Small-Colony Variants in Persistent and Recurrent Staphylococcus aureus Bacteremia
The small-colony variant (SCV) phenotype of Staphylococcus aureus is associated with intracellular persistence and reduced antimicrobial susceptibility, which can lead to therapeutic failure. Since SCVs grow slowly and have a confusing morphology, the identification of infections due to SCV is diffi...
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Veröffentlicht in: | Microbial drug resistance (Larchmont, N.Y.) N.Y.), 2016-10, Vol.22 (7), p.538-544 |
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creator | Kim, Nak-Hyun Kang, Yu Min Han, Woong Dae Park, Kyoung Un Park, Kay-Hyun Yoo, Jae Il Lee, Dong-Gun Park, Chulmin Song, Kyoung-Ho Kim, Eu Suk Park, Sang Won Kim, Nam Joong Oh, Myoung-don Kim, Hong Bin |
description | The small-colony variant (SCV) phenotype of
Staphylococcus aureus
is associated with intracellular persistence and reduced antimicrobial susceptibility, which can lead to therapeutic failure. Since SCVs grow slowly and have a confusing morphology, the identification of infections due to SCV is difficult. We have identified SCVs in two patients who presented with persistent methicillin-resistant
Staphylococcus aureus
(MRSA) bacteremia complicated by surgical site infections after cardiothoracic surgery. Nine blood isolates were collected from the two patients for species identification, antimicrobial susceptibility testing, and phenotypic and genotypic characterization. Colonies on Columbia blood agar were pinpoint, nonpigmented, nonhemolytic, and reverted to normal colonies after 48 hr of incubation on Schaedler agar. Auxotrophy assays revealed hemin dependence. Susceptibility to vancomycin (minimal inhibitory concentrations 1.0 μg/mL) was confirmed by
E
-test and broth microdilution test. All the isolates were identified as MRSA by multiplex polymerase chain reaction specific for the
mec
A,
fem
A, and 16S rRNA genes, and all had the same genotype: Multilocus sequence typing ST5, SCC
mec
type II,
agr
type II, and
spa
type t2460. Moreover pulsed-field gel electrophoresis typing revealed that all nine isolates belonged to the same clone. Mutations in the
relA
gene were not found, and none of the isolates was identified as hVISA by population analysis profiling-AUC ratio. A high level of suspicion is required to detect SCVs, and although it is not common, the possibility of the SCV phenotype has to be considered in persistent
S. aureus
bacteremia. |
doi_str_mv | 10.1089/mdr.2015.0262 |
format | Article |
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Staphylococcus aureus
is associated with intracellular persistence and reduced antimicrobial susceptibility, which can lead to therapeutic failure. Since SCVs grow slowly and have a confusing morphology, the identification of infections due to SCV is difficult. We have identified SCVs in two patients who presented with persistent methicillin-resistant
Staphylococcus aureus
(MRSA) bacteremia complicated by surgical site infections after cardiothoracic surgery. Nine blood isolates were collected from the two patients for species identification, antimicrobial susceptibility testing, and phenotypic and genotypic characterization. Colonies on Columbia blood agar were pinpoint, nonpigmented, nonhemolytic, and reverted to normal colonies after 48 hr of incubation on Schaedler agar. Auxotrophy assays revealed hemin dependence. Susceptibility to vancomycin (minimal inhibitory concentrations 1.0 μg/mL) was confirmed by
E
-test and broth microdilution test. All the isolates were identified as MRSA by multiplex polymerase chain reaction specific for the
mec
A,
fem
A, and 16S rRNA genes, and all had the same genotype: Multilocus sequence typing ST5, SCC
mec
type II,
agr
type II, and
spa
type t2460. Moreover pulsed-field gel electrophoresis typing revealed that all nine isolates belonged to the same clone. Mutations in the
relA
gene were not found, and none of the isolates was identified as hVISA by population analysis profiling-AUC ratio. A high level of suspicion is required to detect SCVs, and although it is not common, the possibility of the SCV phenotype has to be considered in persistent
S. aureus
bacteremia.</description><identifier>ISSN: 1076-6294</identifier><identifier>EISSN: 1931-8448</identifier><identifier>DOI: 10.1089/mdr.2015.0262</identifier><identifier>PMID: 26982169</identifier><language>eng</language><publisher>United States: Mary Ann Liebert, Inc</publisher><subject>Aged ; Anti-Bacterial Agents - pharmacology ; Bacteremia - drug therapy ; Bacteremia - microbiology ; Bacteremia - pathology ; Bacteria ; Bacterial Typing Techniques ; Blood ; Clone Cells ; Drug therapy ; Electrophoresis, Gel, Pulsed-Field ; Genes, Bacterial ; Genotype ; Genotype & phenotype ; Humans ; Male ; Mechanisms ; Methicillin-Resistant Staphylococcus aureus - classification ; Methicillin-Resistant Staphylococcus aureus - drug effects ; Methicillin-Resistant Staphylococcus aureus - genetics ; Methicillin-Resistant Staphylococcus aureus - isolation & purification ; Multilocus Sequence Typing ; Phenotype ; Recurrence ; Staphylococcal Infections - drug therapy ; Staphylococcal Infections - microbiology ; Staphylococcal Infections - pathology ; Staphylococcus aureus ; Staphylococcus infections ; Surgical Wound Infection - drug therapy ; Surgical Wound Infection - microbiology ; Surgical Wound Infection - pathology ; Vancomycin - pharmacology</subject><ispartof>Microbial drug resistance (Larchmont, N.Y.), 2016-10, Vol.22 (7), p.538-544</ispartof><rights>2016, Mary Ann Liebert, Inc.</rights><rights>(©) Copyright 2016, Mary Ann Liebert, Inc.</rights><lds50>peer_reviewed</lds50><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c398t-3db996ef09bdb1dce8f6815e67ae3d6431a02f82526b929f252fc6ea8756d76c3</citedby><cites>FETCH-LOGICAL-c398t-3db996ef09bdb1dce8f6815e67ae3d6431a02f82526b929f252fc6ea8756d76c3</cites></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><link.rule.ids>314,780,784,27924,27925</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/26982169$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Kim, Nak-Hyun</creatorcontrib><creatorcontrib>Kang, Yu Min</creatorcontrib><creatorcontrib>Han, Woong Dae</creatorcontrib><creatorcontrib>Park, Kyoung Un</creatorcontrib><creatorcontrib>Park, Kay-Hyun</creatorcontrib><creatorcontrib>Yoo, Jae Il</creatorcontrib><creatorcontrib>Lee, Dong-Gun</creatorcontrib><creatorcontrib>Park, Chulmin</creatorcontrib><creatorcontrib>Song, Kyoung-Ho</creatorcontrib><creatorcontrib>Kim, Eu Suk</creatorcontrib><creatorcontrib>Park, Sang Won</creatorcontrib><creatorcontrib>Kim, Nam Joong</creatorcontrib><creatorcontrib>Oh, Myoung-don</creatorcontrib><creatorcontrib>Kim, Hong Bin</creatorcontrib><title>Small-Colony Variants in Persistent and Recurrent Staphylococcus aureus Bacteremia</title><title>Microbial drug resistance (Larchmont, N.Y.)</title><addtitle>Microb Drug Resist</addtitle><description>The small-colony variant (SCV) phenotype of
Staphylococcus aureus
is associated with intracellular persistence and reduced antimicrobial susceptibility, which can lead to therapeutic failure. Since SCVs grow slowly and have a confusing morphology, the identification of infections due to SCV is difficult. We have identified SCVs in two patients who presented with persistent methicillin-resistant
Staphylococcus aureus
(MRSA) bacteremia complicated by surgical site infections after cardiothoracic surgery. Nine blood isolates were collected from the two patients for species identification, antimicrobial susceptibility testing, and phenotypic and genotypic characterization. Colonies on Columbia blood agar were pinpoint, nonpigmented, nonhemolytic, and reverted to normal colonies after 48 hr of incubation on Schaedler agar. Auxotrophy assays revealed hemin dependence. Susceptibility to vancomycin (minimal inhibitory concentrations 1.0 μg/mL) was confirmed by
E
-test and broth microdilution test. All the isolates were identified as MRSA by multiplex polymerase chain reaction specific for the
mec
A,
fem
A, and 16S rRNA genes, and all had the same genotype: Multilocus sequence typing ST5, SCC
mec
type II,
agr
type II, and
spa
type t2460. Moreover pulsed-field gel electrophoresis typing revealed that all nine isolates belonged to the same clone. Mutations in the
relA
gene were not found, and none of the isolates was identified as hVISA by population analysis profiling-AUC ratio. A high level of suspicion is required to detect SCVs, and although it is not common, the possibility of the SCV phenotype has to be considered in persistent
S. aureus
bacteremia.</description><subject>Aged</subject><subject>Anti-Bacterial Agents - pharmacology</subject><subject>Bacteremia - drug therapy</subject><subject>Bacteremia - microbiology</subject><subject>Bacteremia - pathology</subject><subject>Bacteria</subject><subject>Bacterial Typing Techniques</subject><subject>Blood</subject><subject>Clone Cells</subject><subject>Drug therapy</subject><subject>Electrophoresis, Gel, Pulsed-Field</subject><subject>Genes, Bacterial</subject><subject>Genotype</subject><subject>Genotype & phenotype</subject><subject>Humans</subject><subject>Male</subject><subject>Mechanisms</subject><subject>Methicillin-Resistant Staphylococcus aureus - classification</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>Multilocus Sequence Typing</subject><subject>Phenotype</subject><subject>Recurrence</subject><subject>Staphylococcal Infections - drug therapy</subject><subject>Staphylococcal Infections - microbiology</subject><subject>Staphylococcal Infections - pathology</subject><subject>Staphylococcus aureus</subject><subject>Staphylococcus infections</subject><subject>Surgical Wound Infection - drug therapy</subject><subject>Surgical Wound Infection - microbiology</subject><subject>Surgical Wound Infection - pathology</subject><subject>Vancomycin - pharmacology</subject><issn>1076-6294</issn><issn>1931-8448</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2016</creationdate><recordtype>article</recordtype><sourceid>EIF</sourceid><sourceid>ABUWG</sourceid><sourceid>AFKRA</sourceid><sourceid>AZQEC</sourceid><sourceid>BENPR</sourceid><sourceid>CCPQU</sourceid><sourceid>DWQXO</sourceid><sourceid>GNUQQ</sourceid><recordid>eNqNkbtPwzAQhy0EouUxsqJILCwptpNc7BEqXlIlUAuskWNfRKrEKXYy9L_HUYGBBaZ76NNPuvsIOWN0xqiQV61xM05ZNqMc-B6ZMpmwWKSp2A89zSEGLtMJOfJ-TSnNGCSHZMJBCs5ATsly1aqmiedd09lt9KZcrWzvo9pGz-h87Xu0faSsiZaoB-fGadWrzfu26XSn9eAjNTgM5UbpHh22tTohB5VqPJ5-1WPyenf7Mn-IF0_3j_PrRawTKfo4MaWUgBWVpSmZ0SgqECxDyBUmBtKEKcorwTMOpeSyCk2lAZXIMzA56OSYXO5yN677GND3RVt7jU2jLHaDL5hIIQ33yuwfKAeA8SMBvfiFrrvB2XDISGUyzzMJgYp3lHad9w6rYuPqVrltwWgxeimCl2L0UoxeAn_-lTqULZof-ltEAJIdMK6VtU2NJbr-j9hPAISZlA</recordid><startdate>20161001</startdate><enddate>20161001</enddate><creator>Kim, Nak-Hyun</creator><creator>Kang, Yu Min</creator><creator>Han, Woong Dae</creator><creator>Park, Kyoung Un</creator><creator>Park, Kay-Hyun</creator><creator>Yoo, Jae Il</creator><creator>Lee, Dong-Gun</creator><creator>Park, Chulmin</creator><creator>Song, Kyoung-Ho</creator><creator>Kim, Eu Suk</creator><creator>Park, Sang Won</creator><creator>Kim, Nam Joong</creator><creator>Oh, Myoung-don</creator><creator>Kim, Hong Bin</creator><general>Mary Ann Liebert, Inc</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>3V.</scope><scope>7QL</scope><scope>7QP</scope><scope>7QR</scope><scope>7T7</scope><scope>7TK</scope><scope>7X7</scope><scope>7XB</scope><scope>88A</scope><scope>88E</scope><scope>88I</scope><scope>8C1</scope><scope>8FD</scope><scope>8FE</scope><scope>8FH</scope><scope>8FI</scope><scope>8FJ</scope><scope>8FK</scope><scope>ABUWG</scope><scope>AEUYN</scope><scope>AFKRA</scope><scope>AZQEC</scope><scope>BBNVY</scope><scope>BENPR</scope><scope>BHPHI</scope><scope>C1K</scope><scope>CCPQU</scope><scope>DWQXO</scope><scope>FR3</scope><scope>FYUFA</scope><scope>GHDGH</scope><scope>GNUQQ</scope><scope>HCIFZ</scope><scope>K9.</scope><scope>LK8</scope><scope>M0S</scope><scope>M1P</scope><scope>M2P</scope><scope>M7N</scope><scope>M7P</scope><scope>P64</scope><scope>PQEST</scope><scope>PQQKQ</scope><scope>PQUKI</scope><scope>Q9U</scope><scope>7X8</scope></search><sort><creationdate>20161001</creationdate><title>Small-Colony Variants in Persistent and Recurrent Staphylococcus aureus Bacteremia</title><author>Kim, Nak-Hyun ; Kang, Yu Min ; Han, Woong Dae ; Park, Kyoung Un ; Park, Kay-Hyun ; Yoo, Jae Il ; Lee, Dong-Gun ; Park, Chulmin ; Song, Kyoung-Ho ; Kim, Eu Suk ; Park, Sang Won ; Kim, Nam Joong ; Oh, Myoung-don ; Kim, Hong Bin</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c398t-3db996ef09bdb1dce8f6815e67ae3d6431a02f82526b929f252fc6ea8756d76c3</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2016</creationdate><topic>Aged</topic><topic>Anti-Bacterial Agents - pharmacology</topic><topic>Bacteremia - drug therapy</topic><topic>Bacteremia - microbiology</topic><topic>Bacteremia - pathology</topic><topic>Bacteria</topic><topic>Bacterial Typing Techniques</topic><topic>Blood</topic><topic>Clone Cells</topic><topic>Drug therapy</topic><topic>Electrophoresis, Gel, Pulsed-Field</topic><topic>Genes, Bacterial</topic><topic>Genotype</topic><topic>Genotype & phenotype</topic><topic>Humans</topic><topic>Male</topic><topic>Mechanisms</topic><topic>Methicillin-Resistant Staphylococcus aureus - classification</topic><topic>Methicillin-Resistant Staphylococcus aureus - drug effects</topic><topic>Methicillin-Resistant Staphylococcus aureus - genetics</topic><topic>Methicillin-Resistant Staphylococcus aureus - isolation & purification</topic><topic>Multilocus Sequence Typing</topic><topic>Phenotype</topic><topic>Recurrence</topic><topic>Staphylococcal Infections - drug therapy</topic><topic>Staphylococcal Infections - microbiology</topic><topic>Staphylococcal Infections - pathology</topic><topic>Staphylococcus aureus</topic><topic>Staphylococcus infections</topic><topic>Surgical Wound Infection - drug therapy</topic><topic>Surgical Wound Infection - microbiology</topic><topic>Surgical Wound Infection - pathology</topic><topic>Vancomycin - pharmacology</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Kim, Nak-Hyun</creatorcontrib><creatorcontrib>Kang, Yu Min</creatorcontrib><creatorcontrib>Han, Woong Dae</creatorcontrib><creatorcontrib>Park, Kyoung Un</creatorcontrib><creatorcontrib>Park, Kay-Hyun</creatorcontrib><creatorcontrib>Yoo, Jae Il</creatorcontrib><creatorcontrib>Lee, Dong-Gun</creatorcontrib><creatorcontrib>Park, Chulmin</creatorcontrib><creatorcontrib>Song, Kyoung-Ho</creatorcontrib><creatorcontrib>Kim, Eu Suk</creatorcontrib><creatorcontrib>Park, Sang Won</creatorcontrib><creatorcontrib>Kim, Nam Joong</creatorcontrib><creatorcontrib>Oh, Myoung-don</creatorcontrib><creatorcontrib>Kim, Hong Bin</creatorcontrib><collection>Medline</collection><collection>MEDLINE</collection><collection>MEDLINE (Ovid)</collection><collection>MEDLINE</collection><collection>MEDLINE</collection><collection>PubMed</collection><collection>CrossRef</collection><collection>ProQuest Central (Corporate)</collection><collection>Bacteriology Abstracts (Microbiology B)</collection><collection>Calcium & Calcified Tissue Abstracts</collection><collection>Chemoreception Abstracts</collection><collection>Industrial and Applied Microbiology Abstracts (Microbiology A)</collection><collection>Neurosciences Abstracts</collection><collection>Health & Medical Collection</collection><collection>ProQuest Central (purchase pre-March 2016)</collection><collection>Biology Database (Alumni Edition)</collection><collection>Medical Database (Alumni Edition)</collection><collection>Science Database (Alumni Edition)</collection><collection>Public Health Database</collection><collection>Technology Research Database</collection><collection>ProQuest SciTech Collection</collection><collection>ProQuest Natural Science Collection</collection><collection>Hospital Premium Collection</collection><collection>Hospital Premium Collection (Alumni Edition)</collection><collection>ProQuest Central (Alumni) (purchase pre-March 2016)</collection><collection>ProQuest Central (Alumni Edition)</collection><collection>ProQuest One Sustainability</collection><collection>ProQuest Central UK/Ireland</collection><collection>ProQuest Central Essentials</collection><collection>Biological Science Collection</collection><collection>ProQuest Central</collection><collection>Natural Science Collection</collection><collection>Environmental Sciences and Pollution Management</collection><collection>ProQuest One Community College</collection><collection>ProQuest Central Korea</collection><collection>Engineering Research Database</collection><collection>Health Research Premium Collection</collection><collection>Health Research Premium Collection (Alumni)</collection><collection>ProQuest Central Student</collection><collection>SciTech Premium Collection</collection><collection>ProQuest Health & Medical Complete (Alumni)</collection><collection>ProQuest Biological Science Collection</collection><collection>Health & Medical Collection (Alumni Edition)</collection><collection>Medical Database</collection><collection>Science Database</collection><collection>Algology Mycology and Protozoology Abstracts (Microbiology C)</collection><collection>Biological Science Database</collection><collection>Biotechnology and BioEngineering Abstracts</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 Basic</collection><collection>MEDLINE - Academic</collection><jtitle>Microbial drug resistance (Larchmont, N.Y.)</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Kim, Nak-Hyun</au><au>Kang, Yu Min</au><au>Han, Woong Dae</au><au>Park, Kyoung Un</au><au>Park, Kay-Hyun</au><au>Yoo, Jae Il</au><au>Lee, Dong-Gun</au><au>Park, Chulmin</au><au>Song, Kyoung-Ho</au><au>Kim, Eu Suk</au><au>Park, Sang Won</au><au>Kim, Nam Joong</au><au>Oh, Myoung-don</au><au>Kim, Hong Bin</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Small-Colony Variants in Persistent and Recurrent Staphylococcus aureus Bacteremia</atitle><jtitle>Microbial drug resistance (Larchmont, N.Y.)</jtitle><addtitle>Microb Drug Resist</addtitle><date>2016-10-01</date><risdate>2016</risdate><volume>22</volume><issue>7</issue><spage>538</spage><epage>544</epage><pages>538-544</pages><issn>1076-6294</issn><eissn>1931-8448</eissn><abstract>The small-colony variant (SCV) phenotype of
Staphylococcus aureus
is associated with intracellular persistence and reduced antimicrobial susceptibility, which can lead to therapeutic failure. Since SCVs grow slowly and have a confusing morphology, the identification of infections due to SCV is difficult. We have identified SCVs in two patients who presented with persistent methicillin-resistant
Staphylococcus aureus
(MRSA) bacteremia complicated by surgical site infections after cardiothoracic surgery. Nine blood isolates were collected from the two patients for species identification, antimicrobial susceptibility testing, and phenotypic and genotypic characterization. Colonies on Columbia blood agar were pinpoint, nonpigmented, nonhemolytic, and reverted to normal colonies after 48 hr of incubation on Schaedler agar. Auxotrophy assays revealed hemin dependence. Susceptibility to vancomycin (minimal inhibitory concentrations 1.0 μg/mL) was confirmed by
E
-test and broth microdilution test. All the isolates were identified as MRSA by multiplex polymerase chain reaction specific for the
mec
A,
fem
A, and 16S rRNA genes, and all had the same genotype: Multilocus sequence typing ST5, SCC
mec
type II,
agr
type II, and
spa
type t2460. Moreover pulsed-field gel electrophoresis typing revealed that all nine isolates belonged to the same clone. Mutations in the
relA
gene were not found, and none of the isolates was identified as hVISA by population analysis profiling-AUC ratio. A high level of suspicion is required to detect SCVs, and although it is not common, the possibility of the SCV phenotype has to be considered in persistent
S. aureus
bacteremia.</abstract><cop>United States</cop><pub>Mary Ann Liebert, Inc</pub><pmid>26982169</pmid><doi>10.1089/mdr.2015.0262</doi><tpages>7</tpages></addata></record> |
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subjects | Aged Anti-Bacterial Agents - pharmacology Bacteremia - drug therapy Bacteremia - microbiology Bacteremia - pathology Bacteria Bacterial Typing Techniques Blood Clone Cells Drug therapy Electrophoresis, Gel, Pulsed-Field Genes, Bacterial Genotype Genotype & phenotype Humans Male Mechanisms Methicillin-Resistant Staphylococcus aureus - classification Methicillin-Resistant Staphylococcus aureus - drug effects Methicillin-Resistant Staphylococcus aureus - genetics Methicillin-Resistant Staphylococcus aureus - isolation & purification Multilocus Sequence Typing Phenotype Recurrence Staphylococcal Infections - drug therapy Staphylococcal Infections - microbiology Staphylococcal Infections - pathology Staphylococcus aureus Staphylococcus infections Surgical Wound Infection - drug therapy Surgical Wound Infection - microbiology Surgical Wound Infection - pathology Vancomycin - pharmacology |
title | Small-Colony Variants in Persistent and Recurrent Staphylococcus aureus Bacteremia |
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