Insights into bunyavirus architecture from electron cryotomography of Uukuniemi virus
Bunyaviridae is a large family of viruses that have gained attention as "emerging viruses" because many members cause serious disease in humans, with an increasing number of outbreaks. These negative-strand RNA viruses possess a membrane envelope covered by glycoproteins. The virions are p...
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Veröffentlicht in: | Proceedings of the National Academy of Sciences - PNAS 2008-02, Vol.105 (7), p.2375-2379 |
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description | Bunyaviridae is a large family of viruses that have gained attention as "emerging viruses" because many members cause serious disease in humans, with an increasing number of outbreaks. These negative-strand RNA viruses possess a membrane envelope covered by glycoproteins. The virions are pleiomorphic and thus have not been amenable to structural characterization using common techniques that involve averaging of electron microscopic images. Here, we determined the three-dimensional structure of a member of the Bunyaviridae family by using electron cryotomography. The genome, incorporated as a complex with the nucleoprotein inside the virions, was seen as a thread-like structure partially interacting with the viral membrane. Although no ordered nucleocapsid was observed, lateral interactions between the two membrane glycoproteins determine the structure of the viral particles. In the most regular particles, the glycoprotein protrusions, or "spikes," were seen to be arranged on an icosahedral lattice, with T = 12 triangulation. This arrangement has not yet been proven for a virus. Two distinctly different spike conformations were observed, which were shown to depend on pH. This finding is reminiscent of the fusion proteins of alpha-, flavi-, and influenza viruses, in which conformational changes occur in the low pH of the endosome to facilitate fusion of the viral and host membrane during viral entry. |
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These negative-strand RNA viruses possess a membrane envelope covered by glycoproteins. The virions are pleiomorphic and thus have not been amenable to structural characterization using common techniques that involve averaging of electron microscopic images. Here, we determined the three-dimensional structure of a member of the Bunyaviridae family by using electron cryotomography. The genome, incorporated as a complex with the nucleoprotein inside the virions, was seen as a thread-like structure partially interacting with the viral membrane. Although no ordered nucleocapsid was observed, lateral interactions between the two membrane glycoproteins determine the structure of the viral particles. In the most regular particles, the glycoprotein protrusions, or "spikes," were seen to be arranged on an icosahedral lattice, with T = 12 triangulation. This arrangement has not yet been proven for a virus. Two distinctly different spike conformations were observed, which were shown to depend on pH. This finding is reminiscent of the fusion proteins of alpha-, flavi-, and influenza viruses, in which conformational changes occur in the low pH of the endosome to facilitate fusion of the viral and host membrane during viral entry.</description><identifier>ISSN: 0027-8424</identifier><identifier>ISSN: 1091-6490</identifier><identifier>EISSN: 1091-6490</identifier><identifier>DOI: 10.1073/pnas.0708738105</identifier><identifier>PMID: 18272496</identifier><language>eng</language><publisher>United States: National Academy of Sciences</publisher><subject>Animals ; Biochemistry ; Biological Sciences ; Bunyaviridae ; Bunyavirus ; Cell Line ; Cell Membrane - metabolism ; Cell Membrane - ultrastructure ; Cricetinae ; Cryoelectron Microscopy ; Electrons ; envelope glycoproteins ; Genomes ; Glycoproteins ; Glycoproteins - chemistry ; Hydrogen-Ion Concentration ; Imaging, Three-Dimensional ; Medicin och hälsovetenskap ; Orthobunyavirus ; Orthobunyavirus - ultrastructure ; Protein Binding ; Protein Conformation ; Ribonucleic acid ; ribonucleoprotein particles ; Ribonucleoproteins - metabolism ; Ribonucleoproteins - ultrastructure ; RNA ; Tomography ; Uukuniemi virus ; Uukuniemi virus - ultrastructure ; Viral morphology ; Virion ; Virions ; Virology ; virus assembly ; virus structure ; Viruses</subject><ispartof>Proceedings of the National Academy of Sciences - PNAS, 2008-02, Vol.105 (7), p.2375-2379</ispartof><rights>Copyright 2008 The National Academy of Sciences of the United States of America</rights><rights>Copyright National Academy of Sciences Feb 19, 2008</rights><rights>2008 by The National Academy of Sciences of the USA</rights><lds50>peer_reviewed</lds50><oa>free_for_read</oa><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c637t-7064f077ba8fdc3a0265a669484dd4cd910ff198b14157c103c8653f2cdfebba3</citedby><cites>FETCH-LOGICAL-c637t-7064f077ba8fdc3a0265a669484dd4cd910ff198b14157c103c8653f2cdfebba3</cites></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Uhttp://www.pnas.org/content/105/7.cover.gif</thumbnail><linktopdf>$$Uhttps://www.jstor.org/stable/pdf/25451474$$EPDF$$P50$$Gjstor$$H</linktopdf><linktohtml>$$Uhttps://www.jstor.org/stable/25451474$$EHTML$$P50$$Gjstor$$H</linktohtml><link.rule.ids>230,314,552,727,780,784,803,885,27924,27925,53791,53793,58017,58250</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/18272496$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink><backlink>$$Uhttps://urn.kb.se/resolve?urn=urn:nbn:se:umu:diva-42007$$DView record from Swedish Publication Index$$Hfree_for_read</backlink><backlink>$$Uhttp://kipublications.ki.se/Default.aspx?queryparsed=id:116659758$$DView record from Swedish Publication Index$$Hfree_for_read</backlink></links><search><creatorcontrib>Överby, A.K</creatorcontrib><creatorcontrib>Pettersson, R.F</creatorcontrib><creatorcontrib>Grünewald, K</creatorcontrib><creatorcontrib>Huiskonen, J.T</creatorcontrib><title>Insights into bunyavirus architecture from electron cryotomography of Uukuniemi virus</title><title>Proceedings of the National Academy of Sciences - PNAS</title><addtitle>Proc Natl Acad Sci U S A</addtitle><description>Bunyaviridae is a large family of viruses that have gained attention as "emerging viruses" because many members cause serious disease in humans, with an increasing number of outbreaks. These negative-strand RNA viruses possess a membrane envelope covered by glycoproteins. The virions are pleiomorphic and thus have not been amenable to structural characterization using common techniques that involve averaging of electron microscopic images. Here, we determined the three-dimensional structure of a member of the Bunyaviridae family by using electron cryotomography. The genome, incorporated as a complex with the nucleoprotein inside the virions, was seen as a thread-like structure partially interacting with the viral membrane. Although no ordered nucleocapsid was observed, lateral interactions between the two membrane glycoproteins determine the structure of the viral particles. In the most regular particles, the glycoprotein protrusions, or "spikes," were seen to be arranged on an icosahedral lattice, with T = 12 triangulation. This arrangement has not yet been proven for a virus. Two distinctly different spike conformations were observed, which were shown to depend on pH. This finding is reminiscent of the fusion proteins of alpha-, flavi-, and influenza viruses, in which conformational changes occur in the low pH of the endosome to facilitate fusion of the viral and host membrane during viral entry.</description><subject>Animals</subject><subject>Biochemistry</subject><subject>Biological Sciences</subject><subject>Bunyaviridae</subject><subject>Bunyavirus</subject><subject>Cell Line</subject><subject>Cell Membrane - metabolism</subject><subject>Cell Membrane - ultrastructure</subject><subject>Cricetinae</subject><subject>Cryoelectron Microscopy</subject><subject>Electrons</subject><subject>envelope glycoproteins</subject><subject>Genomes</subject><subject>Glycoproteins</subject><subject>Glycoproteins - chemistry</subject><subject>Hydrogen-Ion Concentration</subject><subject>Imaging, Three-Dimensional</subject><subject>Medicin och hälsovetenskap</subject><subject>Orthobunyavirus</subject><subject>Orthobunyavirus - ultrastructure</subject><subject>Protein Binding</subject><subject>Protein Conformation</subject><subject>Ribonucleic acid</subject><subject>ribonucleoprotein particles</subject><subject>Ribonucleoproteins - metabolism</subject><subject>Ribonucleoproteins - ultrastructure</subject><subject>RNA</subject><subject>Tomography</subject><subject>Uukuniemi virus</subject><subject>Uukuniemi virus - ultrastructure</subject><subject>Viral morphology</subject><subject>Virion</subject><subject>Virions</subject><subject>Virology</subject><subject>virus assembly</subject><subject>virus structure</subject><subject>Viruses</subject><issn>0027-8424</issn><issn>1091-6490</issn><issn>1091-6490</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2008</creationdate><recordtype>article</recordtype><sourceid>EIF</sourceid><sourceid>D8T</sourceid><recordid>eNqFkktv1DAUhSMEomVgzQqIWMCGaa8fsZ0NUlVelSqxgGFrOY4942kSD3ZcmH-Pw4w6LQKxsPz6zvH10S2KpwhOEHByuhlUPAEOghOBoLpXHCOo0ZzRGu4XxwCYzwXF9Kh4FOMaAOpKwMPiCAnMMa3ZcbG4GKJbrsZYumH0ZZOGrbp2IcVSBb1yo9FjCqa0wfel6fIu-KHUYetH3_tlUJvVtvS2XKSrNDjTu_K3-HHxwKoumif7eVYsPrz_ev5pfvn548X52eVcM8LHOQdGLXDeKGFbTRRgVinGaipo21Ld1gisRbVoEEUV1wiIFqwiFuvWmqZRZFbUO9_4w2xSIzfB9SpspVcur30r9-dXbhoyGokQY1XNK5G1b_6pfee-nUkfljL1SVIMOepZ8XaHZ7Y3rTbDGFR398U7N4NbyaW_lhgzgSjNBq_2BsF_TyaOsndRm65Tg_EpSg4EY8zRf0EMgtSUTyW9_ANc-xSGHHhmcmSU4sntdAfp4GMMxt6UjEBOPSSnHpKHHsqK57d_euD3TZOB13tgUh7sKsklJrySNnXdaH6Ot6z-Tmbg2Q5Yx9GHGwJXtEKUT6G92N1b5aVaBhfl4kv-HAEQLKfFyS_F_fB4</recordid><startdate>20080219</startdate><enddate>20080219</enddate><creator>Överby, A.K</creator><creator>Pettersson, R.F</creator><creator>Grünewald, K</creator><creator>Huiskonen, J.T</creator><general>National Academy of Sciences</general><general>National Acad Sciences</general><scope>FBQ</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>7QG</scope><scope>7QL</scope><scope>7QP</scope><scope>7QR</scope><scope>7SN</scope><scope>7SS</scope><scope>7T5</scope><scope>7TK</scope><scope>7TM</scope><scope>7TO</scope><scope>7U9</scope><scope>8FD</scope><scope>C1K</scope><scope>FR3</scope><scope>H94</scope><scope>M7N</scope><scope>P64</scope><scope>RC3</scope><scope>7X8</scope><scope>5PM</scope><scope>ADTPV</scope><scope>AOWAS</scope><scope>D93</scope><scope>D8T</scope><scope>ZZAVC</scope></search><sort><creationdate>20080219</creationdate><title>Insights into bunyavirus architecture from electron cryotomography of Uukuniemi virus</title><author>Överby, A.K ; 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subjects | Animals Biochemistry Biological Sciences Bunyaviridae Bunyavirus Cell Line Cell Membrane - metabolism Cell Membrane - ultrastructure Cricetinae Cryoelectron Microscopy Electrons envelope glycoproteins Genomes Glycoproteins Glycoproteins - chemistry Hydrogen-Ion Concentration Imaging, Three-Dimensional Medicin och hälsovetenskap Orthobunyavirus Orthobunyavirus - ultrastructure Protein Binding Protein Conformation Ribonucleic acid ribonucleoprotein particles Ribonucleoproteins - metabolism Ribonucleoproteins - ultrastructure RNA Tomography Uukuniemi virus Uukuniemi virus - ultrastructure Viral morphology Virion Virions Virology virus assembly virus structure Viruses |
title | Insights into bunyavirus architecture from electron cryotomography of Uukuniemi virus |
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