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PubMed2002

Influence of boar and semen parameters on motility and acrosome integrity in liquid boar semen stored for five days.

Ninety ejaculates from a total of 76 AI boars were extended in Beltsville Thawing Solution (BTS). Boar identity, breed, weight of the ejaculate and sperm concentration were registered. Motility and acrosome integrity were assessed after storage at 16-18 degrees C for 6, 30, 54, 78, and 102 h. Storage time had a significant influence on both motility (p < 0.01) and acrosome integrity (p < 0.001). The Least Square Means for percentage of motility showed a small decline from 79.8% after 6 h of storage to 78.4% at 102 h. Motility at 78 and 102 h was significantly different from motility at 6 h (p < 0.05). The percentage of sperm cells with normal acrosomes declined throughout the experiment. The Least Square Means for 6, 30, 54, 78, and 102 h of storage were 93.9%, 90.6%, 88.0%, 84.8%, and 78.2%, respectively. The decrease in acrosome integrity from one storage time to the next was highly significant throughout the trial (p < 0.001). There was a significant influence of boar (p < 0.001) and sperm concentration (p < 0.01) on motility, while acrosome integrity was affected only by boar (p < 0.001). Breed of the boars and weight of the ejaculate did not influence the dependent variables.

Acrosome↗
PubMedDate not supplied

Classical swine fever virus: clinical, virological, serological and hematological findings after infection of domestic pigs and wild boars with the field isolate "Spante" originating from wild boar.

A classical swine fever virus (CSFV) field isolate originating from wild boar was investigated on its virulence in domestic pigs and wild boar. Three weaner pigs and two wild boars (yearlings) were intranasally inoculated with the isolate "Spante" and tested for clinical, virological, hematological and serological findings until day 31 after infection (p. i.). One day p. i. the piglets were put in contact to three sentinel pigs. During a period of 31 d neither the domestic pigs nor the wild boars showed clinical signs specific for CSF. Two infected weaner pigs became transiently viraemic, transmitted CSFV in nasal secretions, showed a slight leukopenia and reacted serologically positive. The contact infection resulted in a viraemia in two sentinel piglets on day 30. Only one contact animal developed antibodies. None of the wild boars became viraemic, excreted CSFV in nasal secretions or developed antibodies. The CSFV isolate "Spante" represents a low virulent virus. Referring to a significant higher percentage of virologically positive tissue samples after nested PCR compared with the virus isolation, persistence of CSFV is discussed.

Animals↗
PubMed1975

[Effect of the standard of hygiene in the care for breeding boars and of the technic of semen collection on the number of pathogens in the boar ejaculate].

The microbiological examination of 48 ejaculates obtained by an artificial vagina revealed an average number of 178 000 germs per 1 ml of semen (1900 - 758 000). When the technique was changed, the manual method being employed, 23 ejaculates were obtained from the same boars and the microbiological examination revealed 44 200 germs per 1 ml of semen, on an average. In the second part of the trial 85 ejaculates obtained by an artificial vagina from 17 breeding boars were subject to microbiological examination. The average number of germs found in this case was 99 377 (10 000 - 400 000). When boar body was washed with water or with water and soap and rubbed with a sterile cloth, prior to each collection, the number of germs per 1 ml of semen decreased to 6071 (0 - 40 000). The reduction of the number of germs in the ejaculate of washed boars is statistically highly significant, as compared with semen collection from boars without washing. The number of fungus-bearing ejaculates decreased from the original 39.9% to 9.3%.

Animals↗
PubMed1986

Biochemical studies on proacrosin and acrosin from epididymal boar spermatozoa: in vitro translation of boar testicular proacrosin mRNA.

An inactive form of acrosin was extracted from epididymal boar spermatozoa utilizing acid pH conditions. When subjected to activation in alkaline environment, this form turns into an enzymatically active species, which exhibits close-related electrophoretic characteristics. Both the precursor and the activated species, when incubated in the presence of thermolysin, give rise to two fastly moving acrosin molecular forms. In order to establish the nature of the true acrosin zymogen, we isolated poly(A+)-RNA from boar testicles, performed its translation in vitro in the presence of [35S]-methionine and reticulocyte lysate, immunoprecipitated the translation products with anti-boar acrosin antibody, and analyzed them by SDS-polyacrylamide gel electrophoresis and autoradiography. A single translation product of molecular weight 55,000 was detected. It is concluded that the polypeptide chain of the boar zymogen is of 55,000; increases in molecular weight are due to post-translational modifications, like glycosylation.

Acrosin↗
PubMed1984

The effect of pseudorabies (Aujeszky's) virus infection on young mature boars and boar fertility.

This study was designed to determine the effects of experimental inoculation with pseudorabies virus on the reproductive tracts of young adult boars. Pseudorabies virus was inoculated intranasally into 12 boars and intrapreputially into four boars. All animals seroconverted after nasal or preputial inoculation. Semen abnormalities were observed 21 days postinoculation with partial recovery by 50 days postinoculation. Virus was isolated from the preputial sheath of two intrapreputially inoculated boars 12 days postinoculation. It was concluded that pseudorabies virus infection can be established via preputial inoculation and that decreased spermatogenesis and infertility can result.

Animals↗
PubMed1977

Antigens on boar spermatozoa and the effect of antibodies against the spermatozoa and the accessory sexual gland fluids on boar spermatozoa.

Antigens on the acrosomes of boar spermatozoa could be detected by the anti-complement immunofluorescence test, using antisera against spermatozoa and against seminal vesicle and epididymis fluids. Weak fluorescence was observed even on the tail and no fluorescence in the postnuclear segment. Adequate absorption of the complement allowed the sperm-immobilizing test to be used with boar spermatozoa. Using this test, the specificity of the sperm-immobilizing effect on antispermatozoal antibodies was confirmed. The sperm-immobilizing effect and damage to the acrosomes was prevented by absorption of the sera with spermatozoa. Antibodies against the fluid of the boar prostate did not react with antigens on boar spermatozoa.

Agglutination Tests↗
PubMedDate not supplied

[A.I. in pigs: influence of boar seminal plasma on breeding efficiency of diluted boar semen (author's transl)].

Ejaculates from six boars of Danish Landrace were divided into four parts, I, II, III and IV which were treated in the following way: I was diluted 1:4-1:6 with EDTA-diluter, and filled into glass vials (single doses). II was centrifugated at 1800-2000 r.p.m. in 12-15 min.; the centifugate was resuspended in the supernatant and diluted as indicated under I. III and IV were centrifugated at 1800-2000 r.p.m. in 12-15 min. The supernatant was removed by aspiration and the centrifugate diluted with as much EDTA-diluter necessary to produce the same no, of doses of 10 ml as was produced from I and II respectively. The diluted semen was stored at 18-20 degrees C and used on the day of collection. Just before insemination the semen from I, II and III was diluted with IVT-diluter to a final volume of 75 ml. Semen from IV was diluted to the same volume with IVT-diluter with the addition of 50% boar seminal plasma, procured by centrifugation of ejaculates from other boars of the A.I. Centre, and stored at divided by 20 degrees C until use. The results have been set out in Table I. Inseminations with semen from I and II resulted in pregnancy rates of 84,6% and 86,3% and average litter sizes of 10,3 and 10,1 for sows and 9,1 and 9,6 for gilts; inseminations with semen from III and IV resulted in pregnancy rates of 78,9 and 78,2% and average litter sizes of 10,5 and 10,7 for sows and 10,0 and 8,7 for gilts. None of the differences in pregnancy rates between groups were significant. The findings were: 1. By insemination with initially diluted semen without seminal plasma a tendency to a decline in pregnancy rates could be demonstrated. 2. The decline persisted after the addition of 50% boar seminal plasma to the diluter used for the final dilution just before insemination.

Animals↗
PubMed1996

Lectin histochemistry during in vitro capacitation and acrosome reaction in boar spermatozoa: new lectins for evaluating acrosomal status of boar spermatozoa.

Six peroxidase (HRP)-conjugated lectins have been used to analyze the distribution of carbohydrates in ejaculated boar spermatozoa during in vitro capacitation and acrosome reaction in air-dried preparations. The membranes of boar spermatozoa were positive to WGA and Con-A in the acrosome, middle piece and principal piece. PNA labelled the acrosomal region. DBA, UEA-I and LTA bound weakly or not to the spermatozoa. The lectin labelling pattern did not change during the in vitro capacitation. A diminution in the proportion of spermatozoa with acrosome positive to lectins PNA, WGA and Con-A was observed after coincubation with homologous immature oocytes. A positive correlation existed between the percentages of lectins bound to spermatozoa and the triple stain technique. The results show that peroxidase-conjugated lectins may be useful in determining acrosomal integrity of boar spermatozoa during in vitro capacitation and acrosome reaction.

Acrosome↗
PubMed1976

Influence of boar acrosin antibodies produced in rabbit and sheep on chymotrypsinogen activation catalyzed by acrosin from boar, bull, ram, rabbkt and human.

Activation of bovine chymotrypsinogen is catalyzed with increasing velocity by human, rabbit, boar, bull and ram acrosin. Antiboar-acrosin rabbit gamma-globulins cause a significant reduction in the proenzyme activation rate induced by boar and bull acrosin, but only a weak reduction or none if ram or rabbit acrosin is the activating agent. The antiboar-acrosin gamma-globulins from sheep strongly inhibit chymotrypsinogen activation by ram, bull and boar acrosin, and significantly inhibit the human acrosin-catalyzed reaction.

Acrosin↗
PubMed1979

Lipid changes in boar spermatozoa during epididymal maturation with some observations on the flow and composition of boar rete testis fluid.

The flow rate and composition of boar rete testis fluid were similar to those in other species studied previously. The total phospholipid phosphorus and phospholipid fatty acid content of boar spermatozoa decreased during maturation in the epididymis but the level of phospholipid phosphorus was slightly higher in ejaculated spermatozoa than in epididymal spermatozoa. During passage of the spermatozoa from the testis to the cauda epididymidis, loss of the major saturated acids (palmitic, 16:0, and stearic, 18:0) was extensive but partly recovered in the ejaculated spermatozoa. The mass of docosapentaenoic (22:5) and docosahexaenoic (22:6) acids tended to decrease continuously during maturation but the percentage of 22:6 by weight of total phospholipid fatty acid reached a maximum in the epididymis. Ejaculated boar spermatozoa contained considerably more phospholipid and phospholipid fatty acid than did ejaculated bull or ram spermatozoa.

Animals↗
PubMed2004

High resolution DNA flow cytometry of boar sperm cells in identification of boars carrying cytogenetic aberrations.

The cytogenetic quality of boars used for breeding determines the litter outcome and thus has large economical consequences. Traditionally, quality controls based on the examination of simple karyograms are time consuming and sometimes give uncertain results. As an alternative, the use of high-resolution DNA flow cytometry on DAPI-stained sperm cell nuclei (CV </= 1.3%) was investigated as a screening method for the cytogenetic quality of boars. By analyzing a series of 25 animals judged normal by their fertility statistics and a series of seven animals with known reciprocal translocations, a model for identifying sperm cells from cytogenetically aberrant animals was proposed. This model was applied to a series of 50 uncharacterized animals. The model successfully identified a mosaic or chimaeric carrier of an aberrant X chromosome. However, implementation of this technique for screening purposes would necessitate essential improvements in standardization and measurement precision.

Animals↗
PubMed1997

Inhibition of bacterial and boar epididymal sperm immunogenicity by boar seminal immunosuppressive component in mice.

Intravenous deposition of the immunosuppressive component, isolated from boar seminal vesicle secretion, led to suppression of primary and secondary antibody response to boar epididymal spermatozoa and to bacterial antigens. The most effective suppression of the immune response was achieved in female mice treated with immunosuppressive component 3 days before the immunization with antigen. The treatment with immunosuppressor 3 days after the immunization resulted in less effective immunosuppression. After the primary immunization, male mice displayed low sensitivity to epididymal spermatozoa. The production of IgG and IgM antibodies to spermatozoa was depressed for a relatively long period in female mice treated with immunosuppressor. The immunosuppressive components of the reproductive gland secretions may protect sperm cells from the adverse effect of the immune system cells and enhance the chance of conception. However, seminal immunosuppressive components may play an unfavourable role by producing a predisposition in the reproductive tract to bacterial or viral infections.

Animals↗
PubMed1982

Use of boar spermatozoa for artificial insemination. III. Fecundity of boar spermatozoa stored in Beltsville liquid and Kiev extenders for three days at 18 C.

A field trial was conducted on several hundred farms in The Netherlands to compare the fertilizing capacity of boar spermatozoa stored for 1, 2, or 3 d at 18 C in either Kiev or Beltsville liquid extender (BL-1). Two storage volumes (25 and 100 ml) were used. Twelve Dutch Landrace boars, all in routine commercial artificial insemination service, provided the semen in twice-a-week collections. Over an 8-wk period in March and April, 1979, 2,849 sows and gilts were inseminated. Farrowing rates were higher (P less than .0001) with Kiev extender than with BL-1 extender (69.3 vs 60.5%) when semen was used over a 3 d period. The volume at which the semen was extended and stored had no effect on any parameter. Farrowing rate declined significantly when semen stored at 18 C for more than 2 d was used (74.5% vs 64.7% with semen stored for 1 and 3 in Kiev extender; 65.9% vs 52.7% with semen stored for 1 and 3 d in BL-1 extender). The farrowing rate, total number of pigs/litter and live pigs/litter were significantly higher for sows than for gilts inseminated with similar extended semen. On the basis of the results of this trial, Kiev extender appears to be more suitable as a diluent for liquid semen than does BL-1. AI with semen extended and stored for 3 d at 18 C can be expected to result in a lower farrowing rate than AI with semen stored for 1 or 2 d.

Animals↗
PubMed1991

Cryopreservation of boar semen. II: Effect of cooling rate and duration of freezing point plateau on boar semen frozen in mini- and maxi-straws and plastic bags.

The post-thaw motility and the acrosome integrity of semen from 4 boars frozen with a programmable freezing machine, in mini (0.25 ml) and maxi (5 ml) plastic straws and in 10 x 5 cm Teflon FEP-plastic bags (0.12 mm thick, 5 ml), were compared. The freezing of the semen was monitored by way of thermo-couples placed in the straws and the bags. Three freezing programmes were used, namely A: from +5 degrees C, at a rate of 3 degrees C/min, to -6 degrees C, held for 1 min at -6 degrees C, and followed by a cooling rate of 20 degrees C/min to -100 degrees C; B: a similar curve except that there was no holding time at -6 degrees C and that the cooling rate was 30 degrees C/min, and C: from +5 degrees C to -100 degrees C, with a cooling rate of 35 degrees C/min, followed by storage in liquid N2. Despite the freezing curve assayed, both the mini-straws and the bags depicted much shorter freezing point plateaus as compared to the maxi-straws. Post-thaw sperm motility as well as the amount of normal apical ridges were equally significantly higher when semen was frozen in mini-straws or in bags than in maxi-straws. Significant differences in these post-thawing parameters were obtained between the freezing curves used. The stepwise freezing procedure A appeared as the best alternative for boar semen, considering this in vitro evaluation.

Acrosome↗
PubMed1979

[Quantifiable morphokinesis of parts of the hypothalamo-adenohypophyseal-gonadal axis of hormonally desexed boars. 4. Studies on boars that have undergone combined treatment with the steroid test substance 547 and norgestrel].

Steroid test substance 547 and Norgestrel were used in a combination treatment of parts of the hypothalamo-adenohypophyseo-gonadal axis of boars. The quantifiable parameters of the morphokinetic effect thus produced (cell nucleus volumes of Nucleus praeopticus medialis hypothalami and its neurons as well as those of Leydig's cells testicle weight, length and diameter of tube, percentage of Leydig's cells, testicle weight, length and diameter of tube, percentage of Leydig's cells) did not differ significantly from the findings obtained from boars treated with Norgestrel only (cf. Dorst and co-workder, 1978). The same combination treatment, however, differed from exclusive Norgestrel treatment by causing the occurrence of socalled castration cells, which led to the assumption of an anti-androgenic effect of such combination treatment.

Androstenes↗
PubMed1978

[Quantifiable morphokinesis in members of the hypothalamo-adenohypophyseogonadal axis of hormonally castrated boars. 2. Studies on norgestrel treated boars].

Norgestrel treatment of boars differed from analogous chloromandinone acetate treatment in that no significant morphokinetic effect was recordable from all parts of the hypothalamic-adenohypophyseal-gonadal axis. The morphometric parameters as well as the histological pattern obtained of the anterior lobe of the pituitary gland appear to prove that in boar the antigonadotropic effect of norgestrel is lower than that of chloromadinone acetate, with dosage and duration of treatment identical.

Animals↗
PubMed1980

[Investigations of the lysine requirement of fattening boars in dependence on their performance. 3. Influence of energy consumption on the fat and protein retention of the boars].

The results of the carcass analysis show a distinct influence of the duration of keeping on protein retention. The protein percentage was highest with those animals whose lysine requirement was met 100%. A lysine supplement of 20% of the valid norm had no infuence on the percental protein content. In both cases (100% and 120%) 17.1% protein were determined in the carcass. Concerning the daily protein retention, boars whose protein requirement wes met 120% and with a live weight of more than 90 kg achieved more favourable results than those of the norm variant. Up to 90 kg live weight no difference between the two variants could be detected. Animals which received feed rich in energy showed a very high daily protein retention during the first third of the fattening period, which decreased relatively much, however, in the course of growth.

Animals↗