Migration of Nucleocapsids in Vesicular Stomatitis Virus-Infected Cells Is Dependent on both Microtubules and Actin Filaments
The distribution of vesicular stomatitis virus (VSV) nucleocapsids in the cytoplasm of infected cells was analyzed by scanning confocal fluorescence microscopy using a newly developed quantitative approach called the border-to-border distribution method. Nucleocapsids were located near the cell nucl...
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description | The distribution of vesicular stomatitis virus (VSV) nucleocapsids in the cytoplasm of infected cells was analyzed by scanning confocal fluorescence microscopy using a newly developed quantitative approach called the border-to-border distribution method. Nucleocapsids were located near the cell nucleus at early times postinfection (2 h) but were redistributed during infection toward the edges of the cell. This redistribution was inhibited by treatment with nocodazole, colcemid, or cytochalasin D, indicating it is dependent on both microtubules and actin filaments. The role of actin filaments in nucleocapsid mobility was also confirmed by live-cell imaging of fluorescent nucleocapsids of a virus containing P protein fused to enhanced green fluorescent protein. However, in contrast to the overall redistribution in the cytoplasm, the incorporation of nucleocapsids into virions as determined in pulse-chase experiments was dependent on the activity of actin filaments with little if any effect on inhibition of microtubule function. These results indicate that the mechanisms by which nucleocapsids are transported to the farthest reaches of the cell differ from those required for incorporation into virions. This is likely due to the ability of nucleocapsids to follow shorter paths to the plasma membrane mediated by actin filaments.
Nucleocapsids of nonsegmented negative-strand viruses like VSV are assembled in the cytoplasm during genome RNA replication and must migrate to the plasma membrane for assembly into virions. Nucleocapsids are too large to diffuse in the cytoplasm in the time required for virus assembly and must be transported by cytoskeletal elements. Previous results suggested that microtubules were responsible for migration of VSV nucleocapsids to the plasma membrane for virus assembly. Data presented here show that both microtubules and actin filaments are responsible for mobility of nucleocapsids in the cytoplasm, but that actin filaments play a larger role than microtubules in incorporation of nucleocapsids into virions. |
doi_str_mv | 10.1128/JVI.00488-16 |
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Nucleocapsids of nonsegmented negative-strand viruses like VSV are assembled in the cytoplasm during genome RNA replication and must migrate to the plasma membrane for assembly into virions. Nucleocapsids are too large to diffuse in the cytoplasm in the time required for virus assembly and must be transported by cytoskeletal elements. Previous results suggested that microtubules were responsible for migration of VSV nucleocapsids to the plasma membrane for virus assembly. Data presented here show that both microtubules and actin filaments are responsible for mobility of nucleocapsids in the cytoplasm, but that actin filaments play a larger role than microtubules in incorporation of nucleocapsids into virions.</description><identifier>ISSN: 0022-538X</identifier><identifier>EISSN: 1098-5514</identifier><identifier>DOI: 10.1128/JVI.00488-16</identifier><identifier>PMID: 27122580</identifier><language>eng</language><publisher>United States: American Society for Microbiology</publisher><subject>Actin Cytoskeleton - drug effects ; Actin Cytoskeleton - metabolism ; Cell Nucleus - ultrastructure ; Cell Nucleus - virology ; Cytochalasin D - pharmacology ; Cytoplasm - drug effects ; Cytoplasm - metabolism ; Cytoplasm - virology ; Demecolcine - pharmacology ; Green Fluorescent Proteins - genetics ; HeLa Cells ; Humans ; Microscopy, Electron, Scanning - methods ; Microtubules - drug effects ; Microtubules - metabolism ; Nocodazole - pharmacology ; Nucleocapsid - metabolism ; Nucleocapsid - ultrastructure ; Phosphoproteins - genetics ; Spotlight ; Vesicular stomatitis Indiana virus - drug effects ; Vesicular stomatitis Indiana virus - genetics ; Vesicular stomatitis Indiana virus - metabolism ; Vesicular stomatitis virus ; Viral Proteins - drug effects ; Viral Proteins - metabolism ; Viral Structural Proteins - genetics ; Virion - drug effects ; Virion - metabolism ; Virus Assembly - drug effects ; Virus-Cell Interactions</subject><ispartof>Journal of virology, 2016-07, Vol.90 (13), p.6159-6170</ispartof><rights>Copyright © 2016, American Society for Microbiology. All Rights Reserved.</rights><rights>Copyright © 2016, American Society for Microbiology. All Rights Reserved. 2016 American Society for Microbiology</rights><lds50>peer_reviewed</lds50><oa>free_for_read</oa><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c526t-21a2abaceaa8ee859241086b1330528c2e535c80b409185caca87bf0930e634d3</citedby><cites>FETCH-LOGICAL-c526t-21a2abaceaa8ee859241086b1330528c2e535c80b409185caca87bf0930e634d3</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/PMC4907246/pdf/$$EPDF$$P50$$Gpubmedcentral$$H</linktopdf><linktohtml>$$Uhttps://www.ncbi.nlm.nih.gov/pmc/articles/PMC4907246/$$EHTML$$P50$$Gpubmedcentral$$H</linktohtml><link.rule.ids>230,314,727,780,784,885,27923,27924,53790,53792</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/27122580$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><contributor>Dermody, T. S.</contributor><creatorcontrib>Yacovone, Shalane K</creatorcontrib><creatorcontrib>Smelser, Amanda M</creatorcontrib><creatorcontrib>Macosko, Jed C</creatorcontrib><creatorcontrib>Holzwarth, George</creatorcontrib><creatorcontrib>Ornelles, David A</creatorcontrib><creatorcontrib>Lyles, Douglas S</creatorcontrib><title>Migration of Nucleocapsids in Vesicular Stomatitis Virus-Infected Cells Is Dependent on both Microtubules and Actin Filaments</title><title>Journal of virology</title><addtitle>J Virol</addtitle><description>The distribution of vesicular stomatitis virus (VSV) nucleocapsids in the cytoplasm of infected cells was analyzed by scanning confocal fluorescence microscopy using a newly developed quantitative approach called the border-to-border distribution method. Nucleocapsids were located near the cell nucleus at early times postinfection (2 h) but were redistributed during infection toward the edges of the cell. This redistribution was inhibited by treatment with nocodazole, colcemid, or cytochalasin D, indicating it is dependent on both microtubules and actin filaments. The role of actin filaments in nucleocapsid mobility was also confirmed by live-cell imaging of fluorescent nucleocapsids of a virus containing P protein fused to enhanced green fluorescent protein. However, in contrast to the overall redistribution in the cytoplasm, the incorporation of nucleocapsids into virions as determined in pulse-chase experiments was dependent on the activity of actin filaments with little if any effect on inhibition of microtubule function. These results indicate that the mechanisms by which nucleocapsids are transported to the farthest reaches of the cell differ from those required for incorporation into virions. This is likely due to the ability of nucleocapsids to follow shorter paths to the plasma membrane mediated by actin filaments.
Nucleocapsids of nonsegmented negative-strand viruses like VSV are assembled in the cytoplasm during genome RNA replication and must migrate to the plasma membrane for assembly into virions. Nucleocapsids are too large to diffuse in the cytoplasm in the time required for virus assembly and must be transported by cytoskeletal elements. Previous results suggested that microtubules were responsible for migration of VSV nucleocapsids to the plasma membrane for virus assembly. Data presented here show that both microtubules and actin filaments are responsible for mobility of nucleocapsids in the cytoplasm, but that actin filaments play a larger role than microtubules in incorporation of nucleocapsids into virions.</description><subject>Actin Cytoskeleton - drug effects</subject><subject>Actin Cytoskeleton - metabolism</subject><subject>Cell Nucleus - ultrastructure</subject><subject>Cell Nucleus - virology</subject><subject>Cytochalasin D - pharmacology</subject><subject>Cytoplasm - drug effects</subject><subject>Cytoplasm - metabolism</subject><subject>Cytoplasm - virology</subject><subject>Demecolcine - pharmacology</subject><subject>Green Fluorescent Proteins - genetics</subject><subject>HeLa Cells</subject><subject>Humans</subject><subject>Microscopy, Electron, Scanning - methods</subject><subject>Microtubules - drug effects</subject><subject>Microtubules - metabolism</subject><subject>Nocodazole - pharmacology</subject><subject>Nucleocapsid - metabolism</subject><subject>Nucleocapsid - ultrastructure</subject><subject>Phosphoproteins - genetics</subject><subject>Spotlight</subject><subject>Vesicular stomatitis Indiana virus - drug effects</subject><subject>Vesicular stomatitis Indiana virus - genetics</subject><subject>Vesicular stomatitis Indiana virus - metabolism</subject><subject>Vesicular stomatitis virus</subject><subject>Viral Proteins - drug effects</subject><subject>Viral Proteins - metabolism</subject><subject>Viral Structural Proteins - genetics</subject><subject>Virion - drug effects</subject><subject>Virion - metabolism</subject><subject>Virus Assembly - drug effects</subject><subject>Virus-Cell Interactions</subject><issn>0022-538X</issn><issn>1098-5514</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2016</creationdate><recordtype>article</recordtype><sourceid>EIF</sourceid><recordid>eNqFkT1v1TAUhi0EoreFjRl5ZCCtjz8SZ0GqLi1c1MIAXLFZjnPSGiXxre1U6sB_r0tLBRPTGc6j53y8hLwCdgjA9dGn7eaQMal1BfUTsgLW6kopkE_JijHOKyX0jz2yn9JPxkDKWj4ne7wBzpVmK_Lr3F9Em32YaRjo58WNGJzdJd8n6me6xeTdMtpIv-YwFS77RLc-LqnazAO6jD1d4zgmukn0Pe5w7nHOtNi6kC_puXcx5KVbRkzUzj09drlYT_1op8KlF-TZYMeELx_qAfl-evJt_bE6-_Jhsz4-q5zida44WG4769BajahVyyUwXXcgBFNcO45KKKdZJ1kLWjnrrG66gbWCYS1kLw7Iu3vvbukm7F2ZHe1odtFPNt6YYL35tzP7S3MRro1sWcNlXQRvHgQxXC2Yspl8cuVwO2NYkgEN0LJaAf8_2rRKa2hFU9C392j5UkoRh8eNgJm7cE0J1_wO18DdEq__vuIR_pOmuAUKw6GZ</recordid><startdate>20160701</startdate><enddate>20160701</enddate><creator>Yacovone, Shalane K</creator><creator>Smelser, Amanda M</creator><creator>Macosko, Jed C</creator><creator>Holzwarth, George</creator><creator>Ornelles, David A</creator><creator>Lyles, Douglas S</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>20160701</creationdate><title>Migration of Nucleocapsids in Vesicular Stomatitis Virus-Infected Cells Is Dependent on both Microtubules and Actin Filaments</title><author>Yacovone, Shalane K ; Smelser, Amanda M ; Macosko, Jed C ; Holzwarth, George ; Ornelles, David A ; Lyles, Douglas S</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c526t-21a2abaceaa8ee859241086b1330528c2e535c80b409185caca87bf0930e634d3</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2016</creationdate><topic>Actin Cytoskeleton - drug effects</topic><topic>Actin Cytoskeleton - metabolism</topic><topic>Cell Nucleus - ultrastructure</topic><topic>Cell Nucleus - virology</topic><topic>Cytochalasin D - pharmacology</topic><topic>Cytoplasm - drug effects</topic><topic>Cytoplasm - metabolism</topic><topic>Cytoplasm - virology</topic><topic>Demecolcine - pharmacology</topic><topic>Green Fluorescent Proteins - genetics</topic><topic>HeLa Cells</topic><topic>Humans</topic><topic>Microscopy, Electron, Scanning - methods</topic><topic>Microtubules - drug effects</topic><topic>Microtubules - metabolism</topic><topic>Nocodazole - pharmacology</topic><topic>Nucleocapsid - metabolism</topic><topic>Nucleocapsid - ultrastructure</topic><topic>Phosphoproteins - genetics</topic><topic>Spotlight</topic><topic>Vesicular stomatitis Indiana virus - drug effects</topic><topic>Vesicular stomatitis Indiana virus - genetics</topic><topic>Vesicular stomatitis Indiana virus - metabolism</topic><topic>Vesicular stomatitis virus</topic><topic>Viral Proteins - drug effects</topic><topic>Viral Proteins - metabolism</topic><topic>Viral Structural Proteins - genetics</topic><topic>Virion - drug effects</topic><topic>Virion - metabolism</topic><topic>Virus Assembly - drug effects</topic><topic>Virus-Cell Interactions</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Yacovone, Shalane K</creatorcontrib><creatorcontrib>Smelser, Amanda M</creatorcontrib><creatorcontrib>Macosko, Jed C</creatorcontrib><creatorcontrib>Holzwarth, George</creatorcontrib><creatorcontrib>Ornelles, David A</creatorcontrib><creatorcontrib>Lyles, Douglas S</creatorcontrib><collection>Medline</collection><collection>MEDLINE</collection><collection>MEDLINE (Ovid)</collection><collection>MEDLINE</collection><collection>MEDLINE</collection><collection>PubMed</collection><collection>CrossRef</collection><collection>MEDLINE - Academic</collection><collection>Virology and AIDS Abstracts</collection><collection>AIDS and Cancer Research Abstracts</collection><collection>PubMed Central (Full Participant titles)</collection><jtitle>Journal of virology</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Yacovone, Shalane K</au><au>Smelser, Amanda M</au><au>Macosko, Jed C</au><au>Holzwarth, George</au><au>Ornelles, David A</au><au>Lyles, Douglas S</au><au>Dermody, T. S.</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Migration of Nucleocapsids in Vesicular Stomatitis Virus-Infected Cells Is Dependent on both Microtubules and Actin Filaments</atitle><jtitle>Journal of virology</jtitle><addtitle>J Virol</addtitle><date>2016-07-01</date><risdate>2016</risdate><volume>90</volume><issue>13</issue><spage>6159</spage><epage>6170</epage><pages>6159-6170</pages><issn>0022-538X</issn><eissn>1098-5514</eissn><abstract>The distribution of vesicular stomatitis virus (VSV) nucleocapsids in the cytoplasm of infected cells was analyzed by scanning confocal fluorescence microscopy using a newly developed quantitative approach called the border-to-border distribution method. Nucleocapsids were located near the cell nucleus at early times postinfection (2 h) but were redistributed during infection toward the edges of the cell. This redistribution was inhibited by treatment with nocodazole, colcemid, or cytochalasin D, indicating it is dependent on both microtubules and actin filaments. The role of actin filaments in nucleocapsid mobility was also confirmed by live-cell imaging of fluorescent nucleocapsids of a virus containing P protein fused to enhanced green fluorescent protein. However, in contrast to the overall redistribution in the cytoplasm, the incorporation of nucleocapsids into virions as determined in pulse-chase experiments was dependent on the activity of actin filaments with little if any effect on inhibition of microtubule function. These results indicate that the mechanisms by which nucleocapsids are transported to the farthest reaches of the cell differ from those required for incorporation into virions. This is likely due to the ability of nucleocapsids to follow shorter paths to the plasma membrane mediated by actin filaments.
Nucleocapsids of nonsegmented negative-strand viruses like VSV are assembled in the cytoplasm during genome RNA replication and must migrate to the plasma membrane for assembly into virions. Nucleocapsids are too large to diffuse in the cytoplasm in the time required for virus assembly and must be transported by cytoskeletal elements. Previous results suggested that microtubules were responsible for migration of VSV nucleocapsids to the plasma membrane for virus assembly. Data presented here show that both microtubules and actin filaments are responsible for mobility of nucleocapsids in the cytoplasm, but that actin filaments play a larger role than microtubules in incorporation of nucleocapsids into virions.</abstract><cop>United States</cop><pub>American Society for Microbiology</pub><pmid>27122580</pmid><doi>10.1128/JVI.00488-16</doi><tpages>12</tpages><oa>free_for_read</oa></addata></record> |
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subjects | Actin Cytoskeleton - drug effects Actin Cytoskeleton - metabolism Cell Nucleus - ultrastructure Cell Nucleus - virology Cytochalasin D - pharmacology Cytoplasm - drug effects Cytoplasm - metabolism Cytoplasm - virology Demecolcine - pharmacology Green Fluorescent Proteins - genetics HeLa Cells Humans Microscopy, Electron, Scanning - methods Microtubules - drug effects Microtubules - metabolism Nocodazole - pharmacology Nucleocapsid - metabolism Nucleocapsid - ultrastructure Phosphoproteins - genetics Spotlight Vesicular stomatitis Indiana virus - drug effects Vesicular stomatitis Indiana virus - genetics Vesicular stomatitis Indiana virus - metabolism Vesicular stomatitis virus Viral Proteins - drug effects Viral Proteins - metabolism Viral Structural Proteins - genetics Virion - drug effects Virion - metabolism Virus Assembly - drug effects Virus-Cell Interactions |
title | Migration of Nucleocapsids in Vesicular Stomatitis Virus-Infected Cells Is Dependent on both Microtubules and Actin Filaments |
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