Roles of Ionic and Non-Ionic Osmolarities and Different pH Levels on Triggering Sperm Motility in Nile Tilapia (Oreochromis niloticus)
DOI:
https://doi.org/10.24925/turjaf.v13i8.2103-2110.7693Keywords:
Tilapia, Spermatozoa, Motility, Osmolality, pH, VelocityAbstract
Since advantageous properties such as fast growth rate, tolerance to severe water conditions, flesh quality, variations in feeding and high reproductive performances in different habitats, Nile tilapia (Oreochromis niloticus) become a popular cultured fish species all over the world. Even though its worldwide popularity in aquaculture, some ecological conflicts on distribution of Nile tilapia in nature has been debated in many countries like Türkiye, describing as an invasive species. The present study aims to present how osmolality and pH affect sperm activation in Nile tilapia in terms of sperm motility and velocity as well as duration of motility at 12th and 300th seconds post-activation. For this purpose, two successive experiments have been carried out. Firstly, spermatozoa motility was activated both ionic (NaCl, KCl, CaCl2, MgCl2 and NaHCO3) and non-ionic (glucose, urea, and glycine) solutions at 300, 250, 150, 100, and 50 mOsmol/kg. Additionally, motility was also activated by distilled water. Secondly, the role of pH on triggering sperm motility was determined by diluting spermatozoa in NaCl-based activating medium at pH levels ranged from 6 to 10. Spermatozoa showed the highest motility parameters when they were activated in NaCl and NaHCO3 as ionic solutions and glucose as a non-ionic medium at 100 mOsmol/kg. Sperm motility and velocity were found 96±2% and 91±5 μm/s at 12th s and 64±4 % and 52±4 μm/s at 300th s respectively while duration of motility was determined as 1117±53 s (18’37’’±53’’) in NaCl at 100 mOsmol/kg. The results represented that initiation of Nile tilapia motility is directly activated by a hypo-osmotic shock induced by both ionic and non-ionic media, however, contents of the media induced significant differences in motility parameters. Moreover, it has also demonstrated that Nile tilapia spermatozoa can be activated in a wide range of pH including acidic pH values. Consequently, these findings on sperm motility properties of Nile tilapia contribute essential information not only for aquaculture practice, but also for researchers interested in ecological distribution of the species.
References
Alavi, S. M. H., Cosson, J., Karami, M., Abdolhay, H., & Mojazi Amiri, B. (2004). Chemical composition and osmolality of seminal fluid of Acipenser persicus; their physiological relationship with sperm motility. Aquaculture Research, 35(13), 1238-1243. https://doi.org/10.1111/j.1365-2109.2004.01132.x
Alavi, S. M. H., & Cosson, J. (2005). Sperm motility in fishes. I. Effects of temperature and pH: a review. Cell biology international, 29(2), 101-110. https://doi.org/10.1016/j.cellbi.2004.11.021
Alavi, S. M. H., & Cosson, J. (2006). Sperm motility in fishes. (II) Effects of ions and osmolality: a review. Cell biology international, 30(1), 1-14. https://doi.org/10.1016/j.cellbi.2005.06.004
Alavi, S. H., Rodina, M., Viveiros, A. T., Cosson, J., Gela, D., Boryshpolets, S., & Linhart, O. (2009). Effects of osmolality on sperm morphology, motility and flagellar wave parameters in Northern pike (Esox lucius L.). Theriogenology, 72(1), 32-43. https://doi.org/10.1016/j.theriogenology.2009.01.015
Arslan, P., İnnal, D., & Özeren, S. C. (2021). Notes on the Distribution of the Genus Oreochromis in the East Mediterranean Region of Turkey. Commagene Journal of Biology, 5(1), 18-23. https://doi.org/10.31594/commagene.824644
Billard, R., & Cosson, M. P. (1992). Some problems related to the assessment of sperm motility in freshwater fish. Journal of Experimental Zoology, 261(2), 122-131. https://doi.org/10.1002/jez.1402610203
Boitano, S., & Omoto, C. K. (1991). Membrane hyperpolarization activates trout sperm without an increase in intracellular pH. Journal of Cell Science, 98(3), 343-349. https://doi.org/10.1242/jcs.98.3.343
Butts, I. A., Alavi, S. M. H., Mokdad, A., & Pitcher, T. E. (2013). Physiological functions of osmolality and calcium ions on the initiation of sperm motility and swimming performance in redside dace, Clinostomus elongatus. Comparative Biochemistry and Physiology Part A: Molecular & Integrative Physiology, 166(1), 147-157. https://doi.org/10.1016/j.cbpa.2013.05.011
Bwanika, G. N., Makanga, B., Kizito, Y., Chapman, L. J., & Balirwa, J. (2004). Observations on the biology of Nile tilapia, Oreochromis niloticus L., in two Ugandan crater lakes. African Journal of Ecology, 42, 93-101. https://doi.org/10.1111/j.1365-2028.2004.00468.x
Çiçek, E. (2021). Recent status of exotic tilapia species in Turkey. Ege Journal of Fisheries and Aquatic Sciences, 38(1), 111-116. https://doi.org/10.12714/egejfas.38.1.14
Ciereszko, A., Dietrich, G. J., Dietrich, M. A., Nynca, J., Kuźmiński, H., Dobosz, S., & Grudniewska, J. (2010). Effects of pH on sperm motility in several Salmoniformes species: Oncorhynchus mykiss, Salvelinus fontinalis, Salmo trutta, Salmo salar and Thymallus thymallus. Journal of Applied Ichthyology, 26(5), 665-667. https://doi.org/10.1111/j.1439-0426.2010.01536.x
Cosson, J. (2004). The ionic and osmotic factors controlling motility of fish spermatozoa. Aquaculture International, 12(1), 69-85. https://doi.org/10.1023/B:AQUI.0000017189.44263.bc
Cosson, J. (2010). Frenetic activation of fish spermatozoa flagella entails short‐term motility, portending their precocious decadence. Journal of Fish Biology, 76(1), 240-279. https://doi.org/10.1111/j.1095-8649.2009.02504.x
Dadzie, S. (1992). An overview of aquaculture in eastern Africa. Hydrobiologia, 232, 99-110. https://doi.org/10.1007/BF00014618
Dietrich, M. A., Arnold, G. J., Fröhlich, T., & Ciereszko, A. (2014). In-depth proteomic analysis of carp (Cyprinus carpio L) spermatozoa. Comparative Biochemistry and Physiology Part D: Genomics and Proteomics, 12, 10-15. https://doi.org/10.1016/j.cbd.2014.09.003
Dikel, S., Alev, M. V., Kiriş, G. A., & Çelik, M. (2003). Effects of supplemental dietary L-carnitine on the growth of Nile tilapia (Oreochromis niloticus) in cage conditions. Turkish Journal of Veterinary & Animal Sciences, 27(3), 663-669.
Dreanno, C., Cosson, J., Suquet, M., Cibert, C., Fauvel, C., Dorange, G., & Billard, R. (1999). Effects of osmolality, morphology perturbations and intracellular nucleotide content during the movement of sea bass (Dicentrarchus labrax) spermatozoa. Reproduction, 116(1), 113-125. https://doi.org/10.1530/jrf.0.1160113
El-Sayed, F. M., & Fitzsimmons, K. (2023). From Africa to the world-the journey of Nile tilapia. Rev Aquac 15: 6-21. https://doi.org/10.1111/raq.12738
Ergüden, S. A., Ergüden, D., & Ayas, D. (2022). First Record of Invasive Nile Tilapia Oreochromis niloticus (Linnaeus, 1758) (Family: Cichlidae) in Akgöl (Mersin, Türkiye). Natural and Engineering Sciences, 7(3), 294-301. https://doi.org/10.28978/nesciences.1222548
Gatti, J. L., Billard, R., & Christen, R. (1990). Ionic regulation of the plasma membrane potential of rainbow trout (Salmo gairdneri) spermatozoa: role in the initiation of sperm motility. Journal of Cellular Physiology, 143(3), 546-554. https://doi.org/10.1002/jcp.1041430320
İnanan, B. E. (2020). Fertilization rate, motility, lipid peroxidation and pH changes after chilled storage of rainbow trout (Oncorhynchus mykiss) eggs and spermatozoa by a RMPI medium. Aquaculture Research, 51(1), 222-231. https://doi.org/10.1111/are.14368
İnanan, B. E. (2024). Effects of Colchicine and Trypsin Treatments on Metaphase Chromosome Spreading from Larvae and Different Tissues of Adult Female and Male Nile Tilapia. Menba Journal of Fisheries Faculty. 10 (3), 113-118. DOI: 10.58626/menba.1538957
Krasznai, Z., Márián, T., Balkay, L., Gáspár Jr, R., & Trón, L. (1995). Potassium channels regulate hypo-osmotic shock-induced motility of common carp (Cyprinus carpio) sperm. Aquaculture, 129(1-4), 123-128. https://doi.org/10.1016/0044-8486(94)00234-F
Krasznai, Z., Morisawa, M., Morisawa, S., Krasznai, Z. T., Trón, L., Gáspár, R., & Márián, T. (2003). Role of ion channels and membrane potential in the initiation of carp sperm motility. Aquatic Living Resources, 16(5), 445-449. https://doi.org/10.1016/S0990-7440(03)00054-8
Kanyilmaz, M., & İnanan, B. E. (2020). DNA damage, oxidative stress, decreased viability and motility in common carp (Cyprinus carpio L.) spermatozoa induced by tryptophan, phenylalanine and cysteine amino acids during short-term storage. Turkish Journal of Zoology, 44(3), 281-290. https://doi.org/10.3906/zoo-1910-34
Linhart, O., Cosson, J., Mims, S. D., Shelton, W. L., & Rodina, M. (2002). Effects of ions on the motility of fresh and demembranated paddlefish (Polyodon spathula) spermatozoa. Reproduction, 124(5), 713-719. https://doi.org/10.1530/rep.0.1240713
Linhart, O., Walford, J., Sivaloganathan, B. & Lam, T. J. (1999). Effects of osmolality and ions on the motility of stripped and testicular sperm of freshwater- and seawater-acclimated tilapia, Oreochromis mossambicus. Journal of Fish Biology 55, 1344-1358. https://doi.org/10.1111/j.1095-8649.1999.tb02080.x
Linhart, O., Cheng, Y., Rodina, M., Gela, D., Tučková, V., Shelton, W. L., Tinkir, M., Memiş, D. & Xin, M. (2020). AQUA_2020_1080: Sperm management of European catfish (Silurus glanis L.) for effective reproduction and genetic conservation. Aquaculture, 529, 735620.
Mirera, D. O., & Okemwa, D. (2023). Salinity tolerance of Nile tilapia (Oreochromis niloticus) to seawater and growth responses to different feeds and culture systems. Western Indian Ocean Journal of Marine Science, 22(2), 75-85. https://doi.org/10.4314/wiojms.v22i2.6
Morisawa, M. (2008). Adaptation and strategy for fertilization in the sperm of teleost fish. Journal of Applied Ichthyology, 24(4), 362-370. https://doi.org/10.1111/j.1439-0426.2008.01126.x
Morisawa, M., & Suzuki, K. (1980). Osmolality and potassium ion: their roles in initiation of sperm motility in teleosts. Science, 210(4474), 1145-1147. https://doi.org/10.1126/science.7444445
Morisawa, M., Suzuki, K., Shimizu, H., Morisawa, S., & Yasuda, K. (1983). Effects of osmolality and potassium on motility of spermatozoa from freshwater cyprinid fishes. Journal of Experimental Biology, 107(1), 95-103. https://doi.org/10.1242/jeb.107.1.95
Morita, M., Takemura, A. & Okuno, M. (2004). Requirement of Ca2+ on activation of sperm motility in euryhaline tilapia (Oreochromis mossambicus). Journal of Experimental Biology 207, 337-345. https://doi.org/10.1242/jeb.00748
Öğretmen, F., Gölbaşi, S., Inanan, B. E., Kizak, V., & Kayim, M. (2014). Use of clove oil and eugenol to anesthetize fingerling Shabut Barbus grypus. North American Journal of Aquaculture, 76(1), 9-13. https://doi.org/10.1080/15222055.2013.824942
Pinheiro, J. P. S., Windsor, F. M., Wilson, R. W., & Tyler, C. R. (2021). Global variation in freshwater physico‐chemistry and its influence on chemical toxicity in aquatic wildlife. Biological Reviews, 96(4), 1528-1546. https://doi.org/10.1111/brv.12711
Redondo‐Müller, C., Cosson, M. P., Cosson, J., & Billard, R. (1991). In vitro maturation of the potential for movement of carp spermatozoa. Molecular Reproduction and Development, 29(3), 259-270. https://doi.org/10.1002/mrd.1080290308
Rurangwa, E., Kime, D. E., Ollevier, F., & Nash, J. P. (2004). The measurement of sperm motility and factors affecting sperm quality in cultured fish. Aquaculture, 234(1-4), 1-28. https://doi.org/10.1016/j.aquaculture.2003.12.006
Schneider, C. A., Rasband, W. S., & Eliceiri, K. W. (2012). NIH Image to ImageJ: 25 years of image analysis. Nature methods, 9(7), 671-675. https://doi.org/10.1038/nmeth.2089
Yigit, Ü., Taylor, N., Ergün, S., & Yigit, M. (2023). Production efforts for new candidate finfish species in Turkish marine aquaculture. Aquatic Animal Reports, 1(2), 105-112. https://doi.org/10.5281/zenodo.8229352
Vujovic, P., Chirillo, M., & Silverthorn, D. U. (2018). Learning (by) osmosis: an approach to teaching osmolarity and tonicity. Advances in physiology education, 42(4), 626-635. https://doi.org/10.1152/advan.00094.2018
Wilson-Leedy, J. G., & Ingermann, R. L. (2007). Development of a novel CASA system based on open-source software for characterization of zebrafish sperm motility parameters. Theriogenology, 67(3), 661-672. https://doi.org/10.1016/j.theriogenology.2006.10.003
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