Introduction
The use of sex-selected semen technology in the livestock industry offers many advantages for economic gains and increased selection pressure of high-producing animals (Butler et al., Reference Butler, Hutchinson, Cromie and Shalloo2014). However, its use has not become widespread, probably due to the high cost and decreased fertility of sex-sorted semen. The latter is due mainly to two factors, that is decreased number of spermatozoa per insemination dose and direct damage to sperm resulting from the sorting process (Frijters et al., Reference Frijters, Mullaart, Roelofs, van Hoorne, Moreno, Moreno and Merton2009; Carvalho et al., Reference Carvalho, Silva, Sartori and Dode2013). During sorting, sperm are exposed to harsh conditions including the laser light, high pressure and electric charges that may compromise sperm quality and viability (Seidel, Reference Seidel2007; Carvalho et al., Reference Carvalho, Sartori, Machado, Mourão and Dode2010). There is some evidence that the sorting process may damage sperm DNA (Boe-Hansen et al., Reference Boe-Hansen, Morris, Ersbøll, Greve and Christensen2005; Garcia-Herreros et al., Reference Garcia-Herreros, Carter, Villagómez, MacAulay, Rath, King and Lonergan2010; Zhao et al., Reference Zhao, Ren, Zhao, Cui, Hao, Wang, Du, Qin, Liu, Wang and Zhu2014) with the resulting decrease in embryo development rates when sexed semen was used for in vitro fertilization (IVF) (Morton et al., Reference Morton, Herrmann, Sieg, Struckmann, Maxwell, Rath, Evans, Lucas-Hahn, Niemann and Wrenzycki2007; Palma et al., Reference Palma, Olivier, Neumüller and Sinowatz2008). Therefore, it is plausible that the sorting process may also have an effect on sperm protamination and influence the fertility of sex-sorted semen.
Protamines are small cysteine-rich nuclear proteins that replace histones late in spermatogenesis and are responsible for the highly condensed nature and structural organization of chromatin in the sperm nucleus (Miller et al., Reference Miller, Brinkworth and Iles2010; Cree et al., Reference Cree, Balhorn and Brewer2011). The main role of protamines is preserving sperm DNA integrity, therefore defects in sperm protamination may compromise male fertility. In humans, a low protamine content was correlated with increased DNA fragmentation that, in turn, reduced sperm quality and fertility (Aoki et al., Reference Aoki, Liu and Carrell2005). In cattle (Bos indicus), sperm protamine content also displayed a positive correlation with DNA fragmentation (Fortes et al., Reference Fortes, Satake, Corbet, Corbet, Burns, Moore and Boe-Hansen2014) and a negative correlation with field fertility scores in breeding bulls (Dogan et al., Reference Dogan, Vargovic, Oliveira, Belser, Kaya, Moura, Sutovsky, Parrish, Topper and Memili2015). Additionally, heat stress conditions reduced bull sperm protamine content (Rahman et al., Reference Rahman, Vandaele, Rijsselaere, Maes, Hoogewijs, Frijters, Noordman, Granados, Dernelle, Shamsuddin, Parrish and Van Soom2011). However, while the influence of sperm protamination defects on IVF results has been widely studies in humans (Ni et al., Reference Ni, Spiess, Schuppe and Steger2016), there are no studies in cattle relating sperm protamine deficiency to in vitro embryo production (IVEP).
Protamine content has been assessed by fluorescence microscopy imaging of chromomycin A3 (CMA3)-stained sperm samples in both men (Marzeyeh Tavalaee et al., Reference Tavalaee, Razavi and Nasr-Esfahani2009) and bulls (Simões et al., Reference Simões, Feitosa, Mendes, Marques, Nicacio, de Barros, Visintin and Assumpção2009). Therefore, CMA3 identifies defective spermatozoa due to DNA packaging and indirectly evaluates protamine deficiency (Bianchi et al., Reference Bianchi, Manicardi, Bizzaro, Bianchi and Sakkas1993). This method has been optimized using flow cytometry (Tavalaee et al., Reference Tavalaee, Kiani, Arbabian, Deemeh and Esfahani2010; Fathi et al., Reference Fathi, Tavalaee, Kiani, Deemeh, Modaresi and Nasr-Esfahani2011), allowing the assessment of thousands of cells and therefore providing a more statistically significant analysis. The results of sperm protamine deficiency assessment using flow cytometry have been correlated with sperm DNA fragmentation in both men (Tavalaee et al., Reference Tavalaee, Razavi and Nasr-Esfahani2009; Fathi et al., Reference Fathi, Tavalaee, Kiani, Deemeh, Modaresi and Nasr-Esfahani2011) and bulls (Fortes et al., Reference Fortes, Satake, Corbet, Corbet, Burns, Moore and Boe-Hansen2014).
Therefore, the aims of this study were to evaluate whether the sex-sorting process induces defects in sperm protamination and, in turn, the potential consequences on IVEP results in cattle.
Materials and methods
Materials
All reagents used were from Sigma-Aldrich Chemical Co. (St. Louis, MO, USA), unless otherwise stated.
Experiment 1: Evaluation of protamine deficiency in sexed and unsexed semen
The rate of protamine deficiency was measured on sexed and unsexed sperm from each of two bulls (Bos indicus), performing four samples of frozen–thawed sperm, evaluated per each replicate. Protamine content was evaluated using CMA3 stain and flow cytometry as previously described for human sperm (Tavalaee et al., Reference Tavalaee, Kiani, Arbabian, Deemeh and Esfahani2010; Fathi et al., Reference Fathi, Tavalaee, Kiani, Deemeh, Modaresi and Nasr-Esfahani2011) with the modifications detailed below.
Purchased unsexed and sexed male sorted semen straws from two Nellore (Bos indicus) bulls, were thawed at 35°C and washed twice in Ca2+- and Mg2+-free phosphate-buffered saline (PBS) by centrifugation for 10 min at 200 g. Each pellet was resuspended in PBS and split into three aliquots, corresponding to each of the three groups: (i) negative control (untreated and CMA3 unstained); (ii) positive control, treated with the disulfide bridging agent dithiothreitol (DTT; 5 μM) and stained with CMA3; and, (iii) experimental groups of unsexed or sexed sperm stained with CMA3. Negative and positive controls were used to define the parameters of fluorescence detection in the flow cytometer.
DTT is a reducing agent that causes the disruption of protein disulfide bonds and therefore can decondense the sperm nucleus in vitro, making it more accessible to CMA3 staining. DTT was added to positive control samples that were washed twice by centrifugation at 600 g for 5 min and incubated in an equal volume with a 4 M NaCl solution for 15 min at 38.5°C to inactivate the effect of DTT. Positive control and experimental groups were then resuspended in 0.25 mg/ml CMA3 (10 mM MgCl2.6H2O) and incubated at room temperature for 40 min in the dark. Finally, samples were washed once in PBS by centrifugation at 600 g for 5 min and loaded in the flow cytometer.
Briefly, CMA3 dye is a complex of several closely related glycosidic antibiotics derived from Streptomyces griseus. CMA3 competes with protamines for binding sites at the minor grooves of the DNA strand. Therefore, CMA3 has been considered a suitable tool to evaluate protamine deficiency (Carrell, Reference Carrell2012).
Analyses were performed in a flow cytometer (BD FACSCanto II, Franklin Lakes, NJ, USA) using the blue excitation laser (488/15 nm), fluorescence detection filter PE (568/42 nm) and BD FACSuite™ software for data acquisition. For each sexed and unsexed sperm three straws were analyzed, with each replicate consisting of 20,000 cells per group.
Experiment 2: Relationship between sperm protamination and in vitro embryo development
Oocyte collection and in vitro maturation (IVM)
Cow ovaries were obtained at a local abattoir, washed in PBS and transported to the laboratory in 0.9% sodium chloride within 2 h of slaughter and the fluid from 2–8 mm antral follicles was aspirated. Only cumulus–oocyte complexes (COCs) with homogeneous cytoplasm, devoid of darkened vacuoles or granules, and presenting compact and refractive cumulus oophorus cells (Leibfried and First, Reference Leibfried and First1979) were selected for maturation and washed in tissue culture medium 199 (TCM199) HEPES buffer with 10% fetal bovine serum (FBS; Gibco BRL, Grand Island, NY, USA), 80 μg/ml pyruvate, 62.6 μg/ml penicillin and 50 μg/ml gentamicin.
Groups of 20–25 COCs were placed in 100-μl droplets of TCM199 with sodium bicarbonate and supplemented with 10% FBS (v/v), 0.5 μg/ml follicle stimulating hormone (Follitropin; Bioniche Animal Health, Belleville, Ontario, Canada), 50 μg/ml luteinizing hormone (LH; Lutropin; Bioniche Animal Health), 0.5 μg/ml EGF, 22 μg/ml pyruvate and 50 μg/ml gentamicin. Droplets were placed in 35-mm Petri dishes under sterile mineral oil for a 20 h incubation period under a 5% CO2, 20% O2 and 75% N2 in humidified air atmosphere, at 38.5°C.
In vitro fertilization and embryo culture (IVC)
IVF trials were performed with semen from sexed and unsexed sperm from the same two bulls used in Experiment 1, forming four experimental groups. One straw (250 μl) of semen from each bull was thawed in water at 35°C for 30 s. Thawed semen were carefully overlaid on an 800-μl Percoll column consisting of 400 μl 45% and 400 μl 90% Percoll, and centrifuged at 200 g for 7 min for washing. The pellet was recovered and washed again in 800 μl IVF-Tyrode’s albumin lactate pyruvate (Parrish et al., Reference Parrish, Susko-Parrish, Winer and First1988) medium supplemented with 10 μg/ml heparin, 2 μM penicillamine, 1 μM hypotaurine, 0.25 μM epinephrine and 6 mg/ml BSA, by centrifugation at 200 g for 3 min to remove the Percoll residues.
Sperm concentration was determined using a Neubauer chamber and adjusted to 2 × 106 spermatozoa/ml. Sperm were co-incubated with groups of 20–25 COCs in 80-μl droplets of fertilization medium under sterile mineral oil for 24 h. Presumptive zygotes were then subjected to successive pipetting to remove the remaining cumulus oophorus cells and spermatozoa adhered to the zona pellucida, and then transferred to the IVC dish.
Groups of 15–20 presumptive zygotes were co-incubated over a monolayer of granulosa cells in 100-μl droplets of synthetic oviductal fluid medium supplemented with 6 mg/ml BSA, 10% FBS and 50 μg/ml gentamicin (Holm et al., Reference Holm, Booth, Schmidt, Greve and Callesen1999), under sterile mineral oil. Incubation was performed in a 5% CO2, 20% O2 and 75% N2 atmosphere in humidified air at 38.5oC for 7 days. Rates of cleavage and blastocyst formation were evaluated on days 2 and 7 of culture, respectively. On day 7, embryos were also classified by development kinetics into blastocysts (BL), expanded blastocysts (BX), and hatched blastocysts (BH), and by morphological quality into grades 1, 2 or 3 based on Stringfellow and Seidel (Reference Stringfellow and Seidel1998).
Statistical analysis
Rates of CMA3-positive sperm and embryo development were analyzed by two-way analysis of variance followed by Tukey’s mean separation test. Results are reported as the means and their respective standard deviation (SD) values (mean ± SD). The association between the rates of CMA3-positive sperm and embryonic development was analyzed using a linear regression correlation test. All analyses were performed using SigmaPlot v.11.0 software (Systat Software, San Jose, CS, USA), using a significance level of 5% (P < 0.05).
Results
Experiment 1: Sperm protamination was not different between sexed and unsexed bull sperm
Flow cytometry was an accurate method for quantifying CMA-3 fluorescence, given that the percentage of CMA-3-positive staining increased from 0.02% in the negative control to 99.8% in the positive control. Therefore, negative and positive controls were used to gate the interval of fluorescence within which the experimental groups would be analyzed (Fig. 1).
Flow cytometry analysis of CMA3-positive sperm cells. Fluorescence microscopy imaged samples (A–C) and histograms of flow cytometry analysis (D–F) represent frozen–thawed spermatozoa treated with DTT and stained with CMA3 (positive control; A, D), CMA3-stained test spermatozoa (B, E), and CMA3-unstained, with Hoechst 33342 only (negative control; C, F). Scale bars: 25 μm.
Interestingly, bull 2 had a higher percentage of sperm with protamine deficiency than bull 1 for both unsexed (7.27 ± 2.0 versus 1.38 ± 0.1, respectively) and sexed (9.12 ± 0.8 versus 0.35 ± 0.1, respectively) sperm (P < 0.05). However, within subject, the sorting process had no effect on sperm protamination (Fig. 2).
Percentage of CMA3-positive spermatozoa, evaluated by flow cytometry using unsexed and sex-sorted bull sperm. Results represent the mean ± standard deviation of three replicates, totalling 60,000 spermatozoa per group. a,bDifferent superscripts denote significant differences among groups (P < 0.05).
Experiment 2: Sperm protamination influences in vitro embryo development
We also assessed the effect of sperm origin, sexed or unsexed, on embryo development following IVF. As expected, for each bull, sexed spermatozoa yielded lower rates of embryo cleavage than unsexed spermatozoa (P < 0.05; Table 1). However, blastocyst rates did not differ (P > 0.05) between sexed and unsexed sperm for either bull. For 7-day embryos, there was no difference in measures morphological quality among groups.
Rates of embryonic development following IVF with unsexed and sex-sorted spermatozoa from two different bulls
The results represent the average of five replicates ± standard deviation.
a,b,c Different superscripts denote a significant difference within columns (P < 0.05).
* Rates were calculated from the total number of oocytes in each group.
† The rates were calculated from the total number of blastocysts on day 7.
Unsexed sperm from bull 1 yielded higher blastocyst and hatching rates than unsexed semen from bull 2 (P < 0.05). These results would suggest an effect of sperm protamination on blastocyst formation, considering the differences in CMA-3 positive staining levels detected between bulls (Experiment 1). Indeed a significant association was observed between CMA3-positive staining and cleavage rates (R2 85.1, P = 0.003) as with blastocyst hatching rates (R2 87.6, P = 0.006) for unsexed semen from both bulls (Fig. 3). This inferred that these embryo development parameters are inversely correlated with protamine deficiency. In other words, protamine integrity is likely to be related to increased rates of early cleavage and blastocyst development. However, no association was found in sexed semen (P > 0.05), suggesting a negative influence of sex sorting on sperm quality.
Association between sperm protamination and embryo development rates when using unsexed bull sperm. Sperm protamination was assessed by CMA-3 staining. Panels show the correlation rate of CMA3 staining with (A) cleavage or (B) blastocyst hatching rates following IVF with unsexed sperm from two bulls.
Discussion
This study is the first to report the effect of sex sorting on bull sperm protamine content and, in turn, on rates and quality of embryo development following IVF. For this purpose, we compared unsexed and male sexed spermatozoa from two different bulls using CMA-3 and flow cytometry to assess sperm protamination. Reportedly, the sperm sexing process negatively affected all sperm membrane, cytoskeletal and DNA integrity (Xu et al., Reference Xu, Chaubal and Du2009). Therefore, we hypothesized that DNA damage resulting from the sorting process could stem from direct effects on sperm chromatin packaging. However, we found no interference of the sexing process from sperm protamine content in either bull tested.
In humans, sperm protamine deficiency has been correlated with infertility (Iranpour et al., Reference Iranpour, Nasr-Esfahani, Valojerdi and al-Taraihi2000; Aoki and Carrell, Reference Aoki and Carrell2004; Carrell et al., Reference Carrell, Emery and Hammoud2007; Nanassy et al., Reference Nanassy, Liu, Griffin and Carrell2011). Notably, abnormal chromatin compaction resulting from protamine deficiency yielded DNA fragmentation, as well as methylation and epigenetic defects (Tavalaee et al., Reference Tavalaee, Razavi and Nasr-Esfahani2009). The relationship between sperm protamine content and fertility was also evaluated in other species, including cattle (Simões et al., Reference Simões, Feitosa, Mendes, Marques, Nicacio, de Barros, Visintin and Assumpção2009; Fortes et al., Reference Fortes, Satake, Corbet, Corbet, Burns, Moore and Boe-Hansen2014; Dogan et al., Reference Dogan, Vargovic, Oliveira, Belser, Kaya, Moura, Sutovsky, Parrish, Topper and Memili2015). Sperm protamine content in Bos indicus bulls correlated positively with DNA fragmentation index, as determined by sperm chromatin structure assay (Fortes et al., Reference Fortes, Satake, Corbet, Corbet, Burns, Moore and Boe-Hansen2014). Scrotal sac insulation, a model to study the effects of heat stress on bull fertility, reduced sperm protamine content (Rahman et al., Reference Rahman, Vandaele, Rijsselaere, Maes, Hoogewijs, Frijters, Noordman, Granados, Dernelle, Shamsuddin, Parrish and Van Soom2011). Moreover, field fertility scores of breeding bulls were negatively correlated with the percentage of sperm with reduced protamine content and fragmented DNA (Dogan et al., Reference Dogan, Vargovic, Oliveira, Belser, Kaya, Moura, Sutovsky, Parrish, Topper and Memili2015). These studies underscored the importance of sperm protamination and fertility in bull sperm.
In agreement with other groups, we observed individual differences in sperm protamine content, consistent with a bull effect (Simões et al., Reference Simões, Feitosa, Mendes, Marques, Nicacio, de Barros, Visintin and Assumpção2009; Fortes et al., Reference Fortes, Satake, Corbet, Corbet, Burns, Moore and Boe-Hansen2014). Reportedly, the sorting process affected sperm quality, as well as fertility, in a bull-dependent manner (it varied according to individual) (Palma et al., Reference Palma, Olivier, Neumüller and Sinowatz2008; Xu et al., Reference Xu, Chaubal and Du2009). In this study, for unsexed semen, there was a 5.89% difference in CMA3-positive sperm between the two bulls. This difference in protamination levels for unsexed semen was sufficient to affect embryo cleavage, blastocyst development and blastocyst hatching rates, which differed between the two bulls. Notably, the technique used to assess CMA-3 staining can also affect protamination level results. Using fluorescence microscopy to assess CMA-3 positive sperm, there was a 0.002% difference comparing fresh to frozen–thawed bull semen (Simões et al., Reference Simões, Feitosa, Mendes, Marques, Nicacio, de Barros, Visintin and Assumpção2009) and a 0.15% difference between bulls yielding low or high in vitro cleavage and blastocyst development rates (Castro et al., Reference Castro, Siqueira, Hamilton, Mendes, Visintin and Assumpção2018). However, the range 7–14% CMA3-positive sperm, as assessed by flow cytometry, has been reported as normal in testis and epididymal sperm in bulls (Fortes et al., Reference Fortes, Satake, Corbet, Corbet, Burns, Moore and Boe-Hansen2014). This is considerably higher, not only compared with rates reported in previous studies using fluorescence microscopy, but also compared with the CMA3 rates observed in this study in which we used the same assessment technique. These differences may be due partially to the fact that protamination is completed only in the cauda epididymidis. In any case, we speculate that the ratio of protamine deficiency may be underestimated in cattle and more studies are needed to address this question.
It is worth noting that protamination or replacement of histones with protamines during sperm maturation is a crucial process that ensures epigenetic silencing in protamine-bound DNA regions and protection of the male genome up to fertilization (Carrell et al., Reference Carrell, Emery and Hammoud2008). Therefore, abnormalities in protamine content might influence epigenetic signals transmitted by paternal DNA, interfering with embryonic development (Francis et al., Reference Francis, Yelumalai, Jones and Coward2014; Rajabi et al., Reference Rajabi, Mohseni-Kouchesfehani, Mohammadi-Sangcheshmeh, Farifteh-Nobijari and Salehi2016; Giacone et al., Reference Giacone, Cannarella, Mongioì, Alamo, Condorelli, Calogero and La Vignera2019). Notably, while protamine content related to epigenetics and infertility has been widely studied in humans, information is only now being reported for other mammalian species (Ni et al., Reference Ni, Spiess, Schuppe and Steger2016). In this study, the sex-sorting process had an effect on early embryo development, as assessed by cleavage rates following IVF. However, there was no effect on subsequent blastocyst formation rates. Reported results are conflicting. In some studies, no effects of sex sorting on IVEP were observed, although individual bull sperm quality, as assessed by motility and acrosome integrity, did affect IVF results (Carvalho et al., Reference Carvalho, Sartori, Machado, Mourão and Dode2010; Barceló-Fimbres et al., Reference Barceló-Fimbres, Campos-Chillón and Seidel2011; Inaba et al., Reference Inaba, Abe, Geshi, Matoba, Nagai and Somfai2016). However, other groups have reported decreased cleavage and embryo development rates with sex-sorted spermatozoa in cattle (Lu et al., Reference Lu, Cran and Seidel2000; Sartori et al., Reference Sartori, Souza, Guenther, Caraviello, Geiger, Schenk and Wiltbank2004; Bodmer et al., Reference Bodmer, Janett, Hässig, Daas, Reichert and Thun2005; Wilson et al., Reference Wilson, Fricke, Leibfried-Rutledge, Rutledge, Penfield and Weigel2006; Palma et al., Reference Palma, Olivier, Neumüller and Sinowatz2008). Notably, bovine male embryos tend to have faster developmental kinetics than female embryos in vitro (Beyhan et al., Reference Beyhan, Johnson and First1999), and therefore we suspect that the use of male sexed spermatozoa in this study may have partially overcome any untoward effects related to the sexing process. Additional studies would be needed to test this hypothesis.
Interestingly, Puglisi et al. (Reference Puglisi, Vanni, Galli, Balduzzi, Parati, Bongioni, Crotti, Duchi, Galli, Lazzari and Aleandri2006) hypothesized that the sexing process may also select for a particularly study population of spermatozoa. Our data showed that sperm selection did not affect protamine content or blastocyst development following IVF. We hypothesized that oocyte-repair capabilities (Ménézo et al., Reference Ménézo, Dale and Cohen2010; Fernández-Díez et al., Reference Fernández-Díez, González-Rojo, Lombó and Herráez2016) might aid in fixing any damage to sexed spermatozoa following fertilization. However, the entire fertilization process would be influenced by both oocyte quality and the extent of damage to spermatozoa, which is probably related to the bull effect, reflecting the different results in the literature.
For cattle, the number of replicates used here was in accordance with the current literature (Catteeuw et al., Reference Catteeuw, Wydooghe, Mullaart, Knijn and Van Soom2017; Diógenes et al., Reference Diógenes, Guimarães, Leme and Dode2017; Botigelli et al., Reference Botigelli, Schwarz, Zaffalon, Del Collado, Castro, Fernandes and Leal2017, Reference Botigelli, Razzaa, Pioltinea, Fontesa, Schwarzb, Leal and Nogueira2018; Perrini et al., Reference Perrini, Esposti, Cremonesi and Consiglio2018), although adding more animals could help to clarify the influence of the sex-sorting process on protamination, this was not possible as, firstly, we aimed to standardize the protocol to measure it. Therefore, future studies may clarify the influence of bull genotype on protamination of sexed semen. This study adds a reliable protocol for protamination analysis in sexed semen using flow cytometry, as showed by the accuracy and low SD. We hypothesize that while the sex-sorting process had no effect on bull sperm protamine content, protamination defects may interfere with embryo cleavage following IVEP. In conclusion, while the sex-sorting process had no effect on bull sperm protamine content, protamination defects may interfere with embryo cleavage following IVEP.
Acknowledgements
TVGS performed most of the experiments and wrote the manuscript. EBS, AAG and CAS contributed to the flow cytometry analysis. VCB and AJML contributed to the IVEP experiments. STRF and NNCA contributed to the statistical analysis. PPBS and MSC revised the manuscript. SSDS, MSM and OMO designed the study. All the authors read and accepted the manuscript.
Financial support
This study was supported by the Conselho Nacional de Desenvolvimento Científico e Tecnológico (CNPQ) and Bubras Investiments and Participation.
Conflict of interest
Authors report no conflict of interest.
Ethical standards
Not applicable.
