Sperm cryopreservation affects postthaw motility, but not embryogenesis or larval growth in the Brazilian fish Brycon insignis (Characiformes)

• Published in: Theriogenology Vol. 78; no. 4; pp. 803 - 810
• Main Authors: Viveiros, A.T.M, Isaú, Z.A, Caneppele, D, Leal, M.C
• Format: Journal Article
• Language: English
• Published: United States Elsevier Inc 01.09.2012
• Subjects: animal growth; Animals; Aquaculture; body weight; Brazil; CASA; Characiformes; Characiformes - embryology; Characiformes - growth & development; Characiformes - physiology; cryopreservation; Cryopreservation - veterinary; Embryo, Nonmammalian; embryogenesis; Embryonic Development - physiology; endangered species; Female; fish; Freezing; hatching; Larva - growth & development; larvae; larval development; Male; nitrogen; progeny; Semen; Semen Analysis; Semen Preservation - adverse effects; sperm motility; Sperm Motility - physiology; Sperm quality; spermatozoa; Spermatozoa - cytology; Spermatozoa - physiology; Teleost; thawing; vapors; Brazil; Teleost; Sperm quality; CASA; Semen; Freezing
• ISSN: 0093-691X; 1879-3231
• DOI: 10.1016/j.theriogenology.2012.03.028

Sperm cryopreservation is an important method for preserving genetic information and facilitating artificial reproduction. The objective was to investigate whether the cryopreservation process affects postthaw sperm motility, embryogenesis, and larval growth in the fish Brycon insignis. Sperm was diluted in methyl glycol and Beltsville Thawing solution, frozen in a nitrogen vapor vessel (dry shipper) and stored in liquid nitrogen. Half of the samples were evaluated both subjectively (% of motile sperm and motility quality score—arbitrary grading system from 0 [no movement] to 5 [rapidly swimming sperm]) and in a computer-assisted sperm analyzer (CASA; percentage of motile sperm and velocity). The other half was used for fertilization and the evaluation of embryogenesis (cleavage and gastrula stages), hatching rate, percentage of larvae with normal development and larval growth up to 112 days posthatching (dph). Fresh sperm was analyzed subjectively (percentage of motile sperm and motility quality score) and used as the control. In the subjective analysis, sperm motility significantly decreased from 100% motile sperm and quality score of 5 in fresh sperm to 54% motile sperm and quality score of 3 after thawing. Under computer-assisted sperm analyzer evaluation, postthaw sperm had 67% motile sperm, 122 μm/sec of curvilinear velocity, 87 μm/sec of straight-line velocity and 103 μm/sec of average path velocity. There were no significant differences between progenies (pooled data) for the percentage of viable embryos in cleavage (62%) or gastrula stages (24%) or in the hatching rate (24%), percentage of normal hatched larvae (93%), larval body weight (39.8 g), or standard length (12.7 cm) at 112 days posthatching. Based on these findings, cryopreserved sperm can be used as a tool to restore the population of endangered species, such as B. insignis, as well as for aquaculture purposes, without any concern regarding quality of the offspring.