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Flow Cytometric Determination of the Expression of gp 51 Protein of Bovine Leukaemia Virus in Experimentally Infected Sheep Cover

Flow Cytometric Determination of the Expression of gp 51 Protein of Bovine Leukaemia Virus in Experimentally Infected Sheep

Journal of Veterinary Research
Volume 58 (2014): Issue 3 (September 2014)
By:   
Open Access
|Oct 2014
References

References

  1. 1. Adam E., Kerkhofs P., Mammerickx M., Burny A., Droogmans L., Willems L.: Involvement of the cyclic AMP-responsive element binding protein in bovine leukemia virus expressionJ Virol 1994, 68, 5845-5853.
    Open DOISearch in Google Scholar
  2. 2. Aida Y., Miyasaka M., Okada K., Onuma M., Kogure S., Suzuki M., Minoprio P., Levy D., Ikawa Y.: Further phenotypic characterization of target cells for bovine leukemia virus experimental infection in sheep. Am J Vet Res 1989, 50, 19461951.
    Search in Google Scholar
  3. 3. Aida Y., Okada K., Amanuma H.: Phenotype and ontogeny of cells carrying a TAA that is expressed of bovine leukemia virus induced lymphosarcoma. Cancer Res 1993, 53, 429-437.
    Search in Google Scholar
  4. 4. Balič D., Lojkič I., Perskič M., Bedekovič J.: Identification of a new genotype of bovine leukaemia virus. Arch Virol 2013, 157, 1281-1290.
    Open DOISearch in Google Scholar
  5. 5. Birkebak T.A., Palmer G.H., Davis W.C., Knowles D.P., McElwain T.F.: Association of gp51 expression and persistent CD5+ B-lymphocytes lymphocytosis in sheep infected with BLV. Leukemia 1994, 8, 1890-1899.
    Search in Google Scholar
  6. 6. Cantor G.H., Pritchard S.M., Dequiedt F., Willems L., Kettmann R., Davis W.C.: CD5 is dissociated from the B-cell receptor in B- cells from bovine leukemia virus infected persistently lymphocytotic cattle: consequences to B-cell receptor - mediated apoptosis. J Virol 2001, 75, 1689-1696.
    Open DOISearch in Google Scholar
  7. 7. Chevallier N., Berthelemy M., Le Rhun D., Laine V., Levy D., Schwartz-Cornil I.: Bovine leukemia virus-induced lympho-cytosis and increased cell survival mainly involve the CD11b+ B lymphocyte subset in sheep. J Virol 1998, 72, 4413-4420.
    Open DOISearch in Google Scholar
  8. 8. Clevers H., Mac Hugh N., Bensaid A.: Identification of a bovine surface antigen uniquely expressed on CD4-CD8-T cell receptor gamma/delta T+ lymphocytes. Eur J Immunol 1990, 20, 809-817.
    Open DOISearch in Google Scholar
  9. 9. Coffin J.M.: Retroviridae: The viruses and their replication. In:Lippincot-Raven Publishers, Philadelphia, 1997, pp. 641-671.
    Search in Google Scholar
  10. 10. Cockerell G.L., Parodi A.L., Levy D.: Immunocompetence of sheep experimentally infected with bovine leukemia virus. Vet Immunol Immunopathol 1986, 13, 189-196.
    Open DOISearch in Google Scholar
  11. 11. Depelchin A., Letesson J.J., Lostrie-Trussart N., Mammerickx M., Portetelle D., Burny A.: Bovine leukemia virus (BLV) infected B-cells express a marker similar to the CD5 T- cell marker. Immunol Lett 1989, 29, 69-76.
    Open DOISearch in Google Scholar
  12. 12. Djilali S., Parodi A.L.: The BLV- induced leukemia-lymphosarcoma complex in sheep. Vet Immunol Immunopathol 1989, 22, 233-244.
    Open DOISearch in Google Scholar
  13. 13. Gatei M., Brandon R., Naif H., McLennan M., Daniel R., Levin M.: Changes in B and T cell subsets in bovine leukemia virus-infected cattle. Vet Immunol Immunopathol 1989, 23, 139-147.
    Open DOISearch in Google Scholar
  14. 14. Hidalgo B., Bonilla A.: Lymphoproliferation assays in cattle naturally infected with bovine leukemia virus (BLV) and bovine immunodeficiency virus (BIV). J Vet Med B 1996, 43, 325-332.
    Open DOISearch in Google Scholar
  15. 15. Jensen W.A., Rovnak J., Cockerell G.L.:transcription of the bovine leukemia virus tax/rex region in normal and neoplastic lymphocytes of cattle and sheep. J Virol 1991, 65, 2484-2490.
    Open DOISearch in Google Scholar
  16. 16. Jensen W.A., Sheehy S.E., Fox M.H., Davis W.C., Cockerell G.L.:expression of bovine leukemia virus in isolated B-lymphocytes of cattle and sheep. Vet Immunol Immunopathol 1990, 26, 333-342.
    Open DOISearch in Google Scholar
  17. 17. Kettmann R., Dechamps J., Cleuter Y., Ghysdael J., Mammerickx M.: Distribution of bovine leukemia virus proviral DNA sequences in tissue of animals with enzootic bovine leucosis. Leuk Res 1998, 2, 23-32.
    Open DOISearch in Google Scholar
  18. 18. Klener P., Szynal Y., Cleuter M., Merimi H., Duvillier F.: Insightes into gene expression changes impacting B-cell transformation: cross-species microarray analysis of bovine leukemia virus tax-responsive genes in bovine B-cells. J Virol 2006, 55, 690-695.
    Open DOISearch in Google Scholar
  19. 19. Lewin H.A., Bernoco D.: Evidence for BoLA-linked resistance and susceptibility to subclinical progression of bovine leukaemia virus infection. Anim Genet 1986, 17, 197-207.
    Open DOISearch in Google Scholar
  20. 20. Llames L., Goyache J., Domenech A., Montana A.V., Suarez G., Gomez-Lucia E.: Cellular distribution of bovine leukemia virus proteins gp51SU, Pr72(env), and Pr66 (gag-pro) in persistently infected cells. Virus Res 2001, 79, 45-57.
    Open DOISearch in Google Scholar
  21. 21. Mamoun R.Z., Morrisson M., Rebeyrotte B., Busetta B., Kettmann R., Guilleman B.: Sequence variability of bovine leukemia virus env gene and its relevance to the structure and antigenicity of the glycoproteins. J Virol 1990, 64, 4180-4188.
    Open DOISearch in Google Scholar
  22. 22. Meirom R., Moss S., Brenner J.: Bovine leukemia virus gp51 antigen expression is associated with CD5 and IgM markers on infected lymphocytes. Vet Immunol Immunopathol 1997, 59, 113-119.
    Open DOISearch in Google Scholar
  23. 23. Mirsky M.L., Olmstead C.A., Da Y., Levin H.: The prevalence of proviral bovine leukemia virus in peripheral blood mononuclear cells at two subclinical stages of infection. J Virol 1996, 70, 2178-2183.
    Open DOISearch in Google Scholar
  24. 24. Mirsky M.L., Olmstead C., Da Y., Lewin H.: Reduced bovine leukemia virus proviral load in genetically resistant cattle. Animal Genet 1998, 29, 245-252.
    Open DOISearch in Google Scholar
  25. 25. Powers M., Radke K.: Activation of bovine leukemia virus transcription in lymphocytes from infected sheep: rapid transition through early to late gene expression. J Virol 1992, 66, 4769-4777.
    Open DOISearch in Google Scholar
  26. 26. Sagata N., Yasanuga T., Tsuzuku-Kawamura J., Ohishi K., Ogawa Y., Ihawa I.: Complete nucleotide sequence of the genome of bovine leukemia virus; its evolutionary relationship to other retroviruses. Proc Nat Acad Sci USA 1985, 82, 677-682.
    Search in Google Scholar
  27. 27. Schwartz I., Bensaid A., Polack B., Perrin B.:leukocyte tropism of bovine leukemia virus in sheep and cattle. J Virol 1994, 68, 4589-4596.
    Open DOISearch in Google Scholar
  28. 28. Stec J., Grundboeck J., Szczotka M., Reichert M., Rulka J., Kozaczyńska B.: Effect of mitogens on thestimulation of lymphocytes from normal and BLV-infected cattle. Bull Vet Inst Pulawy 1993, 33, 29-35.
    Search in Google Scholar
  29. 29. Stone D.M., McElwain T.F., Davis W.C.: Enhanced B-lymphocyte expression of IL-2R alpha associated with T lymphocytosis in BLV-infected persistently lymphocytotic cows. Leukemia 1994, 8, 1057-1061.
    Search in Google Scholar
  30. 30. Stone D.M., Norton L.K., Davis W.C.: Modulation of bovine leukemia virus associated spontaneous lymphocyte proliferation by monoclonal antibodies to lymphocyte surface molecules. Clin Immunol Immunopathol 1997, 83, 156-164.
    Open DOISearch in Google Scholar
  31. 31. Szczotka M.: Acid phosphatase and non-specific alpha-naphthyl esterase activities in lymphocytes of sheep experimentally infected with bovine leukemia virus (BLV) and in trials of active immunization. Thesis. National Veterinary Research Institute, Pulawy, Poland, 1988.
    Search in Google Scholar
  32. 32. Takashima I., Olson C., Driscoll D.M., Baumgartener L.E.: B-lymphocytes and T lymphocytes in three types of bovine lymphosarcoma. J Natl Cancer Inst 1977, 59, 1205-1209.
    Open DOISearch in Google Scholar
  33. 33. Trainin Z., Brenner J., Meirom R., Ungar-Waron H.: Detrimental effect of bovine leukemia virus (BLV) on the immunological state of cattle. Vet Immunol Immunopathol 1996, 54, 293-302.
    Open DOISearch in Google Scholar
  34. 34. Uchiyama T.: Human T-cell leukemia virus type I (HTLV-I) and human diseases. Ann Rev Immunol 1997, 15, 15-37.
    Open DOISearch in Google Scholar
  35. 35. Udina I.G., Karamysheva E.E., Turkova S.O., Orlova A.R., Sulimova G.E.: Genetic mechanisms of resistance and susceptibility to leukemia in Ayrshire and black pied cattle breeds determined by allelic distribution of gene Bola-DRB3. Genetika 2003, 39, 383-96.
    Search in Google Scholar
  36. 36. Xu A., Van Ejik M., Park C., Levin H.A.: Polymorphism in BoLa-DRB3 ekson 2 correlates with resistance to persistent lymphocytosis caused by bovine leukaemia virus. J Immunol 1993, 12, 6977-6981.
    Search in Google Scholar
DOI: https://doi.org/10.2478/bvip-2014-0055 | Journal eISSN: 2450-8608 (formerly 2300-3235)
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Language: English
Page range: 353 - 361
Submitted on: Dec 6, 2014
Accepted on: Aug 28, 2014
Published on: Oct 1, 2014
Published by: National Veterinary Research Institute in Pulawy
In partnership with: Paradigm Publishing Services
Keywords:
bovine leukosis,
gp51 glycoprotein,
lymphocytes,
flow cytometry
Related subjects:
Life sciences,
Molecular biology,
Microbiology and virology,
Life sciences, other,
Medicine,
Veterinary medicine

© 2014 Maria Szczotka, published by National Veterinary Research Institute in Pulawy
This work is licensed under the Creative Commons Attribution-NonCommercial-NoDerivatives 3.0 License.

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