Clinical, neuropathological and immunohistochemical features of sporadic and variant forms of Creutzfeldt-Jakob disease in the squirrel monkey (Saimiri sciureus)

Journal of General Virology

Volumn 88, Issue 2, 2007, Pages 688-695

  Williams, Lawrence ^a   Brown, Paul ^b   Ironside, James ^c   Gibson, Susan ^c   Will, Robert ^c   Ritchie, Diane ^c   Kreil, Thomas R ^a   Abee, Christian ^a  

^a UNIVERSITY OF TEXAS MD ANDERSON CANCER CENTER   (United States)

^b Western General Hospital ^*

^c UNIVERSITY OF SOUTH ALABAMA   (United States)

Author keywords

[No Author keywords available]

Indexed keywords

PRION PROTEIN;

ADULT; AGED; ANIMAL BEHAVIOR; ANIMAL EXPERIMENT; ANIMAL MODEL; ANIMAL TISSUE; ARTICLE; ATAXIA; BRAIN HOMOGENATE; BRAIN LEVEL; CLINICAL FEATURE; CONTROLLED STUDY; CREUTZFELDT JAKOB DISEASE; CREUTZFELDT JAKOB DISEASE AGENT; DISEASE DURATION; FEMALE; FRONTAL CORTEX; HISTOPATHOLOGY; HUMAN; HUMAN TISSUE; IMMUNOHISTOCHEMISTRY; INCUBATION TIME; INOCULATION; LYMPHOID TISSUE; MALE; MONKEY DISEASE; NEUROPATHOLOGY; NONHUMAN; PRIORITY JOURNAL; PROTEIN LOCALIZATION; SENILE PLAQUE; SPORADIC CREUTZFELDT JAKOB DISEASE; SQUIRREL MONKEY; TREMOR; VARIANT CREUTZFELDT JAKOB DISEASE;

ADOLESCENT; ADULT; AGED, 80 AND OVER; ANIMALS; BRAIN; CREUTZFELDT-JAKOB SYNDROME; DISEASE MODELS, ANIMAL; FEMALE; HUMANS; IMMUNOHISTOCHEMISTRY; MALE; MIDDLE AGED; PRIONS; SAIMIRI;

ANIMALIA; PAN; SAIMIRI; SAIMIRI SCIUREUS;

EID: 33846809059     PISSN: 00221317     EISSN: None     Source Type: Journal    
DOI: 10.1099/vir.0.81957-0     Document Type: Article

References (13)

1. Azzolin, M., Furlati, S., Pellegrini, G. & Trombetti, C. (1998). The Observer 3.0: the first study of behavior of a couple mother-calf of Tursiops truncatus. In Measuring Behavior '98: Second International Conference on Methods and Techniques in Behavioral Research, Groningen, The Netherlands, 18-21 August 1998.
2. Baker, H. F., Ridley, R. M., Wells, G. A. & Ironside, J. W. (1998). Prion protein immunohistochemical staining in the brains of monkeys with transmissible spongiform encephalopathy. Neuropathol Appl Neurobiol 24, 476-486.
3. Brown, P., Preece, M., Brandel, J.-P., Sato, T., McShane, L., Zerr, I., Fletcher, A., Will, R. G., Pocchiari, M. & other authors (2000). Human spongiform encephalopathy: iatrogenic Creutzfeldt-Jakob disease at the millennium. Neurology 55, 1075-1081.
4. Goldfarb, L. G. & Brown, P. (1995). The transmissible spongiform encephalopathies. Annu Rev Med 46, 57-65.
5. Head, M. W., Bunn, T. J., Bishop, M. T., McLoughlin, V., Lowrie, S., McKimmie, C. S., Williams, M. C., McCardle, L., MacKenzie, J. & other authors (2004). Prion protein heterogeneity in sporadic but not variant Creutzfeldt-jakob disease: UK cases 1991-2002. Ann Neurol 55, 851-859.
6. Ironside, J. W., Head, M. W., Bell, J. E., McCardle, L. & Will, R. G. (2000). Laboratory diagnosis of variant Creutzfeldt-jakob disease. Histopathology 37, 1-9.
7. Kovacs, G. G., Trabattoni, G., Hainfellner, J. A., Ironside, J. W., Knight R. S. & Budka, H. (2002). Mutations of the prion protein gene phenotypic spectrum. J Neurol 249, 1567-1582.
8. Lasmézas, C. I., Fournier, J.-G., Nouvel, V., Boa, H., Marce, D., Lamoury, F., Kopp, N., Hauw, J. J., Ironside, J. & other authors (2001). Adaptation of the bovine spongiform encephalopathy agent to primates and comparison with Creutzfeldt-Jakob disease: implications for human health. Proc Natl Acad Sci U S A 98, 4142-4147.
9. Masters, C. L., Rohwer, R. G., Franko, M. C., Brown, P. & Gajdusek, D. C. (1984). The sequential development of spongiform change and gliosis of scrapie in the golden Syrian hamster. J Neuropathol Exp Neurol 43, 242-252.
10. Parchi, P., Giese, A., Capellari, S., Brown, P., Schulz-Schaeffer, W., Windl, O., Zerr, I., Budka, H., Kopp, N. & other authors (1999). Classification of sporadic Creutzfeldt-Jakob disease based on molecular and phenotypic analysis of 300 subjects. Ann Neurol 46, 224-233.
11. Ritchie, D. L., Head, M. W. & Ironside, J. W. (2004). Advances in the detection of prion protein in peripheral tissues of variant Creutzfeldt-Jakob disease patients using paraffin-embedded tissue blotting. Neuropathol Appl Neurobiol 30, 360-368.
12. Will, R. G., Ironside, J. W., Zeidler, M., Cousens, S. N., Estibeiro, K., Alperovitch, A., Poser, S., Pocchiari, M., Hofman, A. & Smith, P. G. (1996). A new variant of Creutzfeldt-Jakob disease in the UK. Lancet 347, 921-925.
13. Will, R. G., Zeidler, M., Stewart, G. E., Macleod, M. A., Ironside, J. W., Cousens, S. N., Mackenzie, J., Estibeiro, K., Green, A. J. & Knight, R. S. (2000). Diagnosis of new variant Creutzfeldt-Jakob disease. Ann Neurol 47, 575-582.