The use of two staining methods for identification of spermatozoon structure in roosters.

Many of the methods used to stain semen result in very pronounced coloring of the sperm, but unfortunately they do not distinguish their individual structures, which play a key role in the fertilization process. Hence the aim of this study was to identify sperm structures using two staining techniques in the semen of roosters from breeding flocks. The subject of the study was the sperm of roosters from a Ross 308 breeding flock. To capture the differences in the dimensions of sperm subjected to the effect of different chemical substances in dyes, microscope slides were stained by two techniques: with an AgNO3 solution and by a differential method (eosin-nigrosin test). Assessment was made of the degree of coloration and the number of details that could be identified in the morphological structure of the sperm. The use of AgNO3 allowed accurate identification of the acrosome, nucleus, and midpiece, which were visible in the slides stained with eosin-nigrosin, but only in dead spermatozoa. The AGNO3 staining technique used in this study reveals the cell nucleus within the head and can be an alternative method to analysis with a scanning electron microscope. This staining technique can be used to stain sperm structures that cannot be seen in other methods of slide preparation, which means that it can be considered for routine use in assessing the fertility of roosters in breeder flocks.

Effect of sperm concentration in an ejaculate on morphometric traits of spermatozoa in Duroc boars.

The experimental material consisted of 75 ejaculates collected form 8 Duroc boars. The ejaculates were divided into three groups according to sperm concentration in an ejaculate. An ejaculate was obtained from each boar monthly and it was used to make microscopic preparations to examine spermatozoa morphology. In each preparation morphometric measurements were taken of fifteen randomly selected spermatozoa characterized by normal morphology. The following measurements of spermatozoa were taken: length and width of the spermatozoa head, head area, length of the flagellum, perimeter of the spermatozoon head and total spermatozoon length. The results were used to calculate indicators of spermatozoa morphology. Moreover, assessments were made of frequency of morphological defects to isolate spermatozoa with primary and secondary abnormalities following the Blom classification system. It was found that the concentration of spermatozoa in the ejaculate influenced the morphometric characteristics of spermatozoa. Ejaculates with low sperm concentrations are characterized by larger spermatozoa as compared to ejaculates with high sperm concentrations. However, sperm concentration in the ejaculate does not much influence the shape of spermatozoa.