Animal Reproduction (AR)
https://www.animal-reproduction.org/article/doi/10.1590/1984-3143-AR2025-0140
Animal Reproduction (AR)
ORIGINAL ARTICLE

Sperm motility parameters as indicators of seminal quality: a comparative study between fish species

Lorena Pacheco da Silva; Stella Indira Rocha Lobato; Rodrigo Yutaka Dishoff Kasai; Letícia Giosa Paulino; Carmen Fila Zeca Manjate; Laís Pedroso Borges; Rosicleire Veríssimo-Silveira; Alexandre Ninhaus-Silveira

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Abstract

This study investigated the patterns of sperm kinetics in two fish species, Piaractus mesopotamicus and Pseudoplatystoma reticulatum and their relationship with seminal quality. Semen samples were collected after hormonal induction, with the aim of identifying indicators of seminal quality and their relationship with reproductive success. The results revealed marked interspecific differences: P. reticulatum exhibited longer-lasting motility (83 ± 31 s) with stable linear movement patterns after activation, while P. mesopotamicus showed more intense but shorter-lasting motility (41 ± 8 s), exhibiting initial circular trajectories that transitioned to linear patterns. In P. reticulatum, positive correlations were found between total motility (MOT), progressivity (PROG), velocities: curvilinear (VCL), straight-line (VSL) and average (VAP), with hatching rate (HR). These are suggested to be reliable predictors of seminal quality. For P. mesopotamicus, multivariate analysis (PCA) indicated that sperm quality was associated with a specific combination of VCL, VAP, and amplitude and lateral displacement of the head (ALH), although no single parameter was directly correlated with HR. These differences reflect distinct evolutionary adaptations to their lotic reproductive environment, associated with effective oocyte fertilization capacity and larval hatching rate. P. mesopotamicus is adapted for rapid fertilization, with higher sperm speed, while P. reticulatum demonstrates more sustained sperm motility. These results highlight the need for species-specific approaches and demonstrate that the simple evaluation of sperm kinetic parameters in fish does not allow seminal qualification, requiring detailed knowledge of sperm movement by species, essential information to optimize the nutritional and reproductive management of breeders, and seminal cryopreservation protocols.

Keywords

aquaculture, CASA, sperm kinetic, reproductive biotechnologies, fish

References

Baldisserotto B. Espécies nativas para piscicultura no Brasil. Santa Maria: UFSM; 2005. p. 303-325.

Balon EK. Reproductive guilds of fishes: a proposal and definition. J Fish Res Board Can. 1975;32(6):821-64. https://doi.org/10.1139/f75-110.

Bartlett MJ, Steeves TE, Gemmell NJ, Rosengrave PC. Sperm competition risk drives rapid ejaculate adjustments mediated by seminal fluid. eLife. 2017;6:e28811. https://doi.org/10.7554/eLife.28811. PMid:29084621.

Bashiyo-Silva C. Indução a espermiação e criopreservação espermática de Brycon cephalus (Gunther. 1869) (Teleostei: Characidae) [dissertation]. Ilha Solteira: Universidade Estadual Paulista; 2014. Portuguese.

Beirão J, Cabrita E, Pérez-Cerezales S, Martínez-Páramo S, Herráez MP. Effect of cryopreservation on fish sperm subpopulations. Cryobiology. 2011;62(1):22-31. https://doi.org/10.1016/j.cryobiol.2010.11.005. PMid:21112321.

Bobe J, Labbé C. Egg and sperm quality in fish. Gen Comp Endocrinol. 2010;165(3):535-48. https://doi.org/10.1016/j.ygcen.2009.02.011. PMid:19272390.

Browne RK, Kaurova SA, Uteshev VK, Shishova NV, McGinnity D, Figiel CR, Cosson J. Sperm motility of externally fertilizing fish and amphibians. Theriogenology. 2015;83(1):1-13. https://doi.org/10.1016/j.theriogenology.2014.09.018. PMid:25442393.

Cabrita E, Martínez-Páramo S, Gavaia PJ, Riesco MF, Valcarce DG, Sarasquete C, Robles V. Factors enhancing fish sperm quality and emerging tools for sperm analysis. Aquaculture. 2014;432:389-401. https://doi.org/10.1016/j.aquaculture.2014.04.034.

Cabrita E, Sarasquete C, Martínez-Páramo S, Robles V, Beirão J, Pérez-Cerezales S, Herráez MP. Cryopreservation of fish sperm: applications and perspectives. J Appl Ichthyology. 2010;26(5):623-35. https://doi.org/10.1111/j.1439-0426.2010.01556.x.

Cosson J, Groison AL, Fauvel C, Suquet M. Description of hake (Merlucius merlucius) spermatozoa: flagellar wave characteristics and motility parameters in various situations. J Appl Ichthyology. 2010;26(5):644-52. https://doi.org/10.1111/j.1439-0426.2010.01563.x.

Cosson J. Fish sperm physiology: structure. factors regulating motility. and motility evaluation. Biol Res Aquat Sci. 2019;11. https://doi.org/10.5772/intechopen.85139.

Costa BB, Rodrigues RB, Povh JA, Sanches EA, Santos Teixeira N, Souza França T, Spica LN, Machado TLF, Benato JL, Stawinski CV, Kasai RYD, Streit DP Jr. Descriptive analysis of the sperm of three South American catfish species maintained ex situ and the influence of morphology on sperm movement. Theriogenology Wild. 2024;4:100080. https://doi.org/10.1016/j.therwi.2024.100080.

Costa BB. Characterization of sperm quality in Brycon hilarii: how does morphology affect sperm movement? Theriogenology Wild. 2022;1:100007. https://doi.org/10.1016/j.therwi.2022.100007.

Crepaldi DV, Teixeira EA, Faria PM, Ribeiro LP, Melo DC, Oliveira DAA, Turra EM, Queiroz BM. Rendimento de carcaça em surubim (Pseudoplatystoma spp.) avaliado por ultra-som. Rev Bras Saude Prod Anim. 2008;9:813-24.

Dzyuba B, Bondarenko O, Fedorov P, Gazo I, Prokopchuk G, Cosson J. Energetics of fish spermatozoa: the proven and the possible. Aquaculture. 2017;472:60-72. https://doi.org/10.1016/j.aquaculture.2016.05.038.

Favero GC, Gimbo RY, Franco Montoya LN, Zanuzzo FS, Urbinati EC. Fasting and refeeding lead to more efficient growth in lean pacu (Piaractus mesopotamicus). Aquacult Res. 2018;49(1):359-66. https://doi.org/10.1111/are.13466.

Ferraz MAMM, Morató R, Yeste M, Arcarons N, Peña AI, Tamargo C, Hidalgo CO, Muiño R, Mogas T. Evaluation of sperm subpopulation structure in relation to in vitro sperm-oocyte interaction of frozen-thawed semen from Holstein bulls. Theriogenology. 2014;81(8):1067-72. https://doi.org/10.1016/j.theriogenology.2014.01.033. PMid:24581584.

Froese R, Pauly D. FishBase [Internet]. 2019 [cited 2026 May 15]. Available from: http://www.fishbase.org

Gallego V, Asturiano JF. Sperm motility in fish: technical applications and perspectives through CASA-Mot systems. Reprod Fertil Dev. 2018;30(6):820-32. https://doi.org/10.1071/RD17460. PMid:29518349.

Gallego V, Cavalcante SS, Fujimoto RY, Carneiro PCF, Azevedo HC, Maria AN. Fish sperm subpopulations: changes after cryopreservation process and relationship with fertilization success in tambaqui (Colossoma macropomum). Theriogenology. 2017;87:16-24. https://doi.org/10.1016/j.theriogenology.2016.08.001. PMid:27616215.

Gallo JM, Rodrigues RB, Fornari DC, Povh JA, Ribeiro RR, Zhang T, de Freitas TR, dos Santos Teixeira N, Streit DP Jr. Does semen quality of Colossoma macropomum change the productivity of larvae during the reproductive period? Aquaculture. 2022;558:738376. https://doi.org/10.1016/j.aquaculture.2022.738376.

Godinho AL, Lamas IR, Godinho HP. Reproductive ecology of Brazilian freshwater fishes. Environ Biol Fishes. 2010;87(2):143-62. https://doi.org/10.1007/s10641-009-9574-4.

Helfman GS, Collette BB, Facey DE, Bowen BW. The diversity of fishes: biology. evolution. and ecology. Hoboken: John Wiley & Sons; 2009.

Humphries P, King AJ, Koehn JD. Fish. flows and flood plains: links between freshwater fishes and their environment in the Murray-Darling River system. Australia. Environ Biol Fishes. 1999;56(1-2):129-51. https://doi.org/10.1023/A:1007536009916.

Kavamoto ET, Fogli da Silveira W. Características físicas, químicas e microscópicas do sêmen do bagre Rhamdia hilarii (Valenciennes 1840) em condições de campo. Bol Inst Pesca. 1986;13:95-100.

Kholodnyy V, Gadêlha H, Cosson J, Boryshpolets S. How do freshwater fish sperm find the egg? The physicochemical factors guiding the gamete encounters of externally fertilizing freshwater fish. Rev Aquacult. 2020;12(2):1165-92. https://doi.org/10.1111/raq.12378.

Kristan J, Zarski D, Blecha M, Policar T, Malinovskyi O, Samarin AM, Kucharczyk D. Fertilizing ability of gametes at different post-activation times and the sperm-oocyte ratio in the artificial reproduction of pikeperch Sander lucioperca. Aquacult Res. 2018;49(4):1383-8. https://doi.org/10.1111/are.13570.

Kucharczyk D, Nowosad J, Kucharczyk DJ, Kupren K, Targońska K, Wyszomirska E, Kujawa R. Out-of-season artificial reproduction of common dace (Leuciscus leuciscus L.) under controlled conditions. Anim Reprod Sci. 2019;202:21-5. https://doi.org/10.1016/j.anireprosci.2019.01.003. PMid:30638693.

Larson DL, Brenden TO, Baker EA, Scribner KT. Changes in lake sturgeon spawning periodicity is associated with prior reproductive effort. Sci Rep. 2025;15(1):3783. https://doi.org/10.1038/s41598-025-87717-x. PMid:39885297.

Levitan DR. Sperm limitation. gamete competition. and sexual selection in external fertilizers. In: Birkhead TR, Møller AP, editors. Sperm competition and sexual selection. San Diego: Academic Press; 1998. p. 173-215.

Liao WB, Huang Y, Zeng Y, Zhong MJ, Luo Y, Lüpold S. Ejaculate evolution in external fertilizers: influenced by sperm competition or sperm limitation? Evolution. 2018;72(1):4-17. https://doi.org/10.1111/evo.13372. PMid:28975611.

Lima RVA, Bernardino G, Val-Sella MV, Fava-De-Moraes F, Schemy RA, Borella MI. Tecido germinativo ovariano e ciclo reprodutivo de pacus (Piaractus mesopotamicus Holmberg. 1887) mantidos em cativeiro. Bol Tec Cepta. 1991;4:1-46.

Lytle DA, Poff NL. Adaptation to natural flow regimes. Trends Ecol Evol. 2004;19(2):94-100. https://doi.org/10.1016/j.tree.2003.10.002. PMid:16701235.

Maria AN, Murgas LDS, Silva MOB, Miliorini AB, Franciscatto RT, Logato PVR. Influência da adição de iodeto de potássio e citrato de sódio na qualidade do sêmen de pacu (Piaractus mesopotamicus-Holmberg. 1887). Cienc Agrotec. 2004;28(1):191-4. https://doi.org/10.1590/S1413-70542004000100025.

Marinović Z, Marinović Z, Šćekić I, Lujić J, Urbányi B, Horváth Á. The effects of cryopreservation and cold storage on sperm subpopulation structure of common carp (Cyprinus carpio L.). Cryobiology. 2021;99:88-94. https://doi.org/10.1016/j.cryobiol.2021.01.007. PMid:33450240.

Merino O, Figueroa E, Valdebenito I, Risopatrón J, Merino M, Farías JG. Change in the swimming pattern of Salmo salar spermatozoa caused by the high temperature of the sperm motility activation medium. Theriogenology. 2024;219:49-58. https://doi.org/10.1016/j.theriogenology.2024.02.008. PMid:38387124.

Miliorini AB, Murgas LDS, Viveiros ATM, Franciscatto RT, Silva MOB, Maria AN. Resfriamento do sêmen de pacu (Piaractus mesopotamicus) à 4 ºC. utilizando diferentes concentrações de dimetilsulfóxido. Rev Bras Reprod Anim. 2002;26(3):209-11. https://doi.org/10.1590/1519-6984.182391.

Muiño R, Tamargo C, Hidalgo CO, Peña AI. Identification of sperm subpopulations with defined motility characteristics in ejaculates from Holstein bulls: effects of cryopreservation and between-bull variation. Anim Reprod Sci. 2008;109(1-4):27-39. https://doi.org/10.1016/j.anireprosci.2007.10.007. PMid:18036750.

Ninhaus-Silveira A, Foresti F, Veríssimo-Silveira R, Senhorini JA. Seminal analysis. cryogenic preservation. and fertility in matrinxã fish. Brycon cephalus (Günther. 1869). Braz Arch Biol Technol. 2006;49(4):651-9. https://doi.org/10.1590/S1516-89132006000500015.

Nowosad J, Sikora M, Kucharczyk D. Survival rates and the occurrence of larval malformations. including Siamese twins. following fertilization of post-ovulatory aged oocytes in ide Leuciscus idus. Dis Aquat Organ. 2018;127(3):237-42. https://doi.org/10.3354/dao03208. PMid:29516863.

Parker GA, Immler S, Pitnick S, Birkhead TR. Sperm competition games: sperm size (mass) and number under raffle and displacement. and the evolution of P2. J Theor Biol. 2010;264(3):1003-23. https://doi.org/10.1016/j.jtbi.2010.03.003. PMid:20206187.

Parker GA, Pizzari T. Sperm competition and ejaculate economics. Biol Rev Camb Philos Soc. 2010;85(4):897-934. https://doi.org/10.1111/j.1469-185X.2010.00140.x. PMid:20560928.

Petrere M Jr. River fisheries in Brazil: a review. Regul Rivers. 1989;4(1):1-16. https://doi.org/10.1002/rrr.3450040102.

R Development Core Team. R: the R project for statistical computing [Internet]. Vienna: R Foundation for Statistical Computing; 2022 [cited 2026 May 15]. Available from: https://www.r-project.org/

Reid SL. La biología de los bagres rayados Pseudoplatystoma fasciatum y P. tigrinum en la cuenca del río Apure. Venezuela. Rev Unellez Cienc Tecnol. 1983;1:13-41.

Resende EK, Catella AC, Nascimento FL, Palmeira SS, Almeida VLL. Biologia do curimbatá (Prochilodus lineatus) pintado (Pseudoplatystoma corruscans) e cachara (Pseudoplatystoma fasciatum) na bacia hidrográfica do rio Miranda, Pantanal do Mato Grosso do Sul. Brasil. Corumbá: Embrapa; 1995.

Romagosa E, Paiva P, Andrade-Talmelli E, Godinho H. Biologia reprodutiva de fêmeas de cachara. Pseudoplatystoma fasciatum (Teleostei. Siluriformes. Pimelodidae). mantidas em cativeiro. Bol Inst Pesca. 2004;29:151-9.

Rosengrave PC, Lymbery RA, Evans JP. Patterns of sperm swimming behaviour depend on male mating tactic and spawning environment in chinook salmon. Sci Rep. 2024;14(1):25680. https://doi.org/10.1038/s41598-024-76115-4. PMid:39465254.

Routray P, Verma DK, Sarkar SK, Sarangi N. Recent advances in carp seed production and milt cryopreservation. Fish Physiol Biochem. 2007;33(4):413-27. https://doi.org/10.1007/s10695-007-9159-0.

Rudolfsen G, Figenschou L, Folstad I, Tveiten H, Figenschou M. Rapid adjustments of sperm characteristics in relation to social status. Proc Biol Sci. 2006;273(1584):325-32. https://doi.org/10.1098/rspb.2005.3305. PMid:16543175.

Rurangwa E, Kime DE, Ollevier F, Nash JP. The measurement of sperm motility and factors affecting sperm quality in cultured fish. Aquaculture. 2004;234(1-4):1-28. https://doi.org/10.1016/j.aquaculture.2003.12.006.

Rurangwa E, Roelants I, Huyskens G, Ebrahimi M, Kime DE, Ollevier F. The minimum effective spermatozoa:egg ratio for artificial insemination and the effects of mercury on sperm motility and fertilization ability in Clarias gariepinus. J Fish Biol. 1998;53(2):402-13. https://doi.org/10.1006/jfbi.1998.0711.

Sanchez MP. Sperm quality and cryopreservation in teleost: effect of seminal plasma component and climate change [thesis]. Botucatu: Universidade Estadual Paulista "Júlio de Mesquita Filho"; 2023.

Snook RR. Sperm in competition: not playing by the numbers. Trends Ecol Evol. 2005;20(1):46-53. https://doi.org/10.1016/j.tree.2004.10.011. PMid:16701340.

Suquet M, Billard R, Cosson J, Normant Y, Fauvel C. Artificial insemination in turbot (Scophthalmus maximus): determination of the optimal sperm to egg ratio and time of gamete contact. Aquaculture. 1995;133(1):83-90. https://doi.org/10.1016/0044-8486(94)00395-5.

Urbinati EC, Gonçalves FD. Pacu (Piaractus mesopotamicus). In: Baldisserotto B, Gomes LC, editors. Espécies nativas para piscicultura no Brasil. 2nd ed. Santa Maria: Editora UFSM; 2005. p. 101-15.

Vazzoler AEAM. Biologia da reprodução de peixes teleósteos: teoria e prática. Maringá: EDUEM; 1996. p. 169.

Viveiros ATM, Nascimento AF, Orfão LH, Isaú ZA. Motility and fertility of the subtropical freshwater fish streaked prochilod (Prochilodus lineatus) sperm cryopreserved in powdered coconut water. Theriogenology. 2010;74(4):551-6. https://doi.org/10.1016/j.theriogenology.2010.03.018. PMid:20494428.

Zajitschek S. Hotzy C. Zajitschek F. Immler S. Short-term variation in sperm competition causes sperm-mediated epigenetic effects on early offspring performance in the zebrafish. Proc R Soc B Biol Sci. 2014;281(1785):20140422. https://doi.org/10.1098/rspb.2014.0422.
 


Submitted date:
09/29/2025

Reviewed date:
07/27/2026

Accepted date:
05/29/2026

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