Assessment of thawed sperm quality from feline species: Ocelot (Leopardus pardalis) and oncilla (Leopardus gutullus)

This study aimed to evaluate the cryopreservation effects on the semen of oncilla (Leopardus guttulus, n = 5, 15 ejaculates) and ocelot (Leopardus pardalis, n = 5, 17 ejaculates) and compare two extenders (commercial and non-commercial extender). An andrological exam was conducted (testicle measurem...

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Veröffentlicht in:Theriogenology 2022-01, Vol.177, p.56-62
Hauptverfasser: Tebet, Jussara Maria, Ferreira de Souza, Fabiana, Mello Martins, Maria Isabel, Chirinéa, Viviane Helena, Candido de Carvalho, Jaqueline, Papa, Frederico Ozanam, Lopes, Maria Denise
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container_issue
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container_title Theriogenology
container_volume 177
creator Tebet, Jussara Maria
Ferreira de Souza, Fabiana
Mello Martins, Maria Isabel
Chirinéa, Viviane Helena
Candido de Carvalho, Jaqueline
Papa, Frederico Ozanam
Lopes, Maria Denise
description This study aimed to evaluate the cryopreservation effects on the semen of oncilla (Leopardus guttulus, n = 5, 15 ejaculates) and ocelot (Leopardus pardalis, n = 5, 17 ejaculates) and compare two extenders (commercial and non-commercial extender). An andrological exam was conducted (testicle measurements and penis evaluation), including semen collection by electroejaculation. After collection, the semen was assessed to volume, color, pH, sperm motility, vigor, sperm number in the ejaculate, viability, membrane integrity, and sperm morphology. Samples were centrifuged (300 g for 10 min) and pellet diluted in two extenders (TRIS/glucose/egg yolk and BotuCRIO®), packed into 0.25 mL French straws (20 × 106 spermatozoa/mL), equilibrated at 5 °C for 1 h (
doi_str_mv 10.1016/j.theriogenology.2021.10.004
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An andrological exam was conducted (testicle measurements and penis evaluation), including semen collection by electroejaculation. After collection, the semen was assessed to volume, color, pH, sperm motility, vigor, sperm number in the ejaculate, viability, membrane integrity, and sperm morphology. Samples were centrifuged (300 g for 10 min) and pellet diluted in two extenders (TRIS/glucose/egg yolk and BotuCRIO®), packed into 0.25 mL French straws (20 × 106 spermatozoa/mL), equilibrated at 5 °C for 1 h (&lt;0.5 °C/min), freezing in nitrogen vapor for 20 min. Thawing was achieved at 46 °C for 15 min. Thawed samples were evaluated to the same characteristics and ultrastructural analysis. There is no difference for extenders, but in ocelot the spermatozoa maintained higher quality after thawing. Major defects were increased in thawed samples, especially acrosome injuries, in both species. Semen contamination by urine was remarkable to oncilla (53% of the ejaculates) which can have reduced sperm cryoresistance of this species. Ultrastructural analysis endorsed morphological analysis under light microscopy and identified cells with acrosome vesiculation. In conclusion, the spermatozoa of ocelot were more cryoresistent and the extender commercial and non-commercial were suitable for their cryopreservation. Other extenders should be investigated for oncilla. [Display omitted] •Spermatozoa of Leopardus pardalis were more cryoresistent and commercial and non-commercial extenders were suitable to freeze the semen.•Motility of the thawed spermatozoa decreased ∼50% in Leopardus gutullus and ∼20% in Leopardus pardalis.•Cryopreservation induced to ultrastructural changes related with acrosome vesiculation.</description><identifier>ISSN: 0093-691X</identifier><identifier>EISSN: 1879-3231</identifier><identifier>DOI: 10.1016/j.theriogenology.2021.10.004</identifier><language>eng</language><publisher>Elsevier Inc</publisher><subject>Acrosome-injury ; Cat ; Cryopreservation ; Cryoresistency ; Wild-animal</subject><ispartof>Theriogenology, 2022-01, Vol.177, p.56-62</ispartof><rights>2021</rights><lds50>peer_reviewed</lds50><oa>free_for_read</oa><woscitedreferencessubscribed>false</woscitedreferencessubscribed><cites>FETCH-LOGICAL-c358t-9f7eaf0455b192f5c7b8327a99bd2670e87ef02f264aa255e1feb85b7c92b54e3</cites><orcidid>0000-0001-8672-9705 ; 0000-0003-4721-1801</orcidid></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><linktohtml>$$Uhttps://dx.doi.org/10.1016/j.theriogenology.2021.10.004$$EHTML$$P50$$Gelsevier$$H</linktohtml><link.rule.ids>314,780,784,3550,27924,27925,45995</link.rule.ids></links><search><creatorcontrib>Tebet, Jussara Maria</creatorcontrib><creatorcontrib>Ferreira de Souza, Fabiana</creatorcontrib><creatorcontrib>Mello Martins, Maria Isabel</creatorcontrib><creatorcontrib>Chirinéa, Viviane Helena</creatorcontrib><creatorcontrib>Candido de Carvalho, Jaqueline</creatorcontrib><creatorcontrib>Papa, Frederico Ozanam</creatorcontrib><creatorcontrib>Lopes, Maria Denise</creatorcontrib><title>Assessment of thawed sperm quality from feline species: Ocelot (Leopardus pardalis) and oncilla (Leopardus gutullus)</title><title>Theriogenology</title><description>This study aimed to evaluate the cryopreservation effects on the semen of oncilla (Leopardus guttulus, n = 5, 15 ejaculates) and ocelot (Leopardus pardalis, n = 5, 17 ejaculates) and compare two extenders (commercial and non-commercial extender). An andrological exam was conducted (testicle measurements and penis evaluation), including semen collection by electroejaculation. After collection, the semen was assessed to volume, color, pH, sperm motility, vigor, sperm number in the ejaculate, viability, membrane integrity, and sperm morphology. Samples were centrifuged (300 g for 10 min) and pellet diluted in two extenders (TRIS/glucose/egg yolk and BotuCRIO®), packed into 0.25 mL French straws (20 × 106 spermatozoa/mL), equilibrated at 5 °C for 1 h (&lt;0.5 °C/min), freezing in nitrogen vapor for 20 min. Thawing was achieved at 46 °C for 15 min. Thawed samples were evaluated to the same characteristics and ultrastructural analysis. There is no difference for extenders, but in ocelot the spermatozoa maintained higher quality after thawing. Major defects were increased in thawed samples, especially acrosome injuries, in both species. Semen contamination by urine was remarkable to oncilla (53% of the ejaculates) which can have reduced sperm cryoresistance of this species. Ultrastructural analysis endorsed morphological analysis under light microscopy and identified cells with acrosome vesiculation. In conclusion, the spermatozoa of ocelot were more cryoresistent and the extender commercial and non-commercial were suitable for their cryopreservation. Other extenders should be investigated for oncilla. 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An andrological exam was conducted (testicle measurements and penis evaluation), including semen collection by electroejaculation. After collection, the semen was assessed to volume, color, pH, sperm motility, vigor, sperm number in the ejaculate, viability, membrane integrity, and sperm morphology. Samples were centrifuged (300 g for 10 min) and pellet diluted in two extenders (TRIS/glucose/egg yolk and BotuCRIO®), packed into 0.25 mL French straws (20 × 106 spermatozoa/mL), equilibrated at 5 °C for 1 h (&lt;0.5 °C/min), freezing in nitrogen vapor for 20 min. Thawing was achieved at 46 °C for 15 min. Thawed samples were evaluated to the same characteristics and ultrastructural analysis. There is no difference for extenders, but in ocelot the spermatozoa maintained higher quality after thawing. Major defects were increased in thawed samples, especially acrosome injuries, in both species. Semen contamination by urine was remarkable to oncilla (53% of the ejaculates) which can have reduced sperm cryoresistance of this species. Ultrastructural analysis endorsed morphological analysis under light microscopy and identified cells with acrosome vesiculation. In conclusion, the spermatozoa of ocelot were more cryoresistent and the extender commercial and non-commercial were suitable for their cryopreservation. Other extenders should be investigated for oncilla. [Display omitted] •Spermatozoa of Leopardus pardalis were more cryoresistent and commercial and non-commercial extenders were suitable to freeze the semen.•Motility of the thawed spermatozoa decreased ∼50% in Leopardus gutullus and ∼20% in Leopardus pardalis.•Cryopreservation induced to ultrastructural changes related with acrosome vesiculation.</abstract><pub>Elsevier Inc</pub><doi>10.1016/j.theriogenology.2021.10.004</doi><tpages>7</tpages><orcidid>https://orcid.org/0000-0001-8672-9705</orcidid><orcidid>https://orcid.org/0000-0003-4721-1801</orcidid><oa>free_for_read</oa></addata></record>
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subjects Acrosome-injury
Cat
Cryopreservation
Cryoresistency
Wild-animal
title Assessment of thawed sperm quality from feline species: Ocelot (Leopardus pardalis) and oncilla (Leopardus gutullus)
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