Abstract
The semen quality of breeder cocks profoundly impacted the numbers of matched layer hens and the economic benefits of the poultry industry. Adequacy and balance of poultry nutrition, especially the energy provision, critically modulated the reproductive potential of breeder cocks, however, the underlying mechanism was still unclear. For the purpose of this study, a total of 90 yellow-feathered 13-week-old roosters with the same age in days and similar body weight (1,437 ± 44.3 g) were selected and randomly divided into the low energy diet (LE), the moderate energy diet (ME), and the high energy diet (HE) treatments. The phenotypic parameters related to reproduction include semen quality, fertility, and hatchability, and the testis morphological parameters, including seminiferous epithelium length (SEL), seminiferous tubule perimeter (STP), seminiferous tubule area (STA), and Johnsen score, were measured to investigate the regulatory effects of different energy diets on reproductive performances. Furthermore, spermatogenesis and sperm motility-related genes, which included the sry-related high mobility group box (SOX) gene family and sperm-associated antigen (SPAG) gene family, and mitochondria apoptosis-related genes, such as Cyt-C, Bcl-2, and Bax, were measured to determine the underlying mechanism of energy on the reproductive performances. The The results showed that the gonadosomatic index and sperm motility in the ME treatment significantly increased compared with the LE treatment. Chickens in the ME treatment showed a preferable performance of testis development, especially a significant increment of SEL and Johnsen Score, compared with the LE and HE treatments. Finally, spermatogenesis-related genes, which included SPAG6, SPAG16, SOX5, SOX6, and SOX13, and apoptosis-related genes of mitochondria, such as the Cyt-C and Bcl-2, were significantly upregulated in the ME treatment. This study concluded that proper energy provision stimulated regular energy metabolism for spermatogenesis and sperm capacitation, which finally increased semen quality and reproductive performances of breeder cocks.
Introduction
Reproductive performance, especially the semen quality of breeder cocks profoundly impacted the development of the poultry industry (1, 2). Roosters in high genetically selected poultry strain successfully matched 80–100 layer-hens, whereas a certain number of Chinese native chicken breeds matched only 10 layer-hens because of the lower semen volume ejaculation and dispirited sperm motility (3). Therefore, proper strategies to enhance spermatogenesis and sperm motility of native breeder cocks are increasingly required.
Spermatogenesis is a complex cell differentiation and sperm synthesis bioprocess which mainly includes the mitotic stage, the meiosis stage, and the spermiogenesis stage (4–7). Mature sperm further undergoes sperm capacitation to ensure adequate sperm motility to complete the fertilization in the female reproductive tract (8, 9). A certain number of genes, which mainly included the sry-related high mobility group box (SOX) gene family (10) and sperm-associated antigen (SPAG) gene family (11, 12), synergistically participated in spermiogenesis and the capacitation process and further determined the semen quality of breeder cocks. All these genes were functionally expressed in testis and were regulated by genetic traits, natural environment management, and nutrition.
Adequacy and balance of poultry nutrition, especially the energy provision, are considered to ensure the achievement of the normal inherent physiological capacity of other nutritional elements during the growth stage of breeder cocks (13–15). Disordered dietary energy significantly interfered with regular energy metabolism, which mainly occurred in the mitochondria in the cell, and further inhibited semen quality (16); however, the underlying mechanism of the effect of mitochondrial energy metabolism on semen quality is still unclear.
The mechanism of energy metabolism occurred in the mitochondria in cells through the electron transport chain (17) to satisfy the energy requirement of both spermatogenesis and the sperm capacitation process. Mitochondria are mainly involved in energy provision during spermatogenesis and the sperm capacitation process and the apoptosis process during the maturity of sperm morphogenesis. T apoptosis-related genes in the mitochondria, including Cyt-C, Bcl-2, and Bax, disordered the gene expression, providing an exorbitant or depressed energy supply (18, 19), which might further interfere regularly with germ cell apoptosis and, therefore, inhibit semen quality (20).
For the present study, yellow-feathered breeder cocks were selected and differential levels of diet energy were provided to investigate the underlying mechanism of energy on semen quality and reproductive performances. We hypothesized that exorbitant or depressed energy provision inhibited the normal energy metabolism and further triggered the apoptosis process to lower spermatogenesis, which finally declined semen quality and reproductive performances.
Materials and methods
Animal care and procedures followed The Chinese Guidelines for Animal Welfare, which was approved by the Animal Care and Use Committee of Jiangxi Agricultural University, Jiangxi, China, with the approval number JXAULL-20211009.
Experimental design
A total of 90 yellow-feathered 13-week-old breeder cocks with the same age in days and similar body weight (1,437 ± 44.3,g) were randomly selected and divided into the low energy diet (LE), the moderate energy diet (ME), and the high energy diet (HE) treatment groups, respectively. Each treatment contained 6 replicates, with 5 birds in each replicate. All birds will receive a 7 days-long adaptation period followed by a 46-weeks feeding process. Chickens were raised in single cages in a fully enclosed house, received artificial ventilation, and 16 h of light per day. A total of 1 g of diet was provided to each bird at 6 a.m. and 3 p.m., respectively. The ingredients and nutritional levels of the diets are shown in Table 1. Other management systems and immunization procedures refer to the rules and management system of the experimental site.
Table 1
| Ingredients | Low energy | Moderate energy | High energy |
|---|---|---|---|
| Corn | 64.26 | 69.58 | 76.35 |
| Soybean meal | 18.12 | 18.08 | 16.68 |
| Wheat bran | 10.98 | 6.59 | 1.19 |
| NaCl | 0.31 | 0.32 | 0.33 |
| Limestone | 1.55 | 1.55 | 1.54 |
| CaHPO4 | 1.77 | 1.80 | 1.85 |
| Zeolite powder | 2.34 | 1.40 | 1.31 |
| Met | 0.22 | 0.22 | 0.20 |
| Lys | 0.05 | 0.06 | 0.10 |
| Thr | - | - | 0.03 |
| Trp | - | - | 0.02 |
| Choline chloride | 0.18 | 0.18 | 0.18 |
| Mineral premixa | 0.20 | 0.20 | 0.20 |
| Vitamin premixb | 0.02 | 0.02 | 0.02 |
| Total | 100.00 | 100.00 | 100.00 |
| Nutrients levels | |||
| CP | 14.00 | 14.00 | 14.00 |
| ME /(MJ/kg) | 11.30 | 11.72 | 12.14 |
| NaCl | 0.35 | 0.35 | 0.35 |
| Ca | 1.00 | 1.00 | 1.00 |
| AP | 0.42 | 0.42 | 0.42 |
| Lys | 0.70 | 0.70 | 0.70 |
| Met | 0.45 | 0.45 | 0.45 |
| Met+Cys | 0.70 | 0.70 | 0.70 |
| Thr | 0.58 | 0.58 | 0.58 |
| Trp | 0.18 | 0.18 | 0.18 |
Ingredients and nutrient composition of experimental diets (DM basis %).
Mineral premix provided per kilogram of diet: Fe 60 mg, Cu 8.7 mg, Mn 90 mg, Zn 85 mg, I 0.5 mg, Se 0.4 mg.
Vitamin premix provided per kilogram of diet: VA 12,000 IU, VD3 3,500 IU, VE 45 mg, VK3 2 mg, VB13 mg, VB212 mg, VB610 mg, VB12 30 mg, biotin 0.2 mg, calcium pantothenate 15 mg, nicotinic acid 30 mg, folic acid 1.5 mg.
Sperm quality and fertility rate measurement
The parameters of semen quality, which mainly included the semen volume, pH, sperm density, sperm motility, and deformity rate, were further measured two times per week from 25 weeks old to 40 weeks old cocks before the mating test was initiated. Semen quality was measured according to the methods described by Sun et al. (21). To simply state, semen samples from each breeder cock were collected around 3 p.m. by the same skilled technician. The sperm collection process was done using the dorso-abdominal massage method, and care was taken in order not to contaminate the pooled semen through alien materials, such as feces and blood, which could reduce the quality of the collected semen (22). Semen volume was measured in a graduated collection tube immediately after the collection. Following, semen samples from each cock were diluted with 0.9% NaCl in a proportion of 1:100 and further used for evaluation of sperm motility, sperm viability, and sperm concentration with a computer-aided semen analysis system (ML-608JZII; Nanning Songjingtianlun Bio-technology Co., Ltd, Guangxi, China). Sperm motility was shown in the ten-point system while sperm viability was shown in the percentage form. The sperm deformity rate (calculated as the percentage of abnormal spermatozoa of the total (500) spermatozoa analyzed) was determined by in vivo staining with crystal violet and examined under light microscopy (Olympus, Tokyo, Japan) at 400× magnification.
Following, one breeder cock with the average semen quality in each replicate (a total of 18 roosters) was selected for fertility and hatchability measurement. The roosters were used as semen donors for artificial insemination (AI) in yellow-feathered layer hens of the same age, which were sexually rested for 4 weeks before the AI. The ratio of a rooster to hens was 1:10. AI was first performed on 2 consecutive days and two times again with 4 days in between. Eggs were marked and collected daily from day 2 to 14 after the first insemination and stored at a temperature of 18°C and relative humidity of 75% until incubation. Fertility for each rooster was calculated as the percentage of fertile eggs of the total number of set eggs. Hatchability of set eggs was calculated as the percentage of hatched eggs of the total number of set eggs. The healthy young rate was calculated as the percentage of healthy young chicken/total hatched eggs.
Testis morphological measurement
All roosters used in the mating test were slaughtered at 50 weeks old for the collection of testicular tissue samples, weighed, quickly put into liquid nitrogen, and then transferred to a −80°C ultra-low temperature refrigerator for storage. Another part of testicular tissue was collected for section slicing and histomorphological observation. The left testis was cut into a small piece (1.0 cm in length, 1.0 cm in width, and 0.5 cm in height), followed by fixing in the formalin buffer for 48 h. All samples were further embedded in paraffin blocks, cut into sections of 5 μm thickness, and stained with the hematoxylin-eosin. Fifteen seminiferous tubules from each sample were selected for the measurement of seminiferous epithelium length (SEL), seminiferous tubule perimeter (STP), seminiferous tubule area (STA), and Johnsen score (23). All parameters involved in the development of the seminiferous tubule were measured using Image-Pro-Plus (version 6.0; Media Cybernetics, Inc. Maryland, USA) at 400× magnification.
Spermatogenesis-related genes expression measurement
Spermatogenesis-related genes, which included the sry-related high mobility group box (SOX) gene family and the sperm-associated antigen (SPAG) gene family, were selected as the candidate genes for the measurement of expression through the reverse-transcriptional quantitative PCR (RT-PCR) method to determine the effects of energy treatment on spermatogenesis and sperm motility. The apoptosis-related genes in mitochondria, such as Cyt-c, Bcl-2, and Bax, were further measured to determine the underlying mechanism of energy supply on the development of testis and spermatogenesis. The total RNA of the testis sample was isolated from 30 to 50 mg of the sample using the TRIzol reagent (Invitrogen). Any residual gDNA and protein were removed with DNase I (TaKaRa, Japan) and the RNA clean kit (Tiangen, China), respectively. All sample RNAs were reverse transcribed into cDNA using the PrimeScript RT reagent Kit (Perfect Real Time) (TaKaRa, Japan) according to the instructions of the manufacturer. Quantitative PCR was performed using the ABI 7500 Real-time Detection System (Applied Biosystems) and SYBR Premix Ex Taq (Perfect Real Time) (TaKaRa). β-actin was amplified as an endogenous control. The primers of all candidate genes were designed using the Primer Premier 5.0 software and produced by Shenggong Biotech Co., Ltd. (Shanghai, China). All primers are listed in Table 2. The relative abundance of transcripts was calculated using the 2−ΔΔCT method (24).
Table 2
| Gene name | Accession number | Primer sequence | Product size | Tm |
|---|---|---|---|---|
| SOX5 | NM_001004385.1 | F:TGGGCTAAAGATGAACGG | 187 | 54 |
| R:GCTTGTATTTGTAGTCTGGGT | ||||
| SOX6 | XM_015286513.1 | F:GTCATCTTTGGGTGATACAG | 85 | 54 |
| R:TGAGCATAAATAGGCAGTC | ||||
| SOX9 | NM_204281.1 | F:CGATTACACCGAGCACCAGA | 83 | 57 |
| R:AGGTGAATTGTTAGTAGAGGC | ||||
| SOX13 | XM_015299129.1 | F:AGCAGGTCAACATGCCGTAC | 167 | 59 |
| R:CTTTAGCGTGGGAGGAGGAG | ||||
| SPAG6 | NM_001199586.1 | F:GAGATTATTGGAGGTATGAG | 106 | 56 |
| R:CACCAGCAGCGTAAGTAG | ||||
| SPAG16 | XM_421865.5 | F:AGGGCTATAAAGCAGGGTG | 129 | 58 |
| R:TGGCGAGAATAAGTAACATCAG | ||||
| SPAG17 | XM_015294613.1 | F:CGGCTTATCTATGAATGCT | 165 | 54 |
| R:TGAAGTCGTTCCTCCTCTA | ||||
| β-actin | NM_001199586.1 | F:GAGAAATTGTGCGTGACATCA | 152 | 58 |
| R:CCTGAACCTCTCATTGCCA |
Primers information of genes used in RT-qPCR.
Statistical analysis
The following parameters first received a normal distribution test using the SAS procedure “proc univariate data=test normal” (SAS Institute, Inc., Cary, NC, USA) and subsequently the one-way ANOVA S-N-K test: body weight, testis development parameters in each period, semen quality parameters, and testis morphometric development parameters. The relative abundance of transcripts was calculated using the 2−ΔΔ method, followed by a one-way ANOVA S-N-K test to determine the discrepancy in the expression of genes among all treatments. The result was considered significant when a p-value was < 0.05 while a tendency was considered when 0.05 ≤ P < 0.10.
Results
Effects of differential energy level treatment on gonad development
Testes of breeder cocks were sampled during the pregenital, the fastigium, and the anaphase, respectively. All development information related to different periods of testes is shown in Table 3. The development of testes underwent a primary increment before they turned 40 weeks old, followed by a declining tendency. Testis did not maturely develop at 15 weeks old. The ME treatment showed superior body weight while the LE and HE treatments showed development performances of the testis, although not significant. Gonadosomatic index in the ME treatment significantly increased at 40 weeks old compared with the LE and HE treatments (P < 0.05). No other significant discrepancies were detected among all the three treatments.
Table 3
| Items | Treatments | SEM | P-value | |||
|---|---|---|---|---|---|---|
| Low energy | Moderate energy | High energy | ||||
| 15-Weeks-old | Body weight | 1,571 | 1578 | 1,576 | 38 | 0.612 |
| Left testis weight | 4.48 | 4.39 | 4.37 | 1.06 | 0.343 | |
| Right testis weight | 4.62 | 4.51 | 4.57 | 1.28 | 0.447 | |
| Total Testis weight | 9.1 | 8.9 | 8.94 | 1.13 | 0.411 | |
| Gonadosomatic index | 0.6 | 0.57 | 0.57 | 0.14 | 0.251 | |
| 40-Weeks-old | Body weight | 2,303 | 2,320 | 2,420 | 2,76 | 0.667 |
| Left testis weight | 19.12 | 22.08 | 20.08 | 5.53 | 0.396 | |
| Right testis weight | 18.45 | 20.58 | 19.58 | 4.61 | 0.414 | |
| Testis weight | 37.58 | 40.66 | 38.66 | 5.12 | 0.421 | |
| Gonadosomatic index | 1.63b | 1.75a | 1.59b | 0.08 | 0.026 | |
| 60-Weeks-old | Body weight | 2,732 | 2,786 | 2,822 | 63.2 | 0.532 |
| Left testis weight | 17.79 | 19.79 | 18.79 | 2.16 | 0.243 | |
| Right testis weight | 16.11 | 18.11 | 17.61 | 1.23 | 0.167 | |
| Testis weight | 34.71 | 37.91 | 36.41 | 2.02 | 0.089 | |
| Gonadosomatic index | 1.3 | 1.36 | 1.29 | 0.12 | 0.113 | |
Effects of different energy levels on gonad development in different periods.
Means in the same row parameters showed a significant difference.
Semen quality and fertility rate
The results of semen quality are displayed in Table 4. Sperm motility showed a significant increment in the ME and HE treatments compared with the LE treatment (P < 0.05). Meanwhile, sperm deformity showed a downward trend in ME compared with the LE and HE. No significant differences were detected for other sperm quality parameters among all the three treatments.
Table 4
| Items | Treatments | SEM | P-value | ||
|---|---|---|---|---|---|
| Low energy | Moderate energy | High energy | |||
| Volume(ml) | 0.49 | 0.52 | 0.47 | 0.04 | 0.134 |
| pH | 7.15 | 7.13 | 7.21 | 0.06 | 0.215 |
| Density(109/ml) | 2.13 | 2.10 | 2.08 | 0.04 | 0.467 |
| Motility (ten-point) | 6.37b | 6.87a | 6.77a | 0.31 | 0.048 |
| Viability (%) | 78.6 | 84.3 | 81.1 | 5.56 | 0.134 |
| Deformity rate (%) | 7.88 | 6.96 | 7.54 | 1.03 | 0.087 |
Effects of different energy levels on semen quality.
Means in the same row parameters showed a significant difference, SEM, Standard error of the mean.
Subsequently, a mating test was further conducted to determine the effects of differential energy treatments on the fertility rate and hatchability. As seen in Figure 1, no significant differences were observed among all the three treatments on fertility rate, hatchability, and healthy young rate. ME slightly increased the fertility rate and healthy young rate.
Figure 1
Effects of differential energy treatment on fertility rate, hatchability, and healthy young rate. LE, Low energy level; ME, Moderate energy level; HE, High energy level.
Testis morphology measurement
The measurement of testis morphology, which mainly included the gradient levels of spermatogenic cells in seminiferous tubules, is seen in Figure 2. Meanwhile, all morphological measurements based on the sections further received a discrepancy analysis among all the three treatments, and these results are seen in Table 5. The LE treatment remarkably inhibited the development of testis and postponed sexual maturity because of the significant decline in the SEL, STP, STA, and Johnsen Score than ME or HE at 15 weeks old. HE showed a significant increase in the development of testis before sexual maturity; however, it inhibited the testis development at the metaphase and the anaphase compared with LE and ME. Chickens under ME showed a preferable testis development performance at 40 and 60 weeks compared with the LE and HE. Particularly, the SEL and Johnsen Score significantly increased compared with the other two treatments. No significant changes were detected for other parameters during the raising period.
Figure 2
Effects of differential energy treatment on the morphological development of testes. (A) Seminiferous tubules of the effects of LE level treatment. (B) Seminiferous tubules of the effects of ME level treatment. (C) Seminiferous tubules of the effects of ME level treatment.
Table 5
| Items | Low energy | Moderate energy | High energy | SEM | P-value | |
|---|---|---|---|---|---|---|
| 15-Week-old | SEL(μm) | 10.31c | 52.32b | 61.77a | 5.41 | 0.012 |
| STP (μm) | 194.5c | 228.1b | 257.4a | 18.37 | 0.043 | |
| STA (104 μm2) | 2.35c | 3.08b | 3.77a | 0.31 | 0.007 | |
| Johnsen Score | 2.34c | 5.82 b | 6.41a | 1.08 | 0.001 | |
| 40-Week-old | SEL(μm) | 146.4b | 159.3a | 151.7ab | 13.24 | 0.031 |
| STP(μm) | 596.7 | 628.4 | 613.4 | 36.71 | 0.141 | |
| STA (104 μm2) | 19.95 | 21.38 | 20.77 | 2.31 | 0.203 | |
| Johnsen Score | 7.23b | 8.82a | 8.01ab | 0.98 | 0.023 | |
| 60-Week-old | SEL(μm) | 125.4b | 139.3a | 131.7ab | 13.24 | 0.031 |
| STP(μm) | 576.7 | 620.4 | 603.4 | 46.7 | 0.241 | |
| STA (104 μm2) | 17.95 | 20.38 | 19.77 | 3.41 | 0.273 | |
| Johnsen Score | 6.83b | 8.12a | 7.01b | 0.78 | 0.043 | |
Effects of different energy levels on morphometric development of testis and seminiferous tubules.
Means in the same row parameters showed a significant difference. SEL, seminiferous epithelium length; STP, seminiferous tubule perimeter; STA, seminiferous tubule area; SEM, standard errors of the mean.
Spermatogenesis-related genes expression
Spermatogenesis-related genes, which mainly included the SPAG gene family and the SOX gene family, were selected to determine the underlying mechanism of energy provision on spermatogenesis. Based on the results seen in Figure 3, SPAG6 and SPAG16 expressions were significantly increased in the ME treatment compared with the LE treatment, while SPAG6 was also significantly upregulated in the ME treatment compared with HE. No significant changes were observed in SPAG17 among all the three treatments. Further, the SOX gene family showed a similar expression trend with the SPAG gene family. ME significantly upregulated the expression of SOX6 and SOX13 compared with the other two treatments. Meanwhile, the SOX5 gene expression significantly increased in ME compared with LE. No significant discrepancies were found in SOX 9 among all the three treatments.
Figure 3
Effects of differential energy treatment on the expression of sperm motility-related genes. (A) Effects of differential energy treatment on the expression of the SPAG gene family. (B) Effects of differential energy treatment on the expression of the SOX gene family. LE, Low energy level; ME, Moderate energy level; HE, High energy level.
Mitochondria apoptosis-related genes expression
The apoptosis-related genes of mitochondria, including the Cyt-C, Bcl-2, Bax, and Bcl-2/ Bax, were measured, and the results are seen in Figure 4. Expressions of Cyt-C and Bcl-2 were significantly downregulated in the HE treatment compared with the LE and ME treatments. Meanwhile, Cyt-C was significantly upregulated in ME compared with LE. No significant discrepancy was observed between LE and ME on Bcl-2 gene expression. Bax gene expression showed a complete reverse result compared with Bcl-2, which further causatively resulted in the significant increase of the ratio Bcl-2/ Bax in the ME treatment compared with the other two treatments. No significant discrepancy was observed in Bcl-2/ Bax ratio between LE and HE.
Figure 4
Effects of differential energy treatment on the expression of mitochondria energy metabolism-related genes. LE, Low energy level; ME, Moderate energy level; HE, High energy level.
Discussion
Dietary energy provision critically impacted poultry development and maturity during the chicken raising period. Exorbitant or depressed energy supply restricted a certain number of gene expressions, which, in turn, inhibited spermatogenesis and capacitation, thus causatively inducing the decline of semen quality and reproductive performances. Mitochondria performed an indispensable function in response to the energy alteration during spermatogenesis, which mainly included energy production and spermatogenic cell apoptosis (25). Therefore, the functions of mitochondria were especially concerned to determine the underlying mechanism of dietary energy provision on spermatogenesis and sperm motility of breeder cocks.
Effects of differential energy provision on testis development and spermatogenesis
Testes for males harbored numbers of testicular somatic cells and germlines, which are essential for the propagation of the species (26). Similar to other vertebrates, the development and morphology of testes in birds differentiate during embryogenesis and further become condensed into seminiferous cords (27). However, unlike mammals, the testes of chickens are situated deep in the body cavity, which provided a more stabilized environment for testis development.
The development of testes is regulated by photoperiod, nutrition, and gene expression, which further modulated the hypothalamic–pituitary axis and causatively triggered gonad development. The considerable development of testes around the gonad maturity period was a huge energy consumption course (28), which may be the key factor that induced a significant decrease of testis weight in the LE treatment compared with the ME and HE treatments. Furthermore, more energy was required during spermatogenesis because spermatogenic cells triggered the differentiation process through both mitosis and meiosis, during which Sertoli and Leydig cells synchronously were developed to support the differentiation of germlines to synthesize mature sperms. The development of testis development was stagnated and degraded after the mating period or excessive artificial ejaculations. In this period, abundant energy was deposited into long-chain fatty acids, which depressed the development of testis and spermatogenesis and, therefore, causatively induced the decrease of gonad index and Johnsen Scores.
Moreover, energy provision may further regulate the development of testis and spermatogenesis by regulating the differentially expressed genes related to spermatogenesis (29). Since the members of the SPAG gene family including SPAG6 and SPAG16 and the SOX gene family including SOX5, SOX6, and SOX13 were significantly upregulated in ME compared with LE, this finding was in line with Xinhong et al. (30) and Jiang et al. (31). The expression of SPAG6 in testis is mainly expressed in spermatogenic cells, helping to promote the maturity of spermatogenesis (12). Increased SPAGs expression promoted sperm maturity, therefore increasing the Johnsen Score and sperm motility. In addition, the SOX gene family also executed critical effects during testis formation, spermatogenesis, and capacitation, for these genes were expressed in peak in around 15-week-old roosters to promote the development of testis (32–34), which may further help increase the fertility rate.
Effects of differential energy provision on fertility rate
Fertility rate provided the initial direct indicator to evaluate the reproductive performance of breeder cocks, which was mainly impacted by semen quality, especially sperm motility and deformity and the physiological condition of layer hens (35). In contrast, semen quality significantly correlated with the fertility rate. In our present study, although not significant, the fertility rate in ME showed an obvious increment when compared with LE. The underlying mechanism of energy treatment on fertility rate might be attributed to the following reasons.
The activity of mitochondrial bioprocess remarkably regulated spermatogenesis and played diverse roles in the whole process of gamete production (36). Spermatozoa derive energy from the oxidative metabolism to perform normal physiological functions, although they can survive also by glycolytic energy. Abnormal energy transmission in the mitochondria induced infertile sperm motility, which may further cause a decrease in fertility (37). The regulatory effects of the mitochondria on spermatogenesis might be attributed to the degenerative processes of germ cells to ensure the high quality of spermatozoa and to further the regulatory effects on intrinsic apoptosis (38). Intrinsic apoptosis mediated by mitochondrial signaling was shown to play a crucial role in the modulation of apoptosis during the primordial germ cells (PGCs) maturity to avoid anomalous migration into the gonads. Apoptosis-related genes including the Cyt-C, Bax, and Bcl-2 were expressed abnormally in both the LE and HE treatments, which may restrict the formal maturity of sperms, thus decreasing the fertility rate (39).
In addition, spermatogenic-related genes modulated sperm motility and further impacted the fertility rate. The gene family of sperm flagellar axoneme protein interacted with each other to regulate the motility of flagella and played a decisive role in sperm motility (40), which thereby upregulated the expression of SPAG gene members to help increase the fertility rate. Moreover, the expression levels of SOX5, SOX6, SOX9, and SOX13 in the testes of normal roosters were significantly higher than those of asthenozoospermic roosters. Meanwhile, the SOX gene family significantly promoted sperm flagellar motility (41). When the expression of the SOX gene family was downregulated, the flagellar structure changed, and spermatogenesis, morphology, and motility declined. Meanwhile, the SOX genes interacted with the promoter regions of sperm motility candidate genes such as CATSPER1 (42). The upregulation of the SOX genes may further promote the expression of CATSPER1 gene, thereby increasing sperm motility and fertility rate.
In summary, energy provision to yellow-feathered breeder cocks played a critical role in semen quality and reproductive performances. ME provision stimulated normal energy metabolism and further triggered the normal apoptosis process for spermatogenesis, which finally increased semen quality and reproductive performances.
Funding
This research was funded by the Natural Science Foundation of Jiangsu Province (BK20211121). It was also funded by the JBGS Project of Seed Industry Revitalization in Jiangsu Province (JBGS [2021] 107) and the Special Fund for Independent Innovation of Agricultural Science and Technology in Jiangsu Province of China [CZ (20) 3001].
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Statements
Data availability statement
The original contributions presented in the study are included in the article/supplementary material, further inquiries can be directed to the corresponding author.
Ethics statement
The animal study was reviewed and approved by JXAULL-20211009. Written informed consent was obtained from the owners for the participation of their animals in this study.
Author contributions
FX and JS designed the study. YL, ZLv, and JZ conducted the experiment. SX, LZ, and ZLi contributed to parameter measurement and data analysis. All authors contributed to the article and approved the submitted version. All authors carefully read and are accountable for all aspects of the work.
Acknowledgments
We thank the Nanchang Key Laboratory of Animal Health and Safety Production and Jiangxi Province Key Laboratory of Animal Nutrition/Engineering Research Center of Feed Development.
Conflict of interest
The authors declare that the research was conducted in the absence of any commercial or financial relationships that could be construed as a potential conflict of interest.
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Summary
Keywords
breeder cocks, energy, testis, spermatogenesis, mitochondria
Citation
Xue F, Liu Y, Lv Z, Zhang J, Xiong S, Zha L, Liu Z and Shu J (2022) Regulatory effects of differential dietary energy levels on spermatogenesis and sperm motility of yellow-feathered breeder cocks. Front. Vet. Sci. 9:964620. doi: 10.3389/fvets.2022.964620
Received
08 June 2022
Accepted
28 July 2022
Published
29 September 2022
Volume
9 - 2022
Edited by
Xiaolong Gu, Yunnan Agricultural University, China
Reviewed by
Liang Yang, Institute of Animal Sciences (CAAS), China; Woo-Sung Kwon, Kyungpook National University, South Korea
Updates
Copyright
© 2022 Xue, Liu, Lv, Zhang, Xiong, Zha, Liu and Shu.
This is an open-access article distributed under the terms of the Creative Commons Attribution License (CC BY). The use, distribution or reproduction in other forums is permitted, provided the original author(s) and the copyright owner(s) are credited and that the original publication in this journal is cited, in accordance with accepted academic practice. No use, distribution or reproduction is permitted which does not comply with these terms.
*Correspondence: Jingting Shu shujingting@163.com
†These authors have contributed equally to this work
This article was submitted to Animal Nutrition and Metabolism, a section of the journal Frontiers in Veterinary Science
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