Analysis of prion protein aggregates in blood and brain from pre-clinical and clinical BSE cases
Autor: | F. Dreßen, Martin H. Groschup, Martin Kaatz, Dieter Willbold, Detlev Riesner, A. Oelschlegel, Franziska Henke, Eva Birkmann, Elke Reinartz, Oliver Bannach |
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Rok vydání: | 2013 |
Předmět: |
PrPSc Proteins
General Veterinary animal diseases Bovine spongiform encephalopathy Central nervous system Brain Scrapie General Medicine Biology medicine.disease Microbiology Virology nervous system diseases Encephalopathy Bovine Spongiform Pathogenesis Titer medicine.anatomical_structure Germany Immunology Blood plasma medicine Animals Biomarker (medicine) Cattle Prion protein |
Zdroj: | Veterinary Microbiology. 166:102-108 |
ISSN: | 0378-1135 |
DOI: | 10.1016/j.vetmic.2013.05.021 |
Popis: | Prion diseases are infectious neurodegenerative diseases affecting humans and animals. The food-borne bovine spongiform encephalopathy (BSE) had serious impact on both economy and public health, respectively. To follow the pathogenesis of BSE, oral challenge studies were previously conducted, among others on the Isle of Riems, Germany (Balkema-Buschmann et al., 2011b). In the present work brain and plasma samples from this pathogenesis study were subjected to surface fluorescence distribution analysis (sFIDA). sFIDA is a diagnostic tool that exploits the aggregated state of the disease-related prion protein (PrP) as a biomarker for prion disorders. With the exception of one animal, all tested brain samples from clinical cattle exhibited a high titer of PrP particles. Moreover we could detect PrP aggregates already 16 and 24 months after infection. In contrast to our previous demonstration of PrP particles in blood plasma from scrapie sheep, however, no aggregates could be identified in plasma from pre-clinical and clinical cattle. This is in accordance with other studies suggesting a restriction of the BSE infection to the central nervous system. |
Databáze: | OpenAIRE |
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