Evaluation of allelic frequencies distribution of the BoLA-DRB3 gene polymorphisms within exon 2 using PCR-RFLP
- Authors: Bezborodova N.A1, Bytov M.V1, Martynov N.A1, Sokolova O.V1, Petropavlovsky M.V1, Volskaya S.V1
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Affiliations:
- Ural Federal Agrarian Scientific Research Centre, Ural Branch of Russian Academy of Sciences
- Issue: No 4 (2023)
- Pages: 52-55
- Section: Articles
- URL: https://journals.eco-vector.com/2500-2627/article/view/657837
- DOI: https://doi.org/10.31857/S2500262723040105
- EDN: https://elibrary.ru/JYGBPU
- ID: 657837
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About the authors
N. A Bezborodova
Ural Federal Agrarian Scientific Research Centre, Ural Branch of Russian Academy of Sciences
Email: n-bezborodova@mail.ru
620142, Ekaterinburg, ul. Belinskogo, 112a
M. V Bytov
Ural Federal Agrarian Scientific Research Centre, Ural Branch of Russian Academy of Sciences620142, Ekaterinburg, ul. Belinskogo, 112a
N. A Martynov
Ural Federal Agrarian Scientific Research Centre, Ural Branch of Russian Academy of Sciences620142, Ekaterinburg, ul. Belinskogo, 112a
O. V Sokolova
Ural Federal Agrarian Scientific Research Centre, Ural Branch of Russian Academy of Sciences620142, Ekaterinburg, ul. Belinskogo, 112a
M. V Petropavlovsky
Ural Federal Agrarian Scientific Research Centre, Ural Branch of Russian Academy of Sciences620142, Ekaterinburg, ul. Belinskogo, 112a
S. V Volskaya
Ural Federal Agrarian Scientific Research Centre, Ural Branch of Russian Academy of Sciences620142, Ekaterinburg, ul. Belinskogo, 112a
References
- Характеристика быков-производителей с комплексными генотипами генов BLG и INOS по молочной продуктивности женских предков / Х. Х. Гильманов, С. В. Тюлькин, И. В. Ржанова и др. // Ученые записки казанской государственной академии ветеринарной медицины им. Н.Э. Баумана. 2020. Т. 241. № 1. С. 71-75. doi: 10.31588/2413-4201-1883-241-1-71-76.
- Метаболические заболевания крупного рогатого скота / В. А. Мищенко, А. В. Мищенко, Р. В. Яшин и др. // Ветеринария сегодня. 2021. Т. 10. № 3. С. 184-189. doi. 10.29326/2304-196X-2021-3-38-184-189.
- Review: Genetic selection of high-yielding dairy cattle toward sustainable farming systems in a rapidly changing world / L. F. Brito, N. Bedere, F. Douhard, et al. // Ani-mal. 2021. Vol. 15. URL: https://www.sciencedirect.com/science/article/pii/S175173112100135X?via%3Dihub (дата обращения: 10.02.2022). doi: 10.1016/j.animal.2021.100292.
- Detection and immunobiological characterization of bovine leukemia virus in Russian Federation territory in dependence on geographikal variations / M. V. Petropavlovskiy, I. M. Donnik, N. A. Bezborodova, et al. // Journal of Integrated OMICS. 2019. Vol. 9. No. 1. URL: https://www.jiomics.com/index.php/jiomics/article/view/157 (дата обращения: 10.02.2022) doi: 10.5584/jiomics.v9i1.255.
- Early events following bovine leukaemia virus infection in calves with different alleles of the major histocompatibility complex DRB3 gene / A. Forletti, C. M. Lützelschwab, R. Cepeda, et al. // Veterinary Research. 2020. Vol. 51. No. 1. URL: https://veterinaryresearch.biomedcentral.com/articles/10.1186/s13567-019-0732-1 (дата обращения: 10.02.2022). doi: 10.1186/s13567-019-0732-1.
- Frie M. C., Coussens P. M. Bovine leukemia virus: A major silent threat to proper immune responses in cattle // Veterinary Immunology and Immunopathology. 2015. Vol. 163. No. 3. P. 103-114. doi. 10.1016/j.vetimm.2014.11.014.
- Bovine leukemia virus and cow longevity in Michigan dairy herds / P. C. Bartlett, B. Norby, T. M. Byrem et al. // Journal of Dairy Science. 2013. Vol. 96 No. 3. P. 1591-1597. doi. 10.3168/jds.2012-5930.
- Lifetime effects of infection with bovine leukemia virus on longevity and milk production of dairy cows / O. Nekouei, J. Vanleeuwen, H. Stryhn, et al. // Preventive Veterinary Medicine. 2016. Vol. 133. URL: https://pubmed.ncbi.nlm.nih.gov/27720022/ (дата обращения: 10.02.2022). doi: 10.1016/j.prevetmed.2016.09.011.
- Emanuelson U., Scherling K., Pettersson H. Relation-ships between herd bovine leukemia virus infection status and reproduction, disease incidence, and productivity in Swedish dairy herds // Preventive Veterinary Medicine. 1992. Vol. 12. No. 1. P. 121-131. doi. 10.1016/0167-5877(92)90075-Q.
- Bovine leukemia virus discovered in human blood / G. C. Buehring, A. Delaney, H. Shen, et al. // BMC Infectious Diseases. 2019. Vol. 19. No. 1. URL: https://bmcinfectdis.biomedcentral.com/articles/10.1186/s12879-019-3891-9 (дата обращения: 10.02.2022). doi: 10.1186/s12879-019-3891-9.
- No evidence of bovine leukemia virus proviral DNA and antibodies in human specimens from Japan / M. P. Yamanaka, S. Saito, Y. Hara, et al. // Retrovirology. 2022. Vol. 19. No. 1. URL: https://retrovirology.biomedcentral.com/articles/10.1186/s12977-022-00592-6 (дата обра-щения: 10.02.2022). doi: 10.1186/s12977-022-00592-6.
- Relationship between allelic heterozygosity in BoLA-DRB3 and proviral loads in bovine leukemia virus-infected cattle / H. E. Daous, S. Mitoma, E. Elhanafy, et al. // Animals. 2021. Vol. 11. No. 3. URL: https://www.mdpi.com/2076-2615/11/3/647 (дата обращения: 10.02.2022). doi: 10.3390/ani11030647.
- Morales J., Lopez-Herrera A., Zuluaga J. Association of BoLA DRB3 gene polymorphisms with BoHV-1 infection and zootechnical traits // Open Veterinary Journal. 2020. Vol. 10. No. 3. P. 331-339. doi. 10.4314/ovj.v10i3.12.
- Sequence and PCR-RFLP analysis of 14 novel BoLA-DRB3 alleles / A. Gelhaus, L. Schnittger, D. Mehlitz, et al. // Animal Genetics. 1995. Vol. 26. No. 3. P. 147-153. doi. 10.1111/j.1365-2052.1995.tb03154.x.
- van Eijk M. J. T., Stewart-Haynes J. A., Lewin H. A. Extensive polymorphism of the BoLA-DRB3 gene distinguished by PCR-RFLP // Animal Genetics. 1992. Vol. 23. No. 6. P. 483-496. doi. 10.1111/j.1365-2052.1992.tb00168.x.
- Polymorphism in BoLA-DRB3 exon 2 correlates with resistance to persistent lymphocytosis caused by bovine leukemia virus / A. Xu, M. J. van Eijk, C. Park, et al. // The Journal of Immunology. 1993. Vol. 151. No. 12. P. 6977-6985. doi. 10.4049/jimmunol.151.12.6977.
- Takeshima S. N., Ohno A., Aida Y. Bovine leukemia virus proviral load is more strongly associated with bovine major histocompatibility complex class II DRB3 polymorphism than with DQA1 polymorphism in Hol-stein cow in Japan // Retrovirology. 2019. Vol. 16. No. 1. URL: https://retrovirology.biomedcentral.com/articles/10.1186/s12977-019-0476-z (дата обращения: 10.02.2022). doi: 10.1186/s12977-019-0476-z.
- Связь генотипов BoLA-DRB3 с племенной ценностью по показателям молочной продуктивности в российской популяции молочного скота / А. А. Сермягин, Н. В. Ковалюк, А. Н. Ермилов и др. // Сельскохозяйственная биология. 2016. Т. 51. № 6. С. 775-781. doi. 10.15389/agrobiology.2016.6.775rus.
- Association of BLV infection profiles with alleles of the BoLA-DRB3.2 gene / M. A. Juliarena, M. Poli, L. Sala, et al. // Animal Genetics. 2008. Vol. 39. No. 4. P. 432-438. doi. 10.1111/j.1365-2052.2008.01750.x.
- Identification of bovine leukocyte antigen class II haplotypes associated with variations in bovine leukemia virus proviral load in Japanese Black cattle / T. Miyasaka, S. N. Takeshima, M. Jimba, et al. // Tissue Antigens. 2013. Vol. 81. No. 2. P. 72-82. doi. 10.1111/tan.12041.
- Bovine major histocompatibility complex (BoLA) heterozygote advantage against the outcome of bovine leukemia virus infection / C. W. Lo, S. N. Takeshima, S. Wada, et al. // HLA. 2021. Vol. 98. No. 2. P. 132-139. doi. 10.1111/tan.14285.
- Приоритизация генов, ассоциированных с патогенезом лейкоза у крупного рогатого скота / Н. С. Юдин, Н. Л. Подколодный, Т. А. Агаркова и др. // Вавиловский журнал генетики и селекции. 2018. Т. 22 № 8. С. 1063-1069. doi. 10.18699/VJ18.451.
- BoLA-DRB3 polymorphism is associated with differential susceptibility to bovine leukemia virus-induced lymphoma and proviral load / C. W. Lo, L. Borjigin, S. Saito, et al. //Viruses. 2020. Vol. 12. No. 3. URL: https://www.mdpi.com/1999-4915/12/3/352 (дата обращения: 10.02.2022). doi: 10.3390/v12030352.
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