Abnormal sperm morphology has long been the subject of research by many authors, as in many cases it is a significant factor limiting male fertility. Abnormal morphology can not only reduce the fertilising capacity of sperm, but also affect the development and maintenance of pregnancy (21, 34). Some sperm anomalies that have already been classified may have a genetic basis. These include the Dag defect, first discovered in Jersey bulls.
Sperm with the Dag defect have circular, coiled tails, which is caused by the loss of some of the axial fibres of the tail. The typical arrangement of the tail fibres is disturbed within the coil and is characterised by the lack of 3–5 of them, which are located outside the tail but still within the cell membrane. This defect, referred to in the literature as ‘tight coiling’, ‘tightly coiled Dag’ or a ‘Dag-like defect’, besides coiling present as pronounced folding and fracture of the distal part of the sperm midpiece, sometimes with a distal cytoplasmic droplet (7). Oettlé (30) indicated that sperm with the Dag defect may have a tail coiled to varying degrees without an intact plasma membrane. These coils can be very loose or very tight, or the tail can even surround the sperm head (30). Abnormal axonemes are also typical of this defect. They are recognised by the loss of fibrils and the presence of loose fibrils within the cytoplasmic material (30). The Dag defect is very common in the spermatozoa of bulls, with more than 65% showing this defect in an Indian investigation (37). The authors of that research also found acrosome abnormalities in over 75% of sperm cells, which may confirm the genetic basis of both these types of abnormality. This defect is inherited due to an autosomal recessive factor and arises in the distal part of the epididymal caput (7). Ribeiro and Vale (33) suggest that inbreeding significantly determines the occurrence of this defect in buffalo sperm.
As the Dag defect probably has a genetic basis, and there has as yet been relatively little research on this subject, it is worth considering whether sperm with this anomaly have normal head morphometry. Domestic pigs are a species in which artificial insemination is used intensively. When young breeders are diagnosed early, losses can be limited by replacing a boar with poor reproductive performance and ascertained reduced sperm quality with another male, as boars with fertility problems in a nucleus herd can reduce litter sizes (29). Therefore, the aim of the study was to assess the morphometry of the heads of normal sperm and sperm with the Dag defect in the semen of Duroc breeding boars.
The study was carried out in strict compliance with the recommendations in Directive 63/2010/EU on the protection of animals used for scientific or educational purposes and was approved by the Polish Second Local Ethics Committee in Warsaw (number 51/2015). The study was carried out on 12 Duroc boars used at an animal insemination station. The average age of the animals on the day of sample collection was 310.66 ± 29.94 days and the boars were in the age range of 7 to 26 months. For the first 1.5 years of use, an ejaculate sample was collected each month from each boar to examine sperm morphology. Ten ejaculates were obtained for analysis from each boar manually at about 6 a.m. The semen was kept at room temperature until examination of morphometry, for which it was prepared on slides within 15–20 min of collection. The eosin and gentian violet staining method was used, and smears were prepared for it by carefully dragging a drop of fresh semen across a degreased microscope slide heated to 37°C (25). The slides were allowed to air dry for a minimum of 2 h, and were then preserved in a 96% ethanol solution for 5 min and then stained with a 10% aqueous solution of eosin for 20–60 s. The stained slides were washed in distilled water and stained with gentian violet for 3–5 min, after which they were gently rinsed with distilled water for 2 min to remove debris and then dried. This ensured a clean background, and thus a good contrast against the stained spermatozoa. All reagents used were purchased from Sigma-Aldrich Chemie (Taufkirchen, Germany). Morphometric assessment was performed for 30 well-formed sperm per slide (Fig. 1A) showing no visible defects and all sperm diagnosed with the Dag defect (Fig. 1B).
In total, 3,600 morphologically normal sperm and 838 sperm with the Dag defect were evaluated. The area, perimeter, length and width of the sperm head were measured, and these basic morphometric parameters were used to calculate four additional shape indices characterising the sperm head, i.e. ellipticity, elongation, roughness and regularity using the formulae given in Table 1.
Formulae used to calculate sperm head morphometric measurements
Variable | Formula |
---|---|
Head length (μm) | L |
Head width (μm) | W |
Head perimeter (μm) | P |
Head area (μm2) | A |
Head ellipticity | L/W |
Head elongation | (L−W)/(L+W) |
Head roughness | 4π(A/P2) |
Head regularity | π(L×W/4×A) |
These parameters more precisely characterise the shape of the sperm head. Evaluations of morphometric measurements of the sperm head were performed using the MultiScan image analysis system for information extraction from slide photographs (Computer Scanning Systems, Warsaw, Poland) connected to an Olympus BX50 light microscope (Tokyo, Japan) at 1000 × magnification through a 100 × oil immersion objective and a Jenoptik ProgRes camera (Jena, Germany).
The morphometric measurements of the spermatozoa were stored in a database and exported for further statistical analysis. Statistical differences between the samples were tested using Tukey’s test (Statistica version 10.0, StatSoft Inc., Tulsa, OK, USA) and the level of significance was set at P ≤ 0.05.
Fig. 2 shows the changes in the frequency of sperm with the Dag defect in the semen of the Duroc boars. The data indicate that defective sperm are found in the semen of boars irrespective of their age. In the semen of young males just beginning to be used for breeding, the incidence of sperm with the Dag defect did not exceed 0.2%. An increase in the incidence of sperm with this defect was observed in the semen of older boars aged 17–18 and 21–22 months. However, the percentage of sperm with the Dag defect did not exceed 0.42% at any age.
Table 2 presents the morphometric dimensions of the heads of sperm with normal morphological structure and sperm with the Dag defect. Sperm with this defect had markedly smaller heads. The heads of such sperm were 0.32 μm shorter and 0.19 μm narrower than the heads of sperm with normal tails (P ≤ 0.05). The heads of sperm with the Dag defect also had a 1.1μm smaller perimeter and a 2.5 μm2 smaller surface area than the heads of morphologically normal sperm (P ≤ 0.05).
Morphometric parameters of boar sperm measured manually with MultiScan software
Morphometric parameter | Sperm with normal structure | Sperm with Dag defect |
---|---|---|
Head length (μm) | 8.29a ± 0.33 | 7.97b ± 0.32 |
Head width (μm) | 4.26a ± 0.19 | 4.07b ± 0.18 |
Head perimeter (μm) | 23.39a ± 0.98 | 22.29b ± 0.64 |
Head area (μm2) | 27.79a ± 1.17 | 25.29b ± 0.95 |
Different superscript letters designate significant differences between means within rows at P ≤ 0.05
Table 3 presents indices that derive from the standard sperm head dimensions (length, width, perimeter and surface area) to which Tygerberg strict criteria were applied for a more precise analysis of the shape of the sperm head. The data indicate that the heads of sperm with normal structure had a lower ellipticity index than the heads of sperm with the Dag defect. Ellipticity indicates the degree to which the sperm heads are oval, narrow or conical. There were no differences in elongation, which indicates the roundness of the sperm head. Roughness, which specifies the regularity or amorphous shape of the sperm head, was higher for the heads of sperm with the Dag defect than for the heads of normal sperm (P ≤ 0.05). Regularity indicates the symmetry of the sperm head and the degree to which it is pyriform. The regularity index was 0.02 higher for the heads of sperm with the Dag defect than for the heads of normal sperm (P ≤ 0.05).
Sperm head morphology according to Tygerberg strict criteria in boar sperm
Morphometric parameter | Sperm with normal structure | Sperm with Dag defect |
---|---|---|
Ellipticity | 1.95a ± 0.13 | 1.96a ± 0.14 |
Elongation | 0.32a ± 0.02 | 0.32a ± 0.03 |
Roughness | 0.63a ± 0.04 | 0.64b ± 0.02 |
Regularity | 0.99a ± 0.02 | 1.01b ± 0.03 |
Different superscript letters designate significant differences between means within rows at P ≤ 0.05
According to Barth and Oko (5), Dag defect frequency of up to 4% may indicate testicular and epididymal dysfunction. When the percentage of this defect exceeds 50%, it can have serious consequences involving reduced fertility (5). Research conducted on human material has shown a tendency for coiling sperm to occur in the semen of infertile men (43). However, according to the authors, sperm coiling was not dependent on sperm quantity or hormonal status, but may have been associated with qualitative semen characteristics, a hostile endogenous milieu, and an unknown suboptimal epididymal environment. While certain morphological defects occurring in greater quantities in sperm, such as distal cytoplasmic droplets, do not result in reduced fertility, other abnormalities (e.g. decapitated spermatozoa, the knobbed acrosome defect, nuclear vacuoles, short tails, the Dag defect, or corkscrewed midpieces) are considered serious defects that can impede fertilisation and cause infertility (35). Prochowska
The Dag defect is associated with elevated zinc levels, disturbance in the testicles and/or epididymis, and fever (8). Boar sperm defects involving coiled tails were found to be caused during the passage of sperm from the distal caput to the proximal corpus epididymis, and there was a correlation between the onset of tail-bending and the migration of the cytoplasmic droplet (20). Research by Zheng
Thus far, studies on semen have shown that the morphology of sperm within one ejaculate is highly heterogeneous. Sperm differ in size and shape, while exhibiting normal morphological structure (2, 4, 12). Research by Mandawala
The present study also attempts to analyse the occurrence of sperm with the Dag defect in boar semen by the age of the donor animal, because semen morphology and sperm shape and dimensions change through the reproductive life of the boar (1, 25, 39). Studies by many authors indicate better reproductive results in older boars aged 19–30 months (14, 24) or 30–36 months (22). The present authors (1) showed that as boars age, the percentage of sperm with abnormal morphological structure decreases. Semen collected from the youngest breeders (up to about nine months old) may contain many more sperm with morphological anomalies than the semen of more mature boars over the age of one year. Furthermore, in the semen of young Duroc boars under the age of nine months, the authors found that more than 5% of sperm had heads with major morphological defects, and that their frequency was determined by the high proportion of sperm with proximal protoplasmic droplets on the midpiece. There are studies indicating that the presence of cytoplasmic droplets on the sperm midpiece may be linked to chromatin instability (41) and abnormal sperm head dimensions (15), because the head, neck, midpiece and tail develop simultaneously during spermiogenesis (16). Banaszewska
Varying percentages of sperm with the Dag defect are found in the semen of Duroc boars. Given the origins of this defect and its likely genetic basis, as well as its fairly high frequency in the semen of males of various species, more in-depth analysis seems justified. Moreover, because differences in the head shapes of normal sperm and those with the Dag defect indicate the likelihood of changes not only where the defect was identified, i.e. the midpiece and tail, but also perhaps in the ultrastructure of the head and organisation of chromatin structure (condensation), these potential relationships should also be investigated in further research. In the case of boars intended for breeding, it is important to determine the reproductive performance of males before they join the breeding herd. Ascertainment of a boar’s performance is important because although semen quality improves with the age of the boar, some individuals may have a predisposition to produce sperm with defects, which may result in a long-term reduction in fertilisation capacity or in the death of the embryo at earlier stages of development.