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Change in Emiliania huxleyi Virus Assemblage Diversity but Not in Host Genetic Composition during an Ocean Acidification Mesocosm Experiment
Effects of elevated pCO(2) on Emiliania huxleyi genetic diversity and the viruses that infect E. huxleyi (EhVs) have been investigated in large volume enclosures in a Norwegian fjord. Triplicate enclosures were bubbled with air enriched with CO(2) to 760 ppmv whilst the other three enclosures were b...
Autores principales: | , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
MDPI
2017
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5371796/ https://www.ncbi.nlm.nih.gov/pubmed/28282890 http://dx.doi.org/10.3390/v9030041 |
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author | Highfield, Andrea Joint, Ian Gilbert, Jack A. Crawfurd, Katharine J. Schroeder, Declan C. |
author_facet | Highfield, Andrea Joint, Ian Gilbert, Jack A. Crawfurd, Katharine J. Schroeder, Declan C. |
author_sort | Highfield, Andrea |
collection | PubMed |
description | Effects of elevated pCO(2) on Emiliania huxleyi genetic diversity and the viruses that infect E. huxleyi (EhVs) have been investigated in large volume enclosures in a Norwegian fjord. Triplicate enclosures were bubbled with air enriched with CO(2) to 760 ppmv whilst the other three enclosures were bubbled with air at ambient pCO(2); phytoplankton growth was initiated by the addition of nitrate and phosphate. E. huxleyi was the dominant coccolithophore in all enclosures, but no difference in genetic diversity, based on DGGE analysis using primers specific to the calcium binding protein gene (gpa) were detected in any of the treatments. Chlorophyll concentrations and primary production were lower in the three elevated pCO(2) treatments than in the ambient treatments. However, although coccolithophores numbers were reduced in two of the high-pCO(2) treatments; in the third, there was no suppression of coccolithophores numbers, which were very similar to the three ambient treatments. In contrast, there was considerable variation in genetic diversity in the EhVs, as determined by analysis of the major capsid protein (mcp) gene. EhV diversity was much lower in the high-pCO(2) treatment enclosure that did not show inhibition of E. huxleyi growth. Since virus infection is generally implicated as a major factor in terminating phytoplankton blooms, it is suggested that no study of the effect of ocean acidification in phytoplankton can be complete if it does not include an assessment of viruses. |
format | Online Article Text |
id | pubmed-5371796 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2017 |
publisher | MDPI |
record_format | MEDLINE/PubMed |
spelling | pubmed-53717962017-04-10 Change in Emiliania huxleyi Virus Assemblage Diversity but Not in Host Genetic Composition during an Ocean Acidification Mesocosm Experiment Highfield, Andrea Joint, Ian Gilbert, Jack A. Crawfurd, Katharine J. Schroeder, Declan C. Viruses Article Effects of elevated pCO(2) on Emiliania huxleyi genetic diversity and the viruses that infect E. huxleyi (EhVs) have been investigated in large volume enclosures in a Norwegian fjord. Triplicate enclosures were bubbled with air enriched with CO(2) to 760 ppmv whilst the other three enclosures were bubbled with air at ambient pCO(2); phytoplankton growth was initiated by the addition of nitrate and phosphate. E. huxleyi was the dominant coccolithophore in all enclosures, but no difference in genetic diversity, based on DGGE analysis using primers specific to the calcium binding protein gene (gpa) were detected in any of the treatments. Chlorophyll concentrations and primary production were lower in the three elevated pCO(2) treatments than in the ambient treatments. However, although coccolithophores numbers were reduced in two of the high-pCO(2) treatments; in the third, there was no suppression of coccolithophores numbers, which were very similar to the three ambient treatments. In contrast, there was considerable variation in genetic diversity in the EhVs, as determined by analysis of the major capsid protein (mcp) gene. EhV diversity was much lower in the high-pCO(2) treatment enclosure that did not show inhibition of E. huxleyi growth. Since virus infection is generally implicated as a major factor in terminating phytoplankton blooms, it is suggested that no study of the effect of ocean acidification in phytoplankton can be complete if it does not include an assessment of viruses. MDPI 2017-03-08 /pmc/articles/PMC5371796/ /pubmed/28282890 http://dx.doi.org/10.3390/v9030041 Text en © 2017 by the authors. Licensee MDPI, Basel, Switzerland. This article is an open access article distributed under the terms and conditions of the Creative Commons Attribution (CC BY) license (http://creativecommons.org/licenses/by/4.0/). |
spellingShingle | Article Highfield, Andrea Joint, Ian Gilbert, Jack A. Crawfurd, Katharine J. Schroeder, Declan C. Change in Emiliania huxleyi Virus Assemblage Diversity but Not in Host Genetic Composition during an Ocean Acidification Mesocosm Experiment |
title | Change in Emiliania huxleyi Virus Assemblage Diversity but Not in Host Genetic Composition during an Ocean Acidification Mesocosm Experiment |
title_full | Change in Emiliania huxleyi Virus Assemblage Diversity but Not in Host Genetic Composition during an Ocean Acidification Mesocosm Experiment |
title_fullStr | Change in Emiliania huxleyi Virus Assemblage Diversity but Not in Host Genetic Composition during an Ocean Acidification Mesocosm Experiment |
title_full_unstemmed | Change in Emiliania huxleyi Virus Assemblage Diversity but Not in Host Genetic Composition during an Ocean Acidification Mesocosm Experiment |
title_short | Change in Emiliania huxleyi Virus Assemblage Diversity but Not in Host Genetic Composition during an Ocean Acidification Mesocosm Experiment |
title_sort | change in emiliania huxleyi virus assemblage diversity but not in host genetic composition during an ocean acidification mesocosm experiment |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5371796/ https://www.ncbi.nlm.nih.gov/pubmed/28282890 http://dx.doi.org/10.3390/v9030041 |
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