Comparative Genotypes, Staphylococcal Cassette Chromosome mec
This study compares the characteristics of Staphylococcus epidermidis (SE) and Staphylococcus haemolyticus (SH) isolates from epidemiologically unrelated infections in humans (Hu) (28 SE-Hu; 8 SH-Hu) and companion animals (CpA) (12 SE-CpA; 13 SH-CpA). All isolates underwent antimicrobial susceptibil...
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description | This study compares the characteristics of Staphylococcus epidermidis (SE) and Staphylococcus haemolyticus (SH) isolates from epidemiologically unrelated infections in humans (Hu) (28 SE-Hu; 8 SH-Hu) and companion animals (CpA) (12 SE-CpA; 13 SH-CpA). All isolates underwent antimicrobial susceptibility testing, multilocus sequence typing and DNA microarray profiling to detect antimicrobial resistance and SCCmec-associated genes. All methicillin-resistant (MR) isolates (33/40 SE, 20/21 SH) underwent dru and mecA allele typing. Isolates were predominantly assigned to sequence types (STs) within a single clonal complex (CC2, SE, 84.8%; CC1, SH, 95.2%). SCCmec IV predominated among MRSE with ST2-MRSE-IVc common to both Hu (40.9%) and CpA (54.5%). Identical mecA alleles and nontypeable dru types (dts) were identified in one ST2-MRSE-IVc Hu and CpA isolate, however, all mecA alleles and 2/4 dts detected among 18 ST2-MRSE-IVc isolates were closely related, sharing >96.5% DNA sequence homology. Although only one ST-SCCmec type combination (ST1 with a non-typeable [NT] SCCmec NT9 [class C mec and ccrB4]) was common to four MRSH-Hu and one MRSH-CpA, all MRSH isolates were closely related based on similar STs, SCCmec genes (V/V.sub.T or components thereof), mecA alleles and dts. Overall, 39.6% of MR isolates harbored NT SCCmec elements, and ACME was more common amongst MRSE and CpA isolates. Multidrug resistance (MDR) was detected among 96.7% of isolates but they differed in the prevalence of specific macrolide, aminoglycoside and trimethoprim resistance genes amongst SE and SH isolates. Ciprofloxacin, rifampicin, chloramphenicol [fexA, cat-pC221], tetracycline [tet(K)], aminoglycosides [aadD, aphA3] and fusidic acid [fusB] resistance was significantly more common amongst CpA isolates. SE and SH isolates causing infections in Hu and CpA hosts belong predominantly to STs within a single lineage, harboring similar but variable SCCmec genes, mecA alleles and dts. Host and staphylococcal species-specific characteristics were identified in relation to antimicrobial resistance genes and phenotypes, SCCmec and ACME. |
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All isolates underwent antimicrobial susceptibility testing, multilocus sequence typing and DNA microarray profiling to detect antimicrobial resistance and SCCmec-associated genes. All methicillin-resistant (MR) isolates (33/40 SE, 20/21 SH) underwent dru and mecA allele typing. Isolates were predominantly assigned to sequence types (STs) within a single clonal complex (CC2, SE, 84.8%; CC1, SH, 95.2%). SCCmec IV predominated among MRSE with ST2-MRSE-IVc common to both Hu (40.9%) and CpA (54.5%). Identical mecA alleles and nontypeable dru types (dts) were identified in one ST2-MRSE-IVc Hu and CpA isolate, however, all mecA alleles and 2/4 dts detected among 18 ST2-MRSE-IVc isolates were closely related, sharing >96.5% DNA sequence homology. Although only one ST-SCCmec type combination (ST1 with a non-typeable [NT] SCCmec NT9 [class C mec and ccrB4]) was common to four MRSH-Hu and one MRSH-CpA, all MRSH isolates were closely related based on similar STs, SCCmec genes (V/V.sub.T or components thereof), mecA alleles and dts. Overall, 39.6% of MR isolates harbored NT SCCmec elements, and ACME was more common amongst MRSE and CpA isolates. Multidrug resistance (MDR) was detected among 96.7% of isolates but they differed in the prevalence of specific macrolide, aminoglycoside and trimethoprim resistance genes amongst SE and SH isolates. Ciprofloxacin, rifampicin, chloramphenicol [fexA, cat-pC221], tetracycline [tet(K)], aminoglycosides [aadD, aphA3] and fusidic acid [fusB] resistance was significantly more common amongst CpA isolates. SE and SH isolates causing infections in Hu and CpA hosts belong predominantly to STs within a single lineage, harboring similar but variable SCCmec genes, mecA alleles and dts. Host and staphylococcal species-specific characteristics were identified in relation to antimicrobial resistance genes and phenotypes, SCCmec and ACME.</description><identifier>ISSN: 1932-6203</identifier><identifier>EISSN: 1932-6203</identifier><identifier>DOI: 10.1371/journal.pone.0138079</identifier><language>eng</language><publisher>Public Library of Science</publisher><subject>Accountants ; Antibacterial agents ; DNA microarrays ; DNA sequencing ; Genes ; Genetic aspects ; Health aspects ; Infection ; Microbial drug resistance ; Staphylococcal infections</subject><ispartof>PloS one, 2015-09, Vol.10 (9), p.e0138079</ispartof><rights>COPYRIGHT 2015 Public Library of Science</rights><lds50>peer_reviewed</lds50><woscitedreferencessubscribed>false</woscitedreferencessubscribed></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><link.rule.ids>314,776,780,860,27901,27902</link.rule.ids></links><search><creatorcontrib>McManus, Brenda A</creatorcontrib><creatorcontrib>Coleman, David C</creatorcontrib><creatorcontrib>Deasy, Emily C</creatorcontrib><creatorcontrib>Brennan, Gráinne I</creatorcontrib><creatorcontrib>O' Connell, Brian</creatorcontrib><creatorcontrib>Monecke, Stefan</creatorcontrib><creatorcontrib>Ehricht, Ralf</creatorcontrib><creatorcontrib>Leggett, Bernadette</creatorcontrib><creatorcontrib>Leonard, Nola</creatorcontrib><creatorcontrib>Shore, Anna C</creatorcontrib><title>Comparative Genotypes, Staphylococcal Cassette Chromosome mec</title><title>PloS one</title><description>This study compares the characteristics of Staphylococcus epidermidis (SE) and Staphylococcus haemolyticus (SH) isolates from epidemiologically unrelated infections in humans (Hu) (28 SE-Hu; 8 SH-Hu) and companion animals (CpA) (12 SE-CpA; 13 SH-CpA). All isolates underwent antimicrobial susceptibility testing, multilocus sequence typing and DNA microarray profiling to detect antimicrobial resistance and SCCmec-associated genes. All methicillin-resistant (MR) isolates (33/40 SE, 20/21 SH) underwent dru and mecA allele typing. Isolates were predominantly assigned to sequence types (STs) within a single clonal complex (CC2, SE, 84.8%; CC1, SH, 95.2%). SCCmec IV predominated among MRSE with ST2-MRSE-IVc common to both Hu (40.9%) and CpA (54.5%). Identical mecA alleles and nontypeable dru types (dts) were identified in one ST2-MRSE-IVc Hu and CpA isolate, however, all mecA alleles and 2/4 dts detected among 18 ST2-MRSE-IVc isolates were closely related, sharing >96.5% DNA sequence homology. Although only one ST-SCCmec type combination (ST1 with a non-typeable [NT] SCCmec NT9 [class C mec and ccrB4]) was common to four MRSH-Hu and one MRSH-CpA, all MRSH isolates were closely related based on similar STs, SCCmec genes (V/V.sub.T or components thereof), mecA alleles and dts. Overall, 39.6% of MR isolates harbored NT SCCmec elements, and ACME was more common amongst MRSE and CpA isolates. Multidrug resistance (MDR) was detected among 96.7% of isolates but they differed in the prevalence of specific macrolide, aminoglycoside and trimethoprim resistance genes amongst SE and SH isolates. Ciprofloxacin, rifampicin, chloramphenicol [fexA, cat-pC221], tetracycline [tet(K)], aminoglycosides [aadD, aphA3] and fusidic acid [fusB] resistance was significantly more common amongst CpA isolates. SE and SH isolates causing infections in Hu and CpA hosts belong predominantly to STs within a single lineage, harboring similar but variable SCCmec genes, mecA alleles and dts. Host and staphylococcal species-specific characteristics were identified in relation to antimicrobial resistance genes and phenotypes, SCCmec and ACME.</description><subject>Accountants</subject><subject>Antibacterial agents</subject><subject>DNA microarrays</subject><subject>DNA sequencing</subject><subject>Genes</subject><subject>Genetic aspects</subject><subject>Health aspects</subject><subject>Infection</subject><subject>Microbial drug resistance</subject><subject>Staphylococcal infections</subject><issn>1932-6203</issn><issn>1932-6203</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2015</creationdate><recordtype>article</recordtype><recordid>eNqFzEFLwzAYxvEgCs7pN_DQkyDY-aZJk74HD6PoHAwGbngdaXzbbqRNWTJx396DHubJ0_M__HgYu-Uw4ULzx50_7HvjJoPvaQJcFKDxjI04iixVGYjzk75kVyHsAHJRKDViT6XvBrM3cftJyYx6H48DhYdkFc3QHp233lrjktKEQDFSUrZ73_ngO0o6stfsojYu0M3vjtn65XldvqaL5WxeThdpgwhpXimJmjjkBRaiQo6AQhrBNRouhVIojSasgANYVWEtPzCTwgotaw0SxJjd_9w2xtFm21vfR_qKjTmEsJmv3jZTmRWYa-T_2eX7X3t3YlsyLrbBu0Pc-j6cwm9qkWfo</recordid><startdate>20150917</startdate><enddate>20150917</enddate><creator>McManus, Brenda A</creator><creator>Coleman, David C</creator><creator>Deasy, Emily C</creator><creator>Brennan, Gráinne I</creator><creator>O' Connell, Brian</creator><creator>Monecke, Stefan</creator><creator>Ehricht, Ralf</creator><creator>Leggett, Bernadette</creator><creator>Leonard, Nola</creator><creator>Shore, Anna C</creator><general>Public Library of Science</general><scope>IOV</scope><scope>ISR</scope></search><sort><creationdate>20150917</creationdate><title>Comparative Genotypes, Staphylococcal Cassette Chromosome mec</title><author>McManus, Brenda A ; Coleman, David C ; Deasy, Emily C ; Brennan, Gráinne I ; O' Connell, Brian ; Monecke, Stefan ; Ehricht, Ralf ; Leggett, Bernadette ; Leonard, Nola ; Shore, Anna C</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-g990-5b6497e1058983b9190934a3179a1436694a7e9b0100c6b9f4d9243c374f70403</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2015</creationdate><topic>Accountants</topic><topic>Antibacterial agents</topic><topic>DNA microarrays</topic><topic>DNA sequencing</topic><topic>Genes</topic><topic>Genetic aspects</topic><topic>Health aspects</topic><topic>Infection</topic><topic>Microbial drug resistance</topic><topic>Staphylococcal infections</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>McManus, Brenda A</creatorcontrib><creatorcontrib>Coleman, David C</creatorcontrib><creatorcontrib>Deasy, Emily C</creatorcontrib><creatorcontrib>Brennan, Gráinne I</creatorcontrib><creatorcontrib>O' Connell, Brian</creatorcontrib><creatorcontrib>Monecke, Stefan</creatorcontrib><creatorcontrib>Ehricht, Ralf</creatorcontrib><creatorcontrib>Leggett, Bernadette</creatorcontrib><creatorcontrib>Leonard, Nola</creatorcontrib><creatorcontrib>Shore, Anna C</creatorcontrib><collection>Gale In Context: Opposing Viewpoints</collection><collection>Gale In Context: Science</collection><jtitle>PloS one</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>McManus, Brenda A</au><au>Coleman, David C</au><au>Deasy, Emily C</au><au>Brennan, Gráinne I</au><au>O' Connell, Brian</au><au>Monecke, Stefan</au><au>Ehricht, Ralf</au><au>Leggett, Bernadette</au><au>Leonard, Nola</au><au>Shore, Anna C</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Comparative Genotypes, Staphylococcal Cassette Chromosome mec</atitle><jtitle>PloS one</jtitle><date>2015-09-17</date><risdate>2015</risdate><volume>10</volume><issue>9</issue><spage>e0138079</spage><pages>e0138079-</pages><issn>1932-6203</issn><eissn>1932-6203</eissn><abstract>This study compares the characteristics of Staphylococcus epidermidis (SE) and Staphylococcus haemolyticus (SH) isolates from epidemiologically unrelated infections in humans (Hu) (28 SE-Hu; 8 SH-Hu) and companion animals (CpA) (12 SE-CpA; 13 SH-CpA). All isolates underwent antimicrobial susceptibility testing, multilocus sequence typing and DNA microarray profiling to detect antimicrobial resistance and SCCmec-associated genes. All methicillin-resistant (MR) isolates (33/40 SE, 20/21 SH) underwent dru and mecA allele typing. Isolates were predominantly assigned to sequence types (STs) within a single clonal complex (CC2, SE, 84.8%; CC1, SH, 95.2%). SCCmec IV predominated among MRSE with ST2-MRSE-IVc common to both Hu (40.9%) and CpA (54.5%). Identical mecA alleles and nontypeable dru types (dts) were identified in one ST2-MRSE-IVc Hu and CpA isolate, however, all mecA alleles and 2/4 dts detected among 18 ST2-MRSE-IVc isolates were closely related, sharing >96.5% DNA sequence homology. Although only one ST-SCCmec type combination (ST1 with a non-typeable [NT] SCCmec NT9 [class C mec and ccrB4]) was common to four MRSH-Hu and one MRSH-CpA, all MRSH isolates were closely related based on similar STs, SCCmec genes (V/V.sub.T or components thereof), mecA alleles and dts. Overall, 39.6% of MR isolates harbored NT SCCmec elements, and ACME was more common amongst MRSE and CpA isolates. Multidrug resistance (MDR) was detected among 96.7% of isolates but they differed in the prevalence of specific macrolide, aminoglycoside and trimethoprim resistance genes amongst SE and SH isolates. Ciprofloxacin, rifampicin, chloramphenicol [fexA, cat-pC221], tetracycline [tet(K)], aminoglycosides [aadD, aphA3] and fusidic acid [fusB] resistance was significantly more common amongst CpA isolates. SE and SH isolates causing infections in Hu and CpA hosts belong predominantly to STs within a single lineage, harboring similar but variable SCCmec genes, mecA alleles and dts. Host and staphylococcal species-specific characteristics were identified in relation to antimicrobial resistance genes and phenotypes, SCCmec and ACME.</abstract><pub>Public Library of Science</pub><doi>10.1371/journal.pone.0138079</doi><tpages>e0138079</tpages></addata></record> |
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subjects | Accountants Antibacterial agents DNA microarrays DNA sequencing Genes Genetic aspects Health aspects Infection Microbial drug resistance Staphylococcal infections |
title | Comparative Genotypes, Staphylococcal Cassette Chromosome mec |
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