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Viruses of a key coral symbiont exhibit temperature-driven productivity across a reefscape
Viruses can affect coral health by infecting their symbiotic dinoflagellate partners (Symbiodiniaceae). Yet, viral dynamics in coral colonies exposed to environmental stress have not been studied at the reef scale, particularly within individual viral lineages. We sequenced the viral major capsid pr...
Autores principales: | , , , , , , , , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Nature Publishing Group UK
2023
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10068613/ https://www.ncbi.nlm.nih.gov/pubmed/37009785 http://dx.doi.org/10.1038/s43705-023-00227-7 |
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author | Howe-Kerr, Lauren I. Grupstra, Carsten G. B. Rabbitt, Kristen M. Conetta, Dennis Coy, Samantha R. Klinges, J. Grace Maher, Rebecca L. McConnell, Kaitlin M. Meiling, Sonora S. Messyasz, Adriana Schmeltzer, Emily R. Seabrook, Sarah Sims, Jordan A. Veglia, Alex J. Thurber, Andrew R. Thurber, Rebecca L. Vega Correa, Adrienne M. S. |
author_facet | Howe-Kerr, Lauren I. Grupstra, Carsten G. B. Rabbitt, Kristen M. Conetta, Dennis Coy, Samantha R. Klinges, J. Grace Maher, Rebecca L. McConnell, Kaitlin M. Meiling, Sonora S. Messyasz, Adriana Schmeltzer, Emily R. Seabrook, Sarah Sims, Jordan A. Veglia, Alex J. Thurber, Andrew R. Thurber, Rebecca L. Vega Correa, Adrienne M. S. |
author_sort | Howe-Kerr, Lauren I. |
collection | PubMed |
description | Viruses can affect coral health by infecting their symbiotic dinoflagellate partners (Symbiodiniaceae). Yet, viral dynamics in coral colonies exposed to environmental stress have not been studied at the reef scale, particularly within individual viral lineages. We sequenced the viral major capsid protein (mcp) gene of positive-sense single-stranded RNA viruses known to infect symbiotic dinoflagellates (‘dinoRNAVs’) to analyze their dynamics in the reef-building coral, Porites lobata. We repeatedly sampled 54 colonies harboring Cladocopium C15 dinoflagellates, across three environmentally distinct reef zones (fringing reef, back reef, and forereef) around the island of Moorea, French Polynesia over a 3-year period and spanning a reef-wide thermal stress event. By the end of the sampling period, 28% (5/18) of corals in the fringing reef experienced partial mortality versus 78% (14/18) of corals in the forereef. Over 90% (50/54) of colonies had detectable dinoRNAV infections. Reef zone influenced the composition and richness of viral mcp amino acid types (‘aminotypes’), with the fringing reef containing the highest aminotype richness. The reef-wide thermal stress event significantly increased aminotype dispersion, and this pattern was strongest in the colonies that experienced partial mortality. These findings demonstrate that dinoRNAV infections respond to environmental fluctuations experienced in situ on reefs. Further, viral productivity will likely increase as ocean temperatures continue to rise, potentially impacting the foundational symbiosis underpinning coral reef ecosystems. |
format | Online Article Text |
id | pubmed-10068613 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2023 |
publisher | Nature Publishing Group UK |
record_format | MEDLINE/PubMed |
spelling | pubmed-100686132023-04-04 Viruses of a key coral symbiont exhibit temperature-driven productivity across a reefscape Howe-Kerr, Lauren I. Grupstra, Carsten G. B. Rabbitt, Kristen M. Conetta, Dennis Coy, Samantha R. Klinges, J. Grace Maher, Rebecca L. McConnell, Kaitlin M. Meiling, Sonora S. Messyasz, Adriana Schmeltzer, Emily R. Seabrook, Sarah Sims, Jordan A. Veglia, Alex J. Thurber, Andrew R. Thurber, Rebecca L. Vega Correa, Adrienne M. S. ISME Commun Article Viruses can affect coral health by infecting their symbiotic dinoflagellate partners (Symbiodiniaceae). Yet, viral dynamics in coral colonies exposed to environmental stress have not been studied at the reef scale, particularly within individual viral lineages. We sequenced the viral major capsid protein (mcp) gene of positive-sense single-stranded RNA viruses known to infect symbiotic dinoflagellates (‘dinoRNAVs’) to analyze their dynamics in the reef-building coral, Porites lobata. We repeatedly sampled 54 colonies harboring Cladocopium C15 dinoflagellates, across three environmentally distinct reef zones (fringing reef, back reef, and forereef) around the island of Moorea, French Polynesia over a 3-year period and spanning a reef-wide thermal stress event. By the end of the sampling period, 28% (5/18) of corals in the fringing reef experienced partial mortality versus 78% (14/18) of corals in the forereef. Over 90% (50/54) of colonies had detectable dinoRNAV infections. Reef zone influenced the composition and richness of viral mcp amino acid types (‘aminotypes’), with the fringing reef containing the highest aminotype richness. The reef-wide thermal stress event significantly increased aminotype dispersion, and this pattern was strongest in the colonies that experienced partial mortality. These findings demonstrate that dinoRNAV infections respond to environmental fluctuations experienced in situ on reefs. Further, viral productivity will likely increase as ocean temperatures continue to rise, potentially impacting the foundational symbiosis underpinning coral reef ecosystems. Nature Publishing Group UK 2023-04-03 /pmc/articles/PMC10068613/ /pubmed/37009785 http://dx.doi.org/10.1038/s43705-023-00227-7 Text en © The Author(s) 2023 https://creativecommons.org/licenses/by/4.0/Open Access This article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons license, and indicate if changes were made. The images or other third party material in this article are included in the article’s Creative Commons license, unless indicated otherwise in a credit line to the material. If material is not included in the article’s Creative Commons license and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this license, visit http://creativecommons.org/licenses/by/4.0/ (https://creativecommons.org/licenses/by/4.0/) . |
spellingShingle | Article Howe-Kerr, Lauren I. Grupstra, Carsten G. B. Rabbitt, Kristen M. Conetta, Dennis Coy, Samantha R. Klinges, J. Grace Maher, Rebecca L. McConnell, Kaitlin M. Meiling, Sonora S. Messyasz, Adriana Schmeltzer, Emily R. Seabrook, Sarah Sims, Jordan A. Veglia, Alex J. Thurber, Andrew R. Thurber, Rebecca L. Vega Correa, Adrienne M. S. Viruses of a key coral symbiont exhibit temperature-driven productivity across a reefscape |
title | Viruses of a key coral symbiont exhibit temperature-driven productivity across a reefscape |
title_full | Viruses of a key coral symbiont exhibit temperature-driven productivity across a reefscape |
title_fullStr | Viruses of a key coral symbiont exhibit temperature-driven productivity across a reefscape |
title_full_unstemmed | Viruses of a key coral symbiont exhibit temperature-driven productivity across a reefscape |
title_short | Viruses of a key coral symbiont exhibit temperature-driven productivity across a reefscape |
title_sort | viruses of a key coral symbiont exhibit temperature-driven productivity across a reefscape |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10068613/ https://www.ncbi.nlm.nih.gov/pubmed/37009785 http://dx.doi.org/10.1038/s43705-023-00227-7 |
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