Bull Semen Research Articles

PRESENT SCENARIO OF LIVESTOCK BREEDING AND MANAGEMENT PRACTICES IN THE NORTHERN PART OF BANGLADESH

<p><strong>Background: </strong>Bangladesh has a rich heritage of livestock rearing. The management and breeding practices differ across the country. <strong>Objectives:</strong> To study the present scenario of breeding and management practices of livestock at northern Teesta river basin based Lalmonirhat district in Bangladesh. <strong>Methodology: </strong>Total 100 farmers were selected using random sampling technique from 5 upazilas of Lalmonirhat district during July to December, 2022. Data were analyzed using SPSS 23.0 statistical package. <strong>Results: </strong>Results showed that most of the farmers (65%) at the northern part of Bangladesh were middle-aged, 41% of them completed secondary education, and their occupation was mainly agriculture (55%). About 37.78% of respondents supplied roadside grass as roughage to their livestock. Maximum number of respondents (60.24%) supplied hand mixed feed as a source of concentrate whereas 39.76% of respondents used commercial feed. 96% of farmers practiced artificial insemination to inseminate their cows and heifers while in goat nearly all respondent farmers (98.41%) practiced natural mating. Among the breeding companies, 41.41% farmers preferred semen from the Bangladesh Rural Advancement Committee (BRAC), followed by Advanced Chemical Industries (ACI) (30.30%), Government (Department of Livestock Services (DLS) (22.22%), and others (6.07%). About 41.76% respondents used 50% Sahiwal - 50% local genotype bull to breed the cows whereas 23.08% respondents used 100% Sahiwal, 18.68% used 75% Holstein Friesian-25% local, 5.49% used 100% Holstein Friesian, 3.30% used 50% Holstein Friesian-50% Local and only 3.30% used 87.5% Holstein Friesian-12.5% Local genotype bull semen, respectively.<strong> </strong>On the other hand, most of the farmers (98.41%) chosen Black Bengal breeding buck during breeding and remaining used crossbred (Black Bengal Goat- Jamunapari) to breed their does. The actual price of bull semen from Govt. (DLS) was 30 Bangladeshi Taka (BDT) on average for all the breeds whereas, the price ranged 110-200 BDT depending on cattle breeds and bull/bucks Identification (ID) in different private enterprises. Farmers had to pay on an average<strong> </strong>181.18 BDT for DLS originated semen in addition to that BRAC Artificial Insemination (AI) workers took an average of 425.61 BDT from farmers to inseminate their cows. The average milk yield/d was 1.82±0.14, 3.35±0.40, and 2.74±0.27 liters for local, HF crossbred and Sahiwal crossbred respectively in that region. The prevalence of repeat breeding incidences was 13.74%, 14.21%, and 15.17%, for Local, Sahiwal crossbred, and Holstein Friesian crossbred genotypes respectively. The highest incidence of disease was found as Lumpy Skin Disease (14.67%) followed by Foot and Mouth Disease (FMD) (11.98%) and other parasitic and metabolic diseases. In the study area, it was found that maximum number of the respondents (95%) faced excessive feed price problem along with some other problems. <strong>Implications: </strong>Government intervention is necessary to improve the situation of livestock production in the country. <strong>Conclusion:</strong> This study showed the overall scenario of livestock production, breeding, and management in the northern part of Bangladesh which could be helpful for the govt., Non-governmental organizations (NGO’s) and policymakers to take realistic steps for the improvement of livestock production in the northern part of Bangladesh.</p>

MAP3K1, SPEF2 and PLCZ1 genes association with fertility and semen quality traits of AI bulls in Andhra Pradesh

Bull fertility plays an important role in improving the economic value of the herd and is measured in terms of semen quality traits, which is influenced by both genetic and non-genetic factors. Polymorphism of MAP3K1/ CviQI (rs463712269), SPEF2/HpyCH4V (rs722354121) and PLCZ1/AvaII (rs208019489) and their association with scrotal circumference, sperm motility and plasma membrane integrity, respectively were studied on 239 bulls of different breeds reared in different frozen semen bull stations. The MAP3K1/CviQ1 assay revealed that T allele was more frequent in Ongole and Murrah population. RFLP at SPEF2/ HpyCH4V locus indicated fixation of T allele in both the exotic purebred cattle (Holstein Friesian and Jersey) whereas selective advantage of C allele was observed in Murrah buffaloes. Except in Holstein Friesian crossbred, other cattle genetic groups were with CC genotype for PLCZ1/AvaII assay and the Murrah population had low genetic diversity and heterozygosity excess. The PLCZ1/ AvaII genotypes had significant influence on the plasma membrane integrity of sperm in Holstein Friesian, Jersey and Ongole bulls. The plasma membrane integrity of sperm was reported to be high in heterozygotes (CG) of Jersey and Ongole cattle. The present study, concluded the importance of PLCZ1 gene as a marker for semen quality assessment and selection in bulls.

Evaluation of the effectiveness of the use of exosomes in the regulation of the mitochondrial membrane potential of frozen/thawed spermatozoa.

Numerous studies confirm the involvement of extracellular vesicles (EVs) in the regulation of physiological processes of mammalian sperm cells. It has been proven that they take part in the processes of capacitation, acrosonmal reaction, and anti-oxidation. Despite growing interest in the biomedical potential (including the search for new reproductive biomarkers) of EVs, the role of extracellular seminal vesicles in maintaining semen quality during cryopreservation has not yet been established. Therefore, the objective of this experiment was to evaluate the effectiveness of the use in the regulation of the mitochondrial membrane potential of bovine sperm and to explain the mechanisms of EV action during cell cryopreservation. Exosomes were isolated from bull semen plasma, measured, and used for extender supplementation. Semen samples were collected from Simmental bulls, diluted, and pre-evaluated. Then they were divided into equal fractions that did not contain EVs or were supplemented with 0.75; 1.5 and 2.25 mg/ml of EVs. The test samples were frozen/thawed and the mitochondrial membrane potential, DNA integrity, and viability were evaluated. EVs have been established to have a positive effect on cryopreserved sperm structures. The most favourable level of EVs was 1.5 mg / ml, which can be successfully to improve cell cryostability during freezing/thawing. In this study, exosomes isolated from the sperm plasma and supplemented with a concentrated dose in the extender for sperm freezing were shown to significantly improve cryostability of cells by supporting the potentials of the mitochondrial membrane and protecting the cytoplasmic membrane of spermatozoa.

PERSPECTIVE: Semen additives for improving frozen-thawed buffalo and cattle semen ‐ a review

This comprehensive review delves into the evolving landscape of assisted reproductive technologies (ARTs) in bovine species, particularly focusing on the pivotal roles of semen additives in the cryopreservation of buffalo and cattle semen. In developing nations, where ARTs are still emerging, these techniques significantly influence bovine reproductive strategies. In contrast, developed regions have embraced them as primary approaches for dairy buffalo and cattle breeding. Semen cryopreservation, while offering advantages like extended storage and genetic propagation, also presents challenges. These include diminished sperm quality due to reactive oxygen species (ROS) production, alterations in sperm structure, and temperature fluctuations. Further, the effect of cryopreservation differs between cattle and buffaloes, with the latter exhibiting poorer semen viability and fertility due to inherent lipid composition susceptibilities. The generation and implications of ROS, especially hydrogen peroxide, contribute significantly to sperm DNA damage and functional impairments. To counteract these challenges, research has intensified on semen additives, aiming to bolster semen quality and protect against oxidative stress-induced damage. As the field advances, the review emphasizes the need for optimized cryopreservation techniques and tailored antioxidant strategies to harness the full potential of ARTs in bovine breeding programs.

Effect of Adding Different Levels of Nano-Zinc Oxide in Tris Diluent on some Traits of Chilled Semen of Bulls from the Artificial Insemination Center in Iraq

Effect of Adding Different Levels of Nano-Zinc Oxide in Tris Diluent on some Traits of Chilled Semen of Bulls from the Artificial Insemination Center in Iraq

Seminal characteristics and efficacy of egg yolk free semen extender on cryopreservation of Murrah buffalo bull semen

The experiment was undertaken to study the efficacy of egg yolk free semen extender on cryopreservation of buffalo semen. A total of 24 semen ejaculates from Murrah bulls (5 to 6 years) maintained at Central Semen Station, Anjora, Durg, Chhattisgarh were divided into two aliquots and were diluted using Tris-fructose-egg yolk-glycerol (TFYG) and egg yolk free commercial extender (EYFCE, AndroMed). The overall average Murrah bull fresh semen volume (mL), sperm concentration (million/mL), initial progressive motility (%), live sperm (%), abnormal spermatozoa (%), intact acrosome (%) and HOS reactive sperm (%) were 4.90±0.49, 1286.92±100.23, 75.00±0.67, 81.45±0.61, 10.70±0.51, 80.16±0.43 and 68.83±0.40, respectively. There was significant difference between bulls in semen volume (P<0.01), individual motility (P<0.01) and total sperm abnormalities (P<0.05). The semen extended with TFYG and EYFC extenders were cryopreserved in french mini-straw (0.25 mL) using programmable bio-freezer. The mean values of post thaw motility (%), live sperm (%), abnormal sperm (%), intact acrosome (%), HOST (%) of Murrah bull semen extended with TFYG and EYFCE were 45.83±0.77 vs 49.16±1.33, 57.41±0.54 vs 58.62±0.73, 12.54±0.46 vs 12.45±0.63, 69.62±0.82 vs 71.45±0.64 and 56.45±0.52 vs 57.37±0.55, respectively. Post thaw motility, live spermatozoa and intact acrosome were significantly higher (P<0.01) in frozen thawed semen extended with as EYFCE compared to TFYG in Murrah bull semen. It is concluded that EYFCE results in improvement in post thaw semen characteristics viz. post thaw motility, live sperm percent and intact acrosome.

Reproductive Evaluation of Beef Cattle Inseminated with Frozen Semen of Wagyu Cattle in Situbondo District

Evaluation of the success of Artificial Insemination (AI) aims to determine the value of reproductive efficiency of a livestock group. This study aimed to evaluate the success of AI using frozen semen of Wagyu cattle based on S/C, NRR, CR, CvR, and weaning rate in Situbondo District. The material used was secondary data in the form of AI data from 184 beef cows that have been inseminated with frozen semen of Wagyu cattle in Situbondo District. The method used was quantitative research. The results showed that reproductive evaluation of cows that have been inseminated with frozen semen of Wagyu cattle had S/C value of 2, NRR1 of 64%, NRR2 of 55%, CR of 49%, CvR of 53%, and weaning rate of 44%.

Evaluation of the morphological and functional state of cryopreserved sperm of bulls at different periods of long-term storage

Objective. To study the morphological andfunctional state of cryopreserved sperm of bulls during storage for 6 - 27 years at a temperature of - 196 C in liquid nitrogen in a comparative aspect. Methods. The object of the study was cryopreserved semen of bulls stored for 6 - 10 or 20 - 27 years. In the study of the qualitative parameters offrozen- thawed spermatozoa, the method of visual assessment for motility and survival, the method ofers differential staining with trypan blue/Gymza dyes to determine the morphological and functional integrity of cell membranes and the test for the ability to bind to vesicular explants of bovine oviductal epithelial cells in vitro were used. Results. It was found that the extension of the storage period of spermatozoa to 20 - 27years had no significant effect on the functional characteristics o f spermatozoa in terms of motility, survival and absolute survival. The method of differential staining showed that the proportion of live sperm with an intact acrosome in the total distribution did not differ significantly in both studied storage periods and ranged from 61.6 - 63.9 %. The proportion of dead cells also did not differ significantly and was 26.4 % when stored for up to 10 years and 21.7 % when stored for more than 20 years. No significant difference was found in the overall assessment of the percentage of sperm with varying degrees of acrosomal membrane damage. This figure was 22.5 and 26.0 %, respectively. At the same time, when the shelf life of cryopreserved sperm was extended to 20 - 27 years, a significant increase in the percentage of live sperm with a missing acrosome was observed (p<0.01). It was determined that the index of sperm binding to explants of epithelial cells of the oviduct in vitro was significantly higher when storedfor 6-10 years and was 227.9±32.3 against 114.6±19.5 when stored for 20 - 27 years (p<0.05). Conclusions. The use of the traditional method of assessing sperm quality by indicators of sperm motility, survival and absolute sperm survival did not reveal any differences when storing cryopreserved sperm for 6 - 27 years. At the same time, the differential staining method showed a significant increase of 7.2% in the proportion of live sperm with a missing acrosome when the storage period was extended from 6 - 10 to 20 - 27 years. The in vitro test for sperm binding to oviduct epithelial cells showed a significant decrease of almost 2 times in the index of sperm binding to cellular explants during long-term storage. This may indicate a decrease in the ability of such sperm to fertilise. Keywords: bulls, sperm, cryopreservation, long-term storage, differential colouration, oviduct, sperm binding.

Cattle Artificial Insemination Service in Developing Countries: Efficiency, Major Challenges and Economic Loss: A Review

This review paper summarizes information on the efficiency, major challenges and economic loss of cattle Artificial Insemination (AI) service in developing countries. Efficiency of AI service can be measured by number of services per conception (NSC), conception rate at first insemination, and calving rate (CR). The optimum recommended NSC for profitable dairy cow ranges from 1.0-2.0. The averages of NSC of the conventional AI (1.73) and fixed time AI (1.78) in the reviewed publications were in the ranges of the recommendations of NSC. The NSC varies with animal breeds, animal factor (body condition score, age and parity), semen factor (handling procedure and quality), inseminator factor (knowledge, skill and experience), production systems, management level provided and AI breeding methods. The NSC and calving rate vary with conventional AI and fixed time AI breeding methods. Likewise, calving rate (CR) is influenced by poor semen quality, poor semen handling procedure, inadequate insemination skill, poor oestrus detection and wrong time of insemination. The average success rate (CR) of conventional AI (35.15%) in the reviewed publications is far below the success rates reported in some developing countries. Nevertheless, widespread use and longtime use of AI service on selected genotype(s) can cause cattle biodiversity loss. Dairy producers incur additional costs when cows fail to conceive at their first AI services. Moreover, challenges of AI service comprised of feed scarcity, animal diseases, climate change, poor AI infrastructure, poor livestock husbandry practices, weak livestock extension systems and incapability of Artificial Insemination Technicians (AITs). This calls designing suitable interventions to improve the efficiency of AI services. Adequate feed and high level of management should be provided to the breedable cows and heifers. AI service centers should be established as per the recommended number of breedable cows and heifers. AI inputs including AITs should be always available at each AI service center, and proper AI service recording should be practiced. Sexed semen should be used to enhance the number of replacement heifers, and capacity building should be provided to AITs and community cattle breeders. Radio, television and printed medias should be used to enhance the awareness of the community cattle breeders. Frequent extension support is essential for the success rate of the AI service.

The Effects of Different Thawing Procedures on Spermatological Parameters of Frozen Bull Sperm

One of the most crucial elements influencing the efficacy of artificial insemination applications is semen quality. It is known that post-thaw semen quality was affected by thawing method. Errors made during the thawing process can compromise the motility, viability, morphology and DNA integrity of spermatozoa after thawing. This study was conducted to investigate the effects of four distinct thawing procedures on post-thaw semen quality in bulls. The first group was designated as 24°C (n=8); the straws in this group were thawed in a water bath at 24°C for 60 seconds. Second group was designated as 32°C (n=8); the straws in this group were thawed in a water bath at 32°C for 60 seconds. Third group was designated as 38°C (n=8); the straws in this group were thawed in a water bath at 38°C for 30 seconds. And the fourth group was designated as 70°C (n=8); the straws in this group were thawed in a water bath at 70°C for 7 seconds. Following the thawing process, motility, sperm morphology, viability, and DNA damage rate in spermatozoa were evaluated. Results showed that in 32°C group and 24°C group sperm motility significantly decreased when compared to 70°C and 38°C groups. Additionally, the 24°C group exhibited a significantly elevated DNA damage rate compared to the 70°C group, while no differences were observed in the other groups. In conclusion, the most ideal thawing procedures are at 70°C for 7 seconds and at 38°C for 30 seconds are recommended to get optimum sperm quality from frozen bull semen after thawing.

Effect of autologous platelet-rich plasma on the fertility and quality of cryopreserved buffalo bull semen: a comparative study using OptiXcell® and tris egg yolk extenders

BackgroundBuffalo spermatozoa have a distinct membrane structure that makes them more vulnerable to cryopreservation, resulting in lower-quality post-thawed sperm. This decreases the success rate of artificial insemination in buffaloes. Understanding and addressing these specific vulnerabilities are essential for improving reproductive techniques in buffalo populations. The properties of cryopreserved buffalo bull semen were examined in this study regarding the impact of adding autologous platelet-rich plasma (PRP) to OptiXcell® or Tris egg yolk-based extenders. Ten buffalo bulls were used to collect semen. Each bull’s ejaculate was separated into two main equal amounts, each of which was then diluted with either OptiXcell® or Tris egg yolk-based extender, supplemented with various PRP concentrations (5%, 10%, and 15%), and the control (0%), before being cryopreserved according to established protocols. Following equilibration and thawing, the quality and functionality of the sperm were evaluated, along with the antioxidant enzyme activities (GSH and TAC), malondialdehyde (MDA) content, and in vivo fertilization rate of the thawed semen.ResultsAll PRP concentrations in both extenders, particularly 10% PRP, improved the quality and functionality of the sperm in both equilibrated and frozen-thawed semen. Additionally, the antioxidant enzyme activities in both extenders were higher in the PRP-supplemented groups compared to the control group in thawed semen (P < 0.05). All post-thaw sperm quality, antioxidant enzyme activities, and functionality aside from DNA integrity were higher (P < 0.05) in the PRP-supplemented OptiXcell® than in the PRP-supplemented Tris egg yolk-based extender. The fertility of cryopreserved semen in the extenders supplemented with 10% and 15% PRP increased (P < 0.05) significantly more than that of the control extenders, with 10% PRP being the optimum concentration in OptiXcell® (80%) compared to that of Tris egg yolk-based extender (66.67%) and control of two extenders (53.33% and 46.67%, respectively).ConclusionsEven though autologous PRP-supplemented extenders have a protective impact on equilibrated and cryopreserved semen, 10% PRP-supplemented OptiXcell® extenders are more effective at preserving post-thaw semen quality, functionality, and antioxidant capacity, which increases the in vivo fertility of buffalo bulls.

Impact of Zinc Supplementation on Tharparkar Bull Semen Quality: Comparative Study of Commercial and Lab Extenders

Impact of Zinc Supplementation on Tharparkar Bull Semen Quality: Comparative Study of Commercial and Lab Extenders

Analysis of Factors Affecting the Success of Beef Cattle Artificial Insemination (AI) in Jepon District, Blora Regency

Abstract This study aims to investigate the factors that influence the success of artificial insemination, the effect of successful artificial insemination on livestock rearing, and the income of beef cattle farmers in Palon Village, Jepon District, Blora Regency. The research method is quantitative descriptive with a survey approach. Primary data were obtained through direct observations, interviews, and questionnaires with beef cattle farmers in Palon Village and inseminators of the Food, Agriculture, Livestock, and Fisheries Office (DP4) of Blora Regency, while secondary data were obtained from DP4 and the Statistics Indonesia (BPS) of Blora Regency. Multiple linear regression and beef cattle farming analysis were used in this study. The findings show that the number of repeat breeding cases in Palon Village remains significantly high. Several factors were identified as influencing the success of artificial insemination, including female livestock characteristics, thawing and handling semen, breeder conditions, and inseminators’ skills and attitudes. Livestock health, administration of anthelmintics and vitamins, rectal palpation examination, body condition score, age of the breeder, feed, and the origin or breed of the livestock are all important characteristics of female livestock. The handling and thawing of semen were discovered to be critical factors influencing the type of straw used. Farmer conditions, which include age, education level, length of time involved in beef cattle farming, basic livelihood, and the number of owners, also play a role. Age, experience in the field, and the extent of training received were discovered to influence the success of artificial insemination. Repeated mating contributes to increased maintenance costs and the costs associated with artificial insemination in beef cattle.

Automation of bull semen analysis through the development of a modular open technology device for cryopreservation

Automation of bull semen analysis through the development of a modular open technology device for cryopreservation

Study of the expression level influence of aquaporin genes on the quality of semen of Holstein bulls

Study of the expression level influence of aquaporin genes on the quality of semen of Holstein bulls

Role of trace minerals in bull reproductive physiology and semen quality

Testicular dysfunction is often associated with an imbalance in antioxidant/oxidant homeostasis, leading to negative effects of oxidative stress on germ cell proliferation, steroidogenesis, and sperm function. Trace minerals (TM) are involved in basic homeostatic and enzymatic processes like free radical detoxification, cellular respiration, carbohydrates, lipids, nucleic acids, synthesis and metabolism of proteins, and stabilization of membranes and DNA. Dietary source of TM is necessary to support these processes. Supplementing cattle with TM is nowadays a common practice to help support growth, reproduction, and immunity. This review provides information on roles of TM in bulls testicular and sperm functions, and effects of TM mineral supplementation on bull reproductive parameters.

Impact of various cryo-preservation steps on sperm rheotaxis and sperm kinematics in bull

Semen cryopreservation is an important tool that has massively contributed to the progression of animal reproduction, especially in cattle. Nonetheless, a large part of the sperm population suffers from cryostress and loses fertility during the process. Although bovine semen cryopreservation is more advanced than any other species, there are still some missing links in the technology knowledge. The aim of the current study was to detect the effect of cryopreservation steps on sperm rheotaxis. Semen samples were collected from sex bulls and analyzed inside a microfluidic platform with CASA after each step of cryopreservation, including control, dilution with yolk citrate, cryoprotectant addition, and cooling or freezing. The results showed that positive rheotaxis % (PR) was not affected during cryopreservation. On the contrary, the sperm kinematics of the positive rheotactic sperm undergo significant changes, as velocity parameters (VCL, VSL, and VAP) were lower in both the cryoprotectant adding and cooling/freezing steps than in the control and yolk citrate dilution steps, while progression parameters (LIN and BCF) were higher in the cryoprotectant and cooling/freezing steps than in the control and yolk citrate dilution steps. Beside these results, an interesting phenomenon of sperm backward positive rheotaxis has been observed. The results of backward sperm rheotaxis samples revealed a significant decrease in PR%, while all sperm kinematics except BCF were significantly higher than normal rheotaxis samples. Based on these results, we conclude that positive rheotactic sperm cells are the elite of the sperm population; however, they still get some sublethal cryodamage, as shown by alterations in sperm kinematics. We also suggest that the sperm-positive rheotaxis mechanism is a mixture of an active and passive process rather than a passive physical one.

Supplementation with MitoTEMPO before cryopreservation improves sperm quality and fertility potential of Piedmontese beef bull semen.

The purpose of this study was to improve the quality of frozen-thawed Piedmontese bull semen by incorporating MitoTEMPO (MT) in extended semen before cryopreservation. Semen was collected from 4 fertile bulls, using an artificial vagina, once weekly for 6 consecutive weeks. Semen samples were pooled, diluted with Bullxcell® extender, and supplemented with different concentrations of MT (0 as control, 5, 10, 20, 40, and 80 μM) before cooling, equilibration, and freezing procedures. The frozen-thawed semen was assessed for motility, vitality, acrosome intactness, plasma membrane integrity, DNA integrity, apoptosis, mitochondrial membrane potential, intracellular ROS level and in vitro fertilizing capability. The results showed that MT at concentrations of 10, 20, and 40 μM improved the total, progressive, and rapid motility directly after thawing while, at the highest tested concentration (80 μM), it decreased the progressive and rapid motility after 1, 2, and 3 h of incubation. The sperm kinetics including STR and LIN were noticeably increased at concentrations of 10, 20, and 40 μM directly after thawing (0 h), whereas the MT effect was variable on the other sperm kinetics during the different incubation periods. MitoTEMPO improved the sperm vitality at all tested concentrations, while the acrosomal and DNA integrity were improved at 20 μM and the mitochondrial membrane potentials was increased at 80 μM. The cleavage and blastocyst formation rates were significantly increased by using semen treated with 20 μM MT compared with controls. These findings suggest a potential use of MT mainly at a concentration of 20 μM as an additive in the cryopreservation media of bull semen to improve sperm quality.

Deciphering genetic diversity in conserved cattle bulls to achieve sustainable development goals

The primary objective of Sustainable Development Goal target 2.5 established by the United Nations is to ensure the preservation of genetic diversity in domesticated animals. The ICAR-National Bureau of Animal Genetic Resources in India has been actively engaged in the conservation of cattle and buffalo bull semen for long-term storage. This present study aimed to assess the genetic diversity present in the conserved cattle bull semen, which would aid in determining the most suitable strategy for future conservation management. A total of 192 bull semen belonging to 19 cattle breeds were selected to evaluate genetic diversity using 17 pairs of FAO recommended microsatellite primers. Total 267 alleles were detected across all the samples which indicates substantial amount of allelic variation is being maintained in conserved bulls. Further, all cattle bulls semen conserved showed higher observed heterozygosity than expected heterozygosity which indicates excess genetic diversity in all the populations. The FST, F IT and FIS value across the loci and population is 0.146 ± 0.009, 0.054 ± 0.038, and − 0.105 ± 0.035, respectively, which suggests lack of inbreeding in conserved cattle bull semen. This study has established genetic diversity in conserved cattle semen samples to achieve sustainable development goals. In addition, it provides compelling evidence that the current approach for conserving cattle bull semen is heading in the correct direction.

Recovery ability of sperm after freezing of pasundan bull semen

The purpose of this study is to look at Pasundan bulls’ sperm-freezing capacity for recovery. Three bulls’ sperm were collected using an artificial vagina. According to the normal operating protocols of the Center for Artificial Insemination Breeding and Development of Beef Cattle, Ciamis, West Java, fresh semen with sperm motility of 70% was frozen using a tris egg yolk extender. Evaluations of the percentage of motility, viability, and plasma membrane integrity were done under fresh, equilibrium, and post-thawing conditions to determine sperm destruction and the capacity of sperm to recover in each phase. Using the statistical package SPSS Version 25 application, descriptive statistics were used to examine all of the data. The findings indicated that the percentages of motility, viability, and plasma membrane integrity decreased during the freezing procedure. The motility, viability, and plasma membrane integrity of pasundan bovine semen recovered at rates of 64.29, 78.97, and 63.13%, respectively, following the freezing procedure. Based on recovery rates, it is demonstrated that pasundan bull semen has strong resistance and successful survival rates throughout the freezing procedure.