Genomic Heterogeneity of Methicillin Resistant Staphylococcus aureus Associated with Variation in Severity of Illness among Children with Acute Hematogenous Osteomyelitis
The association between severity of illness of children with osteomyelitis caused by Methicillin-resistant Staphylococcus aureus (MRSA) and genomic variation of the causative organism has not been previously investigated. The purpose of this study is to assess genomic heterogeneity among MRSA isolat...
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description | The association between severity of illness of children with osteomyelitis caused by Methicillin-resistant Staphylococcus aureus (MRSA) and genomic variation of the causative organism has not been previously investigated. The purpose of this study is to assess genomic heterogeneity among MRSA isolates from children with osteomyelitis who have diverse severity of illness.
Children with osteomyelitis were prospectively studied between 2010 and 2011. Severity of illness of the affected children was determined from clinical and laboratory parameters. MRSA isolates were analyzed with next generation sequencing (NGS) and optical mapping. Sequence data was used for multi-locus sequence typing (MLST), phylogenetic analysis by maximum likelihood (PAML), and identification of virulence genes and single nucleotide polymorphisms (SNP) relative to reference strains.
The twelve children studied demonstrated severity of illness scores ranging from 0 (mild) to 9 (severe). All isolates were USA300, ST 8, SCC mec IVa MRSA by MLST. The isolates differed from reference strains by 2 insertions (40 Kb each) and 2 deletions (10 and 25 Kb) but had no rearrangements or copy number variations. There was a higher occurrence of virulence genes among study isolates when compared to the reference strains (p = 0.0124). There were an average of 11 nonsynonymous SNPs per strain. PAML demonstrated heterogeneity of study isolates from each other and from the reference strains.
Genomic heterogeneity exists among MRSA isolates causing osteomyelitis among children in a single community. These variations may play a role in the pathogenesis of variation in clinical severity among these children. |
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Children with osteomyelitis were prospectively studied between 2010 and 2011. Severity of illness of the affected children was determined from clinical and laboratory parameters. MRSA isolates were analyzed with next generation sequencing (NGS) and optical mapping. Sequence data was used for multi-locus sequence typing (MLST), phylogenetic analysis by maximum likelihood (PAML), and identification of virulence genes and single nucleotide polymorphisms (SNP) relative to reference strains.
The twelve children studied demonstrated severity of illness scores ranging from 0 (mild) to 9 (severe). All isolates were USA300, ST 8, SCC mec IVa MRSA by MLST. The isolates differed from reference strains by 2 insertions (40 Kb each) and 2 deletions (10 and 25 Kb) but had no rearrangements or copy number variations. There was a higher occurrence of virulence genes among study isolates when compared to the reference strains (p = 0.0124). There were an average of 11 nonsynonymous SNPs per strain. PAML demonstrated heterogeneity of study isolates from each other and from the reference strains.
Genomic heterogeneity exists among MRSA isolates causing osteomyelitis among children in a single community. These variations may play a role in the pathogenesis of variation in clinical severity among these children.</description><identifier>ISSN: 1932-6203</identifier><identifier>EISSN: 1932-6203</identifier><identifier>DOI: 10.1371/journal.pone.0130415</identifier><identifier>PMID: 26086671</identifier><language>eng</language><publisher>United States: Public Library of Science</publisher><subject>Acute Disease ; Adolescent ; Analysis ; Biocompatibility ; Child ; Child, Preschool ; Children ; Chromosomes ; Cladistic analysis ; Copy number ; Demography ; Drug resistance ; Gene expression ; Gene mapping ; Genes ; Genetic Heterogeneity ; Genomes ; Genomics ; Heterogeneity ; High-Throughput Nucleotide Sequencing ; Hospitals ; Humans ; Illnesses ; Immunology ; Infant ; Laboratories ; Methicillin ; Methicillin-Resistant Staphylococcus aureus - classification ; Methicillin-Resistant Staphylococcus aureus - genetics ; Methicillin-Resistant Staphylococcus aureus - isolation & purification ; Microbial drug resistance ; Multilocus Sequence Typing ; Osteomyelitis ; Osteomyelitis - metabolism ; Osteomyelitis - microbiology ; Osteomyelitis - pathology ; Pathogenesis ; Pathogens ; Pediatric diseases ; Pediatrics ; Phylogeny ; Polymorphism, Single Nucleotide ; Prospective Studies ; Sequence Analysis, DNA ; Severity of Illness Index ; Single nucleotide polymorphisms ; Single-nucleotide polymorphism ; Staphylococcal Infections - metabolism ; Staphylococcal Infections - microbiology ; Staphylococcal Infections - pathology ; Staphylococcus aureus ; Staphylococcus infections ; Strains (organisms) ; Surgery ; Thrombosis ; Variation ; Virulence ; Virulence (Microbiology) ; Virulence - genetics</subject><ispartof>PloS one, 2015-06, Vol.10 (6), p.e0130415-e0130415</ispartof><rights>COPYRIGHT 2015 Public Library of Science</rights><rights>2015 Gaviria-Agudelo et al. This is an open access article distributed under the terms of the Creative Commons Attribution License: http://creativecommons.org/licenses/by/4.0/ (the “License”), which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are credited Notwithstanding the ProQuest Terms and Conditions, you may use this content in accordance with the terms of the License.</rights><rights>2015 Gaviria-Agudelo et al 2015 Gaviria-Agudelo et al</rights><lds50>peer_reviewed</lds50><oa>free_for_read</oa><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c692t-e8210973b668dd61d36f133d55c5c763cab5fbf3160fba9b330ddf35247405783</citedby><cites>FETCH-LOGICAL-c692t-e8210973b668dd61d36f133d55c5c763cab5fbf3160fba9b330ddf35247405783</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/PMC4473274/pdf/$$EPDF$$P50$$Gpubmedcentral$$Hfree_for_read</linktopdf><linktohtml>$$Uhttps://www.ncbi.nlm.nih.gov/pmc/articles/PMC4473274/$$EHTML$$P50$$Gpubmedcentral$$Hfree_for_read</linktohtml><link.rule.ids>230,314,727,780,784,864,885,2100,2926,23865,27923,27924,53790,53792,79371,79372</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/26086671$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><contributor>Becker, Karsten</contributor><creatorcontrib>Gaviria-Agudelo, Claudia</creatorcontrib><creatorcontrib>Aroh, Chukwuemika</creatorcontrib><creatorcontrib>Tareen, Naureen</creatorcontrib><creatorcontrib>Wakeland, Edward K</creatorcontrib><creatorcontrib>Kim, MinSoo</creatorcontrib><creatorcontrib>Copley, Lawson A</creatorcontrib><title>Genomic Heterogeneity of Methicillin Resistant Staphylococcus aureus Associated with Variation in Severity of Illness among Children with Acute Hematogenous Osteomyelitis</title><title>PloS one</title><addtitle>PLoS One</addtitle><description>The association between severity of illness of children with osteomyelitis caused by Methicillin-resistant Staphylococcus aureus (MRSA) and genomic variation of the causative organism has not been previously investigated. The purpose of this study is to assess genomic heterogeneity among MRSA isolates from children with osteomyelitis who have diverse severity of illness.
Children with osteomyelitis were prospectively studied between 2010 and 2011. Severity of illness of the affected children was determined from clinical and laboratory parameters. MRSA isolates were analyzed with next generation sequencing (NGS) and optical mapping. Sequence data was used for multi-locus sequence typing (MLST), phylogenetic analysis by maximum likelihood (PAML), and identification of virulence genes and single nucleotide polymorphisms (SNP) relative to reference strains.
The twelve children studied demonstrated severity of illness scores ranging from 0 (mild) to 9 (severe). All isolates were USA300, ST 8, SCC mec IVa MRSA by MLST. The isolates differed from reference strains by 2 insertions (40 Kb each) and 2 deletions (10 and 25 Kb) but had no rearrangements or copy number variations. There was a higher occurrence of virulence genes among study isolates when compared to the reference strains (p = 0.0124). There were an average of 11 nonsynonymous SNPs per strain. PAML demonstrated heterogeneity of study isolates from each other and from the reference strains.
Genomic heterogeneity exists among MRSA isolates causing osteomyelitis among children in a single community. These variations may play a role in the pathogenesis of variation in clinical severity among these children.</description><subject>Acute Disease</subject><subject>Adolescent</subject><subject>Analysis</subject><subject>Biocompatibility</subject><subject>Child</subject><subject>Child, Preschool</subject><subject>Children</subject><subject>Chromosomes</subject><subject>Cladistic analysis</subject><subject>Copy number</subject><subject>Demography</subject><subject>Drug resistance</subject><subject>Gene expression</subject><subject>Gene mapping</subject><subject>Genes</subject><subject>Genetic Heterogeneity</subject><subject>Genomes</subject><subject>Genomics</subject><subject>Heterogeneity</subject><subject>High-Throughput Nucleotide Sequencing</subject><subject>Hospitals</subject><subject>Humans</subject><subject>Illnesses</subject><subject>Immunology</subject><subject>Infant</subject><subject>Laboratories</subject><subject>Methicillin</subject><subject>Methicillin-Resistant Staphylococcus aureus - classification</subject><subject>Methicillin-Resistant Staphylococcus aureus - genetics</subject><subject>Methicillin-Resistant Staphylococcus aureus - isolation & purification</subject><subject>Microbial drug resistance</subject><subject>Multilocus Sequence Typing</subject><subject>Osteomyelitis</subject><subject>Osteomyelitis - metabolism</subject><subject>Osteomyelitis - microbiology</subject><subject>Osteomyelitis - pathology</subject><subject>Pathogenesis</subject><subject>Pathogens</subject><subject>Pediatric diseases</subject><subject>Pediatrics</subject><subject>Phylogeny</subject><subject>Polymorphism, Single Nucleotide</subject><subject>Prospective Studies</subject><subject>Sequence Analysis, DNA</subject><subject>Severity of Illness Index</subject><subject>Single nucleotide polymorphisms</subject><subject>Single-nucleotide polymorphism</subject><subject>Staphylococcal Infections - metabolism</subject><subject>Staphylococcal Infections - microbiology</subject><subject>Staphylococcal Infections - 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Academic</collection><collection>PubMed Central (Full Participant titles)</collection><collection>DOAJ Directory of Open Access Journals</collection><jtitle>PloS one</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Gaviria-Agudelo, Claudia</au><au>Aroh, Chukwuemika</au><au>Tareen, Naureen</au><au>Wakeland, Edward K</au><au>Kim, MinSoo</au><au>Copley, Lawson A</au><au>Becker, Karsten</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Genomic Heterogeneity of Methicillin Resistant Staphylococcus aureus Associated with Variation in Severity of Illness among Children with Acute Hematogenous Osteomyelitis</atitle><jtitle>PloS one</jtitle><addtitle>PLoS One</addtitle><date>2015-06-18</date><risdate>2015</risdate><volume>10</volume><issue>6</issue><spage>e0130415</spage><epage>e0130415</epage><pages>e0130415-e0130415</pages><issn>1932-6203</issn><eissn>1932-6203</eissn><abstract>The association between severity of illness of children with osteomyelitis caused by Methicillin-resistant Staphylococcus aureus (MRSA) and genomic variation of the causative organism has not been previously investigated. The purpose of this study is to assess genomic heterogeneity among MRSA isolates from children with osteomyelitis who have diverse severity of illness.
Children with osteomyelitis were prospectively studied between 2010 and 2011. Severity of illness of the affected children was determined from clinical and laboratory parameters. MRSA isolates were analyzed with next generation sequencing (NGS) and optical mapping. Sequence data was used for multi-locus sequence typing (MLST), phylogenetic analysis by maximum likelihood (PAML), and identification of virulence genes and single nucleotide polymorphisms (SNP) relative to reference strains.
The twelve children studied demonstrated severity of illness scores ranging from 0 (mild) to 9 (severe). All isolates were USA300, ST 8, SCC mec IVa MRSA by MLST. The isolates differed from reference strains by 2 insertions (40 Kb each) and 2 deletions (10 and 25 Kb) but had no rearrangements or copy number variations. There was a higher occurrence of virulence genes among study isolates when compared to the reference strains (p = 0.0124). There were an average of 11 nonsynonymous SNPs per strain. PAML demonstrated heterogeneity of study isolates from each other and from the reference strains.
Genomic heterogeneity exists among MRSA isolates causing osteomyelitis among children in a single community. These variations may play a role in the pathogenesis of variation in clinical severity among these children.</abstract><cop>United States</cop><pub>Public Library of Science</pub><pmid>26086671</pmid><doi>10.1371/journal.pone.0130415</doi><oa>free_for_read</oa></addata></record> |
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recordid | cdi_plos_journals_1689846048 |
source | MEDLINE; DOAJ Directory of Open Access Journals; Public Library of Science (PLoS); EZB-FREE-00999 freely available EZB journals; PubMed Central; Free Full-Text Journals in Chemistry |
subjects | Acute Disease Adolescent Analysis Biocompatibility Child Child, Preschool Children Chromosomes Cladistic analysis Copy number Demography Drug resistance Gene expression Gene mapping Genes Genetic Heterogeneity Genomes Genomics Heterogeneity High-Throughput Nucleotide Sequencing Hospitals Humans Illnesses Immunology Infant Laboratories Methicillin Methicillin-Resistant Staphylococcus aureus - classification Methicillin-Resistant Staphylococcus aureus - genetics Methicillin-Resistant Staphylococcus aureus - isolation & purification Microbial drug resistance Multilocus Sequence Typing Osteomyelitis Osteomyelitis - metabolism Osteomyelitis - microbiology Osteomyelitis - pathology Pathogenesis Pathogens Pediatric diseases Pediatrics Phylogeny Polymorphism, Single Nucleotide Prospective Studies Sequence Analysis, DNA Severity of Illness Index Single nucleotide polymorphisms Single-nucleotide polymorphism Staphylococcal Infections - metabolism Staphylococcal Infections - microbiology Staphylococcal Infections - pathology Staphylococcus aureus Staphylococcus infections Strains (organisms) Surgery Thrombosis Variation Virulence Virulence (Microbiology) Virulence - genetics |
title | Genomic Heterogeneity of Methicillin Resistant Staphylococcus aureus Associated with Variation in Severity of Illness among Children with Acute Hematogenous Osteomyelitis |
url | https://sfx.bib-bvb.de/sfx_tum?ctx_ver=Z39.88-2004&ctx_enc=info:ofi/enc:UTF-8&ctx_tim=2025-01-12T01%3A58%3A50IST&url_ver=Z39.88-2004&url_ctx_fmt=infofi/fmt:kev:mtx:ctx&rfr_id=info:sid/primo.exlibrisgroup.com:primo3-Article-gale_plos_&rft_val_fmt=info:ofi/fmt:kev:mtx:journal&rft.genre=article&rft.atitle=Genomic%20Heterogeneity%20of%20Methicillin%20Resistant%20Staphylococcus%20aureus%20Associated%20with%20Variation%20in%20Severity%20of%20Illness%20among%20Children%20with%20Acute%20Hematogenous%20Osteomyelitis&rft.jtitle=PloS%20one&rft.au=Gaviria-Agudelo,%20Claudia&rft.date=2015-06-18&rft.volume=10&rft.issue=6&rft.spage=e0130415&rft.epage=e0130415&rft.pages=e0130415-e0130415&rft.issn=1932-6203&rft.eissn=1932-6203&rft_id=info:doi/10.1371/journal.pone.0130415&rft_dat=%3Cgale_plos_%3EA418420410%3C/gale_plos_%3E%3Curl%3E%3C/url%3E&disable_directlink=true&sfx.directlink=off&sfx.report_link=0&rft_id=info:oai/&rft_pqid=1689846048&rft_id=info:pmid/26086671&rft_galeid=A418420410&rft_doaj_id=oai_doaj_org_article_e6187973f92442c3970ab0ffe6e581da&rfr_iscdi=true |