CRYOPRESERVATION OF SPERM OF RED ABALONE (HALIOTIS RUFESCENS)

Abstract Abalone culture, a developing industry in Baja California, Mexico, would benefit from genetic improvement and controlled breeding. The use of cryopreserved sperm would allow germplasm availability, and this study was designed to develop sperm cryopreservation protocols for red abalone Haliotis rufescens. The acute toxic effects of the cryoprotectants dimethyl sulfoxide (DMSO), propylene glycol (PG), and glycerol (GLY) were assessed after suspending sperm in different concentrations, whereby cryoprotectant treatments of 10% DMSO and 10% GLY equilibrated for 10 min yielded the highest range of motile sperm in preliminary freezing trials and were used for cryopreservation studies. To determine effective cooling rates, three freezing chambers were tested. Replicate samples of sperm from 4 males were placed in 0.5-mL French straws and frozen using a commercial freezing chamber (CFC) used for bull sperm, a programmable rate chamber (PRC), and a manually controlled styrofoam chamber (MCC). For the CFC, the cooling rate was 16°C/min, from 4°C to −140°C. For the PRC and MCC, it was 1°C/min, from −20°C to −30°C. The samples were held at −30°C for 5 min before being plunged into liquid nitrogen (−196°C) for storage, and each sample was thawed in a water bath at 45°C for 8 s. The quality of thawed sperm was determined by estimating percent motility, evaluating membrane integrity using a dual-staining technique and flow cytometry, and estimating fertilization rate. Statistical analyses were performed using 2-way ANOVA where chamber and treatment were the independent variables. Sperm quality parameters were independent. For motilities, a significant interaction was noted between the cryoprotective treatment and the chamber type, whereby motilities for DMSO and GLY were higher (P = 0.0055) using MCC. Membrane integrities were significantly lower after using the PRC than the CFC or the MCC (P = 0.0167). The highest post-thaw motility (48 ± 7%) was found using sperm suspended in 10% glycerol and frozen in the MCC. The highest percent of intact membranes (56 ± 11%) was for sperm suspended in 10% glycerol and frozen in the CFC. The highest fertilization rate (29 ± 10%) was with samples frozen with 10% glycerol in the CFC. The use of cryopreserved sperm from red abalone provides an alternative breeding option for culture and the protocols delineated are the first developed for this species.

[1]  F. Lahnsteiner,et al.  Frozen preservation of eggs and embryos of fish , 2004 .

[2]  M. Lezcano,et al.  The use of flow cytometry in the evaluation of cell viability of cryopreserved sperm of the marine shrimp (Litopenaeus vannamei). , 2004, Cryobiology.

[3]  J. Lebel,et al.  Influence of cryoprotective agent and cooling rate on frozen and thawed hemocytes from the Mollusk Haliotis tuberculata. , 2003, Cryobiology.

[4]  P. Mladenov,et al.  Flow cytometric evaluation of mitochondrial function and membrane integrity of marine invertebrate sperm , 2003 .

[5]  Terrence R. Tiersch,et al.  The Use of Dairy Protocols for Sperm Cryopreservation of Blue Catfish Ictalurus furcatus , 2003 .

[6]  J. Gwo,et al.  Semen cryopreservation of small abalone (Haliotis diversicolor supertexa). , 2002, Theriogenology.

[7]  T. Tiersch,et al.  Laboratory studies of cryopreservation of sperm and trochophore larvae of the eastern oyster. , 2001, Cryobiology.

[8]  E. Cabrita,et al.  The use of flow cytometry to assess membrane stability in fresh and cryopreserved trout spermatozoa. , 2001, Cryo letters.

[9]  T. Tiersch,et al.  Flow cytometric evaluation of antibiotic effects on viability and mitochondrial function of refrigerated spermatozoa of Nile tilapia. , 2000, Theriogenology.

[10]  朱明远,et al.  九孔鲍(Haliotis diversicolor)对饵料选择性的研究 , 1999 .

[11]  C. Paniagua-Chávez Cryopreservation of Gametes and Larvae of the Eastern Oyster Crassostrea Virginica. , 1999 .

[12]  D. Kerboeuf,et al.  Flow Cytometric Evaluation of Mitochondrial Activity and Membrane Integrity in Fresh and Cryopreserved Rainbow Trout (Oncorhynchus mykiss) Spermatozoa , 1997 .

[13]  Clark,et al.  彩虹鲍(Haliotis iris)的水解酶 , 1997 .

[14]  R. Yanagimachi,et al.  Fertilization and development of mouse oocytes injected with isolated sperm heads. , 1996, Biology of reproduction.

[15]  H. Tsai,et al.  Cryopreservation of Small Abalone (Haliotis diversicolor) Sperm-Technique and Its Significance , 1994 .

[16]  F. Schildberg,et al.  Temperature Gradients in Freezing Chambers of Rate-Controlled Cooling Machines , 1993 .

[17]  S. Drokin Phospholipids and fatty acids of phospholipids of sperm from several freshwater and marine species of fish , 1993 .

[18]  H. Kurokura,et al.  Lesions of spermatozoa by cryopreservation in oyster Crassostrea gigas , 1990 .

[19]  J. Piironen Factors affecting fertilization rate with cryopreserved sperm of whitefish (Coregonus muksun Pallas) , 1987 .

[20]  V. Vacquier,et al.  Regulation of abalone sperm cyclic AMP concentrations and the acrosome reaction by calcium and methylxanthines. , 1983, Developmental biology.

[21]  W. Holtz,et al.  Cryopreservation of rainbow trout (Salmo gairdneri) sperm: III. Effect of proteins in the diluent, sperm from different males and interval between sperm collection and freezing , 1983 .

[22]  H. Stein,et al.  Cryopreservation of the sperm of some freshwater teleosts , 1978 .