Development of an amphibian sperm biobanking protocol for genetic management and population sustainability

Isabella J Burger; Shaina S Lampert; Carrie K Kouba; Dana J Morin; Andrew J Kouba

doi:10.1093/conphys/coac032

Development of an amphibian sperm biobanking protocol for genetic management and population sustainability

Conserv Physiol. 2022 May 23;10(1):coac032. doi: 10.1093/conphys/coac032. eCollection 2022.

Authors

Isabella J Burger¹, Shaina S Lampert², Carrie K Kouba², Dana J Morin¹, Andrew J Kouba¹

Affiliations

¹ Department of Wildlife, Fisheries and Aquaculture, Mississippi State University, Mississippi State, MS, 39762, USA.
² Department of Biochemistry, Molecular Biology, Entomology, and Plant Pathology, Mississippi State, MS, 39762, USA.

Abstract

Sperm cryopreservation is a vital tool in amphibian assisted reproductive technologies that aids in genetic and population management, specifically for at-risk species. Significant advancements have been made in the cryopreservation of amphibian sperm, yet there is little information on how the cryopreservation process influences fertilization and embryonic development. In this study, we tested several cryoprotective agents (CPAs) and freezing rates on sperm recovery, fertilization potential and embryo development using Fowler's toads (Anaxyrus fowleri) as a model amphibian species for application to at-risk anurans. Three cryoprotectant treatments were tested, which included 10% trehalose + 0.25% bovine serum albumin with (1) 5% N,N-dimethylformamide (DMFA); (2) 10% DMFA; or (3) 10% dimethyl sulfoxide (DMSO). Additionally, sperm in each cryoprotectant was frozen at two different rates, -32 to -45°C/min and -20 to -29°C/min. Post-thaw sperm analysis included motility, morphology, viability, fertilization success and embryo development. Results show that 10% DMFA produced significantly higher (P = 0.005) post-thaw sperm motility than 5% DMFA and was similar to 10% DMSO. Furthermore, sperm frozen at -32 to -45°C/min had significantly higher post-thaw motility (P < 0.001) compared to sperm frozen at -20 to -29°C/min. We also found that embryos fertilized with sperm frozen with 5% DMFA resulted in significantly higher (P = 0.02) cleavage than 10% DMSO, yet there was no other effect of CPA on fertilization or embryo development. Furthermore, embryos fertilized with sperm frozen at -32 to -45°C/min resulted in significantly higher cleavage (P = 0.001), neurulation (P = 0.001) and hatching (P = 0.002) numbers than sperm frozen at a rate of -20 to -29°C/min. Overall, eggs fertilized with frozen-thawed sperm produced 1327 tadpoles. These results provide insight towards a biobanking strategy that can be applied to imperilled species to preserve genetic lineages and bolster offspring genetic diversity for reintroduction.

Keywords: assisted reproductive technologies; cryoprotectant; freezing rate; genome banking; model species.