Flow cytometric analysis of lymphocyte subset kinetics in Bali cattle experimentally infected with Jembrana disease virus

Veterinary Immunology and Immunopathology

Volumn 149, Issue 3-4, 2012, Pages 167-176

  Tenaya, I W Masa ^a,c   Heel, Kathy ^b   Stumbles, Philip A ^a   Wilcox, Graham E ^a  

^a MURDOCH UNIVERSITY   (Australia)

^b UNIVERSITY OF WESTERN AUSTRALIA   (Australia)

^c BPPH Wilayah VI   (Indonesia)

Author keywords

Cattle; Flow cytometry; Immunodeficiency; Jembrana disease virus; Lentivirus; Lymphocyte subpopulations

Indexed keywords

COMPLEMENT COMPONENT C3D RECEPTOR; GAMMA INTERFERON; IMMUNOGLOBULIN G;

ANIMAL CELL; ANIMAL EXPERIMENT; ANTIBODY PRODUCTION; ARTICLE; B LYMPHOCYTE; CATTLE; CD4+ T LYMPHOCYTE; CD8+ T LYMPHOCYTE; CYTOTOXIC T LYMPHOCYTE; FEVER; FLOW CYTOMETRY; IMMUNE RESPONSE; JEMBRANA DISEASE; LENTIVIRUS INFECTION; LEUKOPENIA; LYMPH NODE ENLARGEMENT; LYMPHADENOPATHY; LYMPHOCYTE COUNT; LYMPHOCYTE SUBPOPULATION; NONHUMAN; PERIPHERAL BLOOD MONONUCLEAR CELL; PLASMA CELL; T CELL DEPLETION;

ANIMALS; CATTLE; CATTLE DISEASES; CD4-CD8 RATIO; CD4-POSITIVE T-LYMPHOCYTES; CD8-POSITIVE T-LYMPHOCYTES; FEMALE; FLOW CYTOMETRY; IMMUNOPHENOTYPING; INDONESIA; INTERFERON-GAMMA; LENTIVIRUS INFECTIONS; LENTIVIRUSES, BOVINE; LEUKOCYTES, MONONUCLEAR; LYMPHOCYTE SUBSETS;

BOS; BOS JAVANICUS; BOVINE LENTIVIRUSES; JEMBRANA DISEASE VIRUS; LENTIVIRUS;

EID: 84866345051     PISSN: 01652427     EISSN: 18732534     Source Type: Journal    
DOI: 10.1016/j.vetimm.2012.06.013     Document Type: Article

References (50)

1. Ackley C.D., Yamamoto J.K., Levy N., Pedersen N.C., Cooper M.D. Immunologic abnormalities in pathogen-free cats experimentally infected with feline immunodeficiency virus. J. Virol. 1990, 64:5652-5655.
2. Alcami J. Advances in the immunopathology of HIV infection. Enferm. Infecc. Microbiol. Clin. 2004, 22:486-496.
3. Arokium H., Kamata M., Chen I. Virion-associated Vpr of human immunodeficiency virus type 1 triggers activation of apoptotic events and enhances fas-induced apoptosis in human T cells. J. Virol. 2009, 83:11283-11297.
4. Blankson J.N., Persaud D., Siliciano R.F. The challenge of viral reservoirs in HIV-1 infection. Annu. Rev. Med. 2002, 53:557-593.
5. Brenchley J.M., Hill B.J., Ambrozak D.R., Price D.A., Guenaga F.J., Casazza J.P., Kuruppu J., Yazdani J., Migueles S.A., Connors M., Roederer M., Douek D.C., Koup R.A. T-cell subsets that harbor human immunodeficiency virus (HIV) in vivo: implications for HIV pathogenesis. J. Virol. 2004, 78:1160-1168.
6. Brown C.R., Czapiga M., Kabat J., Dang Q., Ourmanov I., Nishimura Y., Martin M.A., Hirsch V.M. Unique pathology in simian immunodeficiency virus-infected rapid progressor macaques is consistent with a pathogenesis distinct from that of classical AIDS. J. Virol. 2007, 81:5594-5606.
7. Brugger B., Krautkramer E., Tibroni N., Munte C.E., Rauch S., Leibrecht I., Glass B., Breuer S., Geyer M., Kräusslich H.G., Kalbitzer H.R., Wieland F.T., Fackler O.T. Human immunodeficiency virus type 1 Nef protein modulates the lipid composition of virions and host cell membrane microdomains. Retrovirology 2007, 4:70-82.
8. Burkala E.J., Narayani I., Hartaningsih N., Kertayadnya G., Berryman D.I., Wilcox G.E. Recombinant Jembrana disease virus proteins as antigens for the detection of antibody to bovine lentiviruses. J. Virol. Methods 1998, 74:39-46.
9. Cao Y., Qin L., Zhang L., Safrit J., Ho D.D. Virologic and immunologic characterization of long-term survivors of human immunodeficiency virus type 1 infection. N. Engl. J. Med. 1995, 332:201-208.
10. Chadwick B.J., Coelen R.J., Sammels L.M., Kertayadnya G., Wilcox G.E. Genomic sequence analysis identifies Jembrana disease virus as a new bovine lentivirus. J. Gen. Virol. 1995, 76(Pt 1):189-192.
11. Chirmule N., Oyaizu N., Saxinger C., Pahwa S. Nef protein of HIV-1 has B-cell stimulatory activity. AIDS 1994, 8:733-734.
12. Clapham P.R., McKnight A. HIV-1 receptors and cell tropism. Br. Med. Bull. 2001, 58:43-59.
13. Cook S.J., Cook R.F., Montelaro R.C., Issel C.J. Differential responses of Equus caballus and Equus asinus to infection with two pathogenic strains of equine infectious anemia virus. Vet. Microbiol. 2001, 79:93-109.
14. Desport M., Ditcham W.G., Lewis J.R., McNab T.J., Stewart M.E., Hartaningsih N., Wilcox G.E. Analysis of Jembrana disease virus replication dynamics in vivo reveals strain variation and atypical responses to infection. Virology 2009, 386:310-316.
15. Desport M., Tenaya I.W., McLachlan A., McNab T.J., Rachmat J., Hartaningsih N., Wilcox G.E. In vivo infection of IgG-containing cells by Jembrana disease virus during acute infection. Virology 2009, 393:221-227.
16. Dharma D.M., Budiantono A., Campbell R.S., Ladds P.W. Studies on experimental Jembrana disease in Bali cattle. III. Pathol. J. Comp. Pathol. 1991, 105:397-414.
17. Dharma D.M., Ladds P.W., Wilcox G.E., Campbell R.S. Immunopathology of experimental Jembrana disease in Bali cattle. Vet. Immunol. Immunopathol. 1994, 44:31-44.
18. Foster B., Prussin C., Liu F., Whitmire J.K., Whitton J.L. Detection of intracellular cytokines by flow cytometry. Current Protocols in Immunology 2007, Wiley Press, (Chapter 6, Unit 6.24). J.E. Coligan (Ed.).
19. Garvey K.J., Oberste M.S., Elser J.E., Braun M.J., Gonda M.A. Nucleotide sequence and genome organization of biologically active proviruses of the bovine immunodeficiency-like virus. Virology 1990, 175:391-409.
20. + T cells mediate protection of rhesus macaques immunized with attenuated simian-human immunodeficiency virus SHIV89. 6 from vaginal challenge with simian immunodeficiency virus. J. Virol. 2008, 82:11181-11196.
21. + T cells in the genital tract control viral replication and delay progression to AIDS after vaginal SIV challenge in rhesus macaques immunized with virulence attenuated SHIV 89.6. J. Intern. Med. 2009, 265:67-77.
22. Gonda M.A., Oberste M.S., Garvey K.J., Pallansch L.A., Battles J.K., Pifat D.Y., Bess J.W., Nagashima K. Development of the bovine immunodeficiency-like virus as a model of lentivirus disease. Dev. Biol. Stand. 1990, 72:97-110.
23. Hammond S.A., Cook S.J., Lichtenstein D.L., Issel C.J., Montelaro R.C. Maturation of the cellular and humoral immune responses to persistent infection in horses by equine infectious anemia virus is a complex and lengthy process. J. Virol. 1997, 71:3840-3852.
24. Hartaningsih N., Wilcox G.E., Kertayadnya G., Astawa M. Antibody response to Jembrana disease virus in Bali cattle. Vet. Microbiol. 1994, 39:15-23.
25. + T-cell activation and bystander apoptosis induced by human immunodeficiency virus type 1 virions. J. Virol. 2005, 79:6299-6311.
26. + T cells subsequent to signaling through homing receptors is Fas/Fas ligand-mediated. J. Leukoc. Biol. 2007, 81:297-305.
27. Jin X., Bauer D.E., Tuttleton S.E., Lewin S., Gettie A., Blanchard J., Irwin C.E., Safrit J.T., Mittler J., Weinberger L., Kostrikis L.G., Zhang L., Perelson A.S., Ho D.D. Dramatic rise in plasma viremia after CD8(+) T cell depletion in simian immunodeficiency virus-infected macaques. J. Exp. Med. 1999, 189:991-998.
28. Levy J.A. HIV pathogenesis and long-term survival. AIDS 1993, 7:1401-1410.
29. Marsh J.W. The numerous effector functions of Nef. Arch. Biochem. Biophys. 1999, 365:192-198.
30. Mattapallil J.J., Douek D.C., Hill B., Nishimura Y., Martin M., Roederer M. Massive infection and loss of memory CD4+ T cells in multiple tissues during acute SIV infection. Nature 2005, 434:1093-1097.
31. + cytotoxic T lymphocytes from horses with equine infectious anemia virus recognize Env and Gag/PR proteins. J. Virol. 1994, 68:1459-1467.
32. McGuire T.C., Fraser D.G., Mealey R.H. Cytotoxic T lymphocytes in protection against equine infectious anemia virus. Anim. Health Res. Rev. 2004, 5:271-276.
33. Migueles S.A., Connors M. The role of CD4(+) and CD8(+) T Cells in controlling HIV infection. Curr. Infect. Dis. Rep. 2002, 4:461-467.
34. + T lymphocytes during febrile periods in horses experimentally infected with equine infectious anemia virus. Vet. Immunol. Immunopathol. 1999, 67:131-140.
35. Oaks J.L., McGuire T.C., Ulibarri C., Crawford T.B. Equine infectious anemia virus is found in tissue macrophages during subclinical infection. J. Virol. 1998, 72:7263-7269.
36. + T cell clones during primary HIV infection. Proc. Natl. Acad. Sci. U.S.A. 1997, 94:9848-9853.
37. Picker L.J. Immunopathogenesis of acute AIDS virus infection. Curr. Opin. Immunol. 2006, 18:399-405.
38. Qi M., Aiken C. Nef enhances HIV-1 infectivity via association with the virus assembly complex. Virology 2008, 373:287-297.
39. Ramachandran S. Early Observation and Research on Jembrana disease in Bali and other Indonesian islands. Workshop on Jembrana Disease and the Bovine Lentiviruses 1996, 5-9. Australian Center for International Agricultural Research. G.E. Wilcox, S. Soeharsono, D.M.N. Dharma, J.W. Copland (Eds.).
40. Rocchi M.S., Anderson M.J., Eaton S.L., Hamilton S., Finlayson J., Steele P., Barclay G.R., Chianini F. Three-colour flow cytometric detection of PrP in ovine leukocytes. Vet. Immunol. Immunopathol. 2007, 116:172-181.
41. Salk J., Bretscher P.A., Salk P.L., Clerici M., Shearer G.M. A strategy for prophylactic vaccination against HIV. Science 1993, 260:1270-1272.
42. Sellon D.C., Perry S.T., Coggins L., Fuller F.J. Wild-type equine infectious anemia virus replicates in vivo predominantly in tissue macrophages, not in peripheral blood monocytes. J. Virol. 1992, 66:5906-5913.
43. Soeharsono S., Hartaningsih N., Soetrisno M., Kertayadnya G., Wilcox G.E. Studies of experimental Jembrana disease in Bali cattle. I. Transmission and persistence of the infectious agent in ruminants and pigs, and resistance of recovered cattle to re-infection. J. Comp. Pathol. 1990, 103:49-59.
44. Soeharsono S., Wilcox G.E., Dharma D.M., Hartaningsih N., Kertayadnya G., Budiantono A. Species differences in the reaction of cattle to Jembrana disease virus infection. J. Comp. Pathol. 1995, 112:391-402.
45. Soesanto M., Soeharsono S., Budiantono A., Sulistyana K., Tenaya M., Wilcox G.E. Studies on experimental Jembrana disease in Bali cattle. II. Clinical signs and haematological changes. J. Comp. Pathol. 1990, 103:61-71.
46. Sol-Foulon N., Esnault C., Percherancier Y., Porrot F., Metais-Cunha P., Bachelerie F., Schwartz O. The effects of HIV-1 Nef on CD4 surface expression and viral infectivity in lymphoid cells are independent of rafts. J. Biol. Chem. 2004, 279:31398-31408.
47. Stewart M., Desport M., Hartaningsih N., Wilcox G. TaqMan real-time reverse transcription-PCR and JDVp26 antigen capture enzyme-linked immunosorbent assay to quantify Jembrana disease virus load during the acute phase of in vivo infection. J. Clin. Microbiol. 2005, 43:5574-5580.
48. Whetstone C.A., Suarez D.L., Miller J.M., Pesch B.A., Harp J.A. Bovine lentivirus induces early transient B-cell proliferation in experimentally inoculated cattle and appears to be pantropic. J. Virol. 1997, 71:640-644.
49. Wilcox G.E., Chadwick B.J., Kertayadnya G. Recent advances in the understanding of Jembrana disease. Vet. Microbiol. 1995, 46:249-255.
50. Zhang D., Shankar P., Xu Z., Harnishsc B., Chen G., Lange C., Lee S.J., Valdez H. Most antiviral CD8 T cells during chronoc viral infection do not express high levels of perforin and are not directly cytotoxic. Blood 2003, 101:226-234.