Random Plant Viral Variants Attain Temporal Advantages During Systemic Infections and in Turn Resist other Variants of the Same Virus
Infection of plants with viruses containing multiple variants frequently leads to dominance by a few random variants in the systemically infected leaves (SLs), for which a plausible explanation is lacking. We show here that SL dominance by a given viral variant is adequately explained by its fortuit...
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description | Infection of plants with viruses containing multiple variants frequently leads to dominance by a few random variants in the systemically infected leaves (SLs), for which a plausible explanation is lacking. We show here that SL dominance by a given viral variant is adequately explained by its fortuitous lead in systemic spread, coupled with its resistance to superinfection by other variants. We analyzed the fate of a multi-variant turnip crinkle virus (TCV) population in
Arabidopsis
and
N. benthamiana
plants. Both wild-type and RNA silencing-defective plants displayed a similar pattern of random dominance by a few variant genotypes, thus discounting a prominent role for RNA silencing. When introduced to plants sequentially as two subpopulations, a twelve-hour head-start was sufficient for the first set to dominate. Finally, SLs of TCV-infected plants became highly resistant to secondary invasions of another TCV variant. We propose that random distribution of variant foci on inoculated leaves allows different variants to lead systemic movement in different plants. The leading variants then colonize large areas of SLs and resist the superinfection of lagging variants in the same areas. In conclusion, superinfection resistance is the primary driver of random enrichment of viral variants in systemically infected plants. |
doi_str_mv | 10.1038/srep15346 |
format | Article |
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Arabidopsis
and
N. benthamiana
plants. Both wild-type and RNA silencing-defective plants displayed a similar pattern of random dominance by a few variant genotypes, thus discounting a prominent role for RNA silencing. When introduced to plants sequentially as two subpopulations, a twelve-hour head-start was sufficient for the first set to dominate. Finally, SLs of TCV-infected plants became highly resistant to secondary invasions of another TCV variant. We propose that random distribution of variant foci on inoculated leaves allows different variants to lead systemic movement in different plants. The leading variants then colonize large areas of SLs and resist the superinfection of lagging variants in the same areas. In conclusion, superinfection resistance is the primary driver of random enrichment of viral variants in systemically infected plants.</description><identifier>ISSN: 2045-2322</identifier><identifier>EISSN: 2045-2322</identifier><identifier>DOI: 10.1038/srep15346</identifier><identifier>PMID: 26481091</identifier><language>eng</language><publisher>London: Nature Publishing Group UK</publisher><subject>14 ; 14/19 ; 38/23 ; 38/35 ; 38/70 ; 38/71 ; 38/90 ; 631/326/596/2557 ; 631/449/2661/2666 ; Arabidopsis - virology ; Carmovirus - physiology ; Dominance ; Flowers & plants ; Gene Order ; Genetic Variation ; Genome, Viral ; Genotypes ; Humanities and Social Sciences ; Invasions ; Leaves ; Models, Biological ; multidisciplinary ; Plant Diseases - virology ; Plant Leaves - virology ; Plant viruses ; Plant Viruses - physiology ; RNA-mediated interference ; Science ; Subpopulations ; Superinfection ; Systemic diseases ; Viral Interference</subject><ispartof>Scientific reports, 2015-10, Vol.5 (1), p.15346-15346, Article 15346</ispartof><rights>The Author(s) 2015</rights><rights>Copyright Nature Publishing Group Oct 2015</rights><rights>Copyright © 2015, Macmillan Publishers Limited 2015 Macmillan Publishers Limited</rights><lds50>peer_reviewed</lds50><oa>free_for_read</oa><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c438t-2e998af226458b9cdf5ca978a74d24a202d24e6d0029031120b68406b7787cd33</citedby><cites>FETCH-LOGICAL-c438t-2e998af226458b9cdf5ca978a74d24a202d24e6d0029031120b68406b7787cd33</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/PMC4612314/pdf/$$EPDF$$P50$$Gpubmedcentral$$Hfree_for_read</linktopdf><linktohtml>$$Uhttps://www.ncbi.nlm.nih.gov/pmc/articles/PMC4612314/$$EHTML$$P50$$Gpubmedcentral$$Hfree_for_read</linktohtml><link.rule.ids>230,314,727,780,784,864,885,27922,27923,41118,42187,51574,53789,53791</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/26481091$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Zhang, Xiao-Feng</creatorcontrib><creatorcontrib>Guo, Jiangbo</creatorcontrib><creatorcontrib>Zhang, Xiuchun</creatorcontrib><creatorcontrib>Meulia, Tea</creatorcontrib><creatorcontrib>Paul, Pierce</creatorcontrib><creatorcontrib>Madden, Laurence V.</creatorcontrib><creatorcontrib>Li, Dawei</creatorcontrib><creatorcontrib>Qu, Feng</creatorcontrib><title>Random Plant Viral Variants Attain Temporal Advantages During Systemic Infections and in Turn Resist other Variants of the Same Virus</title><title>Scientific reports</title><addtitle>Sci Rep</addtitle><addtitle>Sci Rep</addtitle><description>Infection of plants with viruses containing multiple variants frequently leads to dominance by a few random variants in the systemically infected leaves (SLs), for which a plausible explanation is lacking. We show here that SL dominance by a given viral variant is adequately explained by its fortuitous lead in systemic spread, coupled with its resistance to superinfection by other variants. We analyzed the fate of a multi-variant turnip crinkle virus (TCV) population in
Arabidopsis
and
N. benthamiana
plants. Both wild-type and RNA silencing-defective plants displayed a similar pattern of random dominance by a few variant genotypes, thus discounting a prominent role for RNA silencing. When introduced to plants sequentially as two subpopulations, a twelve-hour head-start was sufficient for the first set to dominate. Finally, SLs of TCV-infected plants became highly resistant to secondary invasions of another TCV variant. We propose that random distribution of variant foci on inoculated leaves allows different variants to lead systemic movement in different plants. The leading variants then colonize large areas of SLs and resist the superinfection of lagging variants in the same areas. In conclusion, superinfection resistance is the primary driver of random enrichment of viral variants in systemically infected plants.</description><subject>14</subject><subject>14/19</subject><subject>38/23</subject><subject>38/35</subject><subject>38/70</subject><subject>38/71</subject><subject>38/90</subject><subject>631/326/596/2557</subject><subject>631/449/2661/2666</subject><subject>Arabidopsis - virology</subject><subject>Carmovirus - physiology</subject><subject>Dominance</subject><subject>Flowers & plants</subject><subject>Gene Order</subject><subject>Genetic Variation</subject><subject>Genome, Viral</subject><subject>Genotypes</subject><subject>Humanities and Social Sciences</subject><subject>Invasions</subject><subject>Leaves</subject><subject>Models, Biological</subject><subject>multidisciplinary</subject><subject>Plant Diseases - virology</subject><subject>Plant Leaves - virology</subject><subject>Plant viruses</subject><subject>Plant Viruses - physiology</subject><subject>RNA-mediated interference</subject><subject>Science</subject><subject>Subpopulations</subject><subject>Superinfection</subject><subject>Systemic diseases</subject><subject>Viral Interference</subject><issn>2045-2322</issn><issn>2045-2322</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2015</creationdate><recordtype>article</recordtype><sourceid>C6C</sourceid><sourceid>EIF</sourceid><sourceid>ABUWG</sourceid><sourceid>AFKRA</sourceid><sourceid>AZQEC</sourceid><sourceid>BENPR</sourceid><sourceid>CCPQU</sourceid><sourceid>DWQXO</sourceid><sourceid>GNUQQ</sourceid><recordid>eNplUU1v1DAQtRCIVksP_AFkiQsgLdiOk9gXpFX5qlQJ1JZeLa8z2bra2MF2KvUH8L-ZaMuygC9jzzy_eTOPkOecveWsUu9ygpHXlWwekWPBZL0UlRCPD-5H5CTnW4anFlpy_ZQciUYqzjQ_Jj8vbOjiQL9tbSj02ie7pdc2eXxluirF-kCvYBjjXFh1d5i3G8j0w5R82NDL-1xg8I6ehR5c8TFkioR0_jWlQC8g-1xoLDeQ_vDGnmKCXtoB5pZTfkae9Hab4eQhLsj3Tx-vTr8sz79-PjtdnS-drFRZCtBa2V6g_Fqttev62lndKtvKTkgrmMAATceY0KziXLB1oyRr1m2rWtdV1YK83_GO03qAzkEoOJcZkx9sujfRevN3Jfgbs4l3RjZcVFwiwasHghR_TJCLGXx2sMXtQZyy4a2omZAMDVmQl_9AbyOuBMczXGlUjco0ol7vUC7FjFb2ezGcmdlfs_cXsS8O1e-Rv91EwJsdII-zO5AOWv7H9gu6Nq-s</recordid><startdate>20151020</startdate><enddate>20151020</enddate><creator>Zhang, Xiao-Feng</creator><creator>Guo, Jiangbo</creator><creator>Zhang, Xiuchun</creator><creator>Meulia, Tea</creator><creator>Paul, Pierce</creator><creator>Madden, Laurence V.</creator><creator>Li, Dawei</creator><creator>Qu, Feng</creator><general>Nature Publishing Group UK</general><general>Nature Publishing Group</general><scope>C6C</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>3V.</scope><scope>7X7</scope><scope>7XB</scope><scope>88A</scope><scope>88E</scope><scope>88I</scope><scope>8FE</scope><scope>8FH</scope><scope>8FI</scope><scope>8FJ</scope><scope>8FK</scope><scope>ABUWG</scope><scope>AEUYN</scope><scope>AFKRA</scope><scope>AZQEC</scope><scope>BBNVY</scope><scope>BENPR</scope><scope>BHPHI</scope><scope>CCPQU</scope><scope>DWQXO</scope><scope>FYUFA</scope><scope>GHDGH</scope><scope>GNUQQ</scope><scope>HCIFZ</scope><scope>K9.</scope><scope>LK8</scope><scope>M0S</scope><scope>M1P</scope><scope>M2P</scope><scope>M7P</scope><scope>PIMPY</scope><scope>PQEST</scope><scope>PQQKQ</scope><scope>PQUKI</scope><scope>Q9U</scope><scope>7X8</scope><scope>5PM</scope></search><sort><creationdate>20151020</creationdate><title>Random Plant Viral Variants Attain Temporal Advantages During Systemic Infections and in Turn Resist other Variants of the Same Virus</title><author>Zhang, Xiao-Feng ; Guo, Jiangbo ; Zhang, Xiuchun ; Meulia, Tea ; Paul, Pierce ; Madden, Laurence V. ; Li, Dawei ; Qu, Feng</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c438t-2e998af226458b9cdf5ca978a74d24a202d24e6d0029031120b68406b7787cd33</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2015</creationdate><topic>14</topic><topic>14/19</topic><topic>38/23</topic><topic>38/35</topic><topic>38/70</topic><topic>38/71</topic><topic>38/90</topic><topic>631/326/596/2557</topic><topic>631/449/2661/2666</topic><topic>Arabidopsis - virology</topic><topic>Carmovirus - physiology</topic><topic>Dominance</topic><topic>Flowers & plants</topic><topic>Gene Order</topic><topic>Genetic Variation</topic><topic>Genome, Viral</topic><topic>Genotypes</topic><topic>Humanities and Social Sciences</topic><topic>Invasions</topic><topic>Leaves</topic><topic>Models, Biological</topic><topic>multidisciplinary</topic><topic>Plant Diseases - virology</topic><topic>Plant Leaves - virology</topic><topic>Plant viruses</topic><topic>Plant Viruses - physiology</topic><topic>RNA-mediated interference</topic><topic>Science</topic><topic>Subpopulations</topic><topic>Superinfection</topic><topic>Systemic diseases</topic><topic>Viral Interference</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Zhang, Xiao-Feng</creatorcontrib><creatorcontrib>Guo, Jiangbo</creatorcontrib><creatorcontrib>Zhang, Xiuchun</creatorcontrib><creatorcontrib>Meulia, Tea</creatorcontrib><creatorcontrib>Paul, Pierce</creatorcontrib><creatorcontrib>Madden, Laurence V.</creatorcontrib><creatorcontrib>Li, Dawei</creatorcontrib><creatorcontrib>Qu, Feng</creatorcontrib><collection>Springer Nature OA Free Journals</collection><collection>Medline</collection><collection>MEDLINE</collection><collection>MEDLINE (Ovid)</collection><collection>MEDLINE</collection><collection>MEDLINE</collection><collection>PubMed</collection><collection>CrossRef</collection><collection>ProQuest Central (Corporate)</collection><collection>Health & Medical Collection</collection><collection>ProQuest Central (purchase pre-March 2016)</collection><collection>Biology Database (Alumni Edition)</collection><collection>Medical Database (Alumni Edition)</collection><collection>Science Database (Alumni Edition)</collection><collection>ProQuest SciTech Collection</collection><collection>ProQuest Natural Science Collection</collection><collection>Hospital Premium Collection</collection><collection>Hospital Premium Collection (Alumni Edition)</collection><collection>ProQuest Central (Alumni) (purchase pre-March 2016)</collection><collection>ProQuest Central (Alumni Edition)</collection><collection>ProQuest One Sustainability</collection><collection>ProQuest Central UK/Ireland</collection><collection>ProQuest Central Essentials</collection><collection>Biological Science Collection</collection><collection>ProQuest Central</collection><collection>Natural Science Collection</collection><collection>ProQuest One Community College</collection><collection>ProQuest Central Korea</collection><collection>Health Research Premium Collection</collection><collection>Health Research Premium Collection (Alumni)</collection><collection>ProQuest Central Student</collection><collection>SciTech Premium Collection</collection><collection>ProQuest Health & Medical Complete (Alumni)</collection><collection>ProQuest Biological Science Collection</collection><collection>Health & Medical Collection (Alumni Edition)</collection><collection>Medical Database</collection><collection>Science Database</collection><collection>Biological Science Database</collection><collection>Publicly Available Content Database</collection><collection>ProQuest One Academic Eastern Edition (DO NOT USE)</collection><collection>ProQuest One Academic</collection><collection>ProQuest One Academic UKI Edition</collection><collection>ProQuest Central Basic</collection><collection>MEDLINE - Academic</collection><collection>PubMed Central (Full Participant titles)</collection><jtitle>Scientific reports</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Zhang, Xiao-Feng</au><au>Guo, Jiangbo</au><au>Zhang, Xiuchun</au><au>Meulia, Tea</au><au>Paul, Pierce</au><au>Madden, Laurence V.</au><au>Li, Dawei</au><au>Qu, Feng</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Random Plant Viral Variants Attain Temporal Advantages During Systemic Infections and in Turn Resist other Variants of the Same Virus</atitle><jtitle>Scientific reports</jtitle><stitle>Sci Rep</stitle><addtitle>Sci Rep</addtitle><date>2015-10-20</date><risdate>2015</risdate><volume>5</volume><issue>1</issue><spage>15346</spage><epage>15346</epage><pages>15346-15346</pages><artnum>15346</artnum><issn>2045-2322</issn><eissn>2045-2322</eissn><abstract>Infection of plants with viruses containing multiple variants frequently leads to dominance by a few random variants in the systemically infected leaves (SLs), for which a plausible explanation is lacking. We show here that SL dominance by a given viral variant is adequately explained by its fortuitous lead in systemic spread, coupled with its resistance to superinfection by other variants. We analyzed the fate of a multi-variant turnip crinkle virus (TCV) population in
Arabidopsis
and
N. benthamiana
plants. Both wild-type and RNA silencing-defective plants displayed a similar pattern of random dominance by a few variant genotypes, thus discounting a prominent role for RNA silencing. When introduced to plants sequentially as two subpopulations, a twelve-hour head-start was sufficient for the first set to dominate. Finally, SLs of TCV-infected plants became highly resistant to secondary invasions of another TCV variant. We propose that random distribution of variant foci on inoculated leaves allows different variants to lead systemic movement in different plants. The leading variants then colonize large areas of SLs and resist the superinfection of lagging variants in the same areas. In conclusion, superinfection resistance is the primary driver of random enrichment of viral variants in systemically infected plants.</abstract><cop>London</cop><pub>Nature Publishing Group UK</pub><pmid>26481091</pmid><doi>10.1038/srep15346</doi><tpages>1</tpages><oa>free_for_read</oa></addata></record> |
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subjects | 14 14/19 38/23 38/35 38/70 38/71 38/90 631/326/596/2557 631/449/2661/2666 Arabidopsis - virology Carmovirus - physiology Dominance Flowers & plants Gene Order Genetic Variation Genome, Viral Genotypes Humanities and Social Sciences Invasions Leaves Models, Biological multidisciplinary Plant Diseases - virology Plant Leaves - virology Plant viruses Plant Viruses - physiology RNA-mediated interference Science Subpopulations Superinfection Systemic diseases Viral Interference |
title | Random Plant Viral Variants Attain Temporal Advantages During Systemic Infections and in Turn Resist other Variants of the Same Virus |
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