methods. However, discrepancies were found according to the Etest and population analysis profiling-area under the concentration-time curve (PAP-AUC) methods used. All strains were susceptible to linezolid, and a few isolates were nonsusceptible to daptomycin. Great genetic diversity was observed within the collection, with 31 pulsed-field gel electrophoresis (PFGE) patterns identified. The outbreak strains were all determined to be heteroresistant to vancomycin and were polyclonal. The study identified two major clones, PFGE patterns E and G, which were found in both NICUs across the 5-year study period. This suggests the persistence of highly successful clones that are well adapted to the hospital environment. hV S. epidermidis seems more common than currently realized in the NICU, and certain hV S. epidermidis clones can become endemic to the NICU. The reservoirs for these clones remain unknown at this time, and identification of the reservoirs is needed to better understand the impact of hV S. epidermidis in the NICU and to inform infection prevention strategies. In addition, there is a need to investigate and validate hV determination protocols for different species of CoNS.</description><subject>Bacteremia - epidemiology</subject><subject>Bacteremia - microbiology</subject><subject>Disease Outbreaks</subject><subject>Drug Resistance, Bacterial</subject><subject>Drug Resistance, Bacterial - drug effects</subject><subject>Electrophoresis, Gel, Pulsed-Field</subject><subject>Epidemiology and Surveillance</subject><subject>Female</subject><subject>Humans</subject><subject>Infant</subject><subject>Infant, Newborn</subject><subject>Intensive Care Units, Neonatal</subject><subject>Male</subject><subject>Microbial Sensitivity Tests</subject><subject>Molecular Epidemiology</subject><subject>Multilocus Sequence Typing</subject><subject>Quebec - epidemiology</subject><subject>Staphylococcal Infections</subject><subject>Staphylococcal Infections - drug therapy</subject><subject>Staphylococcal Infections - epidemiology</subject><subject>Staphylococcal Infections - microbiology</subject><subject>Staphylococcal Infections - mortality</subject><subject>Staphylococcus epidermidis</subject><subject>Staphylococcus epidermidis - drug effects</subject><subject>Staphylococcus epidermidis - isolation & purification</subject><subject>Staphylococcus epidermidis - pathogenicity</subject><subject>Vancomycin</subject><subject>Vancomycin - pharmacology</subject><issn>0066-4804</issn><issn>1098-6596</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2016</creationdate><recordtype>article</recordtype><recordid>eNqNks9rFDEUx4Modlu9eZYcFTo1mUx-zEVYlmoL1R60XsPb_GhTZ5I1yRT2T_C_drZbix4ET-GRDx_ee9-H0CtKTiht1bvlcnVCiGxFQ8UTtKCkV43gvXiKFoQI0XSKdAfosJRbMte8J8_RQSs7QrnsF-jnpzQ4Mw2Q8ekmWDeGNKTrLU4eA_4G0aRxa0JszmN1eXQ2QHX4zM1Fyq6EUiFW_KXC5mY7JJOMmQp2O1Eegw0FX051nR18xyHOws8uRagw4J0ulnDn8Aqyw1cx1BfomYehuJcP7xG6-nD6dXXWXFx-PF8tLxroOK2NtJLzTlkluAXSe2OkEECYt52RXAhBLHjwXFlmDFOy9R1fS0GJt70TirAj9H7v3UzreSDjYs0w6E0OI-StThD03z8x3OjrdKc5Yart-Sx48yDI6cfkStVjKMYNA0SXpqKpYpIxoWj3H2jLCOP03nq8R01OpWTnHzuiRO-C1nPQ-j5oTcWMv93jUMZW36Ypx3lp_2Jf_znxo_j3FbBfCjmzfA</recordid><startdate>20161001</startdate><enddate>20161001</enddate><creator>Chong, Jasmine</creator><creator>Quach, Caroline</creator><creator>Blanchard, Ana C</creator><creator>Poliquin, Philippe Guillaume</creator><creator>Golding, George R</creator><creator>Laferrière, Céline</creator><creator>Lévesque, Simon</creator><general>American Society for Microbiology</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>7X8</scope><scope>7QL</scope><scope>7T7</scope><scope>8FD</scope><scope>C1K</scope><scope>FR3</scope><scope>P64</scope><scope>5PM</scope></search><sort><creationdate>20161001</creationdate><title>Molecular Epidemiology of a Vancomycin-Intermediate Heteroresistant Staphylococcus epidermidis Outbreak in a Neonatal Intensive Care Unit</title><author>Chong, Jasmine ; Quach, Caroline ; Blanchard, Ana C ; Poliquin, Philippe Guillaume ; Golding, George R ; Laferrière, Céline ; Lévesque, Simon</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-a451t-7d75548d865da09fcc766a03fd4c756660dafaf58d3cc3872f45b7610fd9e6803</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2016</creationdate><topic>Bacteremia - epidemiology</topic><topic>Bacteremia - microbiology</topic><topic>Disease Outbreaks</topic><topic>Drug Resistance, Bacterial</topic><topic>Drug Resistance, Bacterial - drug effects</topic><topic>Electrophoresis, Gel, Pulsed-Field</topic><topic>Epidemiology and Surveillance</topic><topic>Female</topic><topic>Humans</topic><topic>Infant</topic><topic>Infant, Newborn</topic><topic>Intensive Care Units, Neonatal</topic><topic>Male</topic><topic>Microbial Sensitivity Tests</topic><topic>Molecular Epidemiology</topic><topic>Multilocus Sequence Typing</topic><topic>Quebec - epidemiology</topic><topic>Staphylococcal Infections</topic><topic>Staphylococcal Infections - drug therapy</topic><topic>Staphylococcal Infections - epidemiology</topic><topic>Staphylococcal Infections - microbiology</topic><topic>Staphylococcal Infections - mortality</topic><topic>Staphylococcus epidermidis</topic><topic>Staphylococcus epidermidis - drug effects</topic><topic>Staphylococcus epidermidis - isolation & purification</topic><topic>Staphylococcus epidermidis - pathogenicity</topic><topic>Vancomycin</topic><topic>Vancomycin - pharmacology</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Chong, Jasmine</creatorcontrib><creatorcontrib>Quach, Caroline</creatorcontrib><creatorcontrib>Blanchard, Ana C</creatorcontrib><creatorcontrib>Poliquin, Philippe Guillaume</creatorcontrib><creatorcontrib>Golding, George R</creatorcontrib><creatorcontrib>Laferrière, Céline</creatorcontrib><creatorcontrib>Lévesque, Simon</creatorcontrib><collection>Medline</collection><collection>MEDLINE</collection><collection>MEDLINE (Ovid)</collection><collection>MEDLINE</collection><collection>MEDLINE</collection><collection>PubMed</collection><collection>CrossRef</collection><collection>MEDLINE - Academic</collection><collection>Bacteriology Abstracts (Microbiology B)</collection><collection>Industrial and Applied Microbiology Abstracts (Microbiology A)</collection><collection>Technology Research Database</collection><collection>Environmental Sciences and Pollution Management</collection><collection>Engineering Research Database</collection><collection>Biotechnology and BioEngineering Abstracts</collection><collection>PubMed Central (Full Participant titles)</collection><jtitle>Antimicrobial agents and chemotherapy</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Chong, Jasmine</au><au>Quach, Caroline</au><au>Blanchard, Ana C</au><au>Poliquin, Philippe Guillaume</au><au>Golding, George R</au><au>Laferrière, Céline</au><au>Lévesque, Simon</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Molecular Epidemiology of a Vancomycin-Intermediate Heteroresistant Staphylococcus epidermidis Outbreak in a Neonatal Intensive Care Unit</atitle><jtitle>Antimicrobial agents and chemotherapy</jtitle><stitle>Antimicrob Agents Chemother</stitle><addtitle>Antimicrob Agents Chemother</addtitle><date>2016-10-01</date><risdate>2016</risdate><volume>60</volume><issue>10</issue><spage>5673</spage><epage>5681</epage><pages>5673-5681</pages><issn>0066-4804</issn><eissn>1098-6596</eissn><abstract>Coagulase-negative staphylococci (CoNS) have become the leading cause of bloodstream infections (BSIs) in intensive care units (ICUs), particularly in premature neonates. Vancomycin-intermediate heteroresistant CoNS (hVICoNS) have been identified as sources of BSIs worldwide, and their potential to emerge as significant pathogens in the neonatal ICU (NICU) remains uncertain. This study describes the molecular epidemiology of an outbreak of vancomycin-heteroresistant (hV) Staphylococcus epidermidis central-line-associated BSI (CLABSI) in a single tertiary care NICU and compares it to a second tertiary care NICU that had not been associated with an outbreak. Between November 2009 and April 2014, 119 S. epidermidis CLABSIs were identified in two tertiary care NICUs in Quebec, Canada. Decreased vancomycin susceptibility was identified in about 88% of all collected strains using Etest methods. However, discrepancies were found according to the Etest and population analysis profiling-area under the concentration-time curve (PAP-AUC) methods used. All strains were susceptible to linezolid, and a few isolates were nonsusceptible to daptomycin. Great genetic diversity was observed within the collection, with 31 pulsed-field gel electrophoresis (PFGE) patterns identified. The outbreak strains were all determined to be heteroresistant to vancomycin and were polyclonal. The study identified two major clones, PFGE patterns E and G, which were found in both NICUs across the 5-year study period. This suggests the persistence of highly successful clones that are well adapted to the hospital environment. hV S. epidermidis seems more common than currently realized in the NICU, and certain hV S. epidermidis clones can become endemic to the NICU. The reservoirs for these clones remain unknown at this time, and identification of the reservoirs is needed to better understand the impact of hV S. epidermidis in the NICU and to inform infection prevention strategies. In addition, there is a need to investigate and validate hV determination protocols for different species of CoNS.</abstract><cop>United States</cop><pub>American Society for Microbiology</pub><pmid>27401579</pmid><doi>10.1128/AAC.00726-16</doi><tpages>9</tpages><oa>free_for_read</oa></addata></record> |
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subjects | Bacteremia - epidemiology Bacteremia - microbiology Disease Outbreaks Drug Resistance, Bacterial Drug Resistance, Bacterial - drug effects Electrophoresis, Gel, Pulsed-Field Epidemiology and Surveillance Female Humans Infant Infant, Newborn Intensive Care Units, Neonatal Male Microbial Sensitivity Tests Molecular Epidemiology Multilocus Sequence Typing Quebec - epidemiology Staphylococcal Infections Staphylococcal Infections - drug therapy Staphylococcal Infections - epidemiology Staphylococcal Infections - microbiology Staphylococcal Infections - mortality Staphylococcus epidermidis Staphylococcus epidermidis - drug effects Staphylococcus epidermidis - isolation & purification Staphylococcus epidermidis - pathogenicity Vancomycin Vancomycin - pharmacology |
title | Molecular Epidemiology of a Vancomycin-Intermediate Heteroresistant Staphylococcus epidermidis Outbreak in a Neonatal Intensive Care Unit |
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