Age related changes in laying pattern and egg weight of different laying hen genotypes.

The aim of the study was to evaluate changes in laying patterns depending on the age of different genotypes of laying hens. In the experiment, six genotypes were evaluated (brown-egg hens Bovans Brown, Bovans Sperwer and Isa Sussex, white-egg hens Dekalb White, and laying hens with tinted shells Moravia Barred and Moravia BSL) in three periods during the laying cycle (the onset of lay between 20 and 26 weeks of age, the middle from 36 to 42 weeks of age and the end of lay between 64 and 70 weeks of age). A significant interaction between genotype and age was apparent in mean sequence length (P<0.001), length of the prime sequence (P<0.001), mean number of sequences (P<0.001) and mean time of oviposition (P˂0.001). The longest lag during the course of the experiment was with Moravia BSL, which was more than 3h; the shortest lag was observed in Bovans Brown, which was less than 1h. The mean time of oviposition was also affected by genotype (P˂0.001). Bovans Brown laid their eggs approximately 3.5h after the lights came on, whereas Moravia BSL laid their eggs almost 6h after the lights came on. Egg weight increased with age (P˂0.001), and the smallest differences in egg weight were with ISA Sussex (5g), whereas the biggest differences were with Moravia BSL (10g).

Energy Status Characteristics of Porcine Oocytes During In Vitro Maturation is Influenced by Their Meiotic Competence.

The characteristics of energy status in porcine oocytes as related to their meiotic competence and in vitro maturation were studied. Cycling pubertal gilts in the early luteal to early follicular phases of the ovarian cycle were used as oocyte donors. The oocytes recovered from medium (MF) or small follicles (SF) were considered meiotically more or less competent, respectively. A half of oocytes from each category was matured by the standard protocol. The oocytes were examined before or after maturation by confocal microscopy, a bioluminescent cell assay and Western blotting. Four experiments, each in triplicate, were performed to assess both SF and MF oocytes in terms of metabolic units formed by mitochondria and lipids, ATP and lipid consumption and lipid droplets with adipose differentiation-related protein (ADRP) expression. The proportion of oocytes with metabolic units, the mean ATP content and the number of lipid droplets per oocyte, and the relative number of lipid droplets with ADRP expression were significantly higher in the MF compared to SF oocytes before maturation. On the other hand, after maturation, there was an increase in the proportion of oocytes with metabolic units and the relative number of lipid droplets with ADRP expression in the SF compared to MF oocytes. In conclusion, specific differences in energy characteristics between porcine oocytes with different meiotic competence were found. Meiotically more competent oocytes are more advanced in terms of energy reserves before maturation, while meiotically less competent oocytes are more active in replenishing energy stores during maturation.

Evaluation of shape variability of stallion sperm heads by means of image analysis and Fourier descriptors.

This study quantified and evaluated the variability of sperm head shape for 10 different stallions. Sperm head shape characteristics including sperm head length to width ratio, position of the center of gravity, curvature, and degree of roundness were assessed and analysed from images using elliptic Fourier descriptors and inverse Fourier transformation. The first four principal components accounted for 88.46-92.33% of the total variance and provided a good summary of the overall data. In the case of the ejaculate with defective sperm heads the components accounted for 97.35-98.21% of variation. The study was able to quantitatively confirm that head length to width ratio, which contributed 48.63-53.48% and 71.30-73.34% to the total variance for normal and defective sperm, respectively, was the predominant determining parameter of sperm head shape. There were no statistical significant relationships between Fourier descriptors and values of sperm concentration and/or motility.

Evaluation of chromatin integrity of motile bovine spermatozoa capacitated in vitro.

The efficiency of in vitro embryo production is highly variable amongst individual sires in cattle. To eliminate that this variability is not caused by sperm chromatin damage caused by separation or capacitacion, chromatin integrity was evaluated. Seventeen of AI bulls with good NRRs but variable embryo production efficiency were used. For each bull, motile spermatozoa were separated on a Percoll gradient, resuspended in IVF-TALP medium and capacitated with or incubated without heparin for 6 h. Samples before and after separation and after 3-h and 6-h capacitacion or incubation were evaluated by the Sperm Chromatin Structure Assay (SCSA) and the proportion of sperm with intact chromatin structure was calculated. Based on changes in the non-DFI-sperm proportion, the sires were categorized as DNA-unstable (DNA-us), DNA-stable (DNA-s) and DNA-most stable (DNA-ms) bulls (n=3, n=5 and n=9, respectively). In DNA-us bulls, separation produced a significant increase of the mean non-DFI-sperm proportion (p

Immunochemical studies on xanthine dehydrogenase of soybean root nodules : Ontogenic changes in the level of enzyme and immunocytochemical localization.

Xanthine dehydrogenase (XDH, EC 1.2.1.37) was purified from root nodules of soybean (Glycine max) and used to prepare a polyclonal rabbit antiserum. Monospecificity of this antiserum was ascertained by sodium dodecyl sulfate-polyacrylamide gel electrophoresis of the immunoprecipate. During root nodule development of soybean, only one form of XDH was detected on an immunological basis. Titration of XDH by immunoelectrophoresis showed that a remarkable increase in the amount of XDH occurred between two and four weeks after inoculation, in parallel with the increase in enzyme activity. Localization of XDH by immunofluorescence indicated that the enzyme was present exclusively in uninfected cells where it appeared to be associated with discrete organellels.