Cryopreservation of Platynereis dumerilii larvae.

Fuente: PubMed
Guardado en:
Detalles Bibliográficos
Autores principales: Paredes, Estefania, Berhane Getachew, Netsanet, Bezares-Calderón, Luis Alberto, Campos, Sara, Belokurov, Andrij, Tessmar-Raible, Kristin
Formato: Artículo científico
Lenguaje:en
Publicado: Cryobiology 2026
Materias:
Acceso en línea:
Etiquetas: Agregar Etiqueta
Sin Etiquetas, Sea el primero en etiquetar este registro!
_version_ 1868266125087735808
author Paredes, Estefania
Berhane Getachew, Netsanet
Bezares-Calderón, Luis Alberto
Campos, Sara
Belokurov, Andrij
Tessmar-Raible, Kristin
author_facet Paredes, Estefania
Berhane Getachew, Netsanet
Bezares-Calderón, Luis Alberto
Campos, Sara
Belokurov, Andrij
Tessmar-Raible, Kristin
Paredes, Estefania
Berhane Getachew, Netsanet
Bezares-Calderón, Luis Alberto
Campos, Sara
Belokurov, Andrij
Tessmar-Raible, Kristin
collection PubMed - marine biology
contents Cryopreservation of Platynereis dumerilii larvae. Paredes, Estefania Berhane Getachew, Netsanet Bezares-Calderón, Luis Alberto Campos, Sara Belokurov, Andrij Tessmar-Raible, Kristin Animals Cryopreservation Larva Cryoprotective Agents Polychaeta Dimethyl Sulfoxide Diatoms Sucrose The marine annelid Platynereis dumerilii is a functional molecular model organism for developmental, evolutionary and chronobiological studies. Research on Platynereis is rapidly growing, and with it, the number of genetic variants that laboratories isolate or generate and must subsequently maintain and propagate. Therefore, there is an urgent need to alleviate the burden of live culture maintenance by developing cryopreservation techniques for this species. We report the first cryopreservation protocol for P. dumerilii larvae, which combined with a careful post-thawing culturing regime, allowed us to obtain animals that survived to adulthood and successfully reproduced. Our experiments show highest survival rate in 6-8 dayold larvae (dpf). Equilibration with cryoprotecting agents takes 1h in 5 % (v/v) Me2SO + 0.1 %(v/w) sucrose, followed by transfer to 0.25 ml straws. The protocol cools larvae at 2.5 °C/min from 20 °C to -35 °C using a programmable freezer, followed by a rapid transfer to liquid N. Larvae are thawed in a water bath at 18 °C. The post-thaw larvae feeding regime consisted of 50 % Tetraselmis + 50 % diatom strains mixture (Grammatophora marina and Nitzschia laevis). The maximum survival obtained with this protocol so far produced 34 % survival after ∼5 months, the average is 8.69 ± 13.08 % (140 days) with a large variability inter-individual batches.
format Artículo científico
id pubmed_41265155
institution PubMed
language en
publishDate 2026
publisher Cryobiology
record_format pubmed
spellingShingle Cryopreservation of Platynereis dumerilii larvae.
Paredes, Estefania
Berhane Getachew, Netsanet
Bezares-Calderón, Luis Alberto
Campos, Sara
Belokurov, Andrij
Tessmar-Raible, Kristin
Animals
Cryopreservation
Larva
Cryoprotective Agents
Polychaeta
Dimethyl Sulfoxide
Diatoms
Sucrose
Cryopreservation of Platynereis dumerilii larvae. Paredes, Estefania Berhane Getachew, Netsanet Bezares-Calderón, Luis Alberto Campos, Sara Belokurov, Andrij Tessmar-Raible, Kristin Animals Cryopreservation Larva Cryoprotective Agents Polychaeta Dimethyl Sulfoxide Diatoms Sucrose The marine annelid Platynereis dumerilii is a functional molecular model organism for developmental, evolutionary and chronobiological studies. Research on Platynereis is rapidly growing, and with it, the number of genetic variants that laboratories isolate or generate and must subsequently maintain and propagate. Therefore, there is an urgent need to alleviate the burden of live culture maintenance by developing cryopreservation techniques for this species. We report the first cryopreservation protocol for P. dumerilii larvae, which combined with a careful post-thawing culturing regime, allowed us to obtain animals that survived to adulthood and successfully reproduced. Our experiments show highest survival rate in 6-8 dayold larvae (dpf). Equilibration with cryoprotecting agents takes 1h in 5 % (v/v) Me2SO + 0.1 %(v/w) sucrose, followed by transfer to 0.25 ml straws. The protocol cools larvae at 2.5 °C/min from 20 °C to -35 °C using a programmable freezer, followed by a rapid transfer to liquid N. Larvae are thawed in a water bath at 18 °C. The post-thaw larvae feeding regime consisted of 50 % Tetraselmis + 50 % diatom strains mixture (Grammatophora marina and Nitzschia laevis). The maximum survival obtained with this protocol so far produced 34 % survival after ∼5 months, the average is 8.69 ± 13.08 % (140 days) with a large variability inter-individual batches.
title Cryopreservation of Platynereis dumerilii larvae.
topic Animals
Cryopreservation
Larva
Cryoprotective Agents
Polychaeta
Dimethyl Sulfoxide
Diatoms
Sucrose
url https://pubmed.ncbi.nlm.nih.gov/41265155/