Characterization of an infectious pancreatic necrosis (IPN) virus carrier cell culture with resistance to superinfection with heterologous viruses
A state of persistence of a non susceptible fish cell line with infectious pancreatic necrosis virus (IPNV) was established in vitro by experimental infection. The persistently infected culture showed sustained production of infectious virus and could be continuously passaged for months. A distinct...
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creator | García, Inmaculada Galiana, Antonio Falcó, Alberto Estepa, Amparo Perez, Luis |
description | A state of persistence of a non susceptible fish cell line with infectious pancreatic necrosis virus (IPNV) was established in vitro by experimental infection. The persistently infected culture showed sustained production of infectious virus and could be continuously passaged for months. A distinct feature of this culture is that only a very small fraction of the cells harbours virus replication, in contrast to other reported IPNV-persistently infected cells from salmonid fish, where nearly all the cells express viral antigens. In spite of the small number of detectable IPNV-infected cells, the carrier culture shows resistance to superinfection with homologous as well as heterologous viruses. Temperature shift-up experiments indicate that viral interference is due to continuous replication of IPNV in the culture. Quantitation of Mx gene expression suggested that the interference phenomenon could be mediated by the activation of the interferon (IFN) system. However, conditioned medium from the IPNV-infected cell cultures only marginally protected other cells against VHSV infection, indicating that other type I IFN-independent mechanism may be underlying the resistance of the persistently infected culture to infection with heterologous viruses. Our study defines a novel in vitro model of IPNV persistence and contributes to the understanding of the widespread distribution of aquabirnaviruses in marine and fresh water environments by establishing a carrier state in non susceptible fish species. |
doi_str_mv | 10.1016/j.vetmic.2010.10.017 |
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The persistently infected culture showed sustained production of infectious virus and could be continuously passaged for months. A distinct feature of this culture is that only a very small fraction of the cells harbours virus replication, in contrast to other reported IPNV-persistently infected cells from salmonid fish, where nearly all the cells express viral antigens. In spite of the small number of detectable IPNV-infected cells, the carrier culture shows resistance to superinfection with homologous as well as heterologous viruses. Temperature shift-up experiments indicate that viral interference is due to continuous replication of IPNV in the culture. Quantitation of Mx gene expression suggested that the interference phenomenon could be mediated by the activation of the interferon (IFN) system. However, conditioned medium from the IPNV-infected cell cultures only marginally protected other cells against VHSV infection, indicating that other type I IFN-independent mechanism may be underlying the resistance of the persistently infected culture to infection with heterologous viruses. Our study defines a novel in vitro model of IPNV persistence and contributes to the understanding of the widespread distribution of aquabirnaviruses in marine and fresh water environments by establishing a carrier state in non susceptible fish species.</description><identifier>ISSN: 0378-1135</identifier><identifier>EISSN: 1873-2542</identifier><identifier>DOI: 10.1016/j.vetmic.2010.10.017</identifier><identifier>PMID: 21109369</identifier><identifier>CODEN: VMICDQ</identifier><language>eng</language><publisher>Amsterdam: Elsevier B.V</publisher><subject>Animals ; Antigens, Viral - analysis ; Biological and medical sciences ; Birnaviridae Infections - immunology ; Birnaviridae Infections - virology ; Carrier culture ; Cell Line ; Culture Media, Conditioned ; Fish Diseases - immunology ; Fish Diseases - virology ; Fundamental and applied biological sciences. Psychology ; Gene Expression Regulation, Viral ; Infectious pancreatic necrosis virus ; Infectious pancreatic necrosis virus - growth & development ; Infectious pancreatic necrosis virus - immunology ; Infectious pancreatic necrosis virus - physiology ; Interferon Type I - immunology ; IPNV persistence ; Microbiology ; Miscellaneous ; Salmonidae ; Salmonidae - virology ; Superinfection - virology ; Superinfection exclusion ; Viral hemorrhagic septicemia virus ; Viral Interference ; Virology ; Virus Replication</subject><ispartof>Veterinary microbiology, 2011-04, Vol.149 (1-2), p.48-55</ispartof><rights>2010 Elsevier B.V.</rights><rights>2015 INIST-CNRS</rights><rights>Copyright © 2010 Elsevier B.V. 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The persistently infected culture showed sustained production of infectious virus and could be continuously passaged for months. A distinct feature of this culture is that only a very small fraction of the cells harbours virus replication, in contrast to other reported IPNV-persistently infected cells from salmonid fish, where nearly all the cells express viral antigens. In spite of the small number of detectable IPNV-infected cells, the carrier culture shows resistance to superinfection with homologous as well as heterologous viruses. Temperature shift-up experiments indicate that viral interference is due to continuous replication of IPNV in the culture. Quantitation of Mx gene expression suggested that the interference phenomenon could be mediated by the activation of the interferon (IFN) system. However, conditioned medium from the IPNV-infected cell cultures only marginally protected other cells against VHSV infection, indicating that other type I IFN-independent mechanism may be underlying the resistance of the persistently infected culture to infection with heterologous viruses. Our study defines a novel in vitro model of IPNV persistence and contributes to the understanding of the widespread distribution of aquabirnaviruses in marine and fresh water environments by establishing a carrier state in non susceptible fish species.</description><subject>Animals</subject><subject>Antigens, Viral - analysis</subject><subject>Biological and medical sciences</subject><subject>Birnaviridae Infections - immunology</subject><subject>Birnaviridae Infections - virology</subject><subject>Carrier culture</subject><subject>Cell Line</subject><subject>Culture Media, Conditioned</subject><subject>Fish Diseases - immunology</subject><subject>Fish Diseases - virology</subject><subject>Fundamental and applied biological sciences. Psychology</subject><subject>Gene Expression Regulation, Viral</subject><subject>Infectious pancreatic necrosis virus</subject><subject>Infectious pancreatic necrosis virus - growth & development</subject><subject>Infectious pancreatic necrosis virus - immunology</subject><subject>Infectious pancreatic necrosis virus - physiology</subject><subject>Interferon Type I - immunology</subject><subject>IPNV persistence</subject><subject>Microbiology</subject><subject>Miscellaneous</subject><subject>Salmonidae</subject><subject>Salmonidae - virology</subject><subject>Superinfection - virology</subject><subject>Superinfection exclusion</subject><subject>Viral hemorrhagic septicemia virus</subject><subject>Viral Interference</subject><subject>Virology</subject><subject>Virus Replication</subject><issn>0378-1135</issn><issn>1873-2542</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2011</creationdate><recordtype>article</recordtype><sourceid>EIF</sourceid><recordid>eNqFkd2O0zAQhSMEYsvCGyDwDQIuUvwf5wYJVfystAIk2Gtr6k62rtKkaydF8Bg8MZNNgTu4suz5Zs74nKJ4LPhScGFf7ZZHHPYxLCW_fVpyUd0pFsJVqpRGy7vFgqvKlUIoc1Y8yHnHOde15feLMykEr5WtF8XP1RYShAFT_AFD7DvWNww6FrsGA93HzA7QhYRUDKzDkPocM3tx8fnjS3aMieoBUoqYWMC2ZWFshzEh-xaHLUtI7EDtyIae5fFAKqe53UxskZT7tr-ehG7HYX5Y3GugzfjodJ4XV-_efl19KC8_vb9Yvbksg9bVUDojjGrWlZRGgAMj1EYGroWUm8Y5Y6pKayss2rUF4OgkCOtqDrqWugZRq_Pi-Tz3kPqbEfPg9zFPn4AOaR3v7OSfpcH_JY2RxCpJpJ7JyaecsPGHFPeQvnvB_RSb3_k5Nj_FNr1SbNT25CQwrve4-dP0OycCnp0AyAHaJpGpMf_lVO2MtIq4pzPXQO_hOhFz9YWUFBe1EY5PG76eCSRrj5SbzyEiRbSJiZLxmz7-e9dfJGbCuw</recordid><startdate>20110421</startdate><enddate>20110421</enddate><creator>García, Inmaculada</creator><creator>Galiana, Antonio</creator><creator>Falcó, Alberto</creator><creator>Estepa, Amparo</creator><creator>Perez, Luis</creator><general>Elsevier B.V</general><general>Amsterdam; New York: Elsevier</general><general>Elsevier</general><scope>FBQ</scope><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>7QO</scope><scope>7U9</scope><scope>8FD</scope><scope>F1W</scope><scope>FR3</scope><scope>H94</scope><scope>H95</scope><scope>H98</scope><scope>L.G</scope><scope>P64</scope></search><sort><creationdate>20110421</creationdate><title>Characterization of an infectious pancreatic necrosis (IPN) virus carrier cell culture with resistance to superinfection with heterologous viruses</title><author>García, Inmaculada ; Galiana, Antonio ; Falcó, Alberto ; Estepa, Amparo ; Perez, Luis</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c447t-85153fb72251a8a513d2c04122df88557744616e6b6aa0e82a16890a49249a193</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2011</creationdate><topic>Animals</topic><topic>Antigens, Viral - analysis</topic><topic>Biological and medical sciences</topic><topic>Birnaviridae Infections - immunology</topic><topic>Birnaviridae Infections - virology</topic><topic>Carrier culture</topic><topic>Cell Line</topic><topic>Culture Media, Conditioned</topic><topic>Fish Diseases - immunology</topic><topic>Fish Diseases - virology</topic><topic>Fundamental and applied biological sciences. Psychology</topic><topic>Gene Expression Regulation, Viral</topic><topic>Infectious pancreatic necrosis virus</topic><topic>Infectious pancreatic necrosis virus - growth & development</topic><topic>Infectious pancreatic necrosis virus - immunology</topic><topic>Infectious pancreatic necrosis virus - physiology</topic><topic>Interferon Type I - immunology</topic><topic>IPNV persistence</topic><topic>Microbiology</topic><topic>Miscellaneous</topic><topic>Salmonidae</topic><topic>Salmonidae - virology</topic><topic>Superinfection - virology</topic><topic>Superinfection exclusion</topic><topic>Viral hemorrhagic septicemia virus</topic><topic>Viral Interference</topic><topic>Virology</topic><topic>Virus Replication</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>García, Inmaculada</creatorcontrib><creatorcontrib>Galiana, Antonio</creatorcontrib><creatorcontrib>Falcó, Alberto</creatorcontrib><creatorcontrib>Estepa, Amparo</creatorcontrib><creatorcontrib>Perez, Luis</creatorcontrib><collection>AGRIS</collection><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>Biotechnology Research Abstracts</collection><collection>Virology and AIDS Abstracts</collection><collection>Technology Research Database</collection><collection>ASFA: Aquatic Sciences and Fisheries Abstracts</collection><collection>Engineering Research Database</collection><collection>AIDS and Cancer Research Abstracts</collection><collection>Aquatic Science & Fisheries Abstracts (ASFA) 1: Biological Sciences & Living Resources</collection><collection>Aquatic Science & Fisheries Abstracts (ASFA) Aquaculture Abstracts</collection><collection>Aquatic Science & Fisheries Abstracts (ASFA) Professional</collection><collection>Biotechnology and BioEngineering Abstracts</collection><jtitle>Veterinary microbiology</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>García, Inmaculada</au><au>Galiana, Antonio</au><au>Falcó, Alberto</au><au>Estepa, Amparo</au><au>Perez, Luis</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Characterization of an infectious pancreatic necrosis (IPN) virus carrier cell culture with resistance to superinfection with heterologous viruses</atitle><jtitle>Veterinary microbiology</jtitle><addtitle>Vet Microbiol</addtitle><date>2011-04-21</date><risdate>2011</risdate><volume>149</volume><issue>1-2</issue><spage>48</spage><epage>55</epage><pages>48-55</pages><issn>0378-1135</issn><eissn>1873-2542</eissn><coden>VMICDQ</coden><abstract>A state of persistence of a non susceptible fish cell line with infectious pancreatic necrosis virus (IPNV) was established in vitro by experimental infection. The persistently infected culture showed sustained production of infectious virus and could be continuously passaged for months. A distinct feature of this culture is that only a very small fraction of the cells harbours virus replication, in contrast to other reported IPNV-persistently infected cells from salmonid fish, where nearly all the cells express viral antigens. In spite of the small number of detectable IPNV-infected cells, the carrier culture shows resistance to superinfection with homologous as well as heterologous viruses. Temperature shift-up experiments indicate that viral interference is due to continuous replication of IPNV in the culture. Quantitation of Mx gene expression suggested that the interference phenomenon could be mediated by the activation of the interferon (IFN) system. However, conditioned medium from the IPNV-infected cell cultures only marginally protected other cells against VHSV infection, indicating that other type I IFN-independent mechanism may be underlying the resistance of the persistently infected culture to infection with heterologous viruses. Our study defines a novel in vitro model of IPNV persistence and contributes to the understanding of the widespread distribution of aquabirnaviruses in marine and fresh water environments by establishing a carrier state in non susceptible fish species.</abstract><cop>Amsterdam</cop><pub>Elsevier B.V</pub><pmid>21109369</pmid><doi>10.1016/j.vetmic.2010.10.017</doi><tpages>8</tpages></addata></record> |
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subjects | Animals Antigens, Viral - analysis Biological and medical sciences Birnaviridae Infections - immunology Birnaviridae Infections - virology Carrier culture Cell Line Culture Media, Conditioned Fish Diseases - immunology Fish Diseases - virology Fundamental and applied biological sciences. Psychology Gene Expression Regulation, Viral Infectious pancreatic necrosis virus Infectious pancreatic necrosis virus - growth & development Infectious pancreatic necrosis virus - immunology Infectious pancreatic necrosis virus - physiology Interferon Type I - immunology IPNV persistence Microbiology Miscellaneous Salmonidae Salmonidae - virology Superinfection - virology Superinfection exclusion Viral hemorrhagic septicemia virus Viral Interference Virology Virus Replication |
title | Characterization of an infectious pancreatic necrosis (IPN) virus carrier cell culture with resistance to superinfection with heterologous viruses |
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