Hostname: page-component-cd9895bd7-7cvxr Total loading time: 0 Render date: 2024-12-28T02:49:46.140Z Has data issue: false hasContentIssue false

Effects of the slow cooling during cryopreservation on the survival and morphology of Taiwan shoveljaw carp (Varicorhinus barbatulus) spermatozoa

Published online by Cambridge University Press:  23 December 2009

Sujune Tsai
Affiliation:
Department of biotechnology, Mingdao University, 369 Wenhua Road, Peetow, Chang Hua 52345, Taiwan
Emma Spikings
Affiliation:
LIRANS Institute of research in the applied natural sciences, University of Bedfordshire, 250 Butterfield, Great Marlings, Luton, Bedfordshire LU2 8DL, UK
Ching-Chiang Hwang
Affiliation:
LIRANS Institute of research in the applied natural sciences, University of Bedfordshire, 250 Butterfield, Great Marlings, Luton, Bedfordshire LU2 8DL, UK
Chiashin Lin
Affiliation:
National museum of marine biology & Aquarium, 2 Houwan Road, Checheng, Pingtung 944, Taiwan
Get access

Abstract

Over the past decades, pollution, overfishing, and habitat degradation have driven the population size of Taiwan shoveljaw carp down markedly in Taiwan. Cryopreservation is a useful tool which could be used to maintain genetic resources to protect and preserve this endemic species. Four cryoprotectants [dimethyl sulphoxide (DMSO), dimethylacetamide (DMA), glycerol and methanol] and six freezing rates (0.5, 1, 2, 4, 8, 16 °C min-1) were tested in order to develop an optimal controlled slow-freezing protocol for Taiwan shoveljaw carp spermatozoa. Samples were subsequently examined under the scanning electron microscope to reveal whether cryopreservation had affected their ultrastructural morphology. The highest survival rate (50.1 ± 2.0%) was observed with a freezing rate of 8 °C min-1 in 1M DMSO, using SYBR-14 + PI staining. Fertility and hatching rate results using frozen-thawed spermatozoa (90.2 ± 2.2% and 22.3 ± 2.5%, respectively) were not significantly different from results with fresh spermatozoa. After cryopreservation, 21.0 ± 1.6% of frozen-thawed spermatozoa had mid-piece swelling and rupture of the head. Cryopreservation might, therefore, slightly affect Taiwan shoveljaw carp spermatozoa in terms of morphological change. However, these alterations could be compensated by using large enough numbers of normally functioning frozen-thawed spermatozoa to achieve a standard equal to fresh spermatozoa. This is the first report of successful cryopreservation of Taiwan shoveljaw carp spermatozoa using a controlled slow-cooling method.

Type
Note
Copyright
© EDP Sciences, IFREMER, IRD, 2009

Access options

Get access to the full version of this content by using one of the access options below. (Log in options will check for institutional or personal access. Content may require purchase if you do not have access.)

References

Andrabi, S.M.H., 2007, Fundamental principles of cryopreservation of Bos taurus and Bos indicus bull spermatozoa. Ind. J. Agric. Biol. 2, 367369.
Babiak, I., Glogowsk, J., Brzuska, E., Szumiec, J., Adamek, J., 1997, Cryopreservation of sperm of common carp Cyprinus carpio. Aquac. Res. 28, 567571. CrossRef
Bokor, Z., Müller, T., Bercsényi, M., Horváth, L., Urbányi, B., Horváth, A., 2007, Cryopreservation of sperm of two European percid species, the pikeperch (Sander lucioperca) and the Volga pikeperch (S. volgensis). Acta. Biol. Hung. 58, 19920. CrossRef
Boryshpolets S., Dzyuba B., Rodina M., Li P., Hulak M., Gela D., Linhart O., 2009 Freeze-thawing as the factor of spontaneous activation of spermatozoa motility in common carp (Cyprinus carpio L.). Cryobiology 59.
Chao, N.H., Liao, I.C., 2001, Cryopreservation of finfish and shellfish gametes and embryos. Aquaculture 197, 161189. CrossRef
Chen, S.L., Liu, X.T., Lu, D.C., Zhang, L.Z., Fu, C.J., Fang, J.P., 1992, Cryopreservation of spermatozoa of silver carp, common carp, blunt snout bream and grass carp. Acta Zool. Sin. 38, 413424.
Christensen, J.M., Tiersch, T.R., 2005, Cryopreservation of channel catfish sperm: effects of cryoprotectant exposure time, cooling rate, thawing conditions, and male-to-male variation. Theriogenology 63, 21032112. CrossRef
Drokin, S.I., 1993, Phospholipid distribution and fatty acid composition of phosphatidylcholine and phosphatidylethanolamine in sperm of some freshwater and marine species of fish. Aquat. Living Resour. 6, 4956. CrossRef
Emaljanova, N.G, Makeeva, A.P., 1985, Ultrastructure of spermatozoids of some cyprinid fishes (Cyprinidae). J. Appl. Ichthyol. 25, 137144.
Flajshans, M., Cosson, J., Rodina, M., Linhart, O., 2004, The application of image cytometry to viability assessment in dual fluorescence-stained fish spermatozoa. Cell Biol. Int. 28, 955959. CrossRef
Garner, D.L, Johnson, L.A, Yue, S.Y, Roth, B.L, Haugland, R.P., 1994, Dual staining assessment of bovine sperm viability using SYBR 14 and propidium iodide. J. Androl. 15, 620629.
Garner, D.L., Johnson, L.A., 1995, Viability assessment of mammalian sperm using SYBR 14 and propidium iodide. Biol. Reprod. 53, 276284. CrossRef
Guest, W.C., Avault, J.W., Roussel, J.D., 1976, Preservation of channel catfish sperm. Trans. Am. Fish. Soc. 3, 469474. 2.0.CO;2>CrossRef
Gwo, J.C., 2000, Cryopreservation of aquatic invertebrate semen: A review. Aquac. Res. 31, 259271. CrossRef
Hammerstedt, R.H., Graham, J.K., Nolan, J., 1990, Cryopreservation of mammalian sperm: what we ask them to survive. J. Androl. 11, 7388.
Horváth, Á., Miskolczi, E., Urbányi, B., 2003, Cryopreservation of common carp sperm. Aquat. Living Resour. 16, 457460. CrossRef
Ji, X.S., Zhao, Y., Chen, S.L., Jiang, Y.L., Wang, H., Song, J.Y., Ding, L., Chen, H.J., 2008, Successful fertilisation of Varicorhinus macrolepis eggs with sperm subjected to two freeze-thaw cycles. Theriogenology 69, 793797. CrossRef
Lahnsteiner, F., Berger, B., Weismann, T., 2003, Effects of media, fertilization technique, extender, straw volume, and sperm to egg ratio on hatchability of cyprinid embryos, using cryopreserved semen. Theriogenology 60, 829841. CrossRef
Lahnsteiner, F., Weismann, T., Patzner, R.A., 1992, Fine structural changes in spermatozoa of the frayling, Thymallus thymallus (Pisces: Teleostei), during routine cryopreservation. Aquaculture 103, 7384. CrossRef
Lin, C., Zhang, T., Rawson, D.M., 2009, Cryopreservation of zebrafish (Danio rerio) blastomeres by controlled slow cooling. Cryoletters 30, 132141.
Linhart, O., Benesovsky, J., 1991, Artificial insemination in asp (Aspius aspius L.). Anim. Sci. 36, 973980.
Liu, Q.H, Zhang, S.C, Xiao, Z.Z, Ding, F.H, Yu, D.D, Xu, X.Z., 2007, Flow cytometry and ultrastructure of cryopreserved red seabream (Pagrus major) sperm. Theriogenology 67, 11681174. CrossRef
Melo, F.C.S.A, Godinho, H.P., 2006, A protocol for cryopreservation of spermatozoa of the fish Brycon orthotaenia. Anim. Reprod. 3, 380385.
Mongkonpunya, K., Chairak, N., Pupipat, T., Tiersch, T.R., 1995, Cryopreservation of Mekong giant catfish sperm. Asian Fish. Sci. 8, 211221
Muchlisin, Z.A., Muhammadar., 2002, Long-term cryopreservation of baung spermatozoa, Mystus nemurus: effect of various cryoprotectants on motility and fertility. Torani 12, 204210.
Muchlisin, Z.A., 2005, Current status of extenders and cryoprotectants on fish spermatozoa cryopreservation. Biodiversitas 6, 6669. CrossRef
Ohta, H., Kawamura, K., Unuma, T., Takegoshi, Y., 2001, Cryopreservation of the sperm of the Japanese bitterling. J. Fish Biol. 58, 670681. CrossRef
Oshima, M., 1920, Notes on freshwater fishes of Formosa, with description of new genera and species. Proc. Acad. Nat. Sci. Phil. 122, 120135.
Perchec-Poupard, G., Gatti, J.L., Jeulin, C., Fierville, F., Billard, R., 1997, Effects of extracellular environment on the osmotic signal transduction involved in activation of motility of carp spermatozoa. J. Reprod. Fert. 110, 315327. CrossRef
Psenicka, M., Rodina, M., Nebesarova, J., Linhar, O., 2006, Ultrastructure of spermatozoa of tench Tinca tinca observed by means of scanning and transmission electron microscopy. Theriogenology 66, 13551363. CrossRef
Suquet, M., Dreanno, C., Fauvel, C., Cosson, J., Billard, R., 2000, Cryopreservation of sperm in marine fish. Aquac. Res. 31, 231243. CrossRef
Tian, Y.S., Chen, S.L., Ji, X.S., Zhai, J.M., Sun, L.J., Chen, C., Su, P.Z., 2008, Cryopreservation of spotted halibut (Verasper variegates) sperm. Aquaculture 284, 268271. CrossRef
Tiersch, T.R., Yang, H., 2009, Current status of sperm cryopreservation in biomedical research fish models: zebrafish, medaka, and Xiphophorus. Comp. Biochem. Physiol. C Toxicol. Pharmacol. 149, 224232.
Tsai, S., Rawson, D.M., Zhang, T., 2008, Studies on cryoprotectant toxicityto early stage zebrafish (Danio rerio) ovarian follicle. Cryoletters 29, 477483.
Van der Straten K.M., Leung L.K., Rossini R., Johnston S.D., 2006, Cryopreservation of spermatozoa of black marlin, Makaira indica (Teleostei: Istiophoridae) Cryoletters 27, 203–209.
Viveiros, A.T.M., Lock, E.J., Woelders, H., Komen, J., 2001, Influence of cooling rates and plunging temperatures in an interrupted slow-freezing procedure for semen of the African catfish Clarias gariepinus. Cryobiology 43, 276287. CrossRef
Watson P.F., 2000, The causes of reduced fertility with cryopreserved semen. Anim. Reprod. Sci. 60/61, 481–492.
Yao, Z., Crim, L.W., Richardson, G.F., Emerson, C.J., 2000, Motility, fertility and ultrastructural changes of ocean pout (Macrozoarces americanus) sperm after cryopreservation. Aquaculture 181, 361375. CrossRef