Glial response in the central nervous system of cats with feline infectious peritonitis

Journal of Feline Medicine and Surgery

Volumn 18, Issue 12, 2016, Pages 1023-1030

  Mesquita, Leonardo P ^a   Hora, Aline S ^a   de Siqueira, Adriana ^a   Salvagni, Fernanda A ^a   Brandão, Paulo E ^a   Maiorka, Paulo C ^a  

^a UNIVERSITY OF SÃO PAULO   (Brazil)

Author keywords

[No Author keywords available]

Indexed keywords

GLIAL FIBRILLARY ACIDIC PROTEIN;

ANIMAL; ASTROCYTE; CAT; CENTRAL NERVOUS SYSTEM INFECTION; DOG; FELINE CORONAVIRUS; FELINE INFECTIOUS PERITONITIS; IMMUNOHISTOCHEMISTRY; MALE; METABOLISM; PATHOGENICITY; PATHOLOGY; VETERINARY; VIROLOGY;

ANIMALS; ASTROCYTES; CATS; CENTRAL NERVOUS SYSTEM INFECTIONS; CORONAVIRUS, FELINE; DOGS; FELINE INFECTIOUS PERITONITIS; GLIAL FIBRILLARY ACIDIC PROTEIN; IMMUNOHISTOCHEMISTRY; MALE;

EID: 85001907623     PISSN: 1098612X     EISSN: 15322750     Source Type: Journal    
DOI: 10.1177/1098612X15615906     Document Type: Article

References (28)

1. Pedersen NC., A review of feline infectious peritonitis virus infection: 1963–2008. J Feline Med Surg 2009; 11: 225–258.
2. Kipar A, Meli ML., Feline infectious peritonitis: still an enigma? Vet Pathol 2014; 51: 505–526.
3. Foley JE, Lapointe J-M, Koblik P. Diagnostic features of clinical neurologic feline infectious peritonitis. J Vet Intern Med 1998; 12: 415–423.
4. Brown CC, Baker DC, Barker IK. Alimentary system. In: Maxie MG, (eds). Jubb, Kennedy and Palmer’s pathology of domestic animals. 5th ed. Oxford: Elsevier, 2007, pp 1–296.
5. Slauson D, Finn J., Meningoencephalitis and panophthalmitis in feline infectious peritonitis. J Am Vet Med Assoc 1972; 160: 729–734.
6. Poncelet L, Coppens A, Peeters D. Detection of antigenic heterogeneity in feline coronavirus nucleocapsid in feline pyogranulomatous meningoencephalitis. Vet Pathol 2008; 45: 140–153.
7. Kipar A, Bellmann S, Kremendahl J. Cellular composition, coronavirus antigen expression and production of specific antibodies in lesions in feline infectious peritonitis. Vet Immunol Immunopathol 1998; 65: 243–257.
8. Berg A-L, Ekman K, Belák S. Cellular composition and interferon-γ expression of the local inflammatory response in feline infectious peritonitis (FIP). Vet Microbiol 2005; 111: 15–23.
9. Kipar A, May H, Menger S. Morphologic features and development of granulomatous vasculitis in feline infectious peritonitis. Vet Pathol 2005; 42: 321–330.
10. Hora AS, Asano KM, Guerra JM. Intrahost diversity of feline coronavirus: a consensus between the circulating virulent/avirulent strains and the internal mutation hypothesis? Sci World J 2013; 2013: 572325.
11. Foley JE, Rand C, Leutenegger C., Inflammation and changes in cytokine levels in neurological feline infectious peritonitis. J Feline Med Surg 2003; 5: 313–322.
12. Gaedke K, Zurbriggen A, Baumgärtner W., Lack of correlation between virus nucleoprotein and mRNA expression and the inflammatory response in demyelinating distemper encephalitis indicates a biphasic disease process. Eur J Vet Pathol 1999; 5: 9–20.
13. Headley SA, Soares IC, Graça DL., Glial fibrillary acidic protein (GFAP)-immunoreactive astrocytes in dogs infected with canine distemper virus. J Comp Pathol 2001; 125: 90–97.
14. Orsini H, Bondan EF, Sanchez M. Marcação imuno-histoquímica da expressão astrocitária de proteína glial fibrilar ácida e de vimentina no sistema nervoso central de cães com cinomose. Arq Neuropsiquiatr 2007; 65: 1070–1077.
15. Melo GD, Machado GF., Glial reactivity in dogs with visceral leishmaniasis: correlation with T-lymphocyte infiltration and with cerebrospinal fluid anti-Leishmania antibody titres. Cell Tissue Res 2011; 346: 293–304.
16. Machado GF, Alessi AC. Glial fibrillary acidic protein (GFAP) immunoreactive astrocytes in the CNS of normal and rabies-infected adult cattle. I. Hippocampus and dentate gyrus. Braz J Vet Res Anim Sci 1997; 34: 345–348.
17. Lemos KR, Alessi AC., Astrócitos imunorreativos à proteína glial fibrilar ácida (GFAP) em sistema nervoso central de equinos normais e de equinos com leucoencefalomalácia. Pesq Vet Bras 1999; 19: 104–108.
18. Poli A, Abramo F, Di Iorio C. Neuropathology in cats experimentally infected with feline immunodeficiency virus: a morphological, immunocytochemical and morphometric study. J Neurovirol 1997; 3: 361–368.
19. Headley SA, Amude AM, Alfieri AF. Molecular detection of canine distemper virus and the immunohistochemical characterization of the neurologic lesions in naturally occurring old dog encephalitis. J Vet Diagn Invest 2007; 21: 588–597.
20. Shin TK, Lee YD, Sim KB., Embryonic intermediate filaments, nestin and vimentin, expression in the spinal cords of rats with experimental autoimmune encephalomyelitis. J Vet Sci 2003; 4: 9–13.
21. Seehusen F, Orlando EA, Wewetzer K. Vimentin-positive astrocytes in canine distemper: a target for canine distemper virus especially in chronic demyelinating lesions? Acta Neuropathol 2007; 114: 597–608.
22. Lazarides E., Intermediate filaments: a chemically heterogeneous, developmentally regulated class of proteins. Annu Rev Biochem 1982; 51: 219–250.
23. Gocht A, Löhler J., Changes in glial cell markers in recent and old demyelinated lesions in central pontine myelinolysis. Acta Neuropathol 1990; 80: 46–58.
24. Eng LF, Ghirnikar RS., GFAP and astrogliosis. Brain Pathol 1994; 4: 229–237.
25. Asensio VC, Campbell IL., Chemokines in the CNS: plurifunctional mediators in diverse states. Trends Neurosci 1999; 4: 504–512.
26. Farina C, Aloisi F, Meinl E., Astrocytes are active players in cerebral innate immunity. Trends Immunol 2007; 28: 138–145.
27. Foley JE, Leutenegger C., A review of coronavirus infection in the central nervous system of cats and mice. J Vet Intern Med 2001; 15: 438–444.
28. Prinz M, Priller J., Microglia and brain macrophages in the molecular age: from origin to neuropsychiatric disease. Nat Rev Neurosci 2014; 15: 300–312.