Hostname: page-component-cd9895bd7-jkksz Total loading time: 0 Render date: 2024-12-27T07:46:58.396Z Has data issue: false hasContentIssue false

Hatchery-scale trials using cryopreserved spermatozoa ofblack-lip pearl oyster, Pinctada margaritifera

Published online by Cambridge University Press:  28 June 2011

Belinda Hui
Affiliation:
Ifremer, Laboratoire Domestication de l’Huître perlière, Centre du Pacifique, BP 7004, 98719 Taravao, Tahiti, Polynésie Française
Vincent Vonau
Affiliation:
Ifremer, Laboratoire Domestication de l’Huître perlière, Centre du Pacifique, BP 7004, 98719 Taravao, Tahiti, Polynésie Française
Jacques Moriceau
Affiliation:
Ifremer, Laboratoire Domestication de l’Huître perlière, Centre du Pacifique, BP 7004, 98719 Taravao, Tahiti, Polynésie Française
Roger Tetumu
Affiliation:
Ifremer, Laboratoire Domestication de l’Huître perlière, Centre du Pacifique, BP 7004, 98719 Taravao, Tahiti, Polynésie Française
Vincent Vanaa
Affiliation:
Ifremer, Laboratoire Domestication de l’Huître perlière, Centre du Pacifique, BP 7004, 98719 Taravao, Tahiti, Polynésie Française
Marina Demoy-Schneider
Affiliation:
Laboratoire Biodiversité terrestre et marine, UMR CNRS EA4239, Université de la Polynésie Française, BP 6570, 98702 Faa’a, Tahiti, Polynésie Française
Marc Suquet
Affiliation:
UMR 100 Physiologie et Ecophysiologie des Mollusques marins, Ifremer, Site expérimentale d’Argenton, 11 Presqu’île du Vivier, 29840 Argenton en Landunvez, France
Gilles Le Moullac*
Affiliation:
Ifremer, Laboratoire Domestication de l’Huître perlière, Centre du Pacifique, BP 7004, 98719 Taravao, Tahiti, Polynésie Française
*
a Corresponding author:Gilles.Le.Moullac@ifremer.fr
Get access

Abstract

Cryopreservation is a valuable tool for genetic improvement programs. Several bivalvemollusc species have already been the subject of such programs and the Tahitian blackpearl oyster industry is now planning the development of selective breeding for desirabletraits in Pinctada margaritifera. The ability to cryopreserve spermatozoawould, therefore, offer significant benefits to the cultured black pearl industry.Spermatozoa were cryopreserved with cryoprotectant agent (CPA) 0.7 M trehalose in 0.8 MMe2SO and a two-step freezing process was used: straws were first maintainedin nitrogen vapour for 10 minutes, then directly plunged into liquid nitrogen and storedfor one week before use. The viability of thawed sperm was 23% lower than that of freshsperm. When using thawed sperm, therefore, a higher sperm/egg ratio of 100 000:1 wasrequired to reach 80% oocyte fertilization, compared with 100:1 for fresh sperm.Nevertheless, this first demonstration of cryopreserved sperm fertility in black pearloyster confirms the hatchery applicability of the cryopreservation technique defined here.Monitoring for larval viability during the first 23 days of life revealed no significantdifferences between the progeny produced with cryopreserved sperm and that produced usingfresh sperm.

Type
Note
Copyright
© EDP Sciences, IFREMER, IRD 2011

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

Acosta-Salmón, H., Jerry, D.J., Southgate, P.C., 2007, Effects of cryoprotectant agents and freezing protocol on motility of black-lip pearl oyster (Pinctada margaritifera L.) spermatozoa. Cryobiology 54, 1318. CrossRefGoogle Scholar
Adams, S.L., Hessian, P.A., Mladenov, P.V., 2003, Flow cytometric evaluation of mitochondrial function and membrane integrity of marine invertebrate sperm. Invertebr. Reprod. Dev. 44, 4551. CrossRefGoogle Scholar
Adams, S.L., Hessian, P.A., Mladenov, P.V., 2004a, Cryopreservation of sea urchin (Evechinus chloroticus) sperm. Cryo Lett. 25, 287300. Google ScholarPubMed
Adams, S.L., Smith, J.F., Roberts, R.D., Janke, A.R., Kaspar, H.F., Tervit, H.R., Pugh, P.A., Webb, S.C., King, N.G., 2004b, Cryopreservation of sperm of the Pacific Oyster (Crassostrea gigas): development of a practical method for commercial spat production. Aquaculture 242, 271282. CrossRefGoogle Scholar
Adams, S.L., Smith, J.F., Roberts, R.D., Janke, A.R., King, N.G., Tervit, H.R., Webb, S.C., 2008, Application of sperm cryopreservation in selective breeding of the Pacific oyster, Crassostrea gigas (Thunberg). Aquac. Res. 39, 14341442. CrossRefGoogle Scholar
Arnaud-Haond, S., Goyard, E., Vonau, V., Herbaut, C., Prou, J., Saulnier, D., 2007, Pearl Formation : Persistence of the Graft During the Entire Process of biomineralization. Mar. Biotechnol. 9, 113116. CrossRefGoogle ScholarPubMed
Bougrier, S., Rabenomanana, L.D., 1986, Cryopreservation of spermatozoa of the Japanese Oyster, Crassostrea gigas. Aquaculture 58, 277280. CrossRefGoogle Scholar
Cabrita, E., Robles, V., Cuñado, S., Wallace, J.C., Sarasquete, C., Herráez,, M.P., 2005, Evaluation of gilthead sea bream, Sparus aurata, sperm quality after cryopreservation in 5ml macrotubes. Cryobiology 50, 273284. CrossRefGoogle Scholar
Fauvel, C., Suquet, M., Dreanno, C., Zonno, V., Menu, B., 1998, Cryopreservation of sea bass (Dicentrarchus labrax) spermatozoa in experimental and production stimulating conditions. Aquat. Living Resour. 11, 387394. CrossRefGoogle Scholar
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. Inter. 28, 955959. CrossRefGoogle ScholarPubMed
Graham, J.K., Kunze, E., Hammerstedt, R.H., 1990, Analysis of sperm cell viability, acrosomal integrity, and mitochondrial function using flow cytometry. Biol. Reprod. 43, 5564. CrossRefGoogle ScholarPubMed
Grzyb, K., Rychlowski, M., Biegniewska, A., Skorkowski, E.F., 2003, Quantitative determination of creatine kinase release from herring (Clupea harengus) spermatozoa induced by tributyltin. Comp. Biochem. Physiol. C 134, 207213. Google ScholarPubMed
Gwo, J.C., Wu, C.Y., Chang, W.S.P., Cheng, H.Y., 2003, Evaluation of damage in Pacific oyster (Crassostrea gigas) spermatozoa before and after cryopreservation using comet assay. Cryo. Lett. 24, 171180. Google Scholar
Heasman, M.P., O’Connor, W.A., Frazer, A.W., 1996, Effects of fertilization and incubation factors on the quality and yield of scallop, Pecten fumatus Reeve larvae. Aquac. Res. 27, 505513. CrossRefGoogle Scholar
Horvat, A., Wayman, W.R., Dean, J.C., Urbanyi, B., Tiersch, T.R., Mims, S.D., Johnson, D., Jenkins, J.A., 2008, Viability and fertilizing capacity of cryopreserved sperm from three North American acipenseriform species: a retrospective study. J. Appl. Ichthyol. 24, 443449. CrossRefGoogle Scholar
Hui B., Demoy-Schneider M., Vonau V., Le Moullac G., Moriceau J., Le Pennec M., Cochard J.C., 2009, Gamete cryopreservation, an asset for a durable pearl farming in French Polynesia. 11th Pacific Science Inter-congress, Tahiti, 2–6 March 2009.
Lyons, L., Jerry, D.R., Southgate, P.C., 2005, Cryopreservation of black-lip pearl oyster (Pinctada margaritifera L.) spermatozoa: effects of cryoprotectants on spermatozoa motility. J. Shellfish Res. 24, 11871190. Google Scholar
Magnesen, T., Bergh, O., Christophersen, G., 2006, Yields of great scallop, Pecten maximus, larvae in a commercial flow-through rearing system in Norway. Aquac. Int. 14, 377394. CrossRefGoogle Scholar
Narita, T., Kawamoto, T., Isowa, K., Aoki, H., Hayashi, M., Komaru, A., Ohta, H., 2007, Effects of cryopreservation methods on post-thaw motility of spermatozoa from the Japanese pearl oyster, Pinctada fucata martensii. Cryobiology 54, 1926. Google Scholar
Narita, T., Kawamoto, T., Isowa, K., Aoki, H., Hayashi, M., Komaru, A., Ohta, H., 2008, Fertility of cryopreserved spermatozoa of the Japanese pearl oyster, Pinctada fucata martensii. Aquaculture 275, 178181. CrossRefGoogle Scholar
Paniagua-Chávez, C.G., Jenkins, J., Segovia, M., Tiersch, T.R., 2006, Assessment of gamete quality for the eastern oyster (Crassostrea virginica) by use of fluorescent dyes. Cryobiology 53, 128138. CrossRefGoogle Scholar
Pouvreau, S., Gangnery, A., Tiapari, J., Lagarde, F., Garnier, M., Bodoy, A., 2000, Gametogenic cycle and reproductive effort of the tropical blacklip pearl oyster, Pinctada margaritifera (Bivalvia: Pteriidae), cultivated in Takapoto atoll (French Polynesia). Aquat. Living Resour. 13, 3748. CrossRefGoogle Scholar
Rico-Villa, B., Woerther, P., Mingant, C., Lepiver, D., Pouvreau, S., Hamon, M., Robert, R., 2008, A flow-through rearing system for ecophysiological studies of Pacific oyster Crassostrea gigas larvae. Aquaculture 282, 5460. CrossRefGoogle Scholar
Santos, A.E., Nascimento, I.A., 1989, Influence of gamete density, salinity and temperature on the normal embryonic development of the mangrove oyster Crassostrea rhizophorae. Aquaculture 73, 295307. Google Scholar
Sarkis, S., Helm, M., Hohn, C., 2006, Larval rearing of calico scallops, Argopecten gibbus, in a flow-through system. Aquac. Int. 14, 527538. CrossRefGoogle Scholar
Smith, J.F., Pugh, P.A., Tervit, H.R., Roberts, R.D., Janke, A.R., Kaspar, H.F., Adams, S.L., 2001, Cryopreservation of shellfish sperm, eggs and embryos. Proc. N. Z. Soc. Anim. Prod. 61, 3134. Google Scholar
Song, Y.P., Suquet, M., Quéau, I., Lebrun, L., 2009, Setting of a procedure for experimental fertilization of Pacific oyster (Crassostrea gigas) oocytes. Aquaculture 287, 311314. CrossRefGoogle Scholar
Wada, S.K., 1963, Studies on the fertilization of Pelecypod gamete. Increase in maturity and accomplishment of fertilization of pearl oyster gametes in ammoniacal sea water. Mem. Fac. Fish. Kagoshima Univ. 12, 92108. Google Scholar
Yankson, K., Moyse, J., 1991, Cryopreservation of the spermatozoa of Crassostrea tulipa and three other oysters. Aquaculture 97, 259267. CrossRefGoogle Scholar