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A gammaherpesvirus establishes persistent infection in neuroblastoma cells
Gammaherpesvirus (γHV) infection of the central nervous system (CNS) has been implicated in diverse neurological diseases, and murine γHV-68 (MHV-68) is known to persist in the brain after cerebral infection. The underlying molecular mechanisms of persistency of virus in the brain are poorly underst...
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Published in: | Molecules and cells 2014, 37(7), , pp.518-525 |
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description | Gammaherpesvirus (γHV) infection of the central nervous system (CNS) has been implicated in diverse neurological diseases, and murine γHV-68 (MHV-68) is known to persist in the brain after cerebral infection. The underlying molecular mechanisms of persistency of virus in the brain are poorly understood. Here, we characterized a unique pattern of MHV-68 persistent infection in neuroblastoma cells. On infection with MHV-68, both murine and human neuroblastoma cells expressed viral lytic proteins and produced virions. However, the infected cells survived productive infection and could be cultured for multiple passages without affecting their cellular growth. Latent infection as well as productive replication was established in these prolonged cultures, and lytic replication was further increased by treatment with lytic inducers. Our results provide a novel system to study persistent infection of γHVs in vitro following de novo infection and suggest application of MHV-68 as a potential gene transfer vector to the brain. |
doi_str_mv | 10.14348/molcells.2014.0024 |
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The underlying molecular mechanisms of persistency of virus in the brain are poorly understood. Here, we characterized a unique pattern of MHV-68 persistent infection in neuroblastoma cells. On infection with MHV-68, both murine and human neuroblastoma cells expressed viral lytic proteins and produced virions. However, the infected cells survived productive infection and could be cultured for multiple passages without affecting their cellular growth. Latent infection as well as productive replication was established in these prolonged cultures, and lytic replication was further increased by treatment with lytic inducers. Our results provide a novel system to study persistent infection of γHVs in vitro following de novo infection and suggest application of MHV-68 as a potential gene transfer vector to the brain.</description><identifier>ISSN: 1016-8478</identifier><identifier>EISSN: 0219-1032</identifier><identifier>DOI: 10.14348/molcells.2014.0024</identifier><identifier>PMID: 25092213</identifier><language>eng</language><publisher>United States: Korean Society for Molecular and Cellular Biology</publisher><subject>Animals ; Brain - pathology ; Brain - virology ; Butyric Acid - pharmacology ; Cell Line, Tumor ; Cell Proliferation ; Gammaherpesvirinae - drug effects ; Gammaherpesvirinae - physiology ; Ganciclovir - pharmacology ; Genetic Vectors ; Herpesviridae Infections - drug therapy ; Herpesviridae Infections - physiopathology ; Humans ; Mice ; Neuroblastoma - drug therapy ; Neuroblastoma - pathology ; Neuroblastoma - virology ; Pyridines - pharmacology ; Virus Latency - drug effects ; Virus Replication - drug effects ; 생물학</subject><ispartof>Molecules and Cells, 2014, 37(7), , pp.518-525</ispartof><rights>Copyright © 2014 by The Korean Society for Molecular and Cellular Biology. All rights reserved. 2014</rights><lds50>peer_reviewed</lds50><oa>free_for_read</oa><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c437t-c4024622dfba63636a54c806d90032bdd8e6d124a46abe492be09e9d83bd5093</citedby><cites>FETCH-LOGICAL-c437t-c4024622dfba63636a54c806d90032bdd8e6d124a46abe492be09e9d83bd5093</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/PMC4132303/pdf/$$EPDF$$P50$$Gpubmedcentral$$H</linktopdf><linktohtml>$$Uhttps://www.ncbi.nlm.nih.gov/pmc/articles/PMC4132303/$$EHTML$$P50$$Gpubmedcentral$$H</linktohtml><link.rule.ids>230,314,723,776,780,881,27900,27901,53765,53767</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/25092213$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink><backlink>$$Uhttps://www.kci.go.kr/kciportal/ci/sereArticleSearch/ciSereArtiView.kci?sereArticleSearchBean.artiId=ART001899462$$DAccess content in National Research Foundation of Korea (NRF)$$Hfree_for_read</backlink></links><search><creatorcontrib>Cho, Hye-Jeong</creatorcontrib><creatorcontrib>Song, Moon Jung</creatorcontrib><title>A gammaherpesvirus establishes persistent infection in neuroblastoma cells</title><title>Molecules and cells</title><addtitle>Mol Cells</addtitle><description>Gammaherpesvirus (γHV) infection of the central nervous system (CNS) has been implicated in diverse neurological diseases, and murine γHV-68 (MHV-68) is known to persist in the brain after cerebral infection. 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Our results provide a novel system to study persistent infection of γHVs in vitro following de novo infection and suggest application of MHV-68 as a potential gene transfer vector to the brain.</description><subject>Animals</subject><subject>Brain - pathology</subject><subject>Brain - virology</subject><subject>Butyric Acid - pharmacology</subject><subject>Cell Line, Tumor</subject><subject>Cell Proliferation</subject><subject>Gammaherpesvirinae - drug effects</subject><subject>Gammaherpesvirinae - physiology</subject><subject>Ganciclovir - pharmacology</subject><subject>Genetic Vectors</subject><subject>Herpesviridae Infections - drug therapy</subject><subject>Herpesviridae Infections - physiopathology</subject><subject>Humans</subject><subject>Mice</subject><subject>Neuroblastoma - drug therapy</subject><subject>Neuroblastoma - pathology</subject><subject>Neuroblastoma - virology</subject><subject>Pyridines - pharmacology</subject><subject>Virus Latency - drug effects</subject><subject>Virus Replication - drug effects</subject><subject>생물학</subject><issn>1016-8478</issn><issn>0219-1032</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2014</creationdate><recordtype>article</recordtype><recordid>eNpVkVtrAjEQhUNpqWL9BYWyb31aO7m47r4URHqxCIXie0g2sxrcG8kq9N83rlVaAplA5jtzkkPIPYUJFVykT1VT5liWfsKAigkAE1dkCIxmMQXOrsmQAk3iVMzSARl7bzWIDCBhPL0lAzaFjDHKh-RjHm1UVaktuhb9wbq9j9B3SpfWb9FHLTpvfYd1F9m6wLyzTR1OUY171-hS-a6pVNQ7uSM3hSo9jn_riKxfX9aL93j1-bZczFdxLvisC3vwmjBmCq0SHpaaijyFxAR7nGljUkwMZUKJRGkUGdMIGWYm5doE23xEHk-ytSvkLreyUbavm0bunJx_rZdyFvhj5_Ops93rCk0eHuFUKVtnK-W-e-7_TW23QeUgBeWMAw8C_CSQu8Z7h8WFpSD7GOQ5BnmMQR5jCNTD37EX5vzp_AcT6If7</recordid><startdate>20140701</startdate><enddate>20140701</enddate><creator>Cho, Hye-Jeong</creator><creator>Song, Moon Jung</creator><general>Korean Society for Molecular and Cellular Biology</general><general>한국분자세포생물학회</general><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>5PM</scope><scope>ACYCR</scope></search><sort><creationdate>20140701</creationdate><title>A gammaherpesvirus establishes persistent infection in neuroblastoma cells</title><author>Cho, Hye-Jeong ; Song, Moon Jung</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c437t-c4024622dfba63636a54c806d90032bdd8e6d124a46abe492be09e9d83bd5093</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2014</creationdate><topic>Animals</topic><topic>Brain - pathology</topic><topic>Brain - virology</topic><topic>Butyric Acid - pharmacology</topic><topic>Cell Line, Tumor</topic><topic>Cell Proliferation</topic><topic>Gammaherpesvirinae - drug effects</topic><topic>Gammaherpesvirinae - physiology</topic><topic>Ganciclovir - pharmacology</topic><topic>Genetic Vectors</topic><topic>Herpesviridae Infections - drug therapy</topic><topic>Herpesviridae Infections - physiopathology</topic><topic>Humans</topic><topic>Mice</topic><topic>Neuroblastoma - drug therapy</topic><topic>Neuroblastoma - pathology</topic><topic>Neuroblastoma - virology</topic><topic>Pyridines - pharmacology</topic><topic>Virus Latency - drug effects</topic><topic>Virus Replication - drug effects</topic><topic>생물학</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Cho, Hye-Jeong</creatorcontrib><creatorcontrib>Song, Moon Jung</creatorcontrib><collection>Medline</collection><collection>MEDLINE</collection><collection>MEDLINE (Ovid)</collection><collection>MEDLINE</collection><collection>MEDLINE</collection><collection>PubMed</collection><collection>CrossRef</collection><collection>PubMed Central (Full Participant titles)</collection><collection>Korean Citation Index</collection><jtitle>Molecules and cells</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Cho, Hye-Jeong</au><au>Song, Moon Jung</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>A gammaherpesvirus establishes persistent infection in neuroblastoma cells</atitle><jtitle>Molecules and cells</jtitle><addtitle>Mol Cells</addtitle><date>2014-07-01</date><risdate>2014</risdate><volume>37</volume><issue>7</issue><spage>518</spage><epage>525</epage><pages>518-525</pages><issn>1016-8478</issn><eissn>0219-1032</eissn><abstract>Gammaherpesvirus (γHV) infection of the central nervous system (CNS) has been implicated in diverse neurological diseases, and murine γHV-68 (MHV-68) is known to persist in the brain after cerebral infection. The underlying molecular mechanisms of persistency of virus in the brain are poorly understood. Here, we characterized a unique pattern of MHV-68 persistent infection in neuroblastoma cells. On infection with MHV-68, both murine and human neuroblastoma cells expressed viral lytic proteins and produced virions. However, the infected cells survived productive infection and could be cultured for multiple passages without affecting their cellular growth. Latent infection as well as productive replication was established in these prolonged cultures, and lytic replication was further increased by treatment with lytic inducers. 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subjects | Animals Brain - pathology Brain - virology Butyric Acid - pharmacology Cell Line, Tumor Cell Proliferation Gammaherpesvirinae - drug effects Gammaherpesvirinae - physiology Ganciclovir - pharmacology Genetic Vectors Herpesviridae Infections - drug therapy Herpesviridae Infections - physiopathology Humans Mice Neuroblastoma - drug therapy Neuroblastoma - pathology Neuroblastoma - virology Pyridines - pharmacology Virus Latency - drug effects Virus Replication - drug effects 생물학 |
title | A gammaherpesvirus establishes persistent infection in neuroblastoma cells |
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