Emergent US adenovirus 3 strains associated with an epidemic and serious disease

Abstract Background Adenovirus type 3 (HAdV3) is one of the most prevalent serotypes detected globally. Variants of HAdV3 have been associated with outbreaks of severe disease. Objectives To better understand genetic diversity of circulating HAdV3s and examine risk factors for severe disease. Study...

Ausführliche Beschreibung

Gespeichert in:
Bibliographische Detailangaben
Veröffentlicht in:Journal of clinical virology 2009-12, Vol.46 (4), p.331-336
Hauptverfasser: Lebeck, Mark G, McCarthy, Troy A, Capuano, Ana W, Schnurr, David P, Landry, Marie L, Setterquist, Sharon F, Heil, Gary L, Kilic, Selim, Gray, Gregory C
Format: Artikel
Sprache:eng
Schlagworte:
Online-Zugang:Volltext
Tags: Tag hinzufügen
Keine Tags, Fügen Sie den ersten Tag hinzu!
container_end_page 336
container_issue 4
container_start_page 331
container_title Journal of clinical virology
container_volume 46
creator Lebeck, Mark G
McCarthy, Troy A
Capuano, Ana W
Schnurr, David P
Landry, Marie L
Setterquist, Sharon F
Heil, Gary L
Kilic, Selim
Gray, Gregory C
description Abstract Background Adenovirus type 3 (HAdV3) is one of the most prevalent serotypes detected globally. Variants of HAdV3 have been associated with outbreaks of severe disease. Objectives To better understand genetic diversity of circulating HAdV3s and examine risk factors for severe disease. Study design Restriction enzyme analysis for genomic characterization of clinical HAdV3 isolates detected by 15 collaborative US laboratories during the period July 2004 to May 2007. Multivariate modeling was employed for statistical analyses. Results The most common HAdV3 types of 516 isolates studied were HAdV3a2 (36.9%), HAdV3a50 (27.1%), HAdV3a51 (18.0%), and HAdV3a17 (4.6%). Non-HAdV3a genome types were rare (1.2%). HAdV3a50 and HAdV3a51 are newly described variants which became more prevalent in 2006 and 2007 and have been associated with at least one epidemic. Their uniqueness was determined by specific banding profiles generated by digests with endonucleases BclI, BglII, and HindIII. Multivariable risk factor modeling demonstrated that children under 2 years of age (OR = 2.7; 95%CI 1.6–4.6), persons with chronic disease (OR = 5.1; 95%CI 2.6–9.8), persons infected with HAdV3a2 (OR = 3.0; 95%CI 1.5–6.0), with HAdV3a50 (OR = 2.5; 95%CI 1.2–5.2), or with multiple or rare strains (OR = 2.8; 95%CI 1.3–6.5) were at increased risk of severe HAdV3 clinical disease. Conclusions In the study period considerable genetic diversity was found among US clinical HAdV3 strains. Novel variants emerged and became prevalent. One such emergent strain may be associated with more severe clinical disease.
doi_str_mv 10.1016/j.jcv.2009.09.023
format Article
fullrecord <record><control><sourceid>proquest_pubme</sourceid><recordid>TN_cdi_pubmedcentral_primary_oai_pubmedcentral_nih_gov_2806089</recordid><sourceformat>XML</sourceformat><sourcesystem>PC</sourcesystem><els_id>1_s2_0_S1386653209004612</els_id><sourcerecordid>21208465</sourcerecordid><originalsourceid>FETCH-LOGICAL-c566t-af3212821573039d556ec68da4c211f85bd1b37f48d8e5af113d7df2a120b523</originalsourceid><addsrcrecordid>eNp9Uttq3DAQFaWlSbf9gL4UvbR98lYXS5YpBEpILxBoIemz0ErjRK4tbzXeLfn7yuySXh4CAxrQmTMz5wwhLzlbc8b1u37d-_1aMNaulxDyETnlppGVanXzuOTS6EorKU7IM8SeMa5k3TwlJ7w1qi4Up-TbxQj5BtJMv19RFyBN-5h3SCXFObuYkDrEyUc3Q6C_4nxLXaKwjQHG6EseKEKOU6kIEcEhPCdPOjcgvDi-K3L98eL6_HN1-fXTl_MPl5VXWs-V66TgwgiuGslkG5TS4LUJrvaC886oTeAb2XS1CQaU6ziXoQmdcFywjRJyRc4OtNvdZoTgywbZDXab4-jynZ1ctP_-pHhrb6a9FYZpZtpC8PZIkKefO8DZjhE9DINLUNaxjay5ZEWmgnzzILLswUxdZF4RfgD6PCFm6O7H4cwuhtneFsPsYphdQshS8-rvPf5UHB0qgNdHgEPvhi675CPe40RRUOp6af7-gIMi-j5CtugjJA8hZvCzDVN8cIyz_6r9EFMsDX_AHWA_7XIqblpuUVhmr5bLWg6LtYzVmgv5Gw5pyHA</addsrcrecordid><sourcetype>Open Access Repository</sourcetype><iscdi>true</iscdi><recordtype>article</recordtype><pqid>21208465</pqid></control><display><type>article</type><title>Emergent US adenovirus 3 strains associated with an epidemic and serious disease</title><source>MEDLINE</source><source>Elsevier ScienceDirect Journals</source><creator>Lebeck, Mark G ; McCarthy, Troy A ; Capuano, Ana W ; Schnurr, David P ; Landry, Marie L ; Setterquist, Sharon F ; Heil, Gary L ; Kilic, Selim ; Gray, Gregory C</creator><creatorcontrib>Lebeck, Mark G ; McCarthy, Troy A ; Capuano, Ana W ; Schnurr, David P ; Landry, Marie L ; Setterquist, Sharon F ; Heil, Gary L ; Kilic, Selim ; Gray, Gregory C</creatorcontrib><description>Abstract Background Adenovirus type 3 (HAdV3) is one of the most prevalent serotypes detected globally. Variants of HAdV3 have been associated with outbreaks of severe disease. Objectives To better understand genetic diversity of circulating HAdV3s and examine risk factors for severe disease. Study design Restriction enzyme analysis for genomic characterization of clinical HAdV3 isolates detected by 15 collaborative US laboratories during the period July 2004 to May 2007. Multivariate modeling was employed for statistical analyses. Results The most common HAdV3 types of 516 isolates studied were HAdV3a2 (36.9%), HAdV3a50 (27.1%), HAdV3a51 (18.0%), and HAdV3a17 (4.6%). Non-HAdV3a genome types were rare (1.2%). HAdV3a50 and HAdV3a51 are newly described variants which became more prevalent in 2006 and 2007 and have been associated with at least one epidemic. Their uniqueness was determined by specific banding profiles generated by digests with endonucleases BclI, BglII, and HindIII. Multivariable risk factor modeling demonstrated that children under 2 years of age (OR = 2.7; 95%CI 1.6–4.6), persons with chronic disease (OR = 5.1; 95%CI 2.6–9.8), persons infected with HAdV3a2 (OR = 3.0; 95%CI 1.5–6.0), with HAdV3a50 (OR = 2.5; 95%CI 1.2–5.2), or with multiple or rare strains (OR = 2.8; 95%CI 1.3–6.5) were at increased risk of severe HAdV3 clinical disease. Conclusions In the study period considerable genetic diversity was found among US clinical HAdV3 strains. Novel variants emerged and became prevalent. One such emergent strain may be associated with more severe clinical disease.</description><identifier>ISSN: 1386-6532</identifier><identifier>EISSN: 1873-5967</identifier><identifier>DOI: 10.1016/j.jcv.2009.09.023</identifier><identifier>PMID: 19854101</identifier><language>eng</language><publisher>Amsterdam: Elsevier B.V</publisher><subject>Adenoviridae ; Adenovirus ; Adenovirus Infections, Human - epidemiology ; Adenovirus Infections, Human - virology ; Adenoviruses, Human - genetics ; Adenoviruses, Human - physiology ; Allergy and Immunology ; Biological and medical sciences ; Child ; Child, Preschool ; Epidemiology ; Female ; Fundamental and applied biological sciences. Psychology ; Genome, Viral - genetics ; Genome, Viral - physiology ; Human viral diseases ; Humans ; Infant ; Infant, Newborn ; Infectious Disease ; Infectious diseases ; Male ; Medical sciences ; Microbiology ; Miscellaneous ; Molecular ; Multivariate Analysis ; Restriction mapping ; Risk Factors ; United States - epidemiology ; Viral diseases ; Virology</subject><ispartof>Journal of clinical virology, 2009-12, Vol.46 (4), p.331-336</ispartof><rights>Elsevier B.V.</rights><rights>2009 Elsevier B.V.</rights><rights>2015 INIST-CNRS</rights><lds50>peer_reviewed</lds50><oa>free_for_read</oa><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c566t-af3212821573039d556ec68da4c211f85bd1b37f48d8e5af113d7df2a120b523</citedby><cites>FETCH-LOGICAL-c566t-af3212821573039d556ec68da4c211f85bd1b37f48d8e5af113d7df2a120b523</cites></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><linktohtml>$$Uhttps://www.sciencedirect.com/science/article/pii/S1386653209004612$$EHTML$$P50$$Gelsevier$$H</linktohtml><link.rule.ids>230,314,776,780,881,3537,27901,27902,65306</link.rule.ids><backlink>$$Uhttp://pascal-francis.inist.fr/vibad/index.php?action=getRecordDetail&amp;idt=22153645$$DView record in Pascal Francis$$Hfree_for_read</backlink><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/19854101$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Lebeck, Mark G</creatorcontrib><creatorcontrib>McCarthy, Troy A</creatorcontrib><creatorcontrib>Capuano, Ana W</creatorcontrib><creatorcontrib>Schnurr, David P</creatorcontrib><creatorcontrib>Landry, Marie L</creatorcontrib><creatorcontrib>Setterquist, Sharon F</creatorcontrib><creatorcontrib>Heil, Gary L</creatorcontrib><creatorcontrib>Kilic, Selim</creatorcontrib><creatorcontrib>Gray, Gregory C</creatorcontrib><title>Emergent US adenovirus 3 strains associated with an epidemic and serious disease</title><title>Journal of clinical virology</title><addtitle>J Clin Virol</addtitle><description>Abstract Background Adenovirus type 3 (HAdV3) is one of the most prevalent serotypes detected globally. Variants of HAdV3 have been associated with outbreaks of severe disease. Objectives To better understand genetic diversity of circulating HAdV3s and examine risk factors for severe disease. Study design Restriction enzyme analysis for genomic characterization of clinical HAdV3 isolates detected by 15 collaborative US laboratories during the period July 2004 to May 2007. Multivariate modeling was employed for statistical analyses. Results The most common HAdV3 types of 516 isolates studied were HAdV3a2 (36.9%), HAdV3a50 (27.1%), HAdV3a51 (18.0%), and HAdV3a17 (4.6%). Non-HAdV3a genome types were rare (1.2%). HAdV3a50 and HAdV3a51 are newly described variants which became more prevalent in 2006 and 2007 and have been associated with at least one epidemic. Their uniqueness was determined by specific banding profiles generated by digests with endonucleases BclI, BglII, and HindIII. Multivariable risk factor modeling demonstrated that children under 2 years of age (OR = 2.7; 95%CI 1.6–4.6), persons with chronic disease (OR = 5.1; 95%CI 2.6–9.8), persons infected with HAdV3a2 (OR = 3.0; 95%CI 1.5–6.0), with HAdV3a50 (OR = 2.5; 95%CI 1.2–5.2), or with multiple or rare strains (OR = 2.8; 95%CI 1.3–6.5) were at increased risk of severe HAdV3 clinical disease. Conclusions In the study period considerable genetic diversity was found among US clinical HAdV3 strains. Novel variants emerged and became prevalent. One such emergent strain may be associated with more severe clinical disease.</description><subject>Adenoviridae</subject><subject>Adenovirus</subject><subject>Adenovirus Infections, Human - epidemiology</subject><subject>Adenovirus Infections, Human - virology</subject><subject>Adenoviruses, Human - genetics</subject><subject>Adenoviruses, Human - physiology</subject><subject>Allergy and Immunology</subject><subject>Biological and medical sciences</subject><subject>Child</subject><subject>Child, Preschool</subject><subject>Epidemiology</subject><subject>Female</subject><subject>Fundamental and applied biological sciences. Psychology</subject><subject>Genome, Viral - genetics</subject><subject>Genome, Viral - physiology</subject><subject>Human viral diseases</subject><subject>Humans</subject><subject>Infant</subject><subject>Infant, Newborn</subject><subject>Infectious Disease</subject><subject>Infectious diseases</subject><subject>Male</subject><subject>Medical sciences</subject><subject>Microbiology</subject><subject>Miscellaneous</subject><subject>Molecular</subject><subject>Multivariate Analysis</subject><subject>Restriction mapping</subject><subject>Risk Factors</subject><subject>United States - epidemiology</subject><subject>Viral diseases</subject><subject>Virology</subject><issn>1386-6532</issn><issn>1873-5967</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2009</creationdate><recordtype>article</recordtype><sourceid>EIF</sourceid><recordid>eNp9Uttq3DAQFaWlSbf9gL4UvbR98lYXS5YpBEpILxBoIemz0ErjRK4tbzXeLfn7yuySXh4CAxrQmTMz5wwhLzlbc8b1u37d-_1aMNaulxDyETnlppGVanXzuOTS6EorKU7IM8SeMa5k3TwlJ7w1qi4Up-TbxQj5BtJMv19RFyBN-5h3SCXFObuYkDrEyUc3Q6C_4nxLXaKwjQHG6EseKEKOU6kIEcEhPCdPOjcgvDi-K3L98eL6_HN1-fXTl_MPl5VXWs-V66TgwgiuGslkG5TS4LUJrvaC886oTeAb2XS1CQaU6ziXoQmdcFywjRJyRc4OtNvdZoTgywbZDXab4-jynZ1ctP_-pHhrb6a9FYZpZtpC8PZIkKefO8DZjhE9DINLUNaxjay5ZEWmgnzzILLswUxdZF4RfgD6PCFm6O7H4cwuhtneFsPsYphdQshS8-rvPf5UHB0qgNdHgEPvhi675CPe40RRUOp6af7-gIMi-j5CtugjJA8hZvCzDVN8cIyz_6r9EFMsDX_AHWA_7XIqblpuUVhmr5bLWg6LtYzVmgv5Gw5pyHA</recordid><startdate>20091201</startdate><enddate>20091201</enddate><creator>Lebeck, Mark G</creator><creator>McCarthy, Troy A</creator><creator>Capuano, Ana W</creator><creator>Schnurr, David P</creator><creator>Landry, Marie L</creator><creator>Setterquist, Sharon F</creator><creator>Heil, Gary L</creator><creator>Kilic, Selim</creator><creator>Gray, Gregory C</creator><general>Elsevier B.V</general><general>Elsevier</general><scope>IQODW</scope><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>7U9</scope><scope>H94</scope><scope>7X8</scope><scope>5PM</scope></search><sort><creationdate>20091201</creationdate><title>Emergent US adenovirus 3 strains associated with an epidemic and serious disease</title><author>Lebeck, Mark G ; McCarthy, Troy A ; Capuano, Ana W ; Schnurr, David P ; Landry, Marie L ; Setterquist, Sharon F ; Heil, Gary L ; Kilic, Selim ; Gray, Gregory C</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c566t-af3212821573039d556ec68da4c211f85bd1b37f48d8e5af113d7df2a120b523</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2009</creationdate><topic>Adenoviridae</topic><topic>Adenovirus</topic><topic>Adenovirus Infections, Human - epidemiology</topic><topic>Adenovirus Infections, Human - virology</topic><topic>Adenoviruses, Human - genetics</topic><topic>Adenoviruses, Human - physiology</topic><topic>Allergy and Immunology</topic><topic>Biological and medical sciences</topic><topic>Child</topic><topic>Child, Preschool</topic><topic>Epidemiology</topic><topic>Female</topic><topic>Fundamental and applied biological sciences. Psychology</topic><topic>Genome, Viral - genetics</topic><topic>Genome, Viral - physiology</topic><topic>Human viral diseases</topic><topic>Humans</topic><topic>Infant</topic><topic>Infant, Newborn</topic><topic>Infectious Disease</topic><topic>Infectious diseases</topic><topic>Male</topic><topic>Medical sciences</topic><topic>Microbiology</topic><topic>Miscellaneous</topic><topic>Molecular</topic><topic>Multivariate Analysis</topic><topic>Restriction mapping</topic><topic>Risk Factors</topic><topic>United States - epidemiology</topic><topic>Viral diseases</topic><topic>Virology</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Lebeck, Mark G</creatorcontrib><creatorcontrib>McCarthy, Troy A</creatorcontrib><creatorcontrib>Capuano, Ana W</creatorcontrib><creatorcontrib>Schnurr, David P</creatorcontrib><creatorcontrib>Landry, Marie L</creatorcontrib><creatorcontrib>Setterquist, Sharon F</creatorcontrib><creatorcontrib>Heil, Gary L</creatorcontrib><creatorcontrib>Kilic, Selim</creatorcontrib><creatorcontrib>Gray, Gregory C</creatorcontrib><collection>Pascal-Francis</collection><collection>Medline</collection><collection>MEDLINE</collection><collection>MEDLINE (Ovid)</collection><collection>MEDLINE</collection><collection>MEDLINE</collection><collection>PubMed</collection><collection>CrossRef</collection><collection>Virology and AIDS Abstracts</collection><collection>AIDS and Cancer Research Abstracts</collection><collection>MEDLINE - Academic</collection><collection>PubMed Central (Full Participant titles)</collection><jtitle>Journal of clinical virology</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Lebeck, Mark G</au><au>McCarthy, Troy A</au><au>Capuano, Ana W</au><au>Schnurr, David P</au><au>Landry, Marie L</au><au>Setterquist, Sharon F</au><au>Heil, Gary L</au><au>Kilic, Selim</au><au>Gray, Gregory C</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Emergent US adenovirus 3 strains associated with an epidemic and serious disease</atitle><jtitle>Journal of clinical virology</jtitle><addtitle>J Clin Virol</addtitle><date>2009-12-01</date><risdate>2009</risdate><volume>46</volume><issue>4</issue><spage>331</spage><epage>336</epage><pages>331-336</pages><issn>1386-6532</issn><eissn>1873-5967</eissn><abstract>Abstract Background Adenovirus type 3 (HAdV3) is one of the most prevalent serotypes detected globally. Variants of HAdV3 have been associated with outbreaks of severe disease. Objectives To better understand genetic diversity of circulating HAdV3s and examine risk factors for severe disease. Study design Restriction enzyme analysis for genomic characterization of clinical HAdV3 isolates detected by 15 collaborative US laboratories during the period July 2004 to May 2007. Multivariate modeling was employed for statistical analyses. Results The most common HAdV3 types of 516 isolates studied were HAdV3a2 (36.9%), HAdV3a50 (27.1%), HAdV3a51 (18.0%), and HAdV3a17 (4.6%). Non-HAdV3a genome types were rare (1.2%). HAdV3a50 and HAdV3a51 are newly described variants which became more prevalent in 2006 and 2007 and have been associated with at least one epidemic. Their uniqueness was determined by specific banding profiles generated by digests with endonucleases BclI, BglII, and HindIII. Multivariable risk factor modeling demonstrated that children under 2 years of age (OR = 2.7; 95%CI 1.6–4.6), persons with chronic disease (OR = 5.1; 95%CI 2.6–9.8), persons infected with HAdV3a2 (OR = 3.0; 95%CI 1.5–6.0), with HAdV3a50 (OR = 2.5; 95%CI 1.2–5.2), or with multiple or rare strains (OR = 2.8; 95%CI 1.3–6.5) were at increased risk of severe HAdV3 clinical disease. Conclusions In the study period considerable genetic diversity was found among US clinical HAdV3 strains. Novel variants emerged and became prevalent. One such emergent strain may be associated with more severe clinical disease.</abstract><cop>Amsterdam</cop><pub>Elsevier B.V</pub><pmid>19854101</pmid><doi>10.1016/j.jcv.2009.09.023</doi><tpages>6</tpages><oa>free_for_read</oa></addata></record>
fulltext fulltext
identifier ISSN: 1386-6532
ispartof Journal of clinical virology, 2009-12, Vol.46 (4), p.331-336
issn 1386-6532
1873-5967
language eng
recordid cdi_pubmedcentral_primary_oai_pubmedcentral_nih_gov_2806089
source MEDLINE; Elsevier ScienceDirect Journals
subjects Adenoviridae
Adenovirus
Adenovirus Infections, Human - epidemiology
Adenovirus Infections, Human - virology
Adenoviruses, Human - genetics
Adenoviruses, Human - physiology
Allergy and Immunology
Biological and medical sciences
Child
Child, Preschool
Epidemiology
Female
Fundamental and applied biological sciences. Psychology
Genome, Viral - genetics
Genome, Viral - physiology
Human viral diseases
Humans
Infant
Infant, Newborn
Infectious Disease
Infectious diseases
Male
Medical sciences
Microbiology
Miscellaneous
Molecular
Multivariate Analysis
Restriction mapping
Risk Factors
United States - epidemiology
Viral diseases
Virology
title Emergent US adenovirus 3 strains associated with an epidemic and serious disease
url https://sfx.bib-bvb.de/sfx_tum?ctx_ver=Z39.88-2004&ctx_enc=info:ofi/enc:UTF-8&ctx_tim=2025-02-06T01%3A00%3A02IST&url_ver=Z39.88-2004&url_ctx_fmt=infofi/fmt:kev:mtx:ctx&rfr_id=info:sid/primo.exlibrisgroup.com:primo3-Article-proquest_pubme&rft_val_fmt=info:ofi/fmt:kev:mtx:journal&rft.genre=article&rft.atitle=Emergent%20US%20adenovirus%203%20strains%20associated%20with%20an%20epidemic%20and%20serious%20disease&rft.jtitle=Journal%20of%20clinical%20virology&rft.au=Lebeck,%20Mark%20G&rft.date=2009-12-01&rft.volume=46&rft.issue=4&rft.spage=331&rft.epage=336&rft.pages=331-336&rft.issn=1386-6532&rft.eissn=1873-5967&rft_id=info:doi/10.1016/j.jcv.2009.09.023&rft_dat=%3Cproquest_pubme%3E21208465%3C/proquest_pubme%3E%3Curl%3E%3C/url%3E&disable_directlink=true&sfx.directlink=off&sfx.report_link=0&rft_id=info:oai/&rft_pqid=21208465&rft_id=info:pmid/19854101&rft_els_id=1_s2_0_S1386653209004612&rfr_iscdi=true