Short-Term Storage of Japanese Koi (Cyprinus carpio var. koi) Sperm on the Egg Fertilization Performance
Keywords:
extender, fertilizing ability, hatching, Nishikigoi, ornamental koi, short duration preservationAbstract
Lack of mature male broodfish, insufficient sperm, and non-synchronized maturation times have always been a hindrance to the breeding program of Japanese koi (Cyprinus carpio var. koi) raised indoors. Therefore, it is believed that the preservation of Japanese koi sperm by short-term storage and cryopreservation could solve this problem. In this study, the appropriate diluent solution, sperm-to-diluent ratio, and storage temperature for short-term storage of Japanese koi sperm were determined, and the efficacy of the short-term stored sperm in fertilizing eggs was evaluated. Milt samples collected from sexually mature males were pooled and tested in modified calcium-free Hank's Balanced Salt Solution (CF-HBSS), modified Mahseer extender, and modified Kurokura extender at 1:1 and 1:5 ratios of sperm to diluent, respectively. Storage temperatures were tested at 4 °C and room temperature. Milt sample without diluent solution served as a control. The percentage of sperm motility was measured daily for one week. For the egg fertilization experiment, Japanese koi eggs were fertilized with sperm on the second day of short-term storage, while a freshly collected sperm sample served as a control. We found that sperm diluted 1:1 with a modified Kurokura extender and stored at 4 °C had a mean sperm motility of 76.00 ± 3.06% on the third day, compared with 54.67 ± 2.91% in the control treatment (P<0.05). Short-term stored spermatozoa showed equivalent egg fertilization ability compared to fresh spermatozoa (control) (P>0.05). In conclusion, the use of a modified Kurokura extender at a 1:1 ratio of sperm to diluent and storage at 4 °C was optimal for short-term storage of Japanese koi sperm, and these sperm still showed equivalent egg fertilization ability to freshly collected sperm after two days of storage. In addition, the current study also determined the appropriate extender solution for cryopreservation of Japanese koi sperm.
Downloads
Metrics
References
Alavi, S.M.H., Linhart, O., Coward, K. & Rodina, M. 2008. Fish spermatology: implication for aquaculture management. In: Fish Spermatology. S.M.H. Alavi, J.J. Cosson, K. Coward & R. Rafiee (Eds.). Alpha Science Ltd, Oxford. pp. 397-460.
Bajer, P. & Sorensen, P. 2010. Recruitment and abundance of an invasive fish, the common carp, is driven by its propensity to invade and reproduce in basins that experience winter-time hypoxia in interconnected lakes. Biological Invasions, 12: 1101-1112. DOI: https://doi.org/10.1007/s10530-009-9528-y
Balon, E.K. 1995. Origin and domestication of the wild carp, Cyprinus carpio: from Roman gourmets to the swimming flowers. Aquaculture, 129: 3-48. DOI: https://doi.org/10.1016/0044-8486(94)00227-F
Bobe, J. & Labbé, C. 2009. Chilled storage of sperm and eggs. In: Methods in Reproductive Aquaculture: Marine and Freshwater Species. E. Cabrita, V. Robles & P. Herráez (Eds.). CRC Press, Boca Raton, London, NY. pp. 219-235. DOI: https://doi.org/10.1201/9780849380549.sec4
Bobe, J. & Labbé, C. 2010. Egg and sperm quality in fish. General and Comparative Endocrinology, 165(3): 535-548. DOI: https://doi.org/10.1016/j.ygcen.2009.02.011
Bozkurt, Y. & Secer, S. 2005. Effect of short-term preservation of mirror carp (Cyprinus carpio) semen on motility, fertilization, and hatching rates. Israeli Journal of Aquaculture - Bamidgeh, 57(3): 207-212. DOI: https://doi.org/10.46989/001c.20407
Bozkurt, Y., Yavas, I. & Karaca, F. 2012. Cryopreservation of Brown Trout (Salmo trutta macrostigma) and Ornamental Koi Carp (Cyprinus carpio) Sperm. In: Current Frontiers in Cryopreservation. I. Katkov (Ed.). InTech, Rijeka, Croatia. pp. 293-304. DOI: https://doi.org/10.5772/32284
Cabrita, E., Robles, V., Sarasquete, C. & Herraez, P. 2011. New Insight on Sperm Quality Evaluation for Broodtscok Improvement. In: Cryopreservation in Aquatic Species, 2nd Edition. T.R. Tiersch & C.C. Green (Eds.). World Aquaculture Society, Baton Rouge, Louisiana. pp. 146-161.
Cejko, B.I., Horváth, Á., Kollár, T., Kása, E., Lujić, J., Marinović, Z., Urbányi, B. & Kowalski, R.K. 2018b. Optimisation of sodium and potassium concentrations and pH in the artificial seminal plasma of common carp Cyprinus carpio L. Fish Physiology and Biochemistry, 44(6): 1435-1442. DOI: https://doi.org/10.1007/s10695-018-0491-3
Cejko, B.I., Sarosiek, B., Krejszeff, S. & Kowalski, R.K. 2018a. Multiple collections of common carp Cyprinus carpio L. semen during the reproductive period and its effects on sperm quality. Animal Reproduction Science, 188(July): 178-188. DOI: https://doi.org/10.1016/j.anireprosci.2017.12.002
Cejko, B.I., Żarski, D., Sarosiek, B., Dryl, K., Palińska-Żarska, K., Skorupa, W. & Kowalski, R.K. 2022. Application of artificial seminal plasma to short-term storage of a large volume of common carp (Cyprinus carpio) sperm for two weeks under controlled conditions. Aquaculture, 546: 737385. DOI: https://doi.org/10.1016/j.aquaculture.2021.737385
Chapman, F.A. 2019. A Semen Extender for the Short-Term Storage of Fish. FA193 Fisheries and Aquatic Sciences Department, UF/IFAS Extension Publications, Gainesville, Florida. pp. 1-3.
Cheng, Y., Zhang, S., Linhartová, Z., Shazada, N.E. & Linhart, O. 2022a. Common carp (Cyprinus carpio) sperm reduction during short-term in vitro storage at 4°C. Animal Reproduction Science, 243: 107017. DOI: https://doi.org/10.1016/j.anireprosci.2022.107017
Cheng, Y., Zhang, S., Linhartová, Z., Shazada, N.E. & Linhart, O. 2022b. Practical use of extender and activation solutions for short-term storage of common carp (Cyprinus carpio) milt in a hatchery. Aquaculture Reports, 24: 101160. DOI: https://doi.org/10.1016/j.aqrep.2022.101160
Chew P.C., Hanan, M.Y., M. Zudaidy, J. & Mohd Fariduddin, O. 2016a. FRI Glami Lemi Bangun Koi Bebas Penyakit. Berita Perikanan Bil. 96, pp. 9.
Chew P.C., Muhamad Zudaidy, J., Hanan, M.Y., Eka, S., Rahimah, Z., Nurul Syafiqa, S. & Mohd Fariduddin, O. 2016c. Growth performances of Japanese koi (cyprinus carpio): comparison between indoor tank and conventional pond production. In: M. Halimah. (Ed.). The Proceedings of the Fisheries Research Seminar 2016, 25-27 October 2016, Batu Maung, Penang. pp. 51-54.
Chew, P.C. 2021. Development of Specific Pathogen Free (SPF) Koi Broodstock. Fisheries Research Institute Annual Report 2021. p. 63.
Chew, P.C., Abd-Rashid, Z., Hassan, R., Asmuni, M. & Chuah, H.P. 2010b. Semen cryo-bank of the Malaysian Mahseer (Tor tambroides and T. douronensis). Journal of Applied Ichthyology, 26(5): 726-731. DOI: https://doi.org/10.1111/j.1439-0426.2010.01552.x
Chew, P.C., Hanan, M.Y., Muhamad Zudaidy, J. & Mohd Fariduddin, O. 2016b. Preliminary results on establishment of disease-free Japanese Koi (Cyprinus carpio L.) stock at FRIGL, Department of Fisheries Malaysia. In: The Proceedings of the Fisheries Research Seminar 2016. Halimah, M. (Ed.). Batu Maung, Penang, pp. 194-197.
Chew, P.C., Hassan, R., Rashid, Z.A., & Chuah, H.P. 2010a. The current status of sperm cryopreservation of the endangered Probarbus jullieni (Sauvage) in Malaysia. Journal of Applied Ichthyology, 26(5): 797-805. DOI: https://doi.org/10.1111/j.1439-0426.2010.01539.x
Contreras, P., Dumorné, K., Ulloa-Rodríguez, P., Merino, O., Figueroa, E., Farías, J.G., Valdebenito, I. & Risopatrón, J. 2020. Effects of short-term storage on sperm function in fish semen: A review. Reviews in Aquaculture, 12(3): 1373-1389. DOI: https://doi.org/10.1111/raq.12387
de Kock, S. & Gomelsky, B. 2015. Japanese Ornamental Koi Carp: Origin, variation and genetics. In: Biology and Ecology of Carp. C. Pietsch & P. Hirsch (Eds.). CRC Press, Boca Raton. pp. 27-53. DOI: https://doi.org/10.1201/b18547-4
Dey, V.K. 2016. The global trade in ornamental fish. INFOFISH International, 4: 52-55.
DOF. 2022. Annual Fisheries Statistics 2022. Department of Fisheries Malaysia, Putrajaya, Malaysia.
Ekici, A., Yamaner, G. & Didem Demircan, M. 2022. Cryopreservation studies in aquaculture from past to present: Scientific techniques and quality controls for commercial applications. In: Cryopreservation - Applications and Challenges, Chapter 1. Quain, M. (Ed.). IntechOpen. DOI: https://doi.org/10.5772/intechopen.108566
Evers, H.G., Pinnegar, J.K. & Taylor, M.I. 2019. Where are they all from? - sources and sustainability in the ornamental freshwater fish trade. Journal of Fish Biology, 94(1): 1-8. DOI: https://doi.org/10.1111/jfb.13930
Ghosh, A.K., Biswas, S., Sarder, L., Sabbir, W. & Rahaman, S.M.B. 2012. Induced breeding, embryonic and larval development of Koi carp (Cyprinus carpio) in Khulna, Bangladesh. Mesopotamian Journal of Marine Science, 27(1): 1-14. DOI: https://doi.org/10.58629/mjms.v27i1.167
Gouda, P., Sinha, M.K. & Parida, S.P. 2020. A study on biology, brood-stock management and induced breeding of Amur common carp, Cyprinus carpio haematopterus (Linnaeus, 1758). Journal of the Indian Society of Coastal Agricultural Research, 38(1): 76-83.
Kalilola, P.J., Williams, M.J., Stewart, P.C., Reichelt, R.E., McNee, A. & Grieve, C. 1993. Australian fisheries resources. Bureau of Resource Sciences, Canberra, Australia. 422 pp.
Kohlmann, K. & Kersten, P. 1999. Genetic variability of German and foreign common carp (Cyprinus carpio L.) populations. Aquaculture, 173: 435-445. DOI: https://doi.org/10.1016/S0044-8486(98)00474-8
Kohlmann, K., Gross, R., Murakaeva, A. & Kersten, P.P. 2003. Genetic variability and structure of common carp (Cyprinus carpio) populations throughout the distribution range inferred from allozyme, microsatellite and mitochondrial DNA markers. Aquatic Living Resources, 16: 421-431. DOI: https://doi.org/10.1016/S0990-7440(03)00082-2
Kuroki, T. 1981. The latest manual to nishikigoi.Shin-Nippon Kyoiku-Tosho Co. Ltd. Japan, 272 pp.
Lahnsteiner, F., Berger, B., Horvath, A., Urbányi, B. & Weismann, T., 2000. Cryopreservation of spermatozoa in cyprinid fishes. Theriogenology, 54: 1477-1498. DOI: https://doi.org/10.1016/S0093-691X(00)00469-6
Liley, R.N., Tamkee, P., Tsai, R. & Hoysak, J.D. 2002. Fertilization dynamics in rainbow trout (Oncorhynchus mykiss): effect of male age social experience and sperm concentration and motility on in vitro fertilization. Canadian Journal of Fisheries and Aquatic Sciences, 59: 144-152. DOI: https://doi.org/10.1139/f01-202
Mabuchi, K., Seno, H., Suzuki, T. & Nishida, M. 2005. Discovery of an ancient lineage of Cyprinus carpio from Lake Biwa, central Japan, based on mtDNA sequence data, with reference to possible multiple origins of koi. Journal of Fish Biology, 66: 1516 -1528. DOI: https://doi.org/10.1111/j.0022-1112.2005.00676.x
Magnotti, C., Cerqueira, V., Lee-Estevez, M., Farias, J., Valdebenito, I. & Figueroa, E. 2016. Cryopreservation and vitrification of fish semen: a review with special emphasis on marine species. Reviews in Aquaculture, 10(1): 15-25. DOI: https://doi.org/10.1111/raq.12145
Magyary, I., Urbányi, B. & Horváth, L. 1996. Cryopreservation of common carp (Cyprinus carpio L.) sperm II. Optimal conditions for fertilization. Journal of Applied Ichthyology, 12: 117-119. DOI: https://doi.org/10.1111/j.1439-0426.1996.tb00073.x
Md. Monirul, I., Abdulla-Al-Asif, & Md. Ruhul, A. 2016. The induced breeding of common carps (Cyprinus carpio) in Bangladesh. Indian Journal of Science, 23(84): 619-632.
Ministry of Agricultural and Agro-Based Industry Malaysia. 2014. MyGAP Malaysia Guidelines - Aquaculture Sector. Crop, Livestock and Fisheries Industry Division, Pusat Pentadbiran Kerajaan Persekutuan, Putrajaya. pp. 21-44.
Ng, C.K. 2017. The ornamental freshwater fish trade in Malaysia. UTAR Agriculture Science Journal 2 (4): 1-18.
Okomoda, V.T., Koh, I.C.C. & Shahreza, S. 2017. A simple technique for accurate estimation of fertilization rate with specific application to Clarias gariepinus (Burchell, 1822). Aquaculture Research, 49(2): 1116-1121. DOI: https://doi.org/10.1111/are.13528
Pérez-Cerezales, S., Martínez-Páramo, S., Cabrita, E., Martínez-Pastor, F., de Paz, P. & Herráez, M.P. 2009. Evaluation of oxidative DNA damage promoted by storage in sperm from sex-reversed rainbow trout. Theriogenology, 71: 605-613. DOI: https://doi.org/10.1016/j.theriogenology.2008.09.057
Tempero, G.W., Ling, N., Hicks, B.J. & Osborne, M.W. 2006. Age composition, growth, and reproduction of koi carp (Cyprinus carpio) in the lower Waikato region, New Zealand. Journal of Marine and Freshwater Research, 40: 571-583. DOI: https://doi.org/10.1080/00288330.2006.9517446
Trigo, P., Merino, O., Figueroa, E., Valdebenito, I., Sánchez, R. & Risopatrón, J. 2015. Effect of short-term semen storage in salmon (Oncorhynchus mykiss) on sperm functional parameters evaluated by flow cytometry. Andrologia, 47: 407-411. DOI: https://doi.org/10.1111/and.12276
Urbanyi B., Horvath A., Varga Z., Horvath L., Magyary I. & Radics, F. 1999. Effect of extenders on sperm cryopreservation of African catfish. Clarias gariepinus (Burchell, 1822). Aquaculture Research, 30: 145-151. DOI: https://doi.org/10.1046/j.1365-2109.1999.00313.x
Viader-Guerrero, M., Guzmán-Villanueva, L.T., Spanopoulos-Zarco, M., Estrada-Godínez, J.A., Maldonado-García, D., Gracia-López, V., Omont, A. & Maldonado-García, M. 2021. Effects of temperature on hatching rate and early larval development of longfin yellowtail Seriola rivoliana. Aquaculture Reports, 21: 100843. DOI: https://doi.org/10.1016/j.aqrep.2021.100843
WHO. 2010. Chapter 2: Counting Sperm Concentration and Total Sperm. In WHO 5th Edition Manual For Semen Analysis. pp.33-45.
Zhang, S., Cheng, Y., Alavi, S.M.H., Shazada, N.E., Rodinová, Z.L.V. & Linhart, O. 2023. Elevated temperature promotes spermatozoa motility kinetics and fertilizing ability following short-term storage: An implication for artificial reproduction of common carp Cyprinus carpio in a hatchery. Aquaculture, 565: 739126. DOI: https://doi.org/10.1016/j.aquaculture.2022.739126
Published
How to Cite
Issue
Section
Any reproduction of figures, tables and illustrations must obtain written permission from the Chief Editor (wicki@ukm.edu.my). No part of the journal may be reproduced without the editor’s permission