期刊论文详细信息
BMC Veterinary Research
Clinical, electroretinographic and histomorphometric evaluation of the retina in sheep with natural scrapie
Pierre-Louis Toutain1  François Schelcher2  Delphine Cayez Gruson1  Olivier Albaric2  Olivier Andreoletti2  Alain Regnier1 
[1] UMR 181 Physiopathologie et Toxicologie Expérimentales, INRA, Ecole Nationale Vétérinaire, 23 chemin des Capelles, B.P. 87614, 31076 Toulouse Cedex 3, France;UMR 1225 Interactions Hôtes-Agents Pathogènes, INRA, Ecole Nationale Vétérinaire, 23 chemin des Capelles, B.P. 87614, 31076 Toulouse Cedex 3, France
关键词: sheep;    scrapie;    retina;    prion;    electroretinography;   
Others  :  1119943
DOI  :  10.1186/1746-6148-7-25
 received in 2010-07-27, accepted in 2011-06-06,  发布年份 2011
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【 摘 要 】

Background

The retina is part of the diencephalon in a peripheral location and may be involved in prion diseases. Retinal function and structural changes were assessed in naturally scrapie-affected red face Manech ewes presenting the classical signs of the disease, and clinically healthy age-matched subjects for controls. Ophthalmic examination was done prior to electroretinography (ERG), which was carried out under conditions that allowed photopic and scotopic activities to be assessed. Histomorphometry of the inner and outer retinal layers was performed post-mortem, and retinas were also examined for evidence of abnormal prion protein (PrPSc) accumulation and glial fibrillary acidic protein (GFAP) upregulation as a marker of gliosis. Scrapie status was determined by examination of brain tissue

Results

Ocular reflexes and ophthalmoscopy did not reveal any difference between scrapie affected and control animals. Although the light-and dark-adapted ERG responses of both rod-and cone-mediated functions had a similar waveform in scrapie-affected and control sheep, a significant reduction in the amplitude of the ERG a-and b-waves was observed in affected animals compared to controls. These functional alterations were correlated with a substantial loss of cells in the outer nuclear layer (ONL), lengthening and disorganization in photoreceptor segments, and substantial reduction in cellularity and thickness of the inner nuclear layer (INL). The degenerative changes in the INL and ONL were most marked in the central and paracentral areas of the scrapie retinas, and were accompanied in all scrapie retinas by PrPSc deposition in the ganglion cell and synaptic layers. GFAP immunoreactivity was mainly increased in the ganglion cell and inner plexiform layers.

Conclusions

No appreciable fundoscopic changes were observed in the scrapie-affected ewes although reproducible changes in retinal function as measured by ERG were observed in these animals. The alterations in the receptoral and post-receptoral pathways corresponded to the degenerative lesions observed in the ONL and INL of the scrapie retinas. The retinal degeneration was associated with prion protein infectivity which presumably spread via the optic nerve.

【 授权许可】

   
2011 Regnier et al; licensee BioMed Central Ltd.

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【 参考文献 】
  • [1]Schreuder BEC: Animal spongiform encephalopathies: An update. part 1. Scrapie and lesser known animal spongiform encephalopathies. Vet Q 1994, 16:174-181.
  • [2]Prusiner SB: Natural and experimental prion diseases of humans and animals. Curr Opin Neurobiol 1992, 2:638-647.
  • [3]Bolton DC, McKinley MP, Prusiner SB: Identification of a protein that purifies with the scrapie prion. Science 1982, 218:1309-1311.
  • [4]Prusiner SB, Bolton DC, Groth DF, Bowman KA, Cochran SP, McKinley MP: Further purification and characterization of scrapie prions. Biochemistry 1982, 21:6942-6950.
  • [5]Prusiner SB, DeArmond SJ: Molecular biology and pathology of scrapie and the prion diseases in humans. Brain Pathol 1991, 1:297-310.
  • [6]Chow RL, Lang RA: Early eye development in vertebrates. Annu Rev Cell Dev Biol 2001, 17:255-296.
  • [7]Hogan RN, Kingsbury DT, Baringer JR, Prusiner SB: Retinal degeneration in experimental Creutzfeldt-Jakob disease. Lab Invest 1983, 49:708-715.
  • [8]Buyukmihci N, Goehring-Harmon F, Marsh RF: Retinal degeneration during clinical scrapie encephalopathy in hamsters. J Comp Neurol 1982, 205:153-160.
  • [9]Kozlowski PB, Moretz RC, Carp RI, Wisniewski HM: Retinal damage in scrapie mice. Acta Neuropathol 1982, 56:9-12.
  • [10]Buyukmihci N, Goehring-Harmon F, Marsh RF: Retinal degeneration in experimental scrapie after intraperitoneal or subcutaneous inoculation of hamsters. Exp Neurol 1985, 88:461-466.
  • [11]Curtis R, Fraser H, Foster JD, Scott JR: The correlation of electroretinographic and histopathological findings in the eyes of mice infected with the 79A strain of scrapie. Neuropathol Appl Neurobiol 1989, 15:75-89.
  • [12]De Seze J, Hache JC, Vermersch P, Arndt CF, Maurage CA, Pasquier F, Laplanche JL, Ruchoux MM, Leys D, Destée A, Petit H: Creutzfeldt-Jakob disease: neurophysiologic visual impairments. Neurology 1998, 51:962-967.
  • [13]Head MW, Northcott V, Rennison K, Ritchie D, McCardle L, Bunn TJR, McLennan NF, Ironside JW, Tullo AB, Bonshek RE: Prion protein accumulation in eyes of patients with sporadic and variant Creutzfeld-Jakob disease. Invest Ophthalmol Vis Sci 2003, 44:342-346.
  • [14]Head MW, Peden AH, Yull HM, Ritchie DL, Bonshek RE, Tullo AB, Ironside JW: Abnormal prion protein in the retina of the most commonly occurring subtype of sporadic Creutzfeldt-Jakob disease. Brit J Ophthalmol 2005, 89:1131-1133.
  • [15]Barnett KC, Palmer AC: Retinopathy in sheep affected with natural scrapie. Res Vet Sci 1971, 12:383-385.
  • [16]Hortells P, Monzón M, Monleón E, Vargas A, Bolea R, Luján L, Badiola JJ: Pathological findings in retina and visual pathways associated to natural scrapie. Brain Res 2006, 1108:188-194.
  • [17]Smith JD, Greenlee JJ, Hamir AN, West Greenlee MH: Altered electroretinogram b-wave in a Sufflok sheep experimentally infected with scrapie. Vet Rec 2009, 165:179-181.
  • [18]Regnier A, Andreoletti O, Cayez D, Schelcher F, Toutain PL: Retinal pathology in natural cases of ovine scrapie. In Proceedings Notes of the American College of Veterinary Ophthalmologists (ACVO) 35th Annual Conference: 20-23 October 2004. Edited by ACVO. Washington DC; 2004:78.
  • [19]Narfström K, Ekesten B: Electroretinographic evaluation of Papillons with and without hereditary retinal degeneration. Am J Vet Res 1998, 59:221-226.
  • [20]Healy AM, Weavers E, McElroy M, Gomez Parada M, Collins JD, O'Doherty E, Sweeney T, Doherty ML: The clinical neurology of scrapie in irish sheep. J Vet Intern Med 2003, 17:908-916.
  • [21]Sokal RR, Rohlf FJ: Biometry: The principles and practice of statistics in biological research. 2nd edition. New York: WH Freeman and Company; 1981.
  • [22]Foster JD, Parnham D, Chong A, Goldmann W, Hunter N: Clinical signs, histopathology and genetics of experimental transmission of BSE and natural scrapie to sheep and goats. Vet Rec 2001, 148:165-171.
  • [23]Benestad SL, Sarradin P, Thu B, Schönheit J, Tranulis MA, Bratberg B: Cases of scrapie with unusual features in Norway and designation of a new type, Nor98. Vet Rec 2003, 153:202-208.
  • [24]Dagleish MP, Rodger SM, Simmons MM, Finlayson J, Buxton D, Chianini F: Atypical scrapie in a sheep in Scotland. Vet Rec 2008, 162:518-519.
  • [25]Foster J, Toovey L, McKenzie C, Chong A, Parnham D, Drummond D, Hunter N: Atypical scrapie in a sheep in a closed UK flock with endemic natural scrapie. Vet Rec 2008, 162:723-725.
  • [26]Mayhew IG, Jolly RD, Pickett BT, Slack PM: Ceroid-lipofuscinosis (Batten's disease): pathogenesis of blindness in the ovine model. Neuropathol Appl Neurobiol 1985, 11:273-290.
  • [27]Van der Lugt JJ, Olivier J, Jordaan P: Status spongiosis, optic neuropathy, and retinal degeneration in Helichrysum argyrosphaerum poisoning in sheep and a goat. Vet Pathol 1996, 33:495-502.
  • [28]Buyukmihci N, Goehring-Harmon F, Marsh RF: Photoreceptor degeneration in experimental transmissible mink encephalopathy of hamsters. Exp Neurol 1987, 96:727-731.
  • [29]Nilsson SEG, Knave BG, Persson HE, Lunt T: The morphology of the sheep retina I. The receptor cells and the pigment epithelium. Acta Ophthalmol 1973, 51:599-611.
  • [30]Smith EL, Witzel DA, Pitts DG: The waveform and scotopic CFF of the sheep electroretinogram. Vision Res 1976, 16:1241-1245.
  • [31]Graydon RJ, Jolly RD: Ceroid-lipofuscinosis (Batten's disease)-Sequential electrophysiologic and pathologic changes in the retina of the ovine model. Invest Ophthalmol Vis Sci 1984, 25:294-301.
  • [32]Strain GM, Claxton MS, Prescott-Mathews JS, LaPhand DJ: Electroretinogram and visual-evoked potential measurements in sheep. Can J Vet Res 1991, 55:1-4.
  • [33]Hood D, Birch D: The a-wave of the human electroretinogram and rod photoreceptor function. Invest Ophthalmol Vis Sci 1990, 31:2070-2081.
  • [34]Stockton RA, Slaughter MM: b-wave of the electroretinogram. A reflection of ON bipolar cell activity. J Gen Physiol 1989, 93:101-122.
  • [35]Wen R, Oakley B II: K+ evoked Müller cell depolarization generates b-wave of electroretinogram in toad retina. Proc Natl Acad Sci USA 1990, 87:2117-2121.
  • [36]Katz BJ, Warner JE, Digre KB, Creel DJ: Selective loss of the electroretinogram B-wave in a patient with Creutzfeldt-Jakob disease. J Neuroophthalmol 2000, 20:116-118.
  • [37]Gouras P: Electroretinography: some basic principles. Invest Ophthalmol Vis Sci 1970, 9:557-569.
  • [38]Sandberg MA, Pawlyk BS, Berson EL: Full-field electroretinograms in miniature poodles with progressive rod-cone degeneration. Invest Ophthalmol Vis Sci 1986, 27:1179-1184.
  • [39]Katz ML, Narfström K, Johnson GS, O'Brien DP: Assessment of retinal function and characterization of lysosomal storage body accumulation in the retinas and brains of Tibetan Terriers with ceroid-lipofuscinosis. Am J Vet Res 2005, 66:67-76.
  • [40]Fraser H: Diversity in the neuropathology of scrapie-like diseases in animals. Br Med Bull 1993, 49:792-809.
  • [41]Hogan RN, Bowman KA, Baringer JR, Prusiner SB: Replication of scrapie prions in hamsters eyes precedes retinal degeneration. Ophthalmic Res 1986, 18:230-235.
  • [42]Fraser H: Neuronal spread of scrapie agent and targeting of lesions within the retino-tectal pathway. Nature 1983, 295:149-150.
  • [43]Smith JD, Greenlee JJ, Hamir AN, West Greenlee MH: Retinal cell types are differentially affected in sheep with scrapie. J Comp Pathol 2008, 138:12-22.
  • [44]Greenlee JJ, Hamir AN, West Greenlee MH: Abnormal prion accumulation associated with retinal pathology in experimentally inoculated scrapie-affected sheep. Vet Pathol 2006, 43:733-739.
  • [45]Ettaiche M, Pichot R, Vincent JP, Chabry J: In vivo cytotoxicity of the prion protein fragment 106-126. J Biol Chem 2000, 275:36487-36490.
  • [46]Bringmann A, Pannicke T, Grosche J, Francke M, Wiedemann P, Osborne NN, Reichenbach A: Müller cells in the healthy and diseased retina. Prog Retin Eye Res 2006, 25:397-424.
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