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Ultrastructural morphogenesis of salmonid alphavirus 1
Studies on the ultrastructural morphogenesis of viruses give an insight into how the host cell mechanisms are utilized for new virion synthesis. A time course examining salmonid alphavirus 1 (SAV 1) assembly was performed by culturing the virus on Chinook salmon embryo cells (CHSE‐214). Different st...
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Published in: | Journal of fish diseases 2012-11, Vol.35 (11), p.799-808 |
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container_title | Journal of fish diseases |
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creator | Herath, T K Ferguson, H W Thompson, K D Adams, A Richards, R H |
description | Studies on the ultrastructural morphogenesis of viruses give an insight into how the host cell mechanisms are utilized for new virion synthesis. A time course examining salmonid alphavirus 1 (SAV 1) assembly was performed by culturing the virus on Chinook salmon embryo cells (CHSE‐214). Different stages of viral replication were observed under electron microscopy. Virus‐like particles were observed inside membrane‐bound vesicles as early as 1 h following contact of the virus with the cells. Membrane‐dependent replication complexes were observed in the cytoplasm of the cells, with spherules found at the periphery of late endosome‐like vacuoles. The use of intracellular membranes for RNA replication is similar to other positive‐sense single‐stranded RNA (+ssRNA) viruses. The number of Golgi apparatus and associated vacuoles characterized by ‘fuzzy’‐coated membranes was greater in virus‐infected cells. The mature enveloped virions started to bud out from the cells at approximately 24 h post‐infection. These observations suggest that the pathway used by SAV 1 for the generation of new virus particles in vitro is comparable to viral replication observed with mammalian alphaviruses but with some interesting differences. |
doi_str_mv | 10.1111/j.1365-2761.2012.01420.x |
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A time course examining salmonid alphavirus 1 (SAV 1) assembly was performed by culturing the virus on Chinook salmon embryo cells (CHSE‐214). Different stages of viral replication were observed under electron microscopy. Virus‐like particles were observed inside membrane‐bound vesicles as early as 1 h following contact of the virus with the cells. Membrane‐dependent replication complexes were observed in the cytoplasm of the cells, with spherules found at the periphery of late endosome‐like vacuoles. The use of intracellular membranes for RNA replication is similar to other positive‐sense single‐stranded RNA (+ssRNA) viruses. The number of Golgi apparatus and associated vacuoles characterized by ‘fuzzy’‐coated membranes was greater in virus‐infected cells. The mature enveloped virions started to bud out from the cells at approximately 24 h post‐infection. These observations suggest that the pathway used by SAV 1 for the generation of new virus particles in vitro is comparable to viral replication observed with mammalian alphaviruses but with some interesting differences.</description><identifier>ISSN: 0140-7775</identifier><identifier>EISSN: 1365-2761</identifier><identifier>DOI: 10.1111/j.1365-2761.2012.01420.x</identifier><identifier>PMID: 22913764</identifier><language>eng</language><publisher>England: Blackwell Publishing Ltd</publisher><subject>Alphavirus - physiology ; Alphavirus - ultrastructure ; Animals ; Atlantic salmon ; Cell Line ; CHSE-214 ; electron microscopy ; Microscopy, Electron, Transmission ; morphogenesis ; Oncorhynchus tshawytscha ; Salmonid alphavirus ; Salmonidae - virology ; ultrastructure ; Virus Replication</subject><ispartof>Journal of fish diseases, 2012-11, Vol.35 (11), p.799-808</ispartof><rights>2012 Blackwell Publishing Ltd</rights><rights>2012 Blackwell Publishing Ltd.</rights><rights>Copyright © 2012 Blackwell Publishing Ltd</rights><lds50>peer_reviewed</lds50><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c4680-6bad309f4aa1d637c5519586699967faf861342a4e685961d5fa19082e4ec9313</citedby><cites>FETCH-LOGICAL-c4680-6bad309f4aa1d637c5519586699967faf861342a4e685961d5fa19082e4ec9313</cites></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><link.rule.ids>314,780,784,27924,27925</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/22913764$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Herath, T K</creatorcontrib><creatorcontrib>Ferguson, H W</creatorcontrib><creatorcontrib>Thompson, K D</creatorcontrib><creatorcontrib>Adams, A</creatorcontrib><creatorcontrib>Richards, R H</creatorcontrib><title>Ultrastructural morphogenesis of salmonid alphavirus 1</title><title>Journal of fish diseases</title><addtitle>J Fish Dis</addtitle><description>Studies on the ultrastructural morphogenesis of viruses give an insight into how the host cell mechanisms are utilized for new virion synthesis. A time course examining salmonid alphavirus 1 (SAV 1) assembly was performed by culturing the virus on Chinook salmon embryo cells (CHSE‐214). Different stages of viral replication were observed under electron microscopy. Virus‐like particles were observed inside membrane‐bound vesicles as early as 1 h following contact of the virus with the cells. Membrane‐dependent replication complexes were observed in the cytoplasm of the cells, with spherules found at the periphery of late endosome‐like vacuoles. The use of intracellular membranes for RNA replication is similar to other positive‐sense single‐stranded RNA (+ssRNA) viruses. The number of Golgi apparatus and associated vacuoles characterized by ‘fuzzy’‐coated membranes was greater in virus‐infected cells. The mature enveloped virions started to bud out from the cells at approximately 24 h post‐infection. These observations suggest that the pathway used by SAV 1 for the generation of new virus particles in vitro is comparable to viral replication observed with mammalian alphaviruses but with some interesting differences.</description><subject>Alphavirus - physiology</subject><subject>Alphavirus - ultrastructure</subject><subject>Animals</subject><subject>Atlantic salmon</subject><subject>Cell Line</subject><subject>CHSE-214</subject><subject>electron microscopy</subject><subject>Microscopy, Electron, Transmission</subject><subject>morphogenesis</subject><subject>Oncorhynchus tshawytscha</subject><subject>Salmonid alphavirus</subject><subject>Salmonidae - virology</subject><subject>ultrastructure</subject><subject>Virus Replication</subject><issn>0140-7775</issn><issn>1365-2761</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2012</creationdate><recordtype>article</recordtype><recordid>eNqNkUtP3DAUhS1EBcPjL6BIbNgk9fXj2l6wQLQMrdB0w2NpmcQpmSaTwU5g-Pf1MHQWXeHNtXy_c658LiEZ0ALS-TovgKPMmUIoGAVWUBCMFqsdMtk2dskkvdJcKSX3yUGMc0pBScA9ss-YAa5QTAjetUNwcQhjOYzBtVnXh-VT_9svfGxi1tdZdG3XL5oqc-3yyb00YYwZHJEvtWujP_6oh-Tu6vvt5XV-82v64_LiJi8Faprjo6s4NbVwDirkqpQSjNSIxhhUtas1AhfMCY9aGoRK1g4M1cwLXxoO_JCcbXyXoX8efRxs18TSt61b-H6MFoBJxlHpz6AAGgXTKqGn_6HzfgyL9BEL1EhluEaeKL2hytDHGHxtl6HpXHhL0Lubndt12nadtl2vwb6vwa6S9ORjwPjY-Wor_Jd7As43wGvT-rdPG9ufV9_Wt6TPN_omDn611bvwx6LiStqH2dROmaBM3c_sjP8F1d2h6g</recordid><startdate>201211</startdate><enddate>201211</enddate><creator>Herath, T K</creator><creator>Ferguson, H W</creator><creator>Thompson, K D</creator><creator>Adams, A</creator><creator>Richards, R H</creator><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>201211</creationdate><title>Ultrastructural morphogenesis of salmonid alphavirus 1</title><author>Herath, T K ; 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A time course examining salmonid alphavirus 1 (SAV 1) assembly was performed by culturing the virus on Chinook salmon embryo cells (CHSE‐214). Different stages of viral replication were observed under electron microscopy. Virus‐like particles were observed inside membrane‐bound vesicles as early as 1 h following contact of the virus with the cells. Membrane‐dependent replication complexes were observed in the cytoplasm of the cells, with spherules found at the periphery of late endosome‐like vacuoles. The use of intracellular membranes for RNA replication is similar to other positive‐sense single‐stranded RNA (+ssRNA) viruses. The number of Golgi apparatus and associated vacuoles characterized by ‘fuzzy’‐coated membranes was greater in virus‐infected cells. The mature enveloped virions started to bud out from the cells at approximately 24 h post‐infection. These observations suggest that the pathway used by SAV 1 for the generation of new virus particles in vitro is comparable to viral replication observed with mammalian alphaviruses but with some interesting differences.</abstract><cop>England</cop><pub>Blackwell Publishing Ltd</pub><pmid>22913764</pmid><doi>10.1111/j.1365-2761.2012.01420.x</doi><tpages>10</tpages></addata></record> |
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subjects | Alphavirus - physiology Alphavirus - ultrastructure Animals Atlantic salmon Cell Line CHSE-214 electron microscopy Microscopy, Electron, Transmission morphogenesis Oncorhynchus tshawytscha Salmonid alphavirus Salmonidae - virology ultrastructure Virus Replication |
title | Ultrastructural morphogenesis of salmonid alphavirus 1 |
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