Successful cryopreservation of coral larvae using vitrification and laser warming

Abstract Climate change has increased the incidence of coral bleaching events, resulting in the loss of ecosystem function and biodiversity on reefs around the world. As reef degradation accelerates, the need for innovative restoration tools has become acute. Despite past successes with ultra-low te...

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Autores principales: Jonathan Daly, Nikolas Zuchowicz, C. Isabel Nuñez Lendo, Kanav Khosla, Claire Lager, E. Michael Henley, John Bischof, F. W. Kleinhans, Chiahsin Lin, Esther C. Peters, Mary Hagedorn
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Publicado: Nature Portfolio 2018
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spelling oai:doaj.org-article:0aab132537b34cdbb0e824faf8b2078c2021-12-02T15:08:57ZSuccessful cryopreservation of coral larvae using vitrification and laser warming10.1038/s41598-018-34035-02045-2322https://doaj.org/article/0aab132537b34cdbb0e824faf8b2078c2018-10-01T00:00:00Zhttps://doi.org/10.1038/s41598-018-34035-0https://doaj.org/toc/2045-2322Abstract Climate change has increased the incidence of coral bleaching events, resulting in the loss of ecosystem function and biodiversity on reefs around the world. As reef degradation accelerates, the need for innovative restoration tools has become acute. Despite past successes with ultra-low temperature storage of coral sperm to conserve genetic diversity, cryopreservation of larvae has remained elusive due to their large volume, membrane complexity, and sensitivity to chilling injury. Here we show for the first time that coral larvae can survive cryopreservation and resume swimming after warming. Vitrification in a 3.5 M cryoprotectant solution (10% v/v propylene glycol, 5% v/v dimethyl sulfoxide, and 1 M trehalose in phosphate buffered saline) followed by warming at a rate of approximately 4,500,000 °C/min with an infrared laser resulted in up to 43% survival of Fungia scutaria larvae on day 2 post-fertilization. Surviving larvae swam and continued to develop for at least 12 hours after laser-warming. This technology will enable biobanking of coral larvae to secure biodiversity, and, if managed in a high-throughput manner where millions of larvae in a species are frozen at one time, could become an invaluable research and conservation tool to help restore and diversify wild reef habitats.Jonathan DalyNikolas ZuchowiczC. Isabel Nuñez LendoKanav KhoslaClaire LagerE. Michael HenleyJohn BischofF. W. KleinhansChiahsin LinEsther C. PetersMary HagedornNature PortfolioarticleCoral LarvaeLaser Heating ExperimentsCryoprotectant SolutionFungia ScutariaLarval VolumeMedicineRScienceQENScientific Reports, Vol 8, Iss 1, Pp 1-10 (2018)
institution DOAJ
collection DOAJ
language EN
topic Coral Larvae
Laser Heating Experiments
Cryoprotectant Solution
Fungia Scutaria
Larval Volume
Medicine
R
Science
Q
spellingShingle Coral Larvae
Laser Heating Experiments
Cryoprotectant Solution
Fungia Scutaria
Larval Volume
Medicine
R
Science
Q
Jonathan Daly
Nikolas Zuchowicz
C. Isabel Nuñez Lendo
Kanav Khosla
Claire Lager
E. Michael Henley
John Bischof
F. W. Kleinhans
Chiahsin Lin
Esther C. Peters
Mary Hagedorn
Successful cryopreservation of coral larvae using vitrification and laser warming
description Abstract Climate change has increased the incidence of coral bleaching events, resulting in the loss of ecosystem function and biodiversity on reefs around the world. As reef degradation accelerates, the need for innovative restoration tools has become acute. Despite past successes with ultra-low temperature storage of coral sperm to conserve genetic diversity, cryopreservation of larvae has remained elusive due to their large volume, membrane complexity, and sensitivity to chilling injury. Here we show for the first time that coral larvae can survive cryopreservation and resume swimming after warming. Vitrification in a 3.5 M cryoprotectant solution (10% v/v propylene glycol, 5% v/v dimethyl sulfoxide, and 1 M trehalose in phosphate buffered saline) followed by warming at a rate of approximately 4,500,000 °C/min with an infrared laser resulted in up to 43% survival of Fungia scutaria larvae on day 2 post-fertilization. Surviving larvae swam and continued to develop for at least 12 hours after laser-warming. This technology will enable biobanking of coral larvae to secure biodiversity, and, if managed in a high-throughput manner where millions of larvae in a species are frozen at one time, could become an invaluable research and conservation tool to help restore and diversify wild reef habitats.
format article
author Jonathan Daly
Nikolas Zuchowicz
C. Isabel Nuñez Lendo
Kanav Khosla
Claire Lager
E. Michael Henley
John Bischof
F. W. Kleinhans
Chiahsin Lin
Esther C. Peters
Mary Hagedorn
author_facet Jonathan Daly
Nikolas Zuchowicz
C. Isabel Nuñez Lendo
Kanav Khosla
Claire Lager
E. Michael Henley
John Bischof
F. W. Kleinhans
Chiahsin Lin
Esther C. Peters
Mary Hagedorn
author_sort Jonathan Daly
title Successful cryopreservation of coral larvae using vitrification and laser warming
title_short Successful cryopreservation of coral larvae using vitrification and laser warming
title_full Successful cryopreservation of coral larvae using vitrification and laser warming
title_fullStr Successful cryopreservation of coral larvae using vitrification and laser warming
title_full_unstemmed Successful cryopreservation of coral larvae using vitrification and laser warming
title_sort successful cryopreservation of coral larvae using vitrification and laser warming
publisher Nature Portfolio
publishDate 2018
url https://doaj.org/article/0aab132537b34cdbb0e824faf8b2078c
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