Perivascular inflammatory cells in ovine Visna/maedi encephalitis and their possible role in virus infection and lesion progression

Journal of NeuroVirology

Volumn 18, Issue 6, 2012, Pages 532-537

  Polledo, Laura ^a   González, Jorge ^a   Benavides, Julio ^a   Martínez Fernández, Beatriz ^a   Ferreras, Ma Carmen ^a   Marín, Juan F García ^a  

^a UNIVERSITY OF LEÓN   (Spain)

Author keywords

Encephalitis; Immunology; Maedi; Neuropathology; Sheep; Visna

Indexed keywords

ANIMAL EXPERIMENT; ANIMAL MODEL; ANIMAL TISSUE; ARTICLE; B LYMPHOCYTE; CANCER INVASION; CD4+ T LYMPHOCYTE; CD8+ T LYMPHOCYTE; CONTROLLED STUDY; DISEASE COURSE; DISEASE SEVERITY; ENCEPHALITIS; INFLAMMATORY CELL; MACROPHAGE; MAEDI VISNA; NONHUMAN; PRIORITY JOURNAL; VIRUS INFECTION;

ANIMALS; ANTIGENS, VIRAL; B-LYMPHOCYTES; BLOOD VESSELS; BRAIN; CD4-POSITIVE T-LYMPHOCYTES; CD8-POSITIVE T-LYMPHOCYTES; ENCEPHALITIS, VIRAL; IMMUNOHISTOCHEMISTRY; IMMUNOPHENOTYPING; MACROPHAGES; SHEEP; SHEEP, DOMESTIC; VISNA; VISNA-MAEDI VIRUS;

OVIS; OVIS ARIES;

EID: 84875742636     PISSN: 13550284     EISSN: 15382443     Source Type: Journal    
DOI: 10.1007/s13365-012-0131-0     Document Type: Article

References (36)

1. Benavides J, Fuertes M, García-Pariente C, Ferreras MC, García Marín JF, Pérez V (2006a) Natural cases of Visna in sheep with myelitis as the sole lesion in the central nervous system. J Comp Pathol 134:219-230
2. Benavides J, Garcia-Pariente C, Fuertes M, Ferreras MC, Garcia-Marin JF, Juste RA, Perez V (2009) Maedi-Visna: the meningoencephalitis in naturally occurring cases. J Comp Pathol 140:1-11
3. Benavides J, García-Pariente C, Gelmetti D, Fuertes M, Ferreras MC, García-Marín JF, Pérez V (2006b) Effects of fixative type and fixation time on the detection of Maedi Visna virus by PCR and immunohistochemistry in paraffin-embedded ovine lung samples. J Virol Methods 137:317-324
4. Benavides J, Gomez N, Gelmetti D, Ferreras MC, Garcia-Pariente C, Fuertes M, Garcia-Marin JF, Perez V (2006c) Diagnosis of the nervous form of Maedi-Visna infection with a high frequency in sheep in Castilla y Leon, Spain. Vet Rec 158:230-235
5. Blacklaws BA (2012) Small ruminant lentiviruses: immunopathogenesis of visna-maedi and caprine arthritis and encephalitis virus. Comp Immunol Microbiol Infect Dis 35:259-269
6. Christodoulopoulos G (2006) Maedi-Visna: clinical review and short reference on the disease status in Mediterranean countries. Small Ruminant Res 62:47-53
7. Craig LE, Sheffer D, Meyer AL, Hauer D, Lechner F, Peterhans E, Adams RJ, Clements JE, Narayan O, Zink MC (1997) Pathogenesis of ovine lentiviral encephalitis: derivation of a neurovirulent strain by in vivo passage. J Neurovirol 3:417-427
8. Cutlip RC, Lehmkuhl HD, Schmerr MJ, Brogden KA (1988) Ovine progressive pneumonia (maedi-visna) in sheep. Vet Microbiol 17:237-250
9. Dawson M (1987) Pathogenesis of maedi-visna. Vet Rec 120:451-454
10. Ebrahimi B, Allsopp TE, Fazakerley JK, Harkiss GD (2000) Phenotypic characterisation and infection of ovine microglial cells with Maedi-Visna virus. J Neurovirol 6:320-328
11. Duval R, Bellet V, Delebassee S, Bosgiraud C (2002a) Implication of caspases during maedi-visna virus-induced apoptosis. J Gen Virol 83:3153-3161
12. Duval R, Delebassee S, Cardot PJ, Bosgiraud C (2002b) Visna virus-induced cytopathic effect in vitro is caused by apoptosis. Arch Virol 147:943-959
13. Esiri MM, Gay D (1990) Immunological and neuropathological significance of the Virchow-Robin space. J Neurol Sci 100:3-8
14. Freel SA, Saunders KO, Tomaras GD (2011) CD8(+) T-cell-mediated control of HIV-1 and SIV infection. Immunol Res 49:135-146
15. Gelmetti D, Gibelli L, Brocchi E, Cammarata G (2000) Using a panel of monoclonal antibodies to detect Maedi virus (MV) in chronic pulmonary distress of sheep. J Virol Methods 88:9-14
16. Georgsson G (1994) Neuropathologic aspects of lentiviral infections. Ann N Y Acad Sci 724:50-67
17. Georgsson G, Houwers DJ, Palsson PA, Petursson G (1989) Expression of viral antigens in the central nervous system of visna-infected sheep: an immunohistochemical study on experimental visna induced by virus strains of increased neurovirulence. Acta Neuropathol 77:299-306
18. Georgsson G, Nathanson N, Palsson PA, Petursson G (1976) The pathology of visna and maedi in sheep. Front Biol 44:61-96
19. Gómez N, González J, Corpa JM, Pérez V, García Marín JF (1999) Diagnóstico de la forma nerviosa del maedi-visna en ovinos de aptitud lechera. Producción Ovina y Caprina 24:393-397
20. Kim WK, Corey S, Alvarez X, Williams K (2003) Monocyte/macrophage traffic in HIV and SIV encephalitis. J Leukoc Biol 74:650-656
21. Kim WK, Corey S, Chesney G, Knight H, Klumpp S, Wuthrich C, Letvin N, Koralnik I, Lackner A, Veasey R, Williams K (2004) Identification of T lymphocytes in simian immunodeficiency virus encephalitis: distribution of CD8+ T cells in association with central nervous system vessels and virus. J Neurovirol 10:315-325
22. Leginagoikoa I, Juste RA, Barandika J, Amorena B, De Andres D, Lujan L, Badiola J, Berriatua E (2006) Extensive rearing hinders Maedi-Visna Virus (MVV) infection in sheep. Vet Res 37:767-778
23. Lujan L, Garcia Marin JF, Fernandez de Luco D, Vargas A, Badiola JJ (1991) Pathological changes in the lungs and mammary glands of sheep and their relationship with maedi-visna infection. Vet Rec 129:51-54
24. Marcondes MC, Burudi EM, Huitron-Resendiz S, Sanchez-Alavez M, Watry D, Zandonatti M, Henriksen SJ, Fox HS (2001) Highly activated CD8(+) T cells in the brain correlate with early central nervous system dysfunction in simian immunodeficiency virus infection. J Immunol 167:5429-5438
25. Panitch H, Petursson G, Georgsson G, Palsson PA, Nathanson N (1976) Pathogenesis of visna. III. Immune responses to central nervous system antigens in experimental allergic encephalomyelitis and visna. Lab Invest 35:452-460
26. Peluso R, Haase A, Stowring L, Edwards M, Ventura P (1985) A Trojan horse mechanism for the spread of visna virus in monocytes. Virology 147:231-236
27. Persidsky Y (1999) Model systems for studies of leukocyte migration across the blood-brain barrier. J Neurovirol 5:579-590
28. Polledo L, Gonzalez J, Benavides J, Morales S, Martinez-Fernandez B, Delgado L, Reina R, Glaria I, Perez V, Ferreras MC, Garcia Marin JF (2011) Patterns of lesion and local host cellular immune response in natural cases of ovine maedi-visna. J Comp Pathol 147:1-10
29. Schmitz JE, Kuroda MJ, Santra S, Sasseville VG, Simon MA, Lifton MA, Racz P, Tenner-Racz K, Dalesandro M, Scallon BJ, Ghrayeb J, Forman MA, Montefiori DC, Rieber EP, Letvin NL, Reimann KA (1999) Control of viremia in simian immunodeficiency virus infection by CD8+ lymphocytes. Science 283:857-860
30. Sigurdsson B, Palsson P, Grimsson H (1957) Visna, a demyelinating transmissible disease of sheep. J Neuropathol Exp Neurol 16:389-403
31. Strazza M, Pirrone V, Wigdahl B, Nonnemacher MR (2011) Breaking down the barrier: the effects of HIV-1 on the blood-brain barrier. Brain Research 1399:96-115
32. Thormar H (2005) Maedi-visna virus and its relationship to human immunodeficiency virus. AIDS Rev 7:233-245
33. Torsteinsdottir S, Andresdottir V, Arnarson H, Petursson G (2007) Immune response to maedi-visna virus. Front Biosci 12:1532-1543
34. Torsteinsdottir S, Georgsson G, Gisladottir E, Rafnar B, Palsson PA, Petursson G (1992) Pathogenesis of central nervous system lesions in visna: cell-mediated immunity and lymphocyte subsets in blood, brain and cerebrospinal fluid. J Neuroimmunol 41:149-158
35. Williams K, Alvarez X, Lackner AA (2001a) Central nervous system perivascular cells are immunoregulatory cells that connect the CNS with the peripheral immune system. Glia 36:156-164
36. Williams KC, Corey S, Westmoreland SV, Pauley D, Knight H, deBakker C, Alvarez X, Lackner AA (2001b) Perivascular macrophages are the primary cell type productively infected by simian immunodeficiency virus in the brains of macaques: implications for the neuropathogenesis of AIDS. J Exp Med 193:905-915