Aquatic birnavirus induces apoptosis through activated caspase-8 and -3 in a zebrafish cell line
In this study, the possible influence of temperature on infectious pancreatic necrosis virus (IPNV)‐induced apoptosis in a zebrafish liver epithelium (ZLE) cell line was investigated. At a lower temperature (18 °C), there was expression of viral proteins VP2 and VP3 at 4 h post‐infection (p.i.). At...
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description | In this study, the possible influence of temperature on infectious pancreatic necrosis virus (IPNV)‐induced apoptosis in a zebrafish liver epithelium (ZLE) cell line was investigated. At a lower temperature (18 °C), there was expression of viral proteins VP2 and VP3 at 4 h post‐infection (p.i.). At this time no expression was found in the high temperature group at 28 °C. The cell survival ratio was 52 and 18% at 24 and 48 h p.i., respectively, during IPNV infection at 18 °C. In addition, we assayed for apoptosis in IPNV‐infected cells with terminal deoxynucleotidyl transferase (TdT)‐mediated end labelling (TUNEL) of DNA at different dosages of virus. We found a ratio of apoptotic cells of 8 and 25% at 12 and 18 h p.i., respectively, in the multiplicity of infection (MOI) 1 group. The MOI 10 group had 20 and 45% apoptotic cells at 12 and 18 h, respectively. Furthermore, at 18 °C IPNV activated the caspase‐8 and 3 from 1.5 to 2 times at 12 and 18 h p.i., respectively. Taken together, these findings suggest that successful virus replication occurs at the low temperature (18 °C) compared with the non‐permissive temperature of 28 °C. Thus, IPNV replication is capable of activating caspase‐8 and ‐3 and inducing host apoptosis. |
doi_str_mv | 10.1111/j.1365-2761.2004.00604.x |
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At a lower temperature (18 °C), there was expression of viral proteins VP2 and VP3 at 4 h post‐infection (p.i.). At this time no expression was found in the high temperature group at 28 °C. The cell survival ratio was 52 and 18% at 24 and 48 h p.i., respectively, during IPNV infection at 18 °C. In addition, we assayed for apoptosis in IPNV‐infected cells with terminal deoxynucleotidyl transferase (TdT)‐mediated end labelling (TUNEL) of DNA at different dosages of virus. We found a ratio of apoptotic cells of 8 and 25% at 12 and 18 h p.i., respectively, in the multiplicity of infection (MOI) 1 group. The MOI 10 group had 20 and 45% apoptotic cells at 12 and 18 h, respectively. Furthermore, at 18 °C IPNV activated the caspase‐8 and 3 from 1.5 to 2 times at 12 and 18 h p.i., respectively. Taken together, these findings suggest that successful virus replication occurs at the low temperature (18 °C) compared with the non‐permissive temperature of 28 °C. Thus, IPNV replication is capable of activating caspase‐8 and ‐3 and inducing host apoptosis.</description><identifier>ISSN: 0140-7775</identifier><identifier>EISSN: 1365-2761</identifier><identifier>DOI: 10.1111/j.1365-2761.2004.00604.x</identifier><identifier>PMID: 15752273</identifier><language>eng</language><publisher>Oxford, UK: Blackwell Science Ltd</publisher><subject>Animals ; apoptosis ; Apoptosis - physiology ; Birnavirus ; Capsid Proteins - metabolism ; Caspase 3 ; Caspase 8 ; caspases ; Caspases - metabolism ; Cell Line ; Danio rerio ; Gene Expression Regulation, Viral ; Immunoblotting ; In Situ Nick-End Labeling ; Infectious pancreatic necrosis virus ; Infectious pancreatic necrosis virus - metabolism ; Infectious pancreatic necrosis virus - physiology ; Liver - pathology ; Liver - virology ; Temperature ; temperature-dependent infection ; TUNEL assay ; Virus Replication - physiology ; Zebrafish - metabolism ; Zebrafish - virology ; zebrafish cell line</subject><ispartof>Journal of fish diseases, 2005-03, Vol.28 (3), p.133-140</ispartof><rights>2005 Blackwell Publishing Ltd</rights><lds50>peer_reviewed</lds50><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c4624-3a66e7e361a1577547cf1aa54fe4ea30b6132717c1ec24fb98e131626167fcc63</citedby><cites>FETCH-LOGICAL-c4624-3a66e7e361a1577547cf1aa54fe4ea30b6132717c1ec24fb98e131626167fcc63</cites></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><linktopdf>$$Uhttps://onlinelibrary.wiley.com/doi/pdf/10.1111%2Fj.1365-2761.2004.00604.x$$EPDF$$P50$$Gwiley$$H</linktopdf><linktohtml>$$Uhttps://onlinelibrary.wiley.com/doi/full/10.1111%2Fj.1365-2761.2004.00604.x$$EHTML$$P50$$Gwiley$$H</linktohtml><link.rule.ids>314,780,784,1417,27924,27925,45574,45575</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/15752273$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Hong, J-R</creatorcontrib><creatorcontrib>Huang, L-J</creatorcontrib><creatorcontrib>Wu, J-L</creatorcontrib><title>Aquatic birnavirus induces apoptosis through activated caspase-8 and -3 in a zebrafish cell line</title><title>Journal of fish diseases</title><addtitle>J Fish Dis</addtitle><description>In this study, the possible influence of temperature on infectious pancreatic necrosis virus (IPNV)‐induced apoptosis in a zebrafish liver epithelium (ZLE) cell line was investigated. At a lower temperature (18 °C), there was expression of viral proteins VP2 and VP3 at 4 h post‐infection (p.i.). At this time no expression was found in the high temperature group at 28 °C. The cell survival ratio was 52 and 18% at 24 and 48 h p.i., respectively, during IPNV infection at 18 °C. In addition, we assayed for apoptosis in IPNV‐infected cells with terminal deoxynucleotidyl transferase (TdT)‐mediated end labelling (TUNEL) of DNA at different dosages of virus. We found a ratio of apoptotic cells of 8 and 25% at 12 and 18 h p.i., respectively, in the multiplicity of infection (MOI) 1 group. The MOI 10 group had 20 and 45% apoptotic cells at 12 and 18 h, respectively. Furthermore, at 18 °C IPNV activated the caspase‐8 and 3 from 1.5 to 2 times at 12 and 18 h p.i., respectively. Taken together, these findings suggest that successful virus replication occurs at the low temperature (18 °C) compared with the non‐permissive temperature of 28 °C. Thus, IPNV replication is capable of activating caspase‐8 and ‐3 and inducing host apoptosis.</description><subject>Animals</subject><subject>apoptosis</subject><subject>Apoptosis - physiology</subject><subject>Birnavirus</subject><subject>Capsid Proteins - metabolism</subject><subject>Caspase 3</subject><subject>Caspase 8</subject><subject>caspases</subject><subject>Caspases - metabolism</subject><subject>Cell Line</subject><subject>Danio rerio</subject><subject>Gene Expression Regulation, Viral</subject><subject>Immunoblotting</subject><subject>In Situ Nick-End Labeling</subject><subject>Infectious pancreatic necrosis virus</subject><subject>Infectious pancreatic necrosis virus - metabolism</subject><subject>Infectious pancreatic necrosis virus - physiology</subject><subject>Liver - pathology</subject><subject>Liver - virology</subject><subject>Temperature</subject><subject>temperature-dependent infection</subject><subject>TUNEL assay</subject><subject>Virus Replication - physiology</subject><subject>Zebrafish - metabolism</subject><subject>Zebrafish - virology</subject><subject>zebrafish cell line</subject><issn>0140-7775</issn><issn>1365-2761</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2005</creationdate><recordtype>article</recordtype><sourceid>EIF</sourceid><recordid>eNqNkcFu1DAQhi0EokvhFZDFgVsWj-3YW4lL1bItqAKpAnE0E--E9ZJNUjspW54ep7sqEhfwwT74-0e_5mOMg5hDPm82c1CmLKQ1MJdC6LkQJt-7R2z28PGYzQRoUVhryyP2LKWNEGBLME_ZEZS2lNKqGft2ejPiEDyvQmzxNsQx8dCuRk-JY9_1Q5dC4sM6duP3NUc_hFscaMU9ph4TFQuO7YoXKoc48l9URaxDWnNPTcOb0NJz9qTGJtGLw3vMvizffT67LK4-Xbw_O70qvDZSFwqNIUvKAOZyttTW14BY6po0oRKVASUtWA_kpa6rkwWBAiMNGFt7b9Qxe72f28fuZqQ0uG1IUwtsqRuTM1afGKXVP0HIoNBCZ_DVX-CmG_OSmuSkyAVLbUSGFnvIxy6lSLXrY9hivHMg3OTKbdykxE1K3OTK3btyuxx9eZg_Vlta_Qke5GTg7R74GRq6--_B7sPy3Nz3L_bxkAbaPcQx_sjLULZ0Xz9eOC2uz5eLy6W7Vr8B_XOvjg</recordid><startdate>200503</startdate><enddate>200503</enddate><creator>Hong, J-R</creator><creator>Huang, L-J</creator><creator>Wu, J-L</creator><general>Blackwell Science Ltd</general><general>Blackwell Publishing Ltd</general><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>7QL</scope><scope>7TN</scope><scope>7U9</scope><scope>8FD</scope><scope>C1K</scope><scope>F1W</scope><scope>FR3</scope><scope>H94</scope><scope>H95</scope><scope>H98</scope><scope>H99</scope><scope>L.F</scope><scope>L.G</scope><scope>M7N</scope><scope>P64</scope><scope>7X8</scope></search><sort><creationdate>200503</creationdate><title>Aquatic birnavirus induces apoptosis through activated caspase-8 and -3 in a zebrafish cell line</title><author>Hong, J-R ; Huang, L-J ; Wu, J-L</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c4624-3a66e7e361a1577547cf1aa54fe4ea30b6132717c1ec24fb98e131626167fcc63</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2005</creationdate><topic>Animals</topic><topic>apoptosis</topic><topic>Apoptosis - physiology</topic><topic>Birnavirus</topic><topic>Capsid Proteins - metabolism</topic><topic>Caspase 3</topic><topic>Caspase 8</topic><topic>caspases</topic><topic>Caspases - metabolism</topic><topic>Cell Line</topic><topic>Danio rerio</topic><topic>Gene Expression Regulation, Viral</topic><topic>Immunoblotting</topic><topic>In Situ Nick-End Labeling</topic><topic>Infectious pancreatic necrosis virus</topic><topic>Infectious pancreatic necrosis virus - metabolism</topic><topic>Infectious pancreatic necrosis virus - physiology</topic><topic>Liver - pathology</topic><topic>Liver - virology</topic><topic>Temperature</topic><topic>temperature-dependent infection</topic><topic>TUNEL assay</topic><topic>Virus Replication - physiology</topic><topic>Zebrafish - metabolism</topic><topic>Zebrafish - virology</topic><topic>zebrafish cell line</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Hong, J-R</creatorcontrib><creatorcontrib>Huang, L-J</creatorcontrib><creatorcontrib>Wu, J-L</creatorcontrib><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>Bacteriology Abstracts (Microbiology B)</collection><collection>Oceanic Abstracts</collection><collection>Virology and AIDS Abstracts</collection><collection>Technology Research Database</collection><collection>Environmental Sciences and Pollution Management</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>ASFA: Marine Biotechnology Abstracts</collection><collection>Aquatic Science & Fisheries Abstracts (ASFA) Marine Biotechnology Abstracts</collection><collection>Aquatic Science & Fisheries Abstracts (ASFA) Professional</collection><collection>Algology Mycology and Protozoology Abstracts (Microbiology C)</collection><collection>Biotechnology and BioEngineering Abstracts</collection><collection>MEDLINE - Academic</collection><jtitle>Journal of fish diseases</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Hong, J-R</au><au>Huang, L-J</au><au>Wu, J-L</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Aquatic birnavirus induces apoptosis through activated caspase-8 and -3 in a zebrafish cell line</atitle><jtitle>Journal of fish diseases</jtitle><addtitle>J Fish Dis</addtitle><date>2005-03</date><risdate>2005</risdate><volume>28</volume><issue>3</issue><spage>133</spage><epage>140</epage><pages>133-140</pages><issn>0140-7775</issn><eissn>1365-2761</eissn><abstract>In this study, the possible influence of temperature on infectious pancreatic necrosis virus (IPNV)‐induced apoptosis in a zebrafish liver epithelium (ZLE) cell line was investigated. At a lower temperature (18 °C), there was expression of viral proteins VP2 and VP3 at 4 h post‐infection (p.i.). At this time no expression was found in the high temperature group at 28 °C. The cell survival ratio was 52 and 18% at 24 and 48 h p.i., respectively, during IPNV infection at 18 °C. In addition, we assayed for apoptosis in IPNV‐infected cells with terminal deoxynucleotidyl transferase (TdT)‐mediated end labelling (TUNEL) of DNA at different dosages of virus. We found a ratio of apoptotic cells of 8 and 25% at 12 and 18 h p.i., respectively, in the multiplicity of infection (MOI) 1 group. The MOI 10 group had 20 and 45% apoptotic cells at 12 and 18 h, respectively. Furthermore, at 18 °C IPNV activated the caspase‐8 and 3 from 1.5 to 2 times at 12 and 18 h p.i., respectively. Taken together, these findings suggest that successful virus replication occurs at the low temperature (18 °C) compared with the non‐permissive temperature of 28 °C. Thus, IPNV replication is capable of activating caspase‐8 and ‐3 and inducing host apoptosis.</abstract><cop>Oxford, UK</cop><pub>Blackwell Science Ltd</pub><pmid>15752273</pmid><doi>10.1111/j.1365-2761.2004.00604.x</doi><tpages>8</tpages></addata></record> |
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subjects | Animals apoptosis Apoptosis - physiology Birnavirus Capsid Proteins - metabolism Caspase 3 Caspase 8 caspases Caspases - metabolism Cell Line Danio rerio Gene Expression Regulation, Viral Immunoblotting In Situ Nick-End Labeling Infectious pancreatic necrosis virus Infectious pancreatic necrosis virus - metabolism Infectious pancreatic necrosis virus - physiology Liver - pathology Liver - virology Temperature temperature-dependent infection TUNEL assay Virus Replication - physiology Zebrafish - metabolism Zebrafish - virology zebrafish cell line |
title | Aquatic birnavirus induces apoptosis through activated caspase-8 and -3 in a zebrafish cell line |
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