TY - JOUR
T1 - Preserving and using germplasm and dissociated embryonic cells for conserving caribbean and pacific coral
AU - Hagedorn, Mary
AU - Carter, Virginia
AU - Martorana, Kelly
AU - Paresa, Malia K.
AU - Acker, Jason
AU - Baums, Iliana B.
AU - Borneman, Eric
AU - Brittsan, Michael
AU - Byers, Michael
AU - Henley, Michael
AU - Laterveer, Michael
AU - Leong, Jo Ann
AU - McCarthy, Megan
AU - Meyers, Stuart
AU - Nelson, Brian D.
AU - Petersen, Dirk
AU - Tiersch, Terrence
AU - Uribe, Rafael Cuevas
AU - Woods, Erik
AU - Wildt, David
N1 - Funding Information:
Mike Brittsan is employed by Columbus Zoo and Aquarium as a Curator, Erik Woods and Michael Byers are scientists employed by General BioTechnology, Micheal Laterveer and Dirk Petersen are Senior Aquarists employed by the Rotterdam Zoo, Brian Nelson is a Senior Aquarist employed by the Fishes Department, New England Aquarium are commercial institutions, however the Mary Hagedorn and David Wildt are Senior Scientists, Michael Henley is an animal keeper employed by the Smithsonian National Zoological Park part of the Smithsonian Institution. The Smithsonian is a Trust Instrumentality which is part federal, part Trust and a 5013C. This work was funded through support from: National Oceanic and Atmospheric Administration (grant # NA07NMF4630109 to MH; grant # NA NA08NMF4630462 to IB); National Science Foundation (OCE – 0825979 to IB); Morris Animal Foundation (grant # D07ZO-053 to MH); Columbus Zoo and Aquarium Conservation Fund (to MH); Rotterdam Zoo, Green Foundation, Clyde and Connie Woodburn Foundation (to SECORE); Smithsonian Institution, Louisiana State University Agricultural Center, University of California Davis and Hawaii Institute of Marine Biology and the Canadian Natural Sciences and Engineering Research Council (NSERC). Nevertheless, this does not alter the authors' adherence to all the PLoS ONE policies on sharing data and materials.
PY - 2012/3/8
Y1 - 2012/3/8
N2 - 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.
AB - 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.
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U2 - 10.1371/journal.pone.0033354
DO - 10.1371/journal.pone.0033354
M3 - Article
C2 - 22413020
AN - SCOPUS:84857875260
SN - 1932-6203
VL - 7
JO - PloS one
JF - PloS one
IS - 3
M1 - e33354
ER -