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Preserving and Using Germplasm and Dissociated Embryonic Cells for Conserving Caribbean and Pacific Coral
Coral reefs are experiencing unprecedented degradation due to human activities, and protecting specific reef habitats may not stop this decline, because the most serious threats are global (i.e., climate change), not local. However, ex situ preservation practices can provide safeguards for coral ree...
Autores principales: | , , , , , , , , , , , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Public Library of Science
2012
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3297639/ https://www.ncbi.nlm.nih.gov/pubmed/22413020 http://dx.doi.org/10.1371/journal.pone.0033354 |
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author | Hagedorn, Mary Carter, Virginia Martorana, Kelly Paresa, Malia K. Acker, Jason Baums, Iliana B. Borneman, Eric Brittsan, Michael Byers, Michael Henley, Michael Laterveer, Michael Leong, Jo-Ann McCarthy, Megan Meyers, Stuart Nelson, Brian D. Petersen, Dirk Tiersch, Terrence Uribe, Rafael Cuevas Woods, Erik Wildt, David |
author_facet | Hagedorn, Mary Carter, Virginia Martorana, Kelly Paresa, Malia K. Acker, Jason Baums, Iliana B. Borneman, Eric Brittsan, Michael Byers, Michael Henley, Michael Laterveer, Michael Leong, Jo-Ann McCarthy, Megan Meyers, Stuart Nelson, Brian D. Petersen, Dirk Tiersch, Terrence Uribe, Rafael Cuevas Woods, Erik Wildt, David |
author_sort | Hagedorn, Mary |
collection | PubMed |
description | Coral reefs are experiencing unprecedented degradation due to human activities, and protecting specific reef habitats may not stop this decline, because the most serious threats are global (i.e., climate change), not local. However, ex situ preservation practices can provide safeguards for coral reef conservation. Specifically, modern advances in cryobiology and genome banking could secure existing species and genetic diversity until genotypes can be introduced into rehabilitated habitats. We assessed the feasibility of recovering viable sperm and embryonic cells post-thaw from two coral species, Acropora palmata and Fungia scutaria that have diffferent evolutionary histories, ecological niches and reproductive strategies. In vitro fertilization (IVF) of conspecific eggs using fresh (control) spermatozoa revealed high levels of fertilization (>90% in A. palmata; >84% in F. scutaria; P>0.05) that were unaffected by tested sperm concentrations. A solution of 10% dimethyl sulfoxide (DMSO) at cooling rates of 20 to 30°C/min most successfully cryopreserved both A. palmata and F. scutaria spermatozoa and allowed producing developing larvae in vitro. IVF success under these conditions was 65% in A. palmata and 53% in F. scutaria on particular nights; however, on subsequent nights, the same process resulted in little or no IVF success. Thus, the window for optimal freezing of high quality spermatozoa was short (∼5 h for one night each spawning cycle). Additionally, cryopreserved F. scutaria embryonic cells had∼50% post-thaw viability as measured by intact membranes. Thus, despite some differences between species, coral spermatozoa and embryonic cells are viable after low temperature (−196°C) storage, preservation and thawing. Based on these results, we have begun systematically banking coral spermatozoa and embryonic cells on a large-scale as a support approach for preserving existing bio- and genetic diversity found in reef systems. |
format | Online Article Text |
id | pubmed-3297639 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2012 |
publisher | Public Library of Science |
record_format | MEDLINE/PubMed |
spelling | pubmed-32976392012-03-12 Preserving and Using Germplasm and Dissociated Embryonic Cells for Conserving Caribbean and Pacific Coral Hagedorn, Mary Carter, Virginia Martorana, Kelly Paresa, Malia K. Acker, Jason Baums, Iliana B. Borneman, Eric Brittsan, Michael Byers, Michael Henley, Michael Laterveer, Michael Leong, Jo-Ann McCarthy, Megan Meyers, Stuart Nelson, Brian D. Petersen, Dirk Tiersch, Terrence Uribe, Rafael Cuevas Woods, Erik Wildt, David PLoS One Research Article Coral reefs are experiencing unprecedented degradation due to human activities, and protecting specific reef habitats may not stop this decline, because the most serious threats are global (i.e., climate change), not local. However, ex situ preservation practices can provide safeguards for coral reef conservation. Specifically, modern advances in cryobiology and genome banking could secure existing species and genetic diversity until genotypes can be introduced into rehabilitated habitats. We assessed the feasibility of recovering viable sperm and embryonic cells post-thaw from two coral species, Acropora palmata and Fungia scutaria that have diffferent evolutionary histories, ecological niches and reproductive strategies. In vitro fertilization (IVF) of conspecific eggs using fresh (control) spermatozoa revealed high levels of fertilization (>90% in A. palmata; >84% in F. scutaria; P>0.05) that were unaffected by tested sperm concentrations. A solution of 10% dimethyl sulfoxide (DMSO) at cooling rates of 20 to 30°C/min most successfully cryopreserved both A. palmata and F. scutaria spermatozoa and allowed producing developing larvae in vitro. IVF success under these conditions was 65% in A. palmata and 53% in F. scutaria on particular nights; however, on subsequent nights, the same process resulted in little or no IVF success. Thus, the window for optimal freezing of high quality spermatozoa was short (∼5 h for one night each spawning cycle). Additionally, cryopreserved F. scutaria embryonic cells had∼50% post-thaw viability as measured by intact membranes. Thus, despite some differences between species, coral spermatozoa and embryonic cells are viable after low temperature (−196°C) storage, preservation and thawing. Based on these results, we have begun systematically banking coral spermatozoa and embryonic cells on a large-scale as a support approach for preserving existing bio- and genetic diversity found in reef systems. Public Library of Science 2012-03-08 /pmc/articles/PMC3297639/ /pubmed/22413020 http://dx.doi.org/10.1371/journal.pone.0033354 Text en This is an open-access article, free of all copyright, and may be freely reproduced, distributed, transmitted, modified, built upon, or otherwise used by anyone for any lawful purpose. The work is made available under the Creative Commons CC0 public domain dedication. https://creativecommons.org/publicdomain/zero/1.0/ This is an open-access article distributed under the terms of the Creative Commons Public Domain declaration, which stipulates that, once placed in the public domain, this work may be freely reproduced, distributed, transmitted, modified, built upon, or otherwise used by anyone for any lawful purpose. |
spellingShingle | Research Article Hagedorn, Mary Carter, Virginia Martorana, Kelly Paresa, Malia K. Acker, Jason Baums, Iliana B. Borneman, Eric Brittsan, Michael Byers, Michael Henley, Michael Laterveer, Michael Leong, Jo-Ann McCarthy, Megan Meyers, Stuart Nelson, Brian D. Petersen, Dirk Tiersch, Terrence Uribe, Rafael Cuevas Woods, Erik Wildt, David Preserving and Using Germplasm and Dissociated Embryonic Cells for Conserving Caribbean and Pacific Coral |
title | Preserving and Using Germplasm and Dissociated Embryonic Cells for Conserving Caribbean and Pacific Coral |
title_full | Preserving and Using Germplasm and Dissociated Embryonic Cells for Conserving Caribbean and Pacific Coral |
title_fullStr | Preserving and Using Germplasm and Dissociated Embryonic Cells for Conserving Caribbean and Pacific Coral |
title_full_unstemmed | Preserving and Using Germplasm and Dissociated Embryonic Cells for Conserving Caribbean and Pacific Coral |
title_short | Preserving and Using Germplasm and Dissociated Embryonic Cells for Conserving Caribbean and Pacific Coral |
title_sort | preserving and using germplasm and dissociated embryonic cells for conserving caribbean and pacific coral |
topic | Research Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3297639/ https://www.ncbi.nlm.nih.gov/pubmed/22413020 http://dx.doi.org/10.1371/journal.pone.0033354 |
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