A molecular epidemiological investigation of methicillin-susceptible Staphylococcus aureus causing bloodstream infections in Ireland, 2006–2017
The prevalence of methicillin-susceptible Staphylococcus aureus (MSSA) bloodstream infections (BSIs) has increased in many countries, including Ireland. This study aimed to investigate the molecular epidemiology of MSSA causing BSIs in Irish hospitals between 2006 and 2017, when MSSA BSIs increased,...
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creator | Deasy, Emily C. Brennan, Gráinne I. Tecklenborg, Sarah C. Umeh, Chioma Coleman, David C. Shore, Anna C. |
description | The prevalence of methicillin-susceptible
Staphylococcus aureus
(MSSA) bloodstream infections (BSIs) has increased in many countries, including Ireland. This study aimed to investigate the molecular epidemiology of MSSA causing BSIs in Irish hospitals between 2006 and 2017, when MSSA BSIs increased, to identify any potential patient or pathogen contributing factors. A total of 252 MSSA isolates from patients in Irish hospitals in 2006/2007, 2011 and 2017 underwent
spa
typing and DNA microarray profiling. Each patient’s gender, age, 14-day mortality and epidemiological context of infection were recorded. Significant increases in community-onset (CO) MSSA BSIs and the average patient’s age and decreases in hospital-onset (HO) MSSA were identified. Although, extensive genetic diversity was detected amongst the isolates, i.e. 24 multilocus sequence type clonal complexes (CCs)/sequence types and 124
spa
types, three CCs (CC30, CC45, CC5) dominated, albeit in different proportions, during the study periods. CC30 declined significantly, in particular
spa
type t021, and was more common amongst HO-MSSA and CC45 and CC8 increased, particularly
spa
types t015 and t008, respectively, and were more common amongst CO-MSSA. Five of the seven most frequent
spa
types were more common amongst CO-MSSA. Although overall multidrug resistance decreased, the prevalence of
erm
(C) increased significantly and virulence genes decreased, mostly notably
egc
,
tst
,
scn
,
sep
and
fnbB
. This study highlights the threat posed by the increasing prevalence of CO-MSSA BSIs and suggests an association with the increasing prevalence of CC45 CO-MSSA, decreasing prevalence of CC30 HO-MSSA, an ageing population and an overall decrease in virulence and resistance genes. |
doi_str_mv | 10.1007/s10096-019-03523-0 |
format | Article |
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Staphylococcus aureus
(MSSA) bloodstream infections (BSIs) has increased in many countries, including Ireland. This study aimed to investigate the molecular epidemiology of MSSA causing BSIs in Irish hospitals between 2006 and 2017, when MSSA BSIs increased, to identify any potential patient or pathogen contributing factors. A total of 252 MSSA isolates from patients in Irish hospitals in 2006/2007, 2011 and 2017 underwent
spa
typing and DNA microarray profiling. Each patient’s gender, age, 14-day mortality and epidemiological context of infection were recorded. Significant increases in community-onset (CO) MSSA BSIs and the average patient’s age and decreases in hospital-onset (HO) MSSA were identified. Although, extensive genetic diversity was detected amongst the isolates, i.e. 24 multilocus sequence type clonal complexes (CCs)/sequence types and 124
spa
types, three CCs (CC30, CC45, CC5) dominated, albeit in different proportions, during the study periods. CC30 declined significantly, in particular
spa
type t021, and was more common amongst HO-MSSA and CC45 and CC8 increased, particularly
spa
types t015 and t008, respectively, and were more common amongst CO-MSSA. Five of the seven most frequent
spa
types were more common amongst CO-MSSA. Although overall multidrug resistance decreased, the prevalence of
erm
(C) increased significantly and virulence genes decreased, mostly notably
egc
,
tst
,
scn
,
sep
and
fnbB
. This study highlights the threat posed by the increasing prevalence of CO-MSSA BSIs and suggests an association with the increasing prevalence of CC45 CO-MSSA, decreasing prevalence of CC30 HO-MSSA, an ageing population and an overall decrease in virulence and resistance genes.</description><identifier>ISSN: 0934-9723</identifier><identifier>EISSN: 1435-4373</identifier><identifier>DOI: 10.1007/s10096-019-03523-0</identifier><identifier>PMID: 30904995</identifier><language>eng</language><publisher>Berlin/Heidelberg: Springer Berlin Heidelberg</publisher><subject>Aging ; Biomedical and Life Sciences ; Biomedicine ; Deoxyribonucleic acid ; DNA ; DNA chips ; DNA fingerprinting ; DNA microarrays ; Epidemiology ; Genes ; Genetic diversity ; Hospitals ; Internal Medicine ; Medical Microbiology ; Methicillin ; Multidrug resistance ; Multilocus sequence typing ; Original Article ; Staphylococcus aureus ; Virulence</subject><ispartof>European journal of clinical microbiology & infectious diseases, 2019-05, Vol.38 (5), p.927-936</ispartof><rights>Springer-Verlag GmbH Germany, part of Springer Nature 2019</rights><rights>European Journal of Clinical Microbiology & Infectious Diseases is a copyright of Springer, (2019). All Rights Reserved.</rights><lds50>peer_reviewed</lds50><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c375t-265bc29054ccfc6c2e040b4366914d60be93cfe7d9c6f52083ae8ebcfc0ac3ed3</citedby><cites>FETCH-LOGICAL-c375t-265bc29054ccfc6c2e040b4366914d60be93cfe7d9c6f52083ae8ebcfc0ac3ed3</cites><orcidid>0000-0002-6667-0918</orcidid></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><linktopdf>$$Uhttps://link.springer.com/content/pdf/10.1007/s10096-019-03523-0$$EPDF$$P50$$Gspringer$$H</linktopdf><linktohtml>$$Uhttps://link.springer.com/10.1007/s10096-019-03523-0$$EHTML$$P50$$Gspringer$$H</linktohtml><link.rule.ids>314,776,780,27901,27902,41464,42533,51294</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/30904995$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Deasy, Emily C.</creatorcontrib><creatorcontrib>Brennan, Gráinne I.</creatorcontrib><creatorcontrib>Tecklenborg, Sarah C.</creatorcontrib><creatorcontrib>Umeh, Chioma</creatorcontrib><creatorcontrib>Coleman, David C.</creatorcontrib><creatorcontrib>Shore, Anna C.</creatorcontrib><title>A molecular epidemiological investigation of methicillin-susceptible Staphylococcus aureus causing bloodstream infections in Ireland, 2006–2017</title><title>European journal of clinical microbiology & infectious diseases</title><addtitle>Eur J Clin Microbiol Infect Dis</addtitle><addtitle>Eur J Clin Microbiol Infect Dis</addtitle><description>The prevalence of methicillin-susceptible
Staphylococcus aureus
(MSSA) bloodstream infections (BSIs) has increased in many countries, including Ireland. This study aimed to investigate the molecular epidemiology of MSSA causing BSIs in Irish hospitals between 2006 and 2017, when MSSA BSIs increased, to identify any potential patient or pathogen contributing factors. A total of 252 MSSA isolates from patients in Irish hospitals in 2006/2007, 2011 and 2017 underwent
spa
typing and DNA microarray profiling. Each patient’s gender, age, 14-day mortality and epidemiological context of infection were recorded. Significant increases in community-onset (CO) MSSA BSIs and the average patient’s age and decreases in hospital-onset (HO) MSSA were identified. Although, extensive genetic diversity was detected amongst the isolates, i.e. 24 multilocus sequence type clonal complexes (CCs)/sequence types and 124
spa
types, three CCs (CC30, CC45, CC5) dominated, albeit in different proportions, during the study periods. CC30 declined significantly, in particular
spa
type t021, and was more common amongst HO-MSSA and CC45 and CC8 increased, particularly
spa
types t015 and t008, respectively, and were more common amongst CO-MSSA. Five of the seven most frequent
spa
types were more common amongst CO-MSSA. Although overall multidrug resistance decreased, the prevalence of
erm
(C) increased significantly and virulence genes decreased, mostly notably
egc
,
tst
,
scn
,
sep
and
fnbB
. This study highlights the threat posed by the increasing prevalence of CO-MSSA BSIs and suggests an association with the increasing prevalence of CC45 CO-MSSA, decreasing prevalence of CC30 HO-MSSA, an ageing population and an overall decrease in virulence and resistance genes.</description><subject>Aging</subject><subject>Biomedical and Life Sciences</subject><subject>Biomedicine</subject><subject>Deoxyribonucleic acid</subject><subject>DNA</subject><subject>DNA chips</subject><subject>DNA fingerprinting</subject><subject>DNA microarrays</subject><subject>Epidemiology</subject><subject>Genes</subject><subject>Genetic diversity</subject><subject>Hospitals</subject><subject>Internal Medicine</subject><subject>Medical Microbiology</subject><subject>Methicillin</subject><subject>Multidrug resistance</subject><subject>Multilocus sequence typing</subject><subject>Original Article</subject><subject>Staphylococcus aureus</subject><subject>Virulence</subject><issn>0934-9723</issn><issn>1435-4373</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2019</creationdate><recordtype>article</recordtype><sourceid>BENPR</sourceid><recordid>eNp9kctuFTEMhiNERQ8HXoAFisSmC6Y4ydyyrCoulSp1AaxHGY_nNFVmMiSTSt3xCqhvyJOQwykgdcHGtuTPv239jL0ScCoAmncxR10XIHQBqpKqgCdsI0pVFaVq1FO2Aa3KQjdSHbPnMd5AHmqb5hk7VqCh1LrasB9nfPKOMDkTOC12oMl653cWjeN2vqW42p1ZrZ-5H_lE67VF65ydi5gi0rLa3hH_vJrl-s559IgpcpMC5YQmRTvveO-8H-IayExZciTcy8Vc8otAzszDWy4B6p_f7yWI5gU7Go2L9PIhb9nXD--_nH8qLq8-XpyfXRaommotZF31KDVUJeKINUqCEvpS1bUW5VBDT1rhSM2gsR4rCa0y1FKfWTCoaFBbdnLQXYL_lvKf3WTzRy4fRD7FTgrdKNmqts3om0fojU9hztftqVqAUFpkSh4oDD7GQGO3BDuZcNcJ6PaGdQfDumxY99uwHLfs9YN06ica_o78cSgD6gDE3Jp3FP7t_o_sL9fgpFI</recordid><startdate>20190501</startdate><enddate>20190501</enddate><creator>Deasy, Emily C.</creator><creator>Brennan, Gráinne I.</creator><creator>Tecklenborg, Sarah C.</creator><creator>Umeh, Chioma</creator><creator>Coleman, David C.</creator><creator>Shore, Anna C.</creator><general>Springer Berlin Heidelberg</general><general>Springer Nature B.V</general><scope>NPM</scope><scope>AAYXX</scope><scope>CITATION</scope><scope>3V.</scope><scope>7QL</scope><scope>7U9</scope><scope>7X7</scope><scope>7XB</scope><scope>88A</scope><scope>88E</scope><scope>8AO</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>FYUFA</scope><scope>GHDGH</scope><scope>GNUQQ</scope><scope>H94</scope><scope>HCIFZ</scope><scope>K9.</scope><scope>LK8</scope><scope>M0S</scope><scope>M1P</scope><scope>M7N</scope><scope>M7P</scope><scope>PQEST</scope><scope>PQQKQ</scope><scope>PQUKI</scope><scope>7X8</scope><orcidid>https://orcid.org/0000-0002-6667-0918</orcidid></search><sort><creationdate>20190501</creationdate><title>A molecular epidemiological investigation of methicillin-susceptible Staphylococcus aureus causing bloodstream infections in Ireland, 2006–2017</title><author>Deasy, Emily C. ; Brennan, Gráinne I. ; Tecklenborg, Sarah C. ; Umeh, Chioma ; Coleman, David C. ; Shore, Anna C.</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c375t-265bc29054ccfc6c2e040b4366914d60be93cfe7d9c6f52083ae8ebcfc0ac3ed3</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2019</creationdate><topic>Aging</topic><topic>Biomedical and Life Sciences</topic><topic>Biomedicine</topic><topic>Deoxyribonucleic acid</topic><topic>DNA</topic><topic>DNA chips</topic><topic>DNA fingerprinting</topic><topic>DNA microarrays</topic><topic>Epidemiology</topic><topic>Genes</topic><topic>Genetic diversity</topic><topic>Hospitals</topic><topic>Internal Medicine</topic><topic>Medical Microbiology</topic><topic>Methicillin</topic><topic>Multidrug resistance</topic><topic>Multilocus sequence typing</topic><topic>Original Article</topic><topic>Staphylococcus aureus</topic><topic>Virulence</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Deasy, Emily C.</creatorcontrib><creatorcontrib>Brennan, Gráinne I.</creatorcontrib><creatorcontrib>Tecklenborg, Sarah C.</creatorcontrib><creatorcontrib>Umeh, Chioma</creatorcontrib><creatorcontrib>Coleman, David C.</creatorcontrib><creatorcontrib>Shore, Anna C.</creatorcontrib><collection>PubMed</collection><collection>CrossRef</collection><collection>ProQuest Central (Corporate)</collection><collection>Bacteriology Abstracts (Microbiology B)</collection><collection>Virology and AIDS 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>ProQuest Pharma Collection</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>Health Research Premium Collection</collection><collection>Health Research Premium Collection (Alumni)</collection><collection>ProQuest Central Student</collection><collection>AIDS and Cancer Research Abstracts</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>Algology Mycology and Protozoology Abstracts (Microbiology C)</collection><collection>Biological Science Database</collection><collection>ProQuest One Academic Eastern Edition (DO NOT USE)</collection><collection>ProQuest One Academic</collection><collection>ProQuest One Academic UKI Edition</collection><collection>MEDLINE - Academic</collection><jtitle>European journal of clinical microbiology & infectious diseases</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Deasy, Emily C.</au><au>Brennan, Gráinne I.</au><au>Tecklenborg, Sarah C.</au><au>Umeh, Chioma</au><au>Coleman, David C.</au><au>Shore, Anna C.</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>A molecular epidemiological investigation of methicillin-susceptible Staphylococcus aureus causing bloodstream infections in Ireland, 2006–2017</atitle><jtitle>European journal of clinical microbiology & infectious diseases</jtitle><stitle>Eur J Clin Microbiol Infect Dis</stitle><addtitle>Eur J Clin Microbiol Infect Dis</addtitle><date>2019-05-01</date><risdate>2019</risdate><volume>38</volume><issue>5</issue><spage>927</spage><epage>936</epage><pages>927-936</pages><issn>0934-9723</issn><eissn>1435-4373</eissn><abstract>The prevalence of methicillin-susceptible
Staphylococcus aureus
(MSSA) bloodstream infections (BSIs) has increased in many countries, including Ireland. This study aimed to investigate the molecular epidemiology of MSSA causing BSIs in Irish hospitals between 2006 and 2017, when MSSA BSIs increased, to identify any potential patient or pathogen contributing factors. A total of 252 MSSA isolates from patients in Irish hospitals in 2006/2007, 2011 and 2017 underwent
spa
typing and DNA microarray profiling. Each patient’s gender, age, 14-day mortality and epidemiological context of infection were recorded. Significant increases in community-onset (CO) MSSA BSIs and the average patient’s age and decreases in hospital-onset (HO) MSSA were identified. Although, extensive genetic diversity was detected amongst the isolates, i.e. 24 multilocus sequence type clonal complexes (CCs)/sequence types and 124
spa
types, three CCs (CC30, CC45, CC5) dominated, albeit in different proportions, during the study periods. CC30 declined significantly, in particular
spa
type t021, and was more common amongst HO-MSSA and CC45 and CC8 increased, particularly
spa
types t015 and t008, respectively, and were more common amongst CO-MSSA. Five of the seven most frequent
spa
types were more common amongst CO-MSSA. Although overall multidrug resistance decreased, the prevalence of
erm
(C) increased significantly and virulence genes decreased, mostly notably
egc
,
tst
,
scn
,
sep
and
fnbB
. This study highlights the threat posed by the increasing prevalence of CO-MSSA BSIs and suggests an association with the increasing prevalence of CC45 CO-MSSA, decreasing prevalence of CC30 HO-MSSA, an ageing population and an overall decrease in virulence and resistance genes.</abstract><cop>Berlin/Heidelberg</cop><pub>Springer Berlin Heidelberg</pub><pmid>30904995</pmid><doi>10.1007/s10096-019-03523-0</doi><tpages>10</tpages><orcidid>https://orcid.org/0000-0002-6667-0918</orcidid></addata></record> |
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subjects | Aging Biomedical and Life Sciences Biomedicine Deoxyribonucleic acid DNA DNA chips DNA fingerprinting DNA microarrays Epidemiology Genes Genetic diversity Hospitals Internal Medicine Medical Microbiology Methicillin Multidrug resistance Multilocus sequence typing Original Article Staphylococcus aureus Virulence |
title | A molecular epidemiological investigation of methicillin-susceptible Staphylococcus aureus causing bloodstream infections in Ireland, 2006–2017 |
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