Literature DB >> 22541324

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

A T M Viveiros1, Z A Isaú, D Caneppele, M C Leal.   

Abstract

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.
Copyright © 2012 Elsevier Inc. All rights reserved.

Entities:  

Mesh:

Year:  2012        PMID: 22541324     DOI: 10.1016/j.theriogenology.2012.03.028

Source DB:  PubMed          Journal:  Theriogenology        ISSN: 0093-691X            Impact factor:   2.740


  4 in total

1.  Sperm cryopreservation reduces offspring growth.

Authors:  David Nusbaumer; Lucas Marques da Cunha; Claus Wedekind
Journal:  Proc Biol Sci       Date:  2019-09-25       Impact factor: 5.349

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

Authors:  Isabella J Burger; Shaina S Lampert; Carrie K Kouba; Dana J Morin; Andrew J Kouba
Journal:  Conserv Physiol       Date:  2022-05-23       Impact factor: 3.252

3.  A novel approach to identifying physical markers of cryo-damage in bull spermatozoa.

Authors:  Sung-Jae Yoon; Woo-Sung Kwon; Md Saidur Rahman; June-Sub Lee; Myung-Geol Pang
Journal:  PLoS One       Date:  2015-05-04       Impact factor: 3.240

4.  Cryobanking of aquatic species.

Authors:  Sonia Martínez-Páramo; Ákos Horváth; Catherine Labbé; Tiantian Zhang; Vanesa Robles; Paz Herráez; Marc Suquet; Serean Adams; Ana Viveiros; Terrence R Tiersch; Elsa Cabrita
Journal:  Aquaculture       Date:  2016-06-01       Impact factor: 4.242

  4 in total

北京卡尤迪生物科技股份有限公司 © 2022-2023.