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RNA elements in open reading frames of the bluetongue virus genome are essential for virus replication
Members of the Reoviridae family are non-enveloped multi-layered viruses with a double stranded RNA genome consisting of 9 to 12 genome segments. Bluetongue virus is the prototype orbivirus (family Reoviridae, genus Orbivirus), causing disease in ruminants, and is spread by Culicoides biting midges....
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Published in: | PloS one 2014-03, Vol.9 (3), p.e92377 |
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description | Members of the Reoviridae family are non-enveloped multi-layered viruses with a double stranded RNA genome consisting of 9 to 12 genome segments. Bluetongue virus is the prototype orbivirus (family Reoviridae, genus Orbivirus), causing disease in ruminants, and is spread by Culicoides biting midges. Obviously, several steps in the Reoviridae family replication cycle require virus specific as well as segment specific recognition by viral proteins, but detailed processes in these interactions are still barely understood. Recently, we have shown that expression of NS3 and NS3a proteins encoded by genome segment 10 of bluetongue virus is not essential for virus replication. This gave us the unique opportunity to investigate the role of RNA sequences in the segment 10 open reading frame in virus replication, independent of its protein products. Reverse genetics was used to generate virus mutants with deletions in the open reading frame of segment 10. Although virus with a deletion between both start codons was not viable, deletions throughout the rest of the open reading frame led to the rescue of replicating virus. However, all bluetongue virus deletion mutants without functional protein expression of segment 10 contained inserts of RNA sequences originating from several viral genome segments. Subsequent studies showed that these RNA inserts act as RNA elements, needed for rescue and replication of virus. Functionality of the inserts is orientation-dependent but is independent from the position in segment 10. This study clearly shows that RNA in the open reading frame of Reoviridae members does not only encode proteins, but is also essential for virus replication. |
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Bluetongue virus is the prototype orbivirus (family Reoviridae, genus Orbivirus), causing disease in ruminants, and is spread by Culicoides biting midges. Obviously, several steps in the Reoviridae family replication cycle require virus specific as well as segment specific recognition by viral proteins, but detailed processes in these interactions are still barely understood. Recently, we have shown that expression of NS3 and NS3a proteins encoded by genome segment 10 of bluetongue virus is not essential for virus replication. This gave us the unique opportunity to investigate the role of RNA sequences in the segment 10 open reading frame in virus replication, independent of its protein products. Reverse genetics was used to generate virus mutants with deletions in the open reading frame of segment 10. Although virus with a deletion between both start codons was not viable, deletions throughout the rest of the open reading frame led to the rescue of replicating virus. However, all bluetongue virus deletion mutants without functional protein expression of segment 10 contained inserts of RNA sequences originating from several viral genome segments. Subsequent studies showed that these RNA inserts act as RNA elements, needed for rescue and replication of virus. Functionality of the inserts is orientation-dependent but is independent from the position in segment 10. This study clearly shows that RNA in the open reading frame of Reoviridae members does not only encode proteins, but is also essential for virus replication.</description><identifier>ISSN: 1932-6203</identifier><identifier>EISSN: 1932-6203</identifier><identifier>DOI: 10.1371/journal.pone.0092377</identifier><identifier>PMID: 24658296</identifier><language>eng</language><publisher>United States: Public Library of Science</publisher><subject>binding ; Biology and life sciences ; Biting ; Bluetongue ; Bluetongue virus - genetics ; Codons ; core ; Cytoplasm ; Deletion mutant ; Double-stranded RNA ; Enzymes ; fever virus ; Gene Deletion ; Gene expression ; Gene sequencing ; Genetics ; Genome, Viral ; Genomes ; Genomics ; insect cells ; Inserts ; intragenic recombination ; Multilayers ; Mutants ; Open Reading Frames ; Plasmids ; Polymerase chain reaction ; protein ns2 ; Proteins ; Replicating ; Replication ; Ribonucleic acid ; RNA ; RNA, Viral - genetics ; RNA-protein interactions ; segment ; Segments ; Veterinary medicine ; Viral proteins ; viral-rna ; Virology ; Virus replication ; Virus Replication - genetics ; Viruses ; vp6 protein</subject><ispartof>PloS one, 2014-03, Vol.9 (3), p.e92377</ispartof><rights>COPYRIGHT 2014 Public Library of Science</rights><rights>2014 Feenstra et al. This is an open-access article distributed under the terms of the Creative Commons Attribution License: http://creativecommons.org/licenses/by/4.0/ (the “License”), which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are credited. Notwithstanding the ProQuest Terms and Conditions, you may use this content in accordance with the terms of the License.</rights><rights>2014 Feenstra et al 2014 Feenstra et al</rights><rights>Wageningen University & Research</rights><lds50>peer_reviewed</lds50><oa>free_for_read</oa><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c743t-ea3af58701fc5c29ea0047535421cba0fc4c6151c5cd6eb9f3e9e94aa90d2643</citedby><cites>FETCH-LOGICAL-c743t-ea3af58701fc5c29ea0047535421cba0fc4c6151c5cd6eb9f3e9e94aa90d2643</cites></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><linktopdf>$$Uhttps://www.proquest.com/docview/1509205478/fulltextPDF?pq-origsite=primo$$EPDF$$P50$$Gproquest$$Hfree_for_read</linktopdf><linktohtml>$$Uhttps://www.proquest.com/docview/1509205478?pq-origsite=primo$$EHTML$$P50$$Gproquest$$Hfree_for_read</linktohtml><link.rule.ids>230,314,727,780,784,885,25753,27924,27925,37012,44590,53791,53793,75126</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/24658296$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><contributor>Attoui, Houssam</contributor><creatorcontrib>Feenstra, Femke</creatorcontrib><creatorcontrib>van Gennip, René G P</creatorcontrib><creatorcontrib>van de Water, Sandra G P</creatorcontrib><creatorcontrib>van Rijn, Piet A</creatorcontrib><title>RNA elements in open reading frames of the bluetongue virus genome are essential for virus replication</title><title>PloS one</title><addtitle>PLoS One</addtitle><description>Members of the Reoviridae family are non-enveloped multi-layered viruses with a double stranded RNA genome consisting of 9 to 12 genome segments. Bluetongue virus is the prototype orbivirus (family Reoviridae, genus Orbivirus), causing disease in ruminants, and is spread by Culicoides biting midges. Obviously, several steps in the Reoviridae family replication cycle require virus specific as well as segment specific recognition by viral proteins, but detailed processes in these interactions are still barely understood. Recently, we have shown that expression of NS3 and NS3a proteins encoded by genome segment 10 of bluetongue virus is not essential for virus replication. This gave us the unique opportunity to investigate the role of RNA sequences in the segment 10 open reading frame in virus replication, independent of its protein products. Reverse genetics was used to generate virus mutants with deletions in the open reading frame of segment 10. Although virus with a deletion between both start codons was not viable, deletions throughout the rest of the open reading frame led to the rescue of replicating virus. 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Bluetongue virus is the prototype orbivirus (family Reoviridae, genus Orbivirus), causing disease in ruminants, and is spread by Culicoides biting midges. Obviously, several steps in the Reoviridae family replication cycle require virus specific as well as segment specific recognition by viral proteins, but detailed processes in these interactions are still barely understood. Recently, we have shown that expression of NS3 and NS3a proteins encoded by genome segment 10 of bluetongue virus is not essential for virus replication. This gave us the unique opportunity to investigate the role of RNA sequences in the segment 10 open reading frame in virus replication, independent of its protein products. Reverse genetics was used to generate virus mutants with deletions in the open reading frame of segment 10. Although virus with a deletion between both start codons was not viable, deletions throughout the rest of the open reading frame led to the rescue of replicating virus. However, all bluetongue virus deletion mutants without functional protein expression of segment 10 contained inserts of RNA sequences originating from several viral genome segments. Subsequent studies showed that these RNA inserts act as RNA elements, needed for rescue and replication of virus. Functionality of the inserts is orientation-dependent but is independent from the position in segment 10. This study clearly shows that RNA in the open reading frame of Reoviridae members does not only encode proteins, but is also essential for virus replication.</abstract><cop>United States</cop><pub>Public Library of Science</pub><pmid>24658296</pmid><doi>10.1371/journal.pone.0092377</doi><tpages>e92377</tpages><oa>free_for_read</oa></addata></record> |
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subjects | binding Biology and life sciences Biting Bluetongue Bluetongue virus - genetics Codons core Cytoplasm Deletion mutant Double-stranded RNA Enzymes fever virus Gene Deletion Gene expression Gene sequencing Genetics Genome, Viral Genomes Genomics insect cells Inserts intragenic recombination Multilayers Mutants Open Reading Frames Plasmids Polymerase chain reaction protein ns2 Proteins Replicating Replication Ribonucleic acid RNA RNA, Viral - genetics RNA-protein interactions segment Segments Veterinary medicine Viral proteins viral-rna Virology Virus replication Virus Replication - genetics Viruses vp6 protein |
title | RNA elements in open reading frames of the bluetongue virus genome are essential for virus replication |
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