Childhood myocarditis and parvovirus B19 genotypes

Abstract Background Human parvovirus B19 (PVB19) infection is occasionally associated with acute myocarditis. Three cases of children with PVB19 virus-associated myocarditis occurred in a very short period and the same geographical region. Objective To elucidate if virological factors could be respo...

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Veröffentlicht in:Journal of clinical virology 2011-01, Vol.50 (1), p.61-64
Hauptverfasser: Dina, Julia, Villedieu, Florence, Labombarda, Fabien, Freymuth, François, de la Gastine, Geoffroy, Jokic, Mikael, Vabret, Astrid
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container_issue 1
container_start_page 61
container_title Journal of clinical virology
container_volume 50
creator Dina, Julia
Villedieu, Florence
Labombarda, Fabien
Freymuth, François
de la Gastine, Geoffroy
Jokic, Mikael
Vabret, Astrid
description Abstract Background Human parvovirus B19 (PVB19) infection is occasionally associated with acute myocarditis. Three cases of children with PVB19 virus-associated myocarditis occurred in a very short period and the same geographical region. Objective To elucidate if virological factors could be responsible for determining the course of infection, a molecular epidemiologic investigation was performed. Study Design The diagnosis of myocarditis was established by histology or echocardiography. In the three cases, the PVB19 DNA was detected in different samples. Eight different regions were amplified by PCR using a high fidelity Taq polymerase and sequenced on both strands. Phylogenetic analyses were performed. First, the genotypes of the PVB19 strains were determined, then the intra-patient viral variability was analysed by sequencing PVB19 detected in different specimens sampled from the same patient at the same moment. Results Nearly complete sequences of the PVB19 virus (4265nt) were obtained from different samples in the three patients. The phylogenetic analyses showed that PVB19 strains identified clustered with genotype 1a PVB19 strains referenced in GenBank. When compared to the referenced strain NC_000883 , the number of substitutions (transitions and transversions) were as follows: 58 for Caen.FRA/19.09, 74 for Caen.FRA/21.09 and 60 for Caen.FRA/24.09. The strains isolated from the same patient showed 100% of similarity. Conclusions Viral myocarditis is a frequently unrecognized cause of post-inflammatory cardiomyopathy. The detailed molecular analyses do not give rise to virological markers associated with myocarditis in these children.
doi_str_mv 10.1016/j.jcv.2010.09.010
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Three cases of children with PVB19 virus-associated myocarditis occurred in a very short period and the same geographical region. Objective To elucidate if virological factors could be responsible for determining the course of infection, a molecular epidemiologic investigation was performed. Study Design The diagnosis of myocarditis was established by histology or echocardiography. In the three cases, the PVB19 DNA was detected in different samples. Eight different regions were amplified by PCR using a high fidelity Taq polymerase and sequenced on both strands. Phylogenetic analyses were performed. First, the genotypes of the PVB19 strains were determined, then the intra-patient viral variability was analysed by sequencing PVB19 detected in different specimens sampled from the same patient at the same moment. Results Nearly complete sequences of the PVB19 virus (4265nt) were obtained from different samples in the three patients. The phylogenetic analyses showed that PVB19 strains identified clustered with genotype 1a PVB19 strains referenced in GenBank. When compared to the referenced strain NC_000883 , the number of substitutions (transitions and transversions) were as follows: 58 for Caen.FRA/19.09, 74 for Caen.FRA/21.09 and 60 for Caen.FRA/24.09. The strains isolated from the same patient showed 100% of similarity. Conclusions Viral myocarditis is a frequently unrecognized cause of post-inflammatory cardiomyopathy. The detailed molecular analyses do not give rise to virological markers associated with myocarditis in these children.</description><identifier>ISSN: 1386-6532</identifier><identifier>EISSN: 1873-5967</identifier><identifier>DOI: 10.1016/j.jcv.2010.09.010</identifier><identifier>PMID: 20952249</identifier><language>eng</language><publisher>Amsterdam: Elsevier B.V</publisher><subject>Acute Disease ; Allergy and Immunology ; B19 genotypes ; Biological and medical sciences ; Child, Preschool ; DNA, Viral - genetics ; Echocardiography ; Female ; Fundamental and applied biological sciences. Psychology ; Genotype ; Human parvovirus B19 ; Human viral diseases ; Humans ; Infant ; Infectious Disease ; Infectious diseases ; Medical sciences ; Microbiology ; Miscellaneous ; Myocarditis ; Myocarditis - physiopathology ; Myocarditis - virology ; Parvoviridae Infections - physiopathology ; Parvoviridae Infections - virology ; Parvovirus B19 ; Parvovirus B19, Human - genetics ; Polymerase Chain Reaction ; Viral diseases ; Virology</subject><ispartof>Journal of clinical virology, 2011-01, Vol.50 (1), p.61-64</ispartof><rights>Elsevier B.V.</rights><rights>2010 Elsevier B.V.</rights><rights>2015 INIST-CNRS</rights><rights>Copyright © 2010 Elsevier B.V. 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Three cases of children with PVB19 virus-associated myocarditis occurred in a very short period and the same geographical region. Objective To elucidate if virological factors could be responsible for determining the course of infection, a molecular epidemiologic investigation was performed. Study Design The diagnosis of myocarditis was established by histology or echocardiography. In the three cases, the PVB19 DNA was detected in different samples. Eight different regions were amplified by PCR using a high fidelity Taq polymerase and sequenced on both strands. Phylogenetic analyses were performed. First, the genotypes of the PVB19 strains were determined, then the intra-patient viral variability was analysed by sequencing PVB19 detected in different specimens sampled from the same patient at the same moment. Results Nearly complete sequences of the PVB19 virus (4265nt) were obtained from different samples in the three patients. The phylogenetic analyses showed that PVB19 strains identified clustered with genotype 1a PVB19 strains referenced in GenBank. When compared to the referenced strain NC_000883 , the number of substitutions (transitions and transversions) were as follows: 58 for Caen.FRA/19.09, 74 for Caen.FRA/21.09 and 60 for Caen.FRA/24.09. The strains isolated from the same patient showed 100% of similarity. Conclusions Viral myocarditis is a frequently unrecognized cause of post-inflammatory cardiomyopathy. The detailed molecular analyses do not give rise to virological markers associated with myocarditis in these children.</description><subject>Acute Disease</subject><subject>Allergy and Immunology</subject><subject>B19 genotypes</subject><subject>Biological and medical sciences</subject><subject>Child, Preschool</subject><subject>DNA, Viral - genetics</subject><subject>Echocardiography</subject><subject>Female</subject><subject>Fundamental and applied biological sciences. Psychology</subject><subject>Genotype</subject><subject>Human parvovirus B19</subject><subject>Human viral diseases</subject><subject>Humans</subject><subject>Infant</subject><subject>Infectious Disease</subject><subject>Infectious diseases</subject><subject>Medical sciences</subject><subject>Microbiology</subject><subject>Miscellaneous</subject><subject>Myocarditis</subject><subject>Myocarditis - physiopathology</subject><subject>Myocarditis - virology</subject><subject>Parvoviridae Infections - physiopathology</subject><subject>Parvoviridae Infections - virology</subject><subject>Parvovirus B19</subject><subject>Parvovirus B19, Human - genetics</subject><subject>Polymerase Chain Reaction</subject><subject>Viral diseases</subject><subject>Virology</subject><issn>1386-6532</issn><issn>1873-5967</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2011</creationdate><recordtype>article</recordtype><sourceid>EIF</sourceid><recordid>eNqNkU9r3DAQxUVoadKkHyCX4EvJyVuN_loECu3StIVADknPQpXHjRyvtZXshf320bLbBHooPY2Efm9m9B4h50AXQEF96Be93ywYLXdqFqUckRNoNK-lUfpVOfNG1Upydkze5txTCpIL_YYcM2okY8KcELZ8CEP7EGNbrbbRu9SGKeTKjW21dmkTNyHNufoMpvqFY5y2a8xn5HXnhozvDvWU_Lj-cr_8Vt_cfv2-_HRTe6HMVHeCO6oQBAAIKsEz1VCqVYdGcM9bDk6j6gwIzYyXErh0wjRNecauLM5PyeW-7zrF3zPmya5C9jgMbsQ4Z9toBhy4-A-SSwDDtS4k7EmfYs4JO7tOYeXS1gK1O09tb4undueppcaWUjQXh-7zzxW2z4o_Jhbg_QFw2buhS270Ib9wXEuQmhXuas9hcW0TMNnsA44e25DQT7aN4Z9rfPxL7YcwhjLwEbeY-zinscRhwWZmqb3bhb_LHiilXJfvPwHsMqWV</recordid><startdate>20110101</startdate><enddate>20110101</enddate><creator>Dina, Julia</creator><creator>Villedieu, Florence</creator><creator>Labombarda, Fabien</creator><creator>Freymuth, François</creator><creator>de la Gastine, Geoffroy</creator><creator>Jokic, Mikael</creator><creator>Vabret, Astrid</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>7X8</scope><scope>7U9</scope><scope>H94</scope></search><sort><creationdate>20110101</creationdate><title>Childhood myocarditis and parvovirus B19 genotypes</title><author>Dina, Julia ; Villedieu, Florence ; Labombarda, Fabien ; Freymuth, François ; de la Gastine, Geoffroy ; Jokic, Mikael ; Vabret, Astrid</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c469t-f43a06e141114051c2680076fe943c3d31a7e6f914729c55135a4988e94ef3863</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2011</creationdate><topic>Acute Disease</topic><topic>Allergy and Immunology</topic><topic>B19 genotypes</topic><topic>Biological and medical sciences</topic><topic>Child, Preschool</topic><topic>DNA, Viral - genetics</topic><topic>Echocardiography</topic><topic>Female</topic><topic>Fundamental and applied biological sciences. Psychology</topic><topic>Genotype</topic><topic>Human parvovirus B19</topic><topic>Human viral diseases</topic><topic>Humans</topic><topic>Infant</topic><topic>Infectious Disease</topic><topic>Infectious diseases</topic><topic>Medical sciences</topic><topic>Microbiology</topic><topic>Miscellaneous</topic><topic>Myocarditis</topic><topic>Myocarditis - physiopathology</topic><topic>Myocarditis - virology</topic><topic>Parvoviridae Infections - physiopathology</topic><topic>Parvoviridae Infections - virology</topic><topic>Parvovirus B19</topic><topic>Parvovirus B19, Human - genetics</topic><topic>Polymerase Chain Reaction</topic><topic>Viral diseases</topic><topic>Virology</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Dina, Julia</creatorcontrib><creatorcontrib>Villedieu, Florence</creatorcontrib><creatorcontrib>Labombarda, Fabien</creatorcontrib><creatorcontrib>Freymuth, François</creatorcontrib><creatorcontrib>de la Gastine, Geoffroy</creatorcontrib><creatorcontrib>Jokic, Mikael</creatorcontrib><creatorcontrib>Vabret, Astrid</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>MEDLINE - Academic</collection><collection>Virology and AIDS Abstracts</collection><collection>AIDS and Cancer Research Abstracts</collection><jtitle>Journal of clinical virology</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Dina, Julia</au><au>Villedieu, Florence</au><au>Labombarda, Fabien</au><au>Freymuth, François</au><au>de la Gastine, Geoffroy</au><au>Jokic, Mikael</au><au>Vabret, Astrid</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Childhood myocarditis and parvovirus B19 genotypes</atitle><jtitle>Journal of clinical virology</jtitle><addtitle>J Clin Virol</addtitle><date>2011-01-01</date><risdate>2011</risdate><volume>50</volume><issue>1</issue><spage>61</spage><epage>64</epage><pages>61-64</pages><issn>1386-6532</issn><eissn>1873-5967</eissn><abstract>Abstract Background Human parvovirus B19 (PVB19) infection is occasionally associated with acute myocarditis. Three cases of children with PVB19 virus-associated myocarditis occurred in a very short period and the same geographical region. Objective To elucidate if virological factors could be responsible for determining the course of infection, a molecular epidemiologic investigation was performed. Study Design The diagnosis of myocarditis was established by histology or echocardiography. In the three cases, the PVB19 DNA was detected in different samples. Eight different regions were amplified by PCR using a high fidelity Taq polymerase and sequenced on both strands. Phylogenetic analyses were performed. First, the genotypes of the PVB19 strains were determined, then the intra-patient viral variability was analysed by sequencing PVB19 detected in different specimens sampled from the same patient at the same moment. Results Nearly complete sequences of the PVB19 virus (4265nt) were obtained from different samples in the three patients. The phylogenetic analyses showed that PVB19 strains identified clustered with genotype 1a PVB19 strains referenced in GenBank. When compared to the referenced strain NC_000883 , the number of substitutions (transitions and transversions) were as follows: 58 for Caen.FRA/19.09, 74 for Caen.FRA/21.09 and 60 for Caen.FRA/24.09. The strains isolated from the same patient showed 100% of similarity. Conclusions Viral myocarditis is a frequently unrecognized cause of post-inflammatory cardiomyopathy. The detailed molecular analyses do not give rise to virological markers associated with myocarditis in these children.</abstract><cop>Amsterdam</cop><pub>Elsevier B.V</pub><pmid>20952249</pmid><doi>10.1016/j.jcv.2010.09.010</doi><tpages>4</tpages></addata></record>
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subjects Acute Disease
Allergy and Immunology
B19 genotypes
Biological and medical sciences
Child, Preschool
DNA, Viral - genetics
Echocardiography
Female
Fundamental and applied biological sciences. Psychology
Genotype
Human parvovirus B19
Human viral diseases
Humans
Infant
Infectious Disease
Infectious diseases
Medical sciences
Microbiology
Miscellaneous
Myocarditis
Myocarditis - physiopathology
Myocarditis - virology
Parvoviridae Infections - physiopathology
Parvoviridae Infections - virology
Parvovirus B19
Parvovirus B19, Human - genetics
Polymerase Chain Reaction
Viral diseases
Virology
title Childhood myocarditis and parvovirus B19 genotypes
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