Literature DB >> 17644982

Challenges in cryopreserving endangered mammal spermatozoa: morphology and the value of acrosomal integrity as markers of cryo-survival.

Budhan Pukazhenthi1, Rachel Santymire, Adrienne Crosier, JoGayle Howard, David E Wildt.   

Abstract

The science of cryobiology is essential to the effective, practical use of semen for assisted breeding to help manage small populations of rare wildlife species. In this review, we describe challenges associated with cryopreserving gametes from wild fauna. Based on more than 25 years of experience across a diversity of mammals, it appears that the primary driving force dictating cryo-survival of a spermatozoon is its initial pre-freeze quality and morphology, especially having a morphologically normal, intact acrosome. This assertion is supported through extensive studies of three animal groups that routinely ejaculate semen containing (1) normal sperm/acrosomal quality (examples, Eld's deer, Cervus eldi and giant panda, Ailuropoda melanoleuca), (2) normal acrosomal quality, but from teratospermic donors (>70% pleiomorphic sperm; cheetah, Acinonyx jubatus and black-footed ferret, Mustela nigripes) and (3) abnormal acrosomal quality and general teratospermia (clouded leopard, Neofelis nebulosa). Data revealed that species producing high quality sperm with > 70% normal, intact acrosomes were best able to survive cryopreservation (-80% intact acrosomes post-thaw). Species that were teratospermic, but with high proportions of intact acrosomes (72 to 88%) in ejaculates varied significantly (4 to 55% intact acrosomes post-thaw) in sperm survival to freeze-thawing. Spermatozoa from the clouded leopard (that was both teratospermic while producing only 11% normal acrosomes in fresh semen) failed to survive cryopreservation despite using an array of conventional and unconventional freezing approaches. These observations (combined with zona penetration assays and artificial insemination results) suggest that proportions of malformed sperm and especially initial structural integrity of the acrosome are more important predictors of sperm survivability post-thaw than initial sperm motility scores.

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Year:  2007        PMID: 17644982

Source DB:  PubMed          Journal:  Soc Reprod Fertil Suppl        ISSN: 1747-3403


  2 in total

1.  Slow freezing, but not vitrification supports complete spermatogenesis in cryopreserved, neonatal sheep testicular xenografts.

Authors:  Budhan S Pukazhenthi; Jennifer Nagashima; Alexander J Travis; Guilherme M Costa; Enrique N Escobar; Luiz R França; David E Wildt
Journal:  PLoS One       Date:  2015-04-29       Impact factor: 3.240

2.  Cryopreservation of ferret (Mustela putorius furo) sperm collected by rectal massage and electroejaculation: Comparison of a decelerating and an accelerating freezing rate protocol.

Authors:  Adolfo Toledano-Díaz; Cristina Castaño; Rosario Velázquez; Paula Bóveda; Antonio López-Sebastián; Eva Martínez-Nevado; Silvia Villaverde-Morcillo; Milagros C Esteso; Julián Santiago-Moreno
Journal:  Vet Med Sci       Date:  2020-10-11
  2 in total

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