CHARACTERISTICS OF FROZEN-THAWED SEMEN FROM BREEDING BULL OF DAIRY AND COMBINED BREEDS
Abstract and keywords
Abstract:
The aim of research is to conduct a comparative study of frozen-thawed semen from breeding bulls of dairy and combined breeds. Objectives: to evaluate the quality of cryopreserved semen at three time points: immediately after thawing, 1 hour after thawing, and 3 hours after thawing; to study the level of sperm DNA fragmentation in bulls of dairy and combined breeds. The object of the study was the semen of sires from breeding enterprises of the Russian Federation. Samples of cryopreserved semen (n = 87) from bulls of dairy breeds (Holstein and Yaroslavl), as well as combined breeds (Simmental and Kostroma) were selected for the study. Sperm motility and DNA structure integrity were studied immediately after thawing, 1 hour after thawing, and 3 hours after thawing. Immediately after thawing, the content of spermatozoa with rectilinear-progressive movement was (48.27 ± 1.896) % for dairy breed bulls and (46.04 ± 1.771) % for combined breeds. After 3 hours, the number of progressively motile sperm decreased to (16.05 ± 1.263) % for dairy breeds and to (12.66 ± 2.829) % for combined breeds. Higher DNA fragmentation was found in the semen of dairy bulls with the following parameters: Tail Moment – 0.291 ± 0.012 and Comet Length – 27.786 ± 0.042, while bulls of combined breeds had lower DNA damage values (Tail Moment – 0.091 ± 0.024, Comet Length – 25.663 ± 0.088). In the sample we studied, combined breed bulls were inferior to dairy breed bulls in sperm survival rate. Dairy bulls exhibited higher values for most parameters characterizing DNA damage compared to bulls of mixed breeds. These interbreed differences should be considered in selection and breeding work and the development of sperm cryopreservation technologies.

Keywords:
stud bulls, bull semen quality, spermatozoa, DNA fragmentation, assisted reproductive technologies
References

1. Roche JR, Burke CR, Crookenden MA, et al. Fertility and the transition dairy cow. Reprod Fertil Dev. 2017;30(1):85-100. DOI:https://doi.org/10.1071/RD17412.

2. Hasler JF. Forty years of embryo transfer in cattle: a review focusing on the journal Theriogenology, the growth of the industry in North America, and personal reminisces. Theriogenology. 2014;81(1):152-169. (In Russ.). DOI:https://doi.org/10.1016/j.theriogenology2013.09.010.

3. Pardede BP, Supriatna I, Yudi Y, et al. Decreased bull fertility: age-related changes in sperm motility and DNA fragmentation. In: E3S Web Conf. The 1st International Conference on Veterinary, Animal, and Environmental Sciences (ICVAES 2019). 2020. Vol. 151. DOI:https://doi.org/10.1051/e3sconf/202015101010.

4. Iolchiev B, Schmidt A, Lukonina O, et al. Chromatin dispersion of spermatozoa of stud bulls depending on age. Animal Husbandry and Fodder Production. 2025;107:255-265. DOI:https://doi.org/10.33284/2658-3135-107-4-255.

5. Naryshkina EN. Variabel'nost' pokazatelya oplodotvoryayushchej sposobnosti semeni bykov-proizvoditelej golshtinskoj porody v plemennyh I tovarnyh stadah. Permskij agrarnyj vestnik. 2021;4(36):124-133. (In Russ.). DOI:https://doi.org/10.47737/2307-2873_2021_36_124. EDN: https://elibrary.ru/DNXBTP.

6. Holodova LV. Analiz oplodotvoryayushchej sposobnosti semeni bykov-proizvoditelej raznyh genotipov. In: Nacionalnaya nauchno-prakticheskaya konferenciya s mezhdunarodnym uchastiem “Aktual'nye problem intensifikacii razvitiya zhivotnovodstva”. Bryansk: Bryanskij GAU; 2022. P. 23–32. (In Russ.). EDN: https://elibrary.ru/GDUYUE.

7. Evenson DP. Sperm Chromatin Structure Assay (SCSA®) for Fertility Assessment. Curr Protoc. 2022;2(8):e508. DOI:https://doi.org/10.1002/cpz1.508.

8. Sharma R, Iovine C, Agarwal A, et al. TUNEL assay – Standardized method for testing sperm DNA fragmentation. Andrologia. 2021;53(2);e13738. DOI:https://doi.org/10.1111/and.13738.

9. Esteves SC, Zini A, Coward RM, et al. Sperm DNA fragmentation testing: Summary evidence and clinical practice recommendations. Andrologia. 2021;53(2);e13874. DOI:https://doi.org/10.1111/and.13874.

10. Amor H, Zeyad A, Alkhaled Y, et al. Relationship between nuclear DNA fragmentation, mitochondrial DNA damage and standard sperm parameters in spermatozoa of fertile and sub-fertile men before and after freeze-thawing procedure. Andrologia. 2018;50(5);e12998. DOI:https://doi.org/10.1111/and.12998.

11. Mohammadi Z, Tavalaee M, Gharagozloo P, et al. Could high DNA stainability (HDS) be a valuable indicator of sperm nuclear integrity? Basic Clin Androl. 2020;30:12. DOI:https://doi.org/10.1186/s12610-020-00110-8.

12. Horta F, Catt S, Ramachandran P, et al. Female ageing affects the DNA repair capacity of oocytes in IVF using a controlled model of sperm DNA damage in mice. Hum Reprod. 2020;35(3):529-544. DOI:https://doi.org/10.1093/humrep/dez308.

13. Wang B, Li Zh, Wang Ch, et al. Zygotic G2/M Cell Cycle Arrest Induced by ATM/Chk1 Activation and DNA Repair in Mouse Embryos Fertilized with Hydrogen Peroxide-Treated Epididymal Mouse Sperm. PloS one. 2013;8:e73987. DOI:https://doi.org/10.1371/journal.pone0073987.

14. Morrell JM, Valeanu AS, Lundeheim N, et al. Sperm quality in frozen beef and dairy bull semen. Acta Vet Scand. 2018;60:41. DOI:https://doi.org/10.1186/s13028-018-0396-2.

15. Collins A, Møller P, Gajski G, et al. Measuring DNA modifications with the comet assay: a compendium of protocols. Nat Protoc. 2023;18(3):929-989. DOI:https://doi.org/10.1038/s41596-022-00754-y.


Login or Create
* Forgot password?