PhD / The aim of this thesis was to investigate the possibility of integrating frozen-thawed boar semen into reproductive technologies and into commercial production of pigs in Australia. This was to be achieved by establishing a semen freezing and AI regime that was of a standard acceptable to industry, and integrating the resultant frozen-thawed sperm into other reproductive technologies, such as flow cytometric sperm sorting and IVF. Initially, a protocol for freezing and thawing boar semen was established, based on the method described by Westendorf et al. (1975) and attempts were made to modify this protocol to improve the post-thaw sperm quality, as determined by in vitro assessment of motility, acrosome integrity and longevity. First, the egg yolk used in the freezing extenders was investigated, and the chicken yolk was replaced with either duck or quail yolk. It was shown that there was no benefit in substituting yolk from duck or quail for the chicken yolk traditionally used in freezing extender. Second, the effect of seminal plasma addition to the freezing extender, or seminal plasma addition to resuspension medium post-thaw was tested. Incorporating whole seminal plasma into the freezing extender at levels above 50% was found to be detrimental to post-thaw sperm quality. Reducing levels to 20% of the final volume improved acrosome integrity, but adversely affected motility of sperm. However, adding 20% seminal plasma to the resuspension medium used after thawing of boar semen had no significant influence on sperm quality compared with resuspension in medium without seminal plasma. The antioxidant catalase, and the iron chelator desferal added to the freezing extender, did not improve post-thaw sperm quality, nor was any benefit seen with addition of these substrates to the resuspension medium post-thaw. However, the bioactive phospholipid PAF and its regulating enzyme PAF:AH appeared to enhance post-thaw motility and acrosome integrity of sperm, respectively, when added to the semen pre-freezing. Unfortunately, due to the restrictions imposed on rPAF:AH as a research drug, it was not possible to test the in vivo effects at this time. After the in vitro experiments were completed, the in vivo fertility of frozen-thawed sperm was tested using the optimal freezing protocol and a novel technology, enabling non-surgical deep intrauterine insemination of sows. The aim was to establish the lowest possible dose of frozen-thawed sperm that could be used, without compromising fertility. Successful pregnancies were achieved with doses as low as 62.5 x 106 frozen-thawed sperm but the farrowing rates were too low to be practicable on a commercial scale. This is the first report of litters born after insemination of such a low dose of frozen-thawed sperm and using the novel DIU insemination technique. However, it was concluded that a double dose of 250 x 106 frozen-thawed sperm was the minimum dose required for maintaining acceptable fertility. Reduction in sperm numbers to such an extent made it possible to consider non-surgical insemination of sex-sorted, frozen-thawed semen. Previously, pregnancies had been achieved only after surgical insemination of sex-sorted boar sperm, or with DIU insemination of unfrozen sperm, immediately after sex-sorting. The low numbers of sex-sorted sperm available restricted the inseminate dose used here to 50 x106 motile sperm. A litter of 5 piglets was born after a low-dose, DIU insemination of sex-sorted, frozen-thawed sperm. This is the first report of piglets born after insemination with sex-sorted frozen-thawed sperm and non-surgical insemination. The low farrowing rate achieved in this experiment prompted the investigation of integrating sex-sorted, frozen-thawed boar sperm into IVF. Morulae were produced after IVF with sex-sorted, frozen-thawed sperm and successfully transferred using non-surgical techniques. This is the first report of pregnancy achieved with non-surgical transfer of embryos produced after IVF and IVC of IVM oocytes with sex-sorted, frozen-thawed boar sperm. Unfortunately, the pregnancy did not hold, and the embryos were lost prior to Day 32, but PCR of non-transferred embryos confirmed successful pre-selection of sex. Overall, this thesis demonstrated that it is still not economically feasible to incorporate frozen-thawed boar semen into the commercial production of pigs although it has considerable application in breeding programmes. However, the development of novel techniques enabling reduction in sperm dose, and for non-surgical transfer of embryos into recipient sows and incorporation of frozen-thawed semen into these technologies means that progress is being made with the integration of reproductive technologies and frozen-thawed semen into the pig industry.

PhD / The aim of this thesis was to investigate the possibility of integrating frozen-thawed boar semen into reproductive technologies and into commercial production of pigs in Australia. This was to be achieved by establishing a semen freezing and AI regime that was of a standard acceptable to industry, and integrating the resultant frozen-thawed sperm into other reproductive technologies, such as flow cytometric sperm sorting and IVF. Initially, a protocol for freezing and thawing boar semen was established, based on the method described by Westendorf et al. (1975) and attempts were made to modify this protocol to improve the post-thaw sperm quality, as determined by in vitro assessment of motility, acrosome integrity and longevity. First, the egg yolk used in the freezing extenders was investigated, and the chicken yolk was replaced with either duck or quail yolk. It was shown that there was no benefit in substituting yolk from duck or quail for the chicken yolk traditionally used in freezing extender. Second, the effect of seminal plasma addition to the freezing extender, or seminal plasma addition to resuspension medium post-thaw was tested. Incorporating whole seminal plasma into the freezing extender at levels above 50% was found to be detrimental to post-thaw sperm quality. Reducing levels to 20% of the final volume improved acrosome integrity, but adversely affected motility of sperm. However, adding 20% seminal plasma to the resuspension medium used after thawing of boar semen had no significant influence on sperm quality compared with resuspension in medium without seminal plasma. The antioxidant catalase, and the iron chelator desferal added to the freezing extender, did not improve post-thaw sperm quality, nor was any benefit seen with addition of these substrates to the resuspension medium post-thaw. However, the bioactive phospholipid PAF and its regulating enzyme PAF:AH appeared to enhance post-thaw motility and acrosome integrity of sperm, respectively, when added to the semen pre-freezing. Unfortunately, due to the restrictions imposed on rPAF:AH as a research drug, it was not possible to test the in vivo effects at this time. After the in vitro experiments were completed, the in vivo fertility of frozen-thawed sperm was tested using the optimal freezing protocol and a novel technology, enabling non-surgical deep intrauterine insemination of sows. The aim was to establish the lowest possible dose of frozen-thawed sperm that could be used, without compromising fertility. Successful pregnancies were achieved with doses as low as 62.5 x 106 frozen-thawed sperm but the farrowing rates were too low to be practicable on a commercial scale. This is the first report of litters born after insemination of such a low dose of frozen-thawed sperm and using the novel DIU insemination technique. However, it was concluded that a double dose of 250 x 106 frozen-thawed sperm was the minimum dose required for maintaining acceptable fertility. Reduction in sperm numbers to such an extent made it possible to consider non-surgical insemination of sex-sorted, frozen-thawed semen. Previously, pregnancies had been achieved only after surgical insemination of sex-sorted boar sperm, or with DIU insemination of unfrozen sperm, immediately after sex-sorting. The low numbers of sex-sorted sperm available restricted the inseminate dose used here to 50 x106 motile sperm. A litter of 5 piglets was born after a low-dose, DIU insemination of sex-sorted, frozen-thawed sperm. This is the first report of piglets born after insemination with sex-sorted frozen-thawed sperm and non-surgical insemination. The low farrowing rate achieved in this experiment prompted the investigation of integrating sex-sorted, frozen-thawed boar sperm into IVF. Morulae were produced after IVF with sex-sorted, frozen-thawed sperm and successfully transferred using non-surgical techniques. This is the first report of pregnancy achieved with non-surgical transfer of embryos produced after IVF and IVC of IVM oocytes with sex-sorted, frozen-thawed boar sperm. Unfortunately, the pregnancy did not hold, and the embryos were lost prior to Day 32, but PCR of non-transferred embryos confirmed successful pre-selection of sex. Overall, this thesis demonstrated that it is still not economically feasible to incorporate frozen-thawed boar semen into the commercial production of pigs although it has considerable application in breeding programmes. However, the development of novel techniques enabling reduction in sperm dose, and for non-surgical transfer of embryos into recipient sows and incorporation of frozen-thawed semen into these technologies means that progress is being made with the integration of reproductive technologies and frozen-thawed semen into the pig industry.

En la siguiente tesis se obtuvieron los siguientes resultados. La adición de plasma seminal a los espermatozoides altamente diluidos ejerce un efecto beneficioso variable dependiendo de la fuente de plasma seminal. El heterodímero PSP-I/PSP-II ejerce un efecto beneficioso sobre los espermatozoides altamente diluidos mediante su adhesión al acrosoma. La incubación produce la migración del heterodímero a la región post-acrosomal, siendo eliminado de la superficie espermática. La adición del heterodímero a los medios de cocultivo entre gametos disminuye significativamente la capacidad fecundante de los espermatozoides. La preincubación de los espermatozoides de verraco tanto frescos como congelados preserva la viabilidad y motilidad espermáticas no afecta a la capacidad fecundante de los espermatozoides frescos de verraco y disminuye la capacidad fecundante de los espermatozoides congelados, la cual puede ser restaurada parcialmente mediante un lavado a través de un gradiente de Percoll. / The addition of 10% of seminal plasma from certain boars maintains or enhances the viability of largely extended boar spermatozoa in vitro. The protective effect of the PSP-I/PSP-II heterodimer on highly-extended boar spermatozoa could be related to the adhesion of the heterodimer to the acrosome. Exposures of the gametes to the heterodimer during in vitro gamete co-incubation significantly decrease the sperm penetration rates and number of spermatozoa per oocytes in denuded oocytes. The effect could be mediated by exposed ZP receptors. Exposure of fresh or frozen-thawed boar spermatozoa to PSP-I/PSP-II preserves sperm viability and motility. Although there is no obvious influence of the heterodimer on the capability of fresh diluted boar spermatozoa to penetrate homologous oocytes, PSP-I/II exerts a deleterious effect when frozen-thawed spermatozoa are used to penetrate IVM-oocytes. A subsequent washing through a Percoll gradient estored sperm function in some of the cells.

La separación espermática por citometría de flujo de los espermatozoides X e Y, es actualmente el único método eficaz para la obtención de descendencia de sexo deseado. En porcino, la selección del sexo de las camadas incrementaría notablemente los beneficios productivos de las explotaciones productoras de animales de alto valor genético al poder manejar los esquemas de selección, desviándolos hacia un sexo u otro según las necesidades de cada explotación. Recientemente, se han realizado avances importantes en la separación espermática mediante esta técnica en porcino. Sin embargo, es necesario un mayor conocimiento de diferentes aspectos relacionados con la eficiencia del proceso, con el efecto del procedimiento sobre la viabilidad y la capacidad fecundante de estos espermatozoides, así como del posible efecto perjudicial del propio proceso de separación sobre el ADN de los espermatozoides de verraco. Esta tesis recoge resultados derivados de experiencias destinadas a estudiar estos aspectos. / Flow cytometric sorting technology based on differential DNA content between X- and Y- spermatozoa is the only effective procedure for achieving offspring of the desired sex. In swine production the application of this method could improve significantly the productive benefits by planning the insemination to produce a specific sex. A detailed knowledge of aspects related to the efficiency of the sperm sorting technique and to aspects related with effects of sorting procedure on the viability and penetration ability of pig oocytes of flow sorted boar spermatozoa, and of the potential damaging effect of the procedure on sperm DNA is necessary to obtain optimal results. This thesis presents the results of experiences about, the usefulness and efficiency of this technology, followed by the analysis of sorted boar spermatozoa motility, viability, penetration ability. Results of mutagenic effect of Hoechst 33342 staining and sorting on sorted boar spermatozoa are also included.