New observations about the fertilisation capacity and latency time of sperm inseminated into the ovary of African catfish (Clarias gariepinus), an oviparous modelfish

In our former study, we proved that sperm injected into the ovary by catheter through the oviduct 10-12 h before hormonally induced ovulation, retains its fertilizing capacity for several hours. Using this method, we produced viable larvae via in vitro fertilisation. The aim of this study was to inv...

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Published in:Aquaculture Vol. 522; p. 735109
Main Authors: Müller, Tamás, Ács, Éva, Beliczky, Gábor, Makk, Judit, Földi, Angéla, Kucska, Balázs, Horváth, László, Ittzés, Áron, Hegyi, Árpád, Szabó, Tamás, Urbányi, Béla, Quyen, Nguyen Ngoc, Orbán, László, Havasi, Máté
Format: Journal Article
Language:English
Published: Elsevier B.V 30-05-2020
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Abstract In our former study, we proved that sperm injected into the ovary by catheter through the oviduct 10-12 h before hormonally induced ovulation, retains its fertilizing capacity for several hours. Using this method, we produced viable larvae via in vitro fertilisation. The aim of this study was to investigate the time-dependent fertilizing capacity of sperm which were introduced into ovary. Sperm samples (2 mL sperm / bodyweight kg) were incubated in gonad lobes 5, 10, 15, 20, 25, 36 and 48 h before the gamete stripping. Ovulation was induced by extracted carp pituitary (CPE) hormonal administration (5 mg CPE / BW kg). There were no statistical differences (p < 0.05) among the hatching rates in the 5-25 h treatment groups, but we observed large individual fluctuations in fertilisation and hatching rate within the groups. However, at 48 h the treated group showed low fertilisation and hatching rate indicating loss of fertilizing capacity. In our second experiment cycle, three different inseminated sperm dosages were tested on fertilisation from the same pooled sperm batch; 2 mL, 1 mL and 0.5 mL sperm volume / BW kg. The 0.5 mL sperm dosage showed statistically (p < 0.05) higher fertilisation and hatching rate indicating that small milt volume was enough to apply for propagation. According to scanning electron microscopic analysis, this is the first observation that there is a chance for ‘internal gametic association’ reproduction strategy in fish species, where there is no direct contact between the two sexes in the spawning. •Sperm was successful incubated in gonad 5, 10, 15, 20, 25, 36, 48 h before gamete stripping.•There were no differences of injected sperm volumes (0.5-2 mL) in fertilisation rate.•First evidence for internal gametic association in real ovulipar fish using sperm injection.
AbstractList In our former study, we proved that sperm injected into the ovary by catheter through the oviduct 10-12 h before hormonally induced ovulation, retains its fertilizing capacity for several hours. Using this method, we produced viable larvae via in vitro fertilisation. The aim of this study was to investigate the time-dependent fertilizing capacity of sperm which were introduced into ovary. Sperm samples (2 mL sperm / bodyweight kg) were incubated in gonad lobes 5, 10, 15, 20, 25, 36 and 48 h before the gamete stripping. Ovulation was induced by extracted carp pituitary (CPE) hormonal administration (5 mg CPE / BW kg). There were no statistical differences (p < 0.05) among the hatching rates in the 5-25 h treatment groups, but we observed large individual fluctuations in fertilisation and hatching rate within the groups. However, at 48 h the treated group showed low fertilisation and hatching rate indicating loss of fertilizing capacity. In our second experiment cycle, three different inseminated sperm dosages were tested on fertilisation from the same pooled sperm batch; 2 mL, 1 mL and 0.5 mL sperm volume / BW kg. The 0.5 mL sperm dosage showed statistically (p < 0.05) higher fertilisation and hatching rate indicating that small milt volume was enough to apply for propagation. According to scanning electron microscopic analysis, this is the first observation that there is a chance for ‘internal gametic association’ reproduction strategy in fish species, where there is no direct contact between the two sexes in the spawning. •Sperm was successful incubated in gonad 5, 10, 15, 20, 25, 36, 48 h before gamete stripping.•There were no differences of injected sperm volumes (0.5-2 mL) in fertilisation rate.•First evidence for internal gametic association in real ovulipar fish using sperm injection.
ArticleNumber 735109
Author Kucska, Balázs
Urbányi, Béla
Ittzés, Áron
Quyen, Nguyen Ngoc
Hegyi, Árpád
Szabó, Tamás
Ács, Éva
Orbán, László
Havasi, Máté
Makk, Judit
Horváth, László
Földi, Angéla
Müller, Tamás
Beliczky, Gábor
Author_xml – sequence: 1
  givenname: Tamás
  surname: Müller
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  email: Muller.Tamas@mkk.szie.hu
  organization: Department of Aquaculture, Faculty of Agricultural and Environmental Sciences, Szent István University, 2100 Gödöllő, Hungary
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  givenname: Éva
  surname: Ács
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  organization: National University of Public Service, Faculty of Water Sciences, 6500 Baja, Bajcsy-Zsilinszky utca 12-14., Hungary
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  givenname: Gábor
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  surname: Kucska
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  organization: Department of Aquaculture, Faculty of Agricultural and Environmental Sciences, Kaposvár University, 7400 Kaposvár, Hungary
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  givenname: László
  surname: Horváth
  fullname: Horváth, László
  organization: Department of Aquaculture, Faculty of Agricultural and Environmental Sciences, Szent István University, 2100 Gödöllő, Hungary
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  givenname: Áron
  surname: Ittzés
  fullname: Ittzés, Áron
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  givenname: Árpád
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  fullname: Hegyi, Árpád
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  givenname: Tamás
  surname: Szabó
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  organization: Department of Aquaculture, Faculty of Agricultural and Environmental Sciences, Szent István University, 2100 Gödöllő, Hungary
– sequence: 11
  givenname: Béla
  surname: Urbányi
  fullname: Urbányi, Béla
  organization: Department of Aquaculture, Faculty of Agricultural and Environmental Sciences, Szent István University, 2100 Gödöllő, Hungary
– sequence: 12
  givenname: Nguyen Ngoc
  surname: Quyen
  fullname: Quyen, Nguyen Ngoc
  organization: Department of Aquaculture, Faculty of Agricultural and Environmental Sciences, Szent István University, 2100 Gödöllő, Hungary
– sequence: 13
  givenname: László
  surname: Orbán
  fullname: Orbán, László
  organization: Frontline Fish Genomics Research Group, Department of Animal Sciences, Georgikon Faculty, University of Pannonia, 8360 Keszthely, Hungary
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  givenname: Máté
  surname: Havasi
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  organization: Department of Animal Sciences, Georgikon Faculty, University of Pannonia, 8360 Keszthely, Hungary
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Keywords Artificial reproduction
Sperm insemination
Sperm injection
In vitro fertilisation
Language English
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Snippet In our former study, we proved that sperm injected into the ovary by catheter through the oviduct 10-12 h before hormonally induced ovulation, retains its...
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SubjectTerms Artificial reproduction
In vitro fertilisation
Sperm injection
Sperm insemination
Title New observations about the fertilisation capacity and latency time of sperm inseminated into the ovary of African catfish (Clarias gariepinus), an oviparous modelfish
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