ЛЕЙКОЗ КРУПНОГО РОГАТОГО СКОТА
Рубрики: ЛЕКЦИИ
Аннотация и ключевые слова
Аннотация (русский):
В аналитической лекции рассмотрены имеющиеся данные по мало обсуждаемым в отечественной литературе аспектам лейкоза крупного рогатого скота. С современных позиций паразитарной системы интерпретированы важнейшие элементы патобиоза ― передача инфекции, патогенез, его клеточные и вирусологические механизма, провирусная нагрузка и практическое значение ее измерения, заражение потомства и роль инфицированного молодняка в распространении лейкоза.

Ключевые слова:
лейкоз, крупный рогатый скот, передача инфекции, патогенез, провирусная нагрузка, лейкоз у молодняка
Текст
Текст произведения (PDF): Читать Скачать
Список литературы

1. Makarov V.V., Grinishin D.P. E`pizootologicheskie perspektivy` lejkoza krupnogo rogatogo skota [Epizootological prospects for the bovine leucosis], Vestnik Rossel`xozakademii [Herald of RAA], 2005, No. 2, pp. 70-73. (In russ.).

2. Makarov V.V., Grinishin D.P. PCzR v diagnostike lejkoza krupnogo rogatogo skota [PCR in diagnostics of the bovine leucosis], Veterinariya [Veterinary medicine], 2005, No. 4, pp. 9-11. (In russ.).

3. Aida Y., Murakami H., Takahashi M., Takeshima S. Mechanisms of pathogenesis induced by bovine leukemia virus as a model for human T-cell leukemia virus, Front. Microbiol., 2013, No. 4, pp. 328. doi: 10.3389 / fmicb.2013.00328

4. EFSA AHAW Panel (EFSA Panel on Animal Health and Welfare), 2015. Scientific opinion on enzootic bovine leukosis, EFSA Journal, 2015, Vol. 13(7), No. 4188, 63 p. doi:10.2903/j.efsa.2015.4188

5. Hanon E., Stinchcombe J., Saito M., Asquith B., Taylor G., Tanaka Y., Weber J., Griffiths G., Bangham C. Fratricide among CD81 T Lymphocytes Naturally Infected with Human T Cell Lymphotropic Virus Type I, Immunity, 2000, Vol. 13, pp. 657-664.

6. Höllsberg P., Mechanisms of T-cell activation by human T-cell lymphotropic virus type I, Microbiology and Molecular Biology Reviews, 1999, No. 63, pp. 308-333.

7. Hoshino H. Cellular factors involved in HTLV-1 entry and pathogenicit. Front. Microbio., 2012, No. 3, pp. 222. doi: 10.3389/fmicb.2012.0022.

8. Gutiérrez G., Merlini R., Alvarez R., Rondelli F., Dynamics of perinatal bovine leukemia virus infection, BMC Veterinary Research, 2014, No. 10(1), pp. 82. doi: 10.1186 / 1746-6148-9-95.

9. Igakura T., Stinchcombe J., Goon P., Taylor G., Weber J., Griffiths G., Tanaka Y., Osame M., Bangham C., Spread of HTLV-I between lymphocytes by virus-induced polarization of the cytoskeleton, Science, 2003, No. 299, pp. 1713-1716.

10. Juliarena M., Barrios C., Lützelschwab C., Esteban E., Bovine leukemia virus: current perspectives, Virus Adaptation and Treatment, 2017, Vol. 9, pp. 13-26. doi.org/10.2147/VAAT.S113947

11. Juliarena M., Gutierrez S., Ceriani C., Determination of proviral load in bovine leukemia virus-infected cattle with and without lymphocytosis, Am. J. Vet. Res., 2007 Nov, No. 68 (11), pp. 1220-5. DOI: 10.2460 / ajvr.68.11.1220

12. Kajiyama W., Kashiwagi J., Ikematsu H., Hayashi H., Nomura H., Okōchi K., Intrafamilial clustering of anti-ATLA-Positive persons, Am J Epldemiol, 1988, No. 124, pp. 800-806.

13. Maguer-Satta V., Duc Dodon M., Human immature thymocytes as target cells of the leukemogenic activity of human T-cell leukemia virus type I, Blood, 1995, No. 86(4), pp. 1444-1452. DOI: 10.1182/blood.

14. Manual of Diagnostic Tests and Vaccines for Terrestrial Animals, 2019 https://www.oie.int/en/standard-setting/terrestrial-manual/access-online/

15. Mazzarello A., Fitch M., Hellerstein M., Chiorazzi N., Measurement of Leukemic B-Cell Growth Kinetics in Patients with Chronic Lymphocytic Leukemia, Methods Mol. Biol., 2019, No. 1881, pp. 129-151. doi: 10.1007 / 978-1-4939-8876-1_11.

16. Mekata H., Sekiguchi S., Konnai S., Kirino Y., Honkawa K., Nonaka N., Horii Y., Norimine J., Evaluation of the natural perinatal transmission of bovine leukaemia virus, Vet. Record., 2015, No. 176(10), pp. 274. http://dx.doi.org/10.1136/vr.102464

17. Mekata H., Yamamoto M., Hayashi T., Kirino Y., Sekiguchi S., Konnai S., Horii Y., Norimine J., Cattle with a low bovine leukemia virus proviral load are rarely an infectious source, Japanese J. of Vet. Res., 2018, No. 66(3), pp. 157-163. doi: 10.14943/jjvr.66.3.157

18. Messmer B., Messmer D., Allen S., Kudalkar P., Cesar D., Murphy E., Koduru P., Ferrarini M., Zupo S., Cutrona G., Damle R., Wasil T., Rai K., Hellerstein M., Chorazzi N., In vivo measurements document the dynamic cellular kinetics of chronic lymphocytic leukemia B cells, J. Clin. Invest. , 2005 Mar, No. 115(3), pp. 755-764.

19. Mirsky M., Olmstead C., Da Y., Lewin H., The prevalence of proviral bovine leukemia virus in peripheral blood mononuclear cells at two subclinical stages of infection, J. Virol., 1996, No. 70 (4), pp. 2178-2183.

20. Panei C.J., Takeshima S.N., Omori T., Nunoya T., Davis W., Ishizaki H., Matoba K., Aida Y., Estimation of bovine leukemia virus (BLV) proviral load harbored by lymphocyte subpopulations in BLV-infected cattle at the subclinical stage of enzootic bovine leucosis using BLV-CoCoMo-qPCR, BMC Vet. Res. 2013;, No. 9, pp. 95. DOI: 10.1186/1746-6148-9-95.

21. Ruiz V., Porta N., Lomónaco M., Trono K., Alvarez I., Bovine Leukemia Virus Infection in Neonatal Calves. Risk Factors and Control Measures. Front. Vet. Sci., 2018, No. 5, pp. 267. doi: 10.3389/fvets.2018.00267.

22. Samitas K., Lötvall J., Bossios A. B cells: from early development to regulating allergic diseases, Arch Immunol Ther Exp (Warsz), 2010, Vol. 58, Is. 3, pp. 209-225. doi:10.1007/s00005-010-0073-2.

23. Schwartz I., Bensaid A., Polack B., Perrin B., Berthelemy M., Levy D., In vivo leukocyte tropism of bovine leukemia virus in sheep and cattle, Journal of Virology, 1994, No. 68 (7), pp. 4589-96, doi: 10.1128/JVI.68.7.4589-4596.1994.

24. Sherer N., Lehmann M., Jimenez-Soto L., Horensavitz C., Pypaert M., Mothes W., Retroviruses can establish filopodial bridges for efficient cell-to-cell transmission, Nat Cell Biol., 2007, No. 9, pp. 310-315. [PubMed: 17293854].

25. Watanuki S., Takeshima S., Borjigin L., Sato H., Bai L., Murakami H., Aida Y., Visualizing bovine leukemia virus (BLV)-infected cells and measuring BLV proviral loads in the milk of BLV seropositive dams. Vet Res., 2019 Nov, Vol. 29, No. 50(1), pp. 102. doi: 10.1186/s13567-019-0724-1.

Войти или Создать
* Забыли пароль?