Cryopreservation of Limnoperna fortunei (golden mussel) sperm with polyethylene glycol

Bio Bureau Biotecnologia Ltda, Rio de Janeiro, Rio de Janeiro, Brasil
Laboratório de Biologia Molecular Ambiental, Instituto de Biofísica Carlos Chagas Filho, Universidade Federal do Rio de Janeiro, Rio de Janeiro, Rio de Janeiro, Brazil
DOI
10.7287/peerj.preprints.27165v2
Subject Areas
Aquaculture, Fisheries and Fish Science, Cell Biology
Keywords
sperm, cryopreservation, Limnoperna fortunei, liquid nitrogen, polyethylene glycol, thawing
Copyright
© 2018 Markovic et al.
Licence
This is an open access article distributed under the terms of the Creative Commons Attribution License, which permits unrestricted use, distribution, reproduction and adaptation in any medium and for any purpose provided that it is properly attributed. For attribution, the original author(s), title, publication source (PeerJ Preprints) and either DOI or URL of the article must be cited.
Cite this article
Markovic M, Alves Americo J, Wajsenzon IJR, Rodrigues da Cunha Y, Vieira Santos de Souza T, de Freitas Rebelo M. 2018. Cryopreservation of Limnoperna fortunei (golden mussel) sperm with polyethylene glycol. PeerJ Preprints 6:e27165v2

Abstract

Background. Insufficient quantities of freshly harvested Limnoperna fortunei gametes and embryos constrain reproduction research in the laboratory. Cryopreservation would allow the accumulation and storage of gametes when they are available. The lack of available cryopreservation protocol for Limnoperna fortunei in the literature led our research group to undertake a study to establish which cryoprotective agents can be might be most useful for cryopreservation of this species’ sperm. Methods. 2%, 5%, and 10% concentration of ethylene glycol, dimethyl sulfoxide, glycerol, and polyethylene glycol 4000 as well as 0.2 M glucose, sucrose, and trehalose (mixed into the 10% concentration of the aforementioned agents) were tested in a 1:1 ratio with sperm, in 0.25 ml straws, frozen in liquid nitrogen. Results. After 48 hours the best survival rate was in the samples with 10% polyethylene glycol 4000, 36.1%, which also resulted in viable sperm after 7 and 15 days.

Author Comment

This is a preprint submission to PeerJ Preprints. The changes which are made between this and previous version of the preprint: the text is organised in two columns and the tables are inserted inside the text. The hyperlink with DOI was added inside the abstract box.

Supplemental Information

Sperm viability with different cryoprotective agents at 0 and 48 hours, and with PEG after 48 hours, 7 and 15 days

DOI: 10.7287/peerj.preprints.27165v2/supp-1