Expression profiling of host and virus during a coccolithophore bloom provides insights into the role of viral infection in promoting carbon export

Abstract The cosmopolitan coccolithophore Emiliania huxleyi is a unicellular eukaryotic alga that forms vast blooms in the oceans impacting large biogeochemical cycles. These blooms are often terminated due to infection by the large dsDNA virus, E. huxleyi virus (EhV). It was recently established th...

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Published in:The ISME Journal
Main Authors: Sheyn, Uri, Rosenwasser, Shilo, Lehahn, Yoav, Barak-Gavish, Noa, Rotkopf, Ron, Bidle, Kay D, Koren, Ilan, Schatz, Daniella, Vardi, Assaf
Format: Article in Journal/Newspaper
Language:English
Published: Oxford University Press (OUP) 2018
Subjects:
Online Access:http://dx.doi.org/10.1038/s41396-017-0004-x
http://www.nature.com/articles/s41396-017-0004-x
http://www.nature.com/articles/s41396-017-0004-x.pdf
https://academic.oup.com/ismej/article-pdf/12/3/704/55852188/41396_2017_article_4.pdf
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spelling croxfordunivpr:10.1038/s41396-017-0004-x 2024-09-15T18:23:52+00:00 Expression profiling of host and virus during a coccolithophore bloom provides insights into the role of viral infection in promoting carbon export Sheyn, Uri Rosenwasser, Shilo Lehahn, Yoav Barak-Gavish, Noa Rotkopf, Ron Bidle, Kay D Koren, Ilan Schatz, Daniella Vardi, Assaf 2018 http://dx.doi.org/10.1038/s41396-017-0004-x http://www.nature.com/articles/s41396-017-0004-x http://www.nature.com/articles/s41396-017-0004-x.pdf https://academic.oup.com/ismej/article-pdf/12/3/704/55852188/41396_2017_article_4.pdf en eng Oxford University Press (OUP) https://academic.oup.com/pages/standard-publication-reuse-rights http://www.springer.com/tdm The ISME Journal volume 12, issue 3, page 704-713 ISSN 1751-7362 1751-7370 journal-article 2018 croxfordunivpr https://doi.org/10.1038/s41396-017-0004-x 2024-08-12T04:22:26Z Abstract The cosmopolitan coccolithophore Emiliania huxleyi is a unicellular eukaryotic alga that forms vast blooms in the oceans impacting large biogeochemical cycles. These blooms are often terminated due to infection by the large dsDNA virus, E. huxleyi virus (EhV). It was recently established that EhV-induced modulation of E. huxleyi metabolism is a key factor for optimal viral infection cycle. Despite the huge ecological importance of this host–virus interaction, the ability to assess its spatial and temporal dynamics and its possible impact on nutrient fluxes is limited by current approaches that focus on quantification of viral abundance and biodiversity. Here, we applied a host and virus gene expression analysis as a sensitive tool to quantify the dynamics of this interaction during a natural E. huxleyi bloom in the North Atlantic. We used viral gene expression profiling as an index for the level of active infection and showed that the latter correlated with water column depth. Intriguingly, this suggests a possible sinking mechanism for removing infected cells as aggregates from the E. huxleyi population in the surface layer into deeper waters. Viral infection was also highly correlated with induction of host metabolic genes involved in host life cycle, sphingolipid, and antioxidant metabolism, providing evidence for modulation of host metabolism under natural conditions. The ability to track and quantify defined phases of infection by monitoring co-expression of viral and host genes, coupled with advance omics approaches, will enable a deeper understanding of the impact that viruses have on the environment. Article in Journal/Newspaper North Atlantic Oxford University Press The ISME Journal 12 3 704 713
institution Open Polar
collection Oxford University Press
op_collection_id croxfordunivpr
language English
description Abstract The cosmopolitan coccolithophore Emiliania huxleyi is a unicellular eukaryotic alga that forms vast blooms in the oceans impacting large biogeochemical cycles. These blooms are often terminated due to infection by the large dsDNA virus, E. huxleyi virus (EhV). It was recently established that EhV-induced modulation of E. huxleyi metabolism is a key factor for optimal viral infection cycle. Despite the huge ecological importance of this host–virus interaction, the ability to assess its spatial and temporal dynamics and its possible impact on nutrient fluxes is limited by current approaches that focus on quantification of viral abundance and biodiversity. Here, we applied a host and virus gene expression analysis as a sensitive tool to quantify the dynamics of this interaction during a natural E. huxleyi bloom in the North Atlantic. We used viral gene expression profiling as an index for the level of active infection and showed that the latter correlated with water column depth. Intriguingly, this suggests a possible sinking mechanism for removing infected cells as aggregates from the E. huxleyi population in the surface layer into deeper waters. Viral infection was also highly correlated with induction of host metabolic genes involved in host life cycle, sphingolipid, and antioxidant metabolism, providing evidence for modulation of host metabolism under natural conditions. The ability to track and quantify defined phases of infection by monitoring co-expression of viral and host genes, coupled with advance omics approaches, will enable a deeper understanding of the impact that viruses have on the environment.
format Article in Journal/Newspaper
author Sheyn, Uri
Rosenwasser, Shilo
Lehahn, Yoav
Barak-Gavish, Noa
Rotkopf, Ron
Bidle, Kay D
Koren, Ilan
Schatz, Daniella
Vardi, Assaf
spellingShingle Sheyn, Uri
Rosenwasser, Shilo
Lehahn, Yoav
Barak-Gavish, Noa
Rotkopf, Ron
Bidle, Kay D
Koren, Ilan
Schatz, Daniella
Vardi, Assaf
Expression profiling of host and virus during a coccolithophore bloom provides insights into the role of viral infection in promoting carbon export
author_facet Sheyn, Uri
Rosenwasser, Shilo
Lehahn, Yoav
Barak-Gavish, Noa
Rotkopf, Ron
Bidle, Kay D
Koren, Ilan
Schatz, Daniella
Vardi, Assaf
author_sort Sheyn, Uri
title Expression profiling of host and virus during a coccolithophore bloom provides insights into the role of viral infection in promoting carbon export
title_short Expression profiling of host and virus during a coccolithophore bloom provides insights into the role of viral infection in promoting carbon export
title_full Expression profiling of host and virus during a coccolithophore bloom provides insights into the role of viral infection in promoting carbon export
title_fullStr Expression profiling of host and virus during a coccolithophore bloom provides insights into the role of viral infection in promoting carbon export
title_full_unstemmed Expression profiling of host and virus during a coccolithophore bloom provides insights into the role of viral infection in promoting carbon export
title_sort expression profiling of host and virus during a coccolithophore bloom provides insights into the role of viral infection in promoting carbon export
publisher Oxford University Press (OUP)
publishDate 2018
url http://dx.doi.org/10.1038/s41396-017-0004-x
http://www.nature.com/articles/s41396-017-0004-x
http://www.nature.com/articles/s41396-017-0004-x.pdf
https://academic.oup.com/ismej/article-pdf/12/3/704/55852188/41396_2017_article_4.pdf
genre North Atlantic
genre_facet North Atlantic
op_source The ISME Journal
volume 12, issue 3, page 704-713
ISSN 1751-7362 1751-7370
op_rights https://academic.oup.com/pages/standard-publication-reuse-rights
http://www.springer.com/tdm
op_doi https://doi.org/10.1038/s41396-017-0004-x
container_title The ISME Journal
container_volume 12
container_issue 3
container_start_page 704
op_container_end_page 713
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