Mimivirus Fibrils Are Important for Viral Attachment to the Microbial World by a Diverse Glycoside Interaction Repertoire
Acanthamoeba polyphaga mimivirus (APMV) is a giant virus from the Mimiviridae family. It has many unusual features, such as a pseudoicosahedral capsid that presents a starfish shape in one of its vertices, through which the ∼ 1.2-Mb double-stranded DNA is released. It also has a dense glycoprotein f...
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creator | Rodrigues, Rodrigo Araújo Lima dos Santos Silva, Ludmila Karen Dornas, Fábio Pio de Oliveira, Danilo Bretas Magalhães, Thais Furtado Ferreira Santos, Daniel Assis Costa, Adriana Oliveira de Macêdo Farias, Luiz Magalhães, Paula Prazeres Bonjardim, Cláudio Antônio Kroon, Erna Geessien La Scola, Bernard Cortines, Juliana Reis Abrahão, Jônatas Santos |
description | Acanthamoeba polyphaga mimivirus (APMV) is a giant virus from the Mimiviridae family. It has many unusual features, such as a pseudoicosahedral capsid that presents a starfish shape in one of its vertices, through which the ∼ 1.2-Mb double-stranded DNA is released. It also has a dense glycoprotein fibril layer covering the capsid that has not yet been functionally characterized. Here, we verified that although these structures are not essential for viral replication, they are truly necessary for viral adhesion to amoebae, its natural host. In the absence of fibrils, APMV had a significantly lower level of attachment to the Acanthamoeba castellanii surface. This adhesion is mediated by glycans, specifically, mannose and N-acetylglucosamine (a monomer of chitin and peptidoglycan), both of which are largely distributed in nature as structural components of several organisms. Indeed, APMV was able to attach to different organisms, such as Gram-positive bacteria, fungi, and arthropods, but not to Gram-negative bacteria. This prompted us to predict that (i) arthropods, mainly insects, might act as mimivirus dispersers and (ii) by attaching to other microorganisms, APMV could be ingested by amoebae, leading to the successful production of viral progeny. To date, this mechanism has never been described in the virosphere.
APMV is a giant virus that is both genetically and structurally complex. Its size is similar to that of small bacteria, and it replicates inside amoebae. The viral capsid is covered by a dense glycoprotein fibril layer, but its function has remained unknown, until now. We found that the fibrils are not essential for mimivirus replication but that they are truly necessary for viral adhesion to the cell surface. This interaction is mediated by glycans, mainly N-acetylglucosamine. We also verified that APMV is able to attach to bacteria, fungi, and arthropods. This indicates that insects might act as mimivirus dispersers and that adhesion to other microorganisms could facilitate viral ingestion by amoebae, a mechanism never before described in the virosphere. |
doi_str_mv | 10.1128/JVI.01976-15 |
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APMV is a giant virus that is both genetically and structurally complex. Its size is similar to that of small bacteria, and it replicates inside amoebae. The viral capsid is covered by a dense glycoprotein fibril layer, but its function has remained unknown, until now. We found that the fibrils are not essential for mimivirus replication but that they are truly necessary for viral adhesion to the cell surface. This interaction is mediated by glycans, mainly N-acetylglucosamine. We also verified that APMV is able to attach to bacteria, fungi, and arthropods. This indicates that insects might act as mimivirus dispersers and that adhesion to other microorganisms could facilitate viral ingestion by amoebae, a mechanism never before described in the virosphere.</description><identifier>ISSN: 0022-538X</identifier><identifier>EISSN: 1098-5514</identifier><identifier>DOI: 10.1128/JVI.01976-15</identifier><identifier>PMID: 26378162</identifier><language>eng</language><publisher>United States: American Society for Microbiology</publisher><subject>Acanthamoeba - physiology ; Acanthamoeba - ultrastructure ; Acanthamoeba - virology ; Acanthamoeba castellanii ; Acanthamoeba polyphaga ; Acetylglucosamine - metabolism ; Analysis of Variance ; Arthropoda ; Asteroidea ; Glycoproteins - metabolism ; Mannose - metabolism ; Microscopy, Electron, Transmission ; Mimiviridae - physiology ; Species Specificity ; Viral Proteins - metabolism ; Virus Attachment ; Virus Replication - physiology ; Virus-Cell Interactions</subject><ispartof>Journal of virology, 2015-12, Vol.89 (23), p.11812-11819</ispartof><rights>Copyright © 2015, American Society for Microbiology. All Rights Reserved.</rights><rights>Copyright © 2015, American Society for Microbiology. All Rights Reserved. 2015 American Society for Microbiology</rights><lds50>peer_reviewed</lds50><oa>free_for_read</oa><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c526t-621c896a743cd08a95c1ec9ac0ae13743a8aede9b5d7c71e5474b4251d51d6f73</citedby><cites>FETCH-LOGICAL-c526t-621c896a743cd08a95c1ec9ac0ae13743a8aede9b5d7c71e5474b4251d51d6f73</cites></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><linktopdf>$$Uhttps://www.ncbi.nlm.nih.gov/pmc/articles/PMC4645322/pdf/$$EPDF$$P50$$Gpubmedcentral$$H</linktopdf><linktohtml>$$Uhttps://www.ncbi.nlm.nih.gov/pmc/articles/PMC4645322/$$EHTML$$P50$$Gpubmedcentral$$H</linktohtml><link.rule.ids>230,314,724,777,781,882,27905,27906,53772,53774</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/26378162$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><contributor>McFadden, G.</contributor><creatorcontrib>Rodrigues, Rodrigo Araújo Lima</creatorcontrib><creatorcontrib>dos Santos Silva, Ludmila Karen</creatorcontrib><creatorcontrib>Dornas, Fábio Pio</creatorcontrib><creatorcontrib>de Oliveira, Danilo Bretas</creatorcontrib><creatorcontrib>Magalhães, Thais Furtado Ferreira</creatorcontrib><creatorcontrib>Santos, Daniel Assis</creatorcontrib><creatorcontrib>Costa, Adriana Oliveira</creatorcontrib><creatorcontrib>de Macêdo Farias, Luiz</creatorcontrib><creatorcontrib>Magalhães, Paula Prazeres</creatorcontrib><creatorcontrib>Bonjardim, Cláudio Antônio</creatorcontrib><creatorcontrib>Kroon, Erna Geessien</creatorcontrib><creatorcontrib>La Scola, Bernard</creatorcontrib><creatorcontrib>Cortines, Juliana Reis</creatorcontrib><creatorcontrib>Abrahão, Jônatas Santos</creatorcontrib><title>Mimivirus Fibrils Are Important for Viral Attachment to the Microbial World by a Diverse Glycoside Interaction Repertoire</title><title>Journal of virology</title><addtitle>J Virol</addtitle><description>Acanthamoeba polyphaga mimivirus (APMV) is a giant virus from the Mimiviridae family. It has many unusual features, such as a pseudoicosahedral capsid that presents a starfish shape in one of its vertices, through which the ∼ 1.2-Mb double-stranded DNA is released. It also has a dense glycoprotein fibril layer covering the capsid that has not yet been functionally characterized. Here, we verified that although these structures are not essential for viral replication, they are truly necessary for viral adhesion to amoebae, its natural host. In the absence of fibrils, APMV had a significantly lower level of attachment to the Acanthamoeba castellanii surface. This adhesion is mediated by glycans, specifically, mannose and N-acetylglucosamine (a monomer of chitin and peptidoglycan), both of which are largely distributed in nature as structural components of several organisms. Indeed, APMV was able to attach to different organisms, such as Gram-positive bacteria, fungi, and arthropods, but not to Gram-negative bacteria. This prompted us to predict that (i) arthropods, mainly insects, might act as mimivirus dispersers and (ii) by attaching to other microorganisms, APMV could be ingested by amoebae, leading to the successful production of viral progeny. To date, this mechanism has never been described in the virosphere.
APMV is a giant virus that is both genetically and structurally complex. Its size is similar to that of small bacteria, and it replicates inside amoebae. The viral capsid is covered by a dense glycoprotein fibril layer, but its function has remained unknown, until now. We found that the fibrils are not essential for mimivirus replication but that they are truly necessary for viral adhesion to the cell surface. This interaction is mediated by glycans, mainly N-acetylglucosamine. We also verified that APMV is able to attach to bacteria, fungi, and arthropods. This indicates that insects might act as mimivirus dispersers and that adhesion to other microorganisms could facilitate viral ingestion by amoebae, a mechanism never before described in the virosphere.</description><subject>Acanthamoeba - physiology</subject><subject>Acanthamoeba - ultrastructure</subject><subject>Acanthamoeba - virology</subject><subject>Acanthamoeba castellanii</subject><subject>Acanthamoeba polyphaga</subject><subject>Acetylglucosamine - metabolism</subject><subject>Analysis of Variance</subject><subject>Arthropoda</subject><subject>Asteroidea</subject><subject>Glycoproteins - metabolism</subject><subject>Mannose - metabolism</subject><subject>Microscopy, Electron, Transmission</subject><subject>Mimiviridae - physiology</subject><subject>Species Specificity</subject><subject>Viral Proteins - metabolism</subject><subject>Virus Attachment</subject><subject>Virus Replication - physiology</subject><subject>Virus-Cell Interactions</subject><issn>0022-538X</issn><issn>1098-5514</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2015</creationdate><recordtype>article</recordtype><sourceid>EIF</sourceid><recordid>eNqNkc1rFEEQxRtRzBq9eZY-enBiV3_OXIQlmriSIIhGb01PT63bMjO96e5d2P8-bRKD3oSCgqofj3r1CHkJ7ASAt28_Xa1OGHRGN6AekQWwrm2UAvmYLBjjvFGi_XFEnuX8izGQUsun5IhrYVrQfEEOl2EK-5B2mZ6FPoUx02VCupq2MRU3F7qOiV6F5Ea6LMX5zYR1WCItG6SXwafYh7r7HtM40P5AHX0f9pgy0vPx4GMOQxWbCybnS4gz_YJbTCWGhM_Jk7UbM76478fk29mHr6cfm4vP56vT5UXjFdel0Rx822lnpPADa12nPKDvnGcOQdSpax0O2PVqMN4AKmlkL7mCoZZeG3FM3t3pbnf9hIOv91c3dpvC5NLBRhfsv5s5bOzPuLf1VUpwXgVe3wukeL3DXOwUssdxdDPGXbZglJC64133H6gA0yoGuqJv7tD6wpwTrh8uAmZ_B2trsPY2WAuq4q_-dvEA_0lS3ABmiKCK</recordid><startdate>20151201</startdate><enddate>20151201</enddate><creator>Rodrigues, Rodrigo Araújo Lima</creator><creator>dos Santos Silva, Ludmila Karen</creator><creator>Dornas, Fábio Pio</creator><creator>de Oliveira, Danilo Bretas</creator><creator>Magalhães, Thais Furtado Ferreira</creator><creator>Santos, Daniel Assis</creator><creator>Costa, Adriana Oliveira</creator><creator>de Macêdo Farias, Luiz</creator><creator>Magalhães, Paula Prazeres</creator><creator>Bonjardim, Cláudio Antônio</creator><creator>Kroon, Erna Geessien</creator><creator>La Scola, Bernard</creator><creator>Cortines, Juliana Reis</creator><creator>Abrahão, Jônatas Santos</creator><general>American Society for Microbiology</general><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>7U9</scope><scope>H94</scope><scope>5PM</scope></search><sort><creationdate>20151201</creationdate><title>Mimivirus Fibrils Are Important for Viral Attachment to the Microbial World by a Diverse Glycoside Interaction Repertoire</title><author>Rodrigues, Rodrigo Araújo Lima ; 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It has many unusual features, such as a pseudoicosahedral capsid that presents a starfish shape in one of its vertices, through which the ∼ 1.2-Mb double-stranded DNA is released. It also has a dense glycoprotein fibril layer covering the capsid that has not yet been functionally characterized. Here, we verified that although these structures are not essential for viral replication, they are truly necessary for viral adhesion to amoebae, its natural host. In the absence of fibrils, APMV had a significantly lower level of attachment to the Acanthamoeba castellanii surface. This adhesion is mediated by glycans, specifically, mannose and N-acetylglucosamine (a monomer of chitin and peptidoglycan), both of which are largely distributed in nature as structural components of several organisms. Indeed, APMV was able to attach to different organisms, such as Gram-positive bacteria, fungi, and arthropods, but not to Gram-negative bacteria. This prompted us to predict that (i) arthropods, mainly insects, might act as mimivirus dispersers and (ii) by attaching to other microorganisms, APMV could be ingested by amoebae, leading to the successful production of viral progeny. To date, this mechanism has never been described in the virosphere.
APMV is a giant virus that is both genetically and structurally complex. Its size is similar to that of small bacteria, and it replicates inside amoebae. The viral capsid is covered by a dense glycoprotein fibril layer, but its function has remained unknown, until now. We found that the fibrils are not essential for mimivirus replication but that they are truly necessary for viral adhesion to the cell surface. This interaction is mediated by glycans, mainly N-acetylglucosamine. We also verified that APMV is able to attach to bacteria, fungi, and arthropods. This indicates that insects might act as mimivirus dispersers and that adhesion to other microorganisms could facilitate viral ingestion by amoebae, a mechanism never before described in the virosphere.</abstract><cop>United States</cop><pub>American Society for Microbiology</pub><pmid>26378162</pmid><doi>10.1128/JVI.01976-15</doi><tpages>8</tpages><oa>free_for_read</oa></addata></record> |
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subjects | Acanthamoeba - physiology Acanthamoeba - ultrastructure Acanthamoeba - virology Acanthamoeba castellanii Acanthamoeba polyphaga Acetylglucosamine - metabolism Analysis of Variance Arthropoda Asteroidea Glycoproteins - metabolism Mannose - metabolism Microscopy, Electron, Transmission Mimiviridae - physiology Species Specificity Viral Proteins - metabolism Virus Attachment Virus Replication - physiology Virus-Cell Interactions |
title | Mimivirus Fibrils Are Important for Viral Attachment to the Microbial World by a Diverse Glycoside Interaction Repertoire |
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