Host–virus dynamics and subcellular controls of cell fate in a natural coccolithophore population

Marine viruses are major evolutionary and biogeochemical drivers in marine microbial foodwebs. However, an in-depth understanding of the cellular mechanisms and the signal transduction pathways mediating host–virus interactions during natural bloom dynamics has remained elusive. We used field-based...

Ausführliche Beschreibung

Gespeichert in:
Bibliographische Detailangaben
Veröffentlicht in:Proceedings of the National Academy of Sciences - PNAS 2012-11, Vol.109 (47), p.19327-19332
Hauptverfasser: Vardi, Assaf, Haramaty, Liti, Van Mooy, Benjamin A. S, Fredricks, Helen F, Kimmance, Susan A, Larsen, Aud, Bidle, Kay D
Format: Artikel
Sprache:eng
Schlagworte:
Online-Zugang:Volltext
Tags: Tag hinzufügen
Keine Tags, Fügen Sie den ersten Tag hinzu!
container_end_page 19332
container_issue 47
container_start_page 19327
container_title Proceedings of the National Academy of Sciences - PNAS
container_volume 109
creator Vardi, Assaf
Haramaty, Liti
Van Mooy, Benjamin A. S
Fredricks, Helen F
Kimmance, Susan A
Larsen, Aud
Bidle, Kay D
description Marine viruses are major evolutionary and biogeochemical drivers in marine microbial foodwebs. However, an in-depth understanding of the cellular mechanisms and the signal transduction pathways mediating host–virus interactions during natural bloom dynamics has remained elusive. We used field-based mesocosms to examine the “arms race” between natural populations of the coccolithophore Emiliania huxleyi and its double-stranded DNA-containing coccolithoviruses (EhVs). Specifically, we examined the dynamics of EhV infection and its regulation of cell fate over the course of bloom development and demise using a diverse suite of molecular tools and in situ fluorescent staining to target different levels of subcellular resolution. We demonstrate the concomitant induction of reactive oxygen species, caspase-specific activity, metacaspase expression, and programmed cell death in response to the accumulation of virus-derived glycosphingolipids upon infection of natural E. huxleyi populations. These subcellular responses to viral infection simultaneously resulted in the enhanced production of transparent exopolymer particles, which can facilitate aggregation and stimulate carbon flux. Our results not only corroborate the critical role for glycosphingolipids and programmed cell death in regulating E. huxleyi –EhV interactions, but also elucidate promising molecular biomarkers and lipid-based proxies for phytoplankton host–virus interactions in natural systems.
doi_str_mv 10.1073/pnas.1208895109
format Article
fullrecord <record><control><sourceid>jstor_pubme</sourceid><recordid>TN_cdi_pubmedcentral_primary_oai_pubmedcentral_nih_gov_3511156</recordid><sourceformat>XML</sourceformat><sourcesystem>PC</sourcesystem><jstor_id>41830208</jstor_id><sourcerecordid>41830208</sourcerecordid><originalsourceid>FETCH-LOGICAL-c558t-8f7b85a208e90d4f1091db336a7c6a2d6e4f8404141e5f9d1af7fb9c36b3219f3</originalsourceid><addsrcrecordid>eNpdkcFu1DAURSMEokNhzQqwxIbNtO_FjmNvKqEKKFIlFtC15Th2x6OMHeykUnf8A3_Il-BohimwsSXf867f1a2qlwhnCC09H4POZ1iDELJBkI-qVTlxzZmEx9UKoG7XgtXspHqW8xYAZCPgaXVSU6SspbiqzFXM068fP-98mjPp74PeeZOJDj3Jc2fsMMyDTsTEMKU4ZBIdWR6J05MlPhBNgp7mpIeCGBMHP23iuInJkjGOZXTyMTyvnjg9ZPvicJ9WNx8_fLu8Wl9_-fT58v312jSNmNbCtZ1odAljJfTMLUn6jlKuW8N13XPLnGDAkKFtnOxRu9Z10lDe0Rqlo6fVxd53nLud7Y0tO-tBjcnvdLpXUXv1rxL8Rt3GO0UbRGx4MXh3MEjx-2zzpHY-L3F1sHHOClFwCS0HWdC3_6HbOKdQ4i0USMZq2hTqfE-ZFHNO1h2XQVBLgWopUD0UWCZe_53hyP9prADkACyTD3ZSsVahpHVbkFd7ZJunmI4MQ0Gh_FT0N3vd6aj0bfJZ3XytATkAUqCc0t-Oy7bt</addsrcrecordid><sourcetype>Open Access Repository</sourcetype><iscdi>true</iscdi><recordtype>article</recordtype><pqid>1180944235</pqid></control><display><type>article</type><title>Host–virus dynamics and subcellular controls of cell fate in a natural coccolithophore population</title><source>MEDLINE</source><source>JSTOR Archive Collection A-Z Listing</source><source>PubMed Central</source><source>Alma/SFX Local Collection</source><source>Free Full-Text Journals in Chemistry</source><creator>Vardi, Assaf ; Haramaty, Liti ; Van Mooy, Benjamin A. S ; Fredricks, Helen F ; Kimmance, Susan A ; Larsen, Aud ; Bidle, Kay D</creator><creatorcontrib>Vardi, Assaf ; Haramaty, Liti ; Van Mooy, Benjamin A. S ; Fredricks, Helen F ; Kimmance, Susan A ; Larsen, Aud ; Bidle, Kay D</creatorcontrib><description>Marine viruses are major evolutionary and biogeochemical drivers in marine microbial foodwebs. However, an in-depth understanding of the cellular mechanisms and the signal transduction pathways mediating host–virus interactions during natural bloom dynamics has remained elusive. We used field-based mesocosms to examine the “arms race” between natural populations of the coccolithophore Emiliania huxleyi and its double-stranded DNA-containing coccolithoviruses (EhVs). Specifically, we examined the dynamics of EhV infection and its regulation of cell fate over the course of bloom development and demise using a diverse suite of molecular tools and in situ fluorescent staining to target different levels of subcellular resolution. We demonstrate the concomitant induction of reactive oxygen species, caspase-specific activity, metacaspase expression, and programmed cell death in response to the accumulation of virus-derived glycosphingolipids upon infection of natural E. huxleyi populations. These subcellular responses to viral infection simultaneously resulted in the enhanced production of transparent exopolymer particles, which can facilitate aggregation and stimulate carbon flux. Our results not only corroborate the critical role for glycosphingolipids and programmed cell death in regulating E. huxleyi –EhV interactions, but also elucidate promising molecular biomarkers and lipid-based proxies for phytoplankton host–virus interactions in natural systems.</description><identifier>ISSN: 0027-8424</identifier><identifier>EISSN: 1091-6490</identifier><identifier>DOI: 10.1073/pnas.1208895109</identifier><identifier>PMID: 23134731</identifier><language>eng</language><publisher>United States: National Academy of Sciences</publisher><subject>Animal populations ; Apoptosis ; Biological Sciences ; biomarkers ; Biopolymers - biosynthesis ; carbon ; Caspases - metabolism ; Cell Lineage ; Cells ; Emiliania huxleyi ; Enzyme Activation ; Eutrophication ; fluorescence ; Glycosphingolipids ; Haploidy ; Haptophyta - cytology ; Haptophyta - enzymology ; Haptophyta - virology ; Host-Pathogen Interactions - physiology ; host-pathogen relationships ; Infections ; Marine ecology ; Molecules ; Mortality ; Norway ; Phycodnaviridae - physiology ; Phytoplankton ; Reactive oxygen species ; Signal transduction ; Sphingolipids ; Subcellular Fractions - virology ; Time Factors ; Viral infections ; Viruses</subject><ispartof>Proceedings of the National Academy of Sciences - PNAS, 2012-11, Vol.109 (47), p.19327-19332</ispartof><rights>copyright © 1993-2008 National Academy of Sciences of the United States of America</rights><rights>Copyright National Academy of Sciences Nov 20, 2012</rights><lds50>peer_reviewed</lds50><oa>free_for_read</oa><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c558t-8f7b85a208e90d4f1091db336a7c6a2d6e4f8404141e5f9d1af7fb9c36b3219f3</citedby><cites>FETCH-LOGICAL-c558t-8f7b85a208e90d4f1091db336a7c6a2d6e4f8404141e5f9d1af7fb9c36b3219f3</cites></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Uhttp://www.pnas.org/content/109/47.cover.gif</thumbnail><linktopdf>$$Uhttps://www.jstor.org/stable/pdf/41830208$$EPDF$$P50$$Gjstor$$H</linktopdf><linktohtml>$$Uhttps://www.jstor.org/stable/41830208$$EHTML$$P50$$Gjstor$$H</linktohtml><link.rule.ids>230,314,727,780,784,803,885,27924,27925,53791,53793,58017,58250</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/23134731$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Vardi, Assaf</creatorcontrib><creatorcontrib>Haramaty, Liti</creatorcontrib><creatorcontrib>Van Mooy, Benjamin A. S</creatorcontrib><creatorcontrib>Fredricks, Helen F</creatorcontrib><creatorcontrib>Kimmance, Susan A</creatorcontrib><creatorcontrib>Larsen, Aud</creatorcontrib><creatorcontrib>Bidle, Kay D</creatorcontrib><title>Host–virus dynamics and subcellular controls of cell fate in a natural coccolithophore population</title><title>Proceedings of the National Academy of Sciences - PNAS</title><addtitle>Proc Natl Acad Sci U S A</addtitle><description>Marine viruses are major evolutionary and biogeochemical drivers in marine microbial foodwebs. However, an in-depth understanding of the cellular mechanisms and the signal transduction pathways mediating host–virus interactions during natural bloom dynamics has remained elusive. We used field-based mesocosms to examine the “arms race” between natural populations of the coccolithophore Emiliania huxleyi and its double-stranded DNA-containing coccolithoviruses (EhVs). Specifically, we examined the dynamics of EhV infection and its regulation of cell fate over the course of bloom development and demise using a diverse suite of molecular tools and in situ fluorescent staining to target different levels of subcellular resolution. We demonstrate the concomitant induction of reactive oxygen species, caspase-specific activity, metacaspase expression, and programmed cell death in response to the accumulation of virus-derived glycosphingolipids upon infection of natural E. huxleyi populations. These subcellular responses to viral infection simultaneously resulted in the enhanced production of transparent exopolymer particles, which can facilitate aggregation and stimulate carbon flux. Our results not only corroborate the critical role for glycosphingolipids and programmed cell death in regulating E. huxleyi –EhV interactions, but also elucidate promising molecular biomarkers and lipid-based proxies for phytoplankton host–virus interactions in natural systems.</description><subject>Animal populations</subject><subject>Apoptosis</subject><subject>Biological Sciences</subject><subject>biomarkers</subject><subject>Biopolymers - biosynthesis</subject><subject>carbon</subject><subject>Caspases - metabolism</subject><subject>Cell Lineage</subject><subject>Cells</subject><subject>Emiliania huxleyi</subject><subject>Enzyme Activation</subject><subject>Eutrophication</subject><subject>fluorescence</subject><subject>Glycosphingolipids</subject><subject>Haploidy</subject><subject>Haptophyta - cytology</subject><subject>Haptophyta - enzymology</subject><subject>Haptophyta - virology</subject><subject>Host-Pathogen Interactions - physiology</subject><subject>host-pathogen relationships</subject><subject>Infections</subject><subject>Marine ecology</subject><subject>Molecules</subject><subject>Mortality</subject><subject>Norway</subject><subject>Phycodnaviridae - physiology</subject><subject>Phytoplankton</subject><subject>Reactive oxygen species</subject><subject>Signal transduction</subject><subject>Sphingolipids</subject><subject>Subcellular Fractions - virology</subject><subject>Time Factors</subject><subject>Viral infections</subject><subject>Viruses</subject><issn>0027-8424</issn><issn>1091-6490</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2012</creationdate><recordtype>article</recordtype><sourceid>EIF</sourceid><recordid>eNpdkcFu1DAURSMEokNhzQqwxIbNtO_FjmNvKqEKKFIlFtC15Th2x6OMHeykUnf8A3_Il-BohimwsSXf867f1a2qlwhnCC09H4POZ1iDELJBkI-qVTlxzZmEx9UKoG7XgtXspHqW8xYAZCPgaXVSU6SspbiqzFXM068fP-98mjPp74PeeZOJDj3Jc2fsMMyDTsTEMKU4ZBIdWR6J05MlPhBNgp7mpIeCGBMHP23iuInJkjGOZXTyMTyvnjg9ZPvicJ9WNx8_fLu8Wl9_-fT58v312jSNmNbCtZ1odAljJfTMLUn6jlKuW8N13XPLnGDAkKFtnOxRu9Z10lDe0Rqlo6fVxd53nLud7Y0tO-tBjcnvdLpXUXv1rxL8Rt3GO0UbRGx4MXh3MEjx-2zzpHY-L3F1sHHOClFwCS0HWdC3_6HbOKdQ4i0USMZq2hTqfE-ZFHNO1h2XQVBLgWopUD0UWCZe_53hyP9prADkACyTD3ZSsVahpHVbkFd7ZJunmI4MQ0Gh_FT0N3vd6aj0bfJZ3XytATkAUqCc0t-Oy7bt</recordid><startdate>20121120</startdate><enddate>20121120</enddate><creator>Vardi, Assaf</creator><creator>Haramaty, Liti</creator><creator>Van Mooy, Benjamin A. S</creator><creator>Fredricks, Helen F</creator><creator>Kimmance, Susan A</creator><creator>Larsen, Aud</creator><creator>Bidle, Kay D</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></search><sort><creationdate>20121120</creationdate><title>Host–virus dynamics and subcellular controls of cell fate in a natural coccolithophore population</title><author>Vardi, Assaf ; Haramaty, Liti ; Van Mooy, Benjamin A. S ; Fredricks, Helen F ; Kimmance, Susan A ; Larsen, Aud ; Bidle, Kay D</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c558t-8f7b85a208e90d4f1091db336a7c6a2d6e4f8404141e5f9d1af7fb9c36b3219f3</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2012</creationdate><topic>Animal populations</topic><topic>Apoptosis</topic><topic>Biological Sciences</topic><topic>biomarkers</topic><topic>Biopolymers - biosynthesis</topic><topic>carbon</topic><topic>Caspases - metabolism</topic><topic>Cell Lineage</topic><topic>Cells</topic><topic>Emiliania huxleyi</topic><topic>Enzyme Activation</topic><topic>Eutrophication</topic><topic>fluorescence</topic><topic>Glycosphingolipids</topic><topic>Haploidy</topic><topic>Haptophyta - cytology</topic><topic>Haptophyta - enzymology</topic><topic>Haptophyta - virology</topic><topic>Host-Pathogen Interactions - physiology</topic><topic>host-pathogen relationships</topic><topic>Infections</topic><topic>Marine ecology</topic><topic>Molecules</topic><topic>Mortality</topic><topic>Norway</topic><topic>Phycodnaviridae - physiology</topic><topic>Phytoplankton</topic><topic>Reactive oxygen species</topic><topic>Signal transduction</topic><topic>Sphingolipids</topic><topic>Subcellular Fractions - virology</topic><topic>Time Factors</topic><topic>Viral infections</topic><topic>Viruses</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Vardi, Assaf</creatorcontrib><creatorcontrib>Haramaty, Liti</creatorcontrib><creatorcontrib>Van Mooy, Benjamin A. S</creatorcontrib><creatorcontrib>Fredricks, Helen F</creatorcontrib><creatorcontrib>Kimmance, Susan A</creatorcontrib><creatorcontrib>Larsen, Aud</creatorcontrib><creatorcontrib>Bidle, Kay D</creatorcontrib><collection>AGRIS</collection><collection>Medline</collection><collection>MEDLINE</collection><collection>MEDLINE (Ovid)</collection><collection>MEDLINE</collection><collection>MEDLINE</collection><collection>PubMed</collection><collection>CrossRef</collection><collection>Animal Behavior Abstracts</collection><collection>Bacteriology Abstracts (Microbiology B)</collection><collection>Calcium &amp; Calcified Tissue Abstracts</collection><collection>Chemoreception Abstracts</collection><collection>Ecology Abstracts</collection><collection>Entomology Abstracts (Full archive)</collection><collection>Immunology Abstracts</collection><collection>Neurosciences Abstracts</collection><collection>Nucleic Acids Abstracts</collection><collection>Oncogenes and Growth Factors Abstracts</collection><collection>Virology and AIDS Abstracts</collection><collection>Technology Research Database</collection><collection>Environmental Sciences and Pollution Management</collection><collection>Engineering Research Database</collection><collection>AIDS and Cancer Research Abstracts</collection><collection>Algology Mycology and Protozoology Abstracts (Microbiology C)</collection><collection>Biotechnology and BioEngineering Abstracts</collection><collection>Genetics Abstracts</collection><collection>MEDLINE - Academic</collection><collection>PubMed Central (Full Participant titles)</collection><jtitle>Proceedings of the National Academy of Sciences - PNAS</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Vardi, Assaf</au><au>Haramaty, Liti</au><au>Van Mooy, Benjamin A. S</au><au>Fredricks, Helen F</au><au>Kimmance, Susan A</au><au>Larsen, Aud</au><au>Bidle, Kay D</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Host–virus dynamics and subcellular controls of cell fate in a natural coccolithophore population</atitle><jtitle>Proceedings of the National Academy of Sciences - PNAS</jtitle><addtitle>Proc Natl Acad Sci U S A</addtitle><date>2012-11-20</date><risdate>2012</risdate><volume>109</volume><issue>47</issue><spage>19327</spage><epage>19332</epage><pages>19327-19332</pages><issn>0027-8424</issn><eissn>1091-6490</eissn><abstract>Marine viruses are major evolutionary and biogeochemical drivers in marine microbial foodwebs. However, an in-depth understanding of the cellular mechanisms and the signal transduction pathways mediating host–virus interactions during natural bloom dynamics has remained elusive. We used field-based mesocosms to examine the “arms race” between natural populations of the coccolithophore Emiliania huxleyi and its double-stranded DNA-containing coccolithoviruses (EhVs). Specifically, we examined the dynamics of EhV infection and its regulation of cell fate over the course of bloom development and demise using a diverse suite of molecular tools and in situ fluorescent staining to target different levels of subcellular resolution. We demonstrate the concomitant induction of reactive oxygen species, caspase-specific activity, metacaspase expression, and programmed cell death in response to the accumulation of virus-derived glycosphingolipids upon infection of natural E. huxleyi populations. These subcellular responses to viral infection simultaneously resulted in the enhanced production of transparent exopolymer particles, which can facilitate aggregation and stimulate carbon flux. Our results not only corroborate the critical role for glycosphingolipids and programmed cell death in regulating E. huxleyi –EhV interactions, but also elucidate promising molecular biomarkers and lipid-based proxies for phytoplankton host–virus interactions in natural systems.</abstract><cop>United States</cop><pub>National Academy of Sciences</pub><pmid>23134731</pmid><doi>10.1073/pnas.1208895109</doi><tpages>6</tpages><oa>free_for_read</oa></addata></record>
fulltext fulltext
identifier ISSN: 0027-8424
ispartof Proceedings of the National Academy of Sciences - PNAS, 2012-11, Vol.109 (47), p.19327-19332
issn 0027-8424
1091-6490
language eng
recordid cdi_pubmedcentral_primary_oai_pubmedcentral_nih_gov_3511156
source MEDLINE; JSTOR Archive Collection A-Z Listing; PubMed Central; Alma/SFX Local Collection; Free Full-Text Journals in Chemistry
subjects Animal populations
Apoptosis
Biological Sciences
biomarkers
Biopolymers - biosynthesis
carbon
Caspases - metabolism
Cell Lineage
Cells
Emiliania huxleyi
Enzyme Activation
Eutrophication
fluorescence
Glycosphingolipids
Haploidy
Haptophyta - cytology
Haptophyta - enzymology
Haptophyta - virology
Host-Pathogen Interactions - physiology
host-pathogen relationships
Infections
Marine ecology
Molecules
Mortality
Norway
Phycodnaviridae - physiology
Phytoplankton
Reactive oxygen species
Signal transduction
Sphingolipids
Subcellular Fractions - virology
Time Factors
Viral infections
Viruses
title Host–virus dynamics and subcellular controls of cell fate in a natural coccolithophore population
url https://sfx.bib-bvb.de/sfx_tum?ctx_ver=Z39.88-2004&ctx_enc=info:ofi/enc:UTF-8&ctx_tim=2025-01-06T18%3A48%3A07IST&url_ver=Z39.88-2004&url_ctx_fmt=infofi/fmt:kev:mtx:ctx&rfr_id=info:sid/primo.exlibrisgroup.com:primo3-Article-jstor_pubme&rft_val_fmt=info:ofi/fmt:kev:mtx:journal&rft.genre=article&rft.atitle=Host%E2%80%93virus%20dynamics%20and%20subcellular%20controls%20of%20cell%20fate%20in%20a%20natural%20coccolithophore%20population&rft.jtitle=Proceedings%20of%20the%20National%20Academy%20of%20Sciences%20-%20PNAS&rft.au=Vardi,%20Assaf&rft.date=2012-11-20&rft.volume=109&rft.issue=47&rft.spage=19327&rft.epage=19332&rft.pages=19327-19332&rft.issn=0027-8424&rft.eissn=1091-6490&rft_id=info:doi/10.1073/pnas.1208895109&rft_dat=%3Cjstor_pubme%3E41830208%3C/jstor_pubme%3E%3Curl%3E%3C/url%3E&disable_directlink=true&sfx.directlink=off&sfx.report_link=0&rft_id=info:oai/&rft_pqid=1180944235&rft_id=info:pmid/23134731&rft_jstor_id=41830208&rfr_iscdi=true