Low level myocardial parvovirus B19 persistence is a frequent finding in patients with heart disease but unrelated to ongoing myocardial injury

While myocardial parvovirus B19 (B19V), aside from enteroviruses (EV) and adenoviruses (ADV), has recently been found often in patients with myocarditis and idiopathic dilated cardiomyopathy (IDC), the pathogenetic significance of B19V genomes in those patients has not yet been sufficiently elucidat...

Ausführliche Beschreibung

Gespeichert in:
Bibliographische Detailangaben
Veröffentlicht in:Journal of medical virology 2010-08, Vol.82 (8), p.1449-1457
Hauptverfasser: Lotze, Ulrich, Egerer, Renate, Glück, Brigitte, Zell, Roland, Sigusch, Holger, Erhardt, Christian, Heim, Albert, Kandolf, Reinhard, Bock, Thomas, Wutzler, Peter, Figulla, Hans-R
Format: Artikel
Sprache:eng
Schlagworte:
Online-Zugang:Volltext
Tags: Tag hinzufügen
Keine Tags, Fügen Sie den ersten Tag hinzu!
container_end_page 1457
container_issue 8
container_start_page 1449
container_title Journal of medical virology
container_volume 82
creator Lotze, Ulrich
Egerer, Renate
Glück, Brigitte
Zell, Roland
Sigusch, Holger
Erhardt, Christian
Heim, Albert
Kandolf, Reinhard
Bock, Thomas
Wutzler, Peter
Figulla, Hans-R
description While myocardial parvovirus B19 (B19V), aside from enteroviruses (EV) and adenoviruses (ADV), has recently been found often in patients with myocarditis and idiopathic dilated cardiomyopathy (IDC), the pathogenetic significance of B19V genomes in those patients has not yet been sufficiently elucidated. In the present study, left ventricular endomyocardial biopsies from 24 patients with left ventricular ejection fraction (LVEF) below 55% due to IDC, and tissue from the right atrial appendage of 10 control patients undergoing bypass surgery with normal LVEF (>55%) were investigated for B19V, ADV, and EV genomes by specific nested polymerase chain reaction (PCR), by real time PCR or by reverse-transcription PCR, respectively. The myocardial tissue samples from the 10 controls were analyzed each in three different virological laboratories for B19V. In the IDC group, the frequency of the myocardial virus genomes found in 54% (13/24) of the patients was as follows: B19V: 50% (12/24), EV: 8% (2/24), including one patient with B19V and EV, and ADV: 0% (0/24). For comparison, the prevalence of B19V genomes was between 30% and 60% in the control group as detected in three different laboratories, but all these control subjects were EV- and ADV-negative. The number of B19V gene copies, however, was very low and similar both in the IDC and control group. In the majority of patients myocardial B19V persistence was associated with a low virus load irrespective of the underlying heart disease so that it may be of no importance in the pathogenesis of IDC. J. Med. Virol. 82:1449-1457, 2010.
doi_str_mv 10.1002/jmv.21821
format Article
fullrecord <record><control><sourceid>proquest_hal_p</sourceid><recordid>TN_cdi_hal_primary_oai_HAL_hal_00552417v1</recordid><sourceformat>XML</sourceformat><sourcesystem>PC</sourcesystem><sourcerecordid>733476937</sourcerecordid><originalsourceid>FETCH-LOGICAL-c4201-2fcf56ad09c577669c35971d8ca025174dcddaf09042918fe7d2119cfb2407cb3</originalsourceid><addsrcrecordid>eNp1kUFv0zAYhi0EYmVw4A-Ab9MO2T47iR0ftzE2oIAQbDtaru20Lmlc7CSlv4K_jEu2woWDZenT8z7W5xehlwROCAA9Xa6GE0oqSh6hCQHBMgGcPEYTIAXLGCPlAXoW4xIAKkHpU3RAoeQUKjpBv6Z-gxs72Aavtl6rYJxq8FqFwQ8u9BGfE4HXNkQXO9tqi13ECtfB_uht2-Hatca1c-zalOlcGkW8cd0CL6wKHTYuWhUtnvUd7ttgG9VZgzuPfTv3u9w_b7p22Yftc_SkVk20L-7vQ3Tz9vLbxXU2_Xz17uJsmumCAsloreuSKQNCl5wzJnReCk5MpRXQkvDCaGNUDQIKKkhVW24oIULXM1oA17P8EB2P3oVq5Dq4lQpb6ZWT12dTuZsBlCUtCB9IYo9Gdh18Wjt2cuWitk2jWuv7KHmeF5yJnP-16uBjDLbeqwnIXVUyVSX_VJXYV_fWfrayZk8-dJOA0xHYuMZu_2-S7z_ePiizMbEr6-c-ocJ3yXjOS3n36UoWIj__8ubDnbxN_OuRr5WXah5clDdf0_fmQCqWQzq_AXrit3c</addsrcrecordid><sourcetype>Open Access Repository</sourcetype><iscdi>true</iscdi><recordtype>article</recordtype><pqid>733476937</pqid></control><display><type>article</type><title>Low level myocardial parvovirus B19 persistence is a frequent finding in patients with heart disease but unrelated to ongoing myocardial injury</title><source>MEDLINE</source><source>Wiley Online Library Journals Frontfile Complete</source><creator>Lotze, Ulrich ; Egerer, Renate ; Glück, Brigitte ; Zell, Roland ; Sigusch, Holger ; Erhardt, Christian ; Heim, Albert ; Kandolf, Reinhard ; Bock, Thomas ; Wutzler, Peter ; Figulla, Hans-R</creator><creatorcontrib>Lotze, Ulrich ; Egerer, Renate ; Glück, Brigitte ; Zell, Roland ; Sigusch, Holger ; Erhardt, Christian ; Heim, Albert ; Kandolf, Reinhard ; Bock, Thomas ; Wutzler, Peter ; Figulla, Hans-R</creatorcontrib><description>While myocardial parvovirus B19 (B19V), aside from enteroviruses (EV) and adenoviruses (ADV), has recently been found often in patients with myocarditis and idiopathic dilated cardiomyopathy (IDC), the pathogenetic significance of B19V genomes in those patients has not yet been sufficiently elucidated. In the present study, left ventricular endomyocardial biopsies from 24 patients with left ventricular ejection fraction (LVEF) below 55% due to IDC, and tissue from the right atrial appendage of 10 control patients undergoing bypass surgery with normal LVEF (&gt;55%) were investigated for B19V, ADV, and EV genomes by specific nested polymerase chain reaction (PCR), by real time PCR or by reverse-transcription PCR, respectively. The myocardial tissue samples from the 10 controls were analyzed each in three different virological laboratories for B19V. In the IDC group, the frequency of the myocardial virus genomes found in 54% (13/24) of the patients was as follows: B19V: 50% (12/24), EV: 8% (2/24), including one patient with B19V and EV, and ADV: 0% (0/24). For comparison, the prevalence of B19V genomes was between 30% and 60% in the control group as detected in three different laboratories, but all these control subjects were EV- and ADV-negative. The number of B19V gene copies, however, was very low and similar both in the IDC and control group. In the majority of patients myocardial B19V persistence was associated with a low virus load irrespective of the underlying heart disease so that it may be of no importance in the pathogenesis of IDC. J. Med. Virol. 82:1449-1457, 2010.</description><identifier>ISSN: 0146-6615</identifier><identifier>EISSN: 1096-9071</identifier><identifier>DOI: 10.1002/jmv.21821</identifier><identifier>PMID: 20572082</identifier><language>eng</language><publisher>Hoboken: Wiley Subscription Services, Inc., A Wiley Company</publisher><subject>Adult ; Aged ; Cardiomyopathy, Dilated - virology ; dilated cardiomyopathy ; Enterovirus - isolation &amp; purification ; Enterovirus Infections - pathology ; Enterovirus Infections - virology ; Female ; Heart - virology ; Humans ; Male ; Middle Aged ; Parvoviridae Infections - pathology ; Parvoviridae Infections - virology ; parvovirus B19 ; Parvovirus B19, Human - isolation &amp; purification ; Parvovirus B19, Human - pathogenicity ; pathogenetic significance ; Viral Load</subject><ispartof>Journal of medical virology, 2010-08, Vol.82 (8), p.1449-1457</ispartof><rights>Copyright © 2010 Wiley‐Liss, Inc.</rights><rights>(c) 2010 Wiley-Liss, Inc.</rights><rights>Distributed under a Creative Commons Attribution 4.0 International License</rights><lds50>peer_reviewed</lds50><oa>free_for_read</oa><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c4201-2fcf56ad09c577669c35971d8ca025174dcddaf09042918fe7d2119cfb2407cb3</citedby><cites>FETCH-LOGICAL-c4201-2fcf56ad09c577669c35971d8ca025174dcddaf09042918fe7d2119cfb2407cb3</cites></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><linktopdf>$$Uhttps://onlinelibrary.wiley.com/doi/pdf/10.1002%2Fjmv.21821$$EPDF$$P50$$Gwiley$$H</linktopdf><linktohtml>$$Uhttps://onlinelibrary.wiley.com/doi/full/10.1002%2Fjmv.21821$$EHTML$$P50$$Gwiley$$H</linktohtml><link.rule.ids>230,314,776,780,881,1411,27901,27902,45550,45551</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/20572082$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink><backlink>$$Uhttps://hal.science/hal-00552417$$DView record in HAL$$Hfree_for_read</backlink></links><search><creatorcontrib>Lotze, Ulrich</creatorcontrib><creatorcontrib>Egerer, Renate</creatorcontrib><creatorcontrib>Glück, Brigitte</creatorcontrib><creatorcontrib>Zell, Roland</creatorcontrib><creatorcontrib>Sigusch, Holger</creatorcontrib><creatorcontrib>Erhardt, Christian</creatorcontrib><creatorcontrib>Heim, Albert</creatorcontrib><creatorcontrib>Kandolf, Reinhard</creatorcontrib><creatorcontrib>Bock, Thomas</creatorcontrib><creatorcontrib>Wutzler, Peter</creatorcontrib><creatorcontrib>Figulla, Hans-R</creatorcontrib><title>Low level myocardial parvovirus B19 persistence is a frequent finding in patients with heart disease but unrelated to ongoing myocardial injury</title><title>Journal of medical virology</title><addtitle>J. Med. Virol</addtitle><description>While myocardial parvovirus B19 (B19V), aside from enteroviruses (EV) and adenoviruses (ADV), has recently been found often in patients with myocarditis and idiopathic dilated cardiomyopathy (IDC), the pathogenetic significance of B19V genomes in those patients has not yet been sufficiently elucidated. In the present study, left ventricular endomyocardial biopsies from 24 patients with left ventricular ejection fraction (LVEF) below 55% due to IDC, and tissue from the right atrial appendage of 10 control patients undergoing bypass surgery with normal LVEF (&gt;55%) were investigated for B19V, ADV, and EV genomes by specific nested polymerase chain reaction (PCR), by real time PCR or by reverse-transcription PCR, respectively. The myocardial tissue samples from the 10 controls were analyzed each in three different virological laboratories for B19V. In the IDC group, the frequency of the myocardial virus genomes found in 54% (13/24) of the patients was as follows: B19V: 50% (12/24), EV: 8% (2/24), including one patient with B19V and EV, and ADV: 0% (0/24). For comparison, the prevalence of B19V genomes was between 30% and 60% in the control group as detected in three different laboratories, but all these control subjects were EV- and ADV-negative. The number of B19V gene copies, however, was very low and similar both in the IDC and control group. In the majority of patients myocardial B19V persistence was associated with a low virus load irrespective of the underlying heart disease so that it may be of no importance in the pathogenesis of IDC. J. Med. Virol. 82:1449-1457, 2010.</description><subject>Adult</subject><subject>Aged</subject><subject>Cardiomyopathy, Dilated - virology</subject><subject>dilated cardiomyopathy</subject><subject>Enterovirus - isolation &amp; purification</subject><subject>Enterovirus Infections - pathology</subject><subject>Enterovirus Infections - virology</subject><subject>Female</subject><subject>Heart - virology</subject><subject>Humans</subject><subject>Male</subject><subject>Middle Aged</subject><subject>Parvoviridae Infections - pathology</subject><subject>Parvoviridae Infections - virology</subject><subject>parvovirus B19</subject><subject>Parvovirus B19, Human - isolation &amp; purification</subject><subject>Parvovirus B19, Human - pathogenicity</subject><subject>pathogenetic significance</subject><subject>Viral Load</subject><issn>0146-6615</issn><issn>1096-9071</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2010</creationdate><recordtype>article</recordtype><sourceid>EIF</sourceid><recordid>eNp1kUFv0zAYhi0EYmVw4A-Ab9MO2T47iR0ftzE2oIAQbDtaru20Lmlc7CSlv4K_jEu2woWDZenT8z7W5xehlwROCAA9Xa6GE0oqSh6hCQHBMgGcPEYTIAXLGCPlAXoW4xIAKkHpU3RAoeQUKjpBv6Z-gxs72Aavtl6rYJxq8FqFwQ8u9BGfE4HXNkQXO9tqi13ECtfB_uht2-Hatca1c-zalOlcGkW8cd0CL6wKHTYuWhUtnvUd7ttgG9VZgzuPfTv3u9w_b7p22Yftc_SkVk20L-7vQ3Tz9vLbxXU2_Xz17uJsmumCAsloreuSKQNCl5wzJnReCk5MpRXQkvDCaGNUDQIKKkhVW24oIULXM1oA17P8EB2P3oVq5Dq4lQpb6ZWT12dTuZsBlCUtCB9IYo9Gdh18Wjt2cuWitk2jWuv7KHmeF5yJnP-16uBjDLbeqwnIXVUyVSX_VJXYV_fWfrayZk8-dJOA0xHYuMZu_2-S7z_ePiizMbEr6-c-ocJ3yXjOS3n36UoWIj__8ubDnbxN_OuRr5WXah5clDdf0_fmQCqWQzq_AXrit3c</recordid><startdate>201008</startdate><enddate>201008</enddate><creator>Lotze, Ulrich</creator><creator>Egerer, Renate</creator><creator>Glück, Brigitte</creator><creator>Zell, Roland</creator><creator>Sigusch, Holger</creator><creator>Erhardt, Christian</creator><creator>Heim, Albert</creator><creator>Kandolf, Reinhard</creator><creator>Bock, Thomas</creator><creator>Wutzler, Peter</creator><creator>Figulla, Hans-R</creator><general>Wiley Subscription Services, Inc., A Wiley Company</general><general>Wiley-Blackwell</general><scope>FBQ</scope><scope>BSCLL</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>1XC</scope><scope>VOOES</scope></search><sort><creationdate>201008</creationdate><title>Low level myocardial parvovirus B19 persistence is a frequent finding in patients with heart disease but unrelated to ongoing myocardial injury</title><author>Lotze, Ulrich ; Egerer, Renate ; Glück, Brigitte ; Zell, Roland ; Sigusch, Holger ; Erhardt, Christian ; Heim, Albert ; Kandolf, Reinhard ; Bock, Thomas ; Wutzler, Peter ; Figulla, Hans-R</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c4201-2fcf56ad09c577669c35971d8ca025174dcddaf09042918fe7d2119cfb2407cb3</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2010</creationdate><topic>Adult</topic><topic>Aged</topic><topic>Cardiomyopathy, Dilated - virology</topic><topic>dilated cardiomyopathy</topic><topic>Enterovirus - isolation &amp; purification</topic><topic>Enterovirus Infections - pathology</topic><topic>Enterovirus Infections - virology</topic><topic>Female</topic><topic>Heart - virology</topic><topic>Humans</topic><topic>Male</topic><topic>Middle Aged</topic><topic>Parvoviridae Infections - pathology</topic><topic>Parvoviridae Infections - virology</topic><topic>parvovirus B19</topic><topic>Parvovirus B19, Human - isolation &amp; purification</topic><topic>Parvovirus B19, Human - pathogenicity</topic><topic>pathogenetic significance</topic><topic>Viral Load</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Lotze, Ulrich</creatorcontrib><creatorcontrib>Egerer, Renate</creatorcontrib><creatorcontrib>Glück, Brigitte</creatorcontrib><creatorcontrib>Zell, Roland</creatorcontrib><creatorcontrib>Sigusch, Holger</creatorcontrib><creatorcontrib>Erhardt, Christian</creatorcontrib><creatorcontrib>Heim, Albert</creatorcontrib><creatorcontrib>Kandolf, Reinhard</creatorcontrib><creatorcontrib>Bock, Thomas</creatorcontrib><creatorcontrib>Wutzler, Peter</creatorcontrib><creatorcontrib>Figulla, Hans-R</creatorcontrib><collection>AGRIS</collection><collection>Istex</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>Hyper Article en Ligne (HAL)</collection><collection>Hyper Article en Ligne (HAL) (Open Access)</collection><jtitle>Journal of medical virology</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Lotze, Ulrich</au><au>Egerer, Renate</au><au>Glück, Brigitte</au><au>Zell, Roland</au><au>Sigusch, Holger</au><au>Erhardt, Christian</au><au>Heim, Albert</au><au>Kandolf, Reinhard</au><au>Bock, Thomas</au><au>Wutzler, Peter</au><au>Figulla, Hans-R</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Low level myocardial parvovirus B19 persistence is a frequent finding in patients with heart disease but unrelated to ongoing myocardial injury</atitle><jtitle>Journal of medical virology</jtitle><addtitle>J. Med. Virol</addtitle><date>2010-08</date><risdate>2010</risdate><volume>82</volume><issue>8</issue><spage>1449</spage><epage>1457</epage><pages>1449-1457</pages><issn>0146-6615</issn><eissn>1096-9071</eissn><abstract>While myocardial parvovirus B19 (B19V), aside from enteroviruses (EV) and adenoviruses (ADV), has recently been found often in patients with myocarditis and idiopathic dilated cardiomyopathy (IDC), the pathogenetic significance of B19V genomes in those patients has not yet been sufficiently elucidated. In the present study, left ventricular endomyocardial biopsies from 24 patients with left ventricular ejection fraction (LVEF) below 55% due to IDC, and tissue from the right atrial appendage of 10 control patients undergoing bypass surgery with normal LVEF (&gt;55%) were investigated for B19V, ADV, and EV genomes by specific nested polymerase chain reaction (PCR), by real time PCR or by reverse-transcription PCR, respectively. The myocardial tissue samples from the 10 controls were analyzed each in three different virological laboratories for B19V. In the IDC group, the frequency of the myocardial virus genomes found in 54% (13/24) of the patients was as follows: B19V: 50% (12/24), EV: 8% (2/24), including one patient with B19V and EV, and ADV: 0% (0/24). For comparison, the prevalence of B19V genomes was between 30% and 60% in the control group as detected in three different laboratories, but all these control subjects were EV- and ADV-negative. The number of B19V gene copies, however, was very low and similar both in the IDC and control group. In the majority of patients myocardial B19V persistence was associated with a low virus load irrespective of the underlying heart disease so that it may be of no importance in the pathogenesis of IDC. J. Med. Virol. 82:1449-1457, 2010.</abstract><cop>Hoboken</cop><pub>Wiley Subscription Services, Inc., A Wiley Company</pub><pmid>20572082</pmid><doi>10.1002/jmv.21821</doi><tpages>9</tpages><oa>free_for_read</oa></addata></record>
fulltext fulltext
identifier ISSN: 0146-6615
ispartof Journal of medical virology, 2010-08, Vol.82 (8), p.1449-1457
issn 0146-6615
1096-9071
language eng
recordid cdi_hal_primary_oai_HAL_hal_00552417v1
source MEDLINE; Wiley Online Library Journals Frontfile Complete
subjects Adult
Aged
Cardiomyopathy, Dilated - virology
dilated cardiomyopathy
Enterovirus - isolation & purification
Enterovirus Infections - pathology
Enterovirus Infections - virology
Female
Heart - virology
Humans
Male
Middle Aged
Parvoviridae Infections - pathology
Parvoviridae Infections - virology
parvovirus B19
Parvovirus B19, Human - isolation & purification
Parvovirus B19, Human - pathogenicity
pathogenetic significance
Viral Load
title Low level myocardial parvovirus B19 persistence is a frequent finding in patients with heart disease but unrelated to ongoing myocardial injury
url https://sfx.bib-bvb.de/sfx_tum?ctx_ver=Z39.88-2004&ctx_enc=info:ofi/enc:UTF-8&ctx_tim=2025-02-05T04%3A57%3A23IST&url_ver=Z39.88-2004&url_ctx_fmt=infofi/fmt:kev:mtx:ctx&rfr_id=info:sid/primo.exlibrisgroup.com:primo3-Article-proquest_hal_p&rft_val_fmt=info:ofi/fmt:kev:mtx:journal&rft.genre=article&rft.atitle=Low%20level%20myocardial%20parvovirus%20B19%20persistence%20is%20a%20frequent%20finding%20in%20patients%20with%20heart%20disease%20but%20unrelated%20to%20ongoing%20myocardial%20injury&rft.jtitle=Journal%20of%20medical%20virology&rft.au=Lotze,%20Ulrich&rft.date=2010-08&rft.volume=82&rft.issue=8&rft.spage=1449&rft.epage=1457&rft.pages=1449-1457&rft.issn=0146-6615&rft.eissn=1096-9071&rft_id=info:doi/10.1002/jmv.21821&rft_dat=%3Cproquest_hal_p%3E733476937%3C/proquest_hal_p%3E%3Curl%3E%3C/url%3E&disable_directlink=true&sfx.directlink=off&sfx.report_link=0&rft_id=info:oai/&rft_pqid=733476937&rft_id=info:pmid/20572082&rfr_iscdi=true