Fibrils from brains of cows with new cattle disease contain scrapie-associated protein
- PMID: 2904126
- DOI: 10.1038/336390a0
Fibrils from brains of cows with new cattle disease contain scrapie-associated protein
Abstract
During the past two years, more than 1,000 cases of a neurological disorder of cattle, bovine spongiform encephalopathy (BSE), have been confirmed from farms throughout Great Britain. The neurological signs and brain pathology of BSE resemble those produced in other species by the pathogens of scrapie and related disorders. The discovery of fibrils similar to scrapie-associated fibrils in detergent extracts o BSE-affected brain supported the clinical and pathological diagnosis of the disease, but has been controversial. Scrapie-associated fibrils are found in brain extracts of all species affected by scrapie and diseases caused by related pathogens. They are pathological aggregates of a neuronal membrane protein termed PrP and a protease-resistant form of PrP is a molecular marker of scrapie-associated fibrils. In this report, we show the major protein of BSE fibrils is the bovine homologue of PrP as judged by its size, protease resistance, immunoreactivity, lectin binding and partial N-terminal protein sequence. This confirms that BSE is a scrapie-like disease.
Similar articles
-
Bovine spongiform encephalopathy: a scrapie-like disease of British cattle.Prog Clin Biol Res. 1989;317:659-67. Prog Clin Biol Res. 1989. PMID: 2574875
-
Ovine infection with the agents of scrapie (CH1641 isolate) and bovine spongiform encephalopathy: immunochemical similarities can be resolved by immunohistochemistry.J Comp Pathol. 2006 Jan;134(1):17-29. doi: 10.1016/j.jcpa.2005.06.005. Epub 2005 Dec 1. J Comp Pathol. 2006. PMID: 16324707
-
Molecular assessment of the potential transmissibilities of BSE and scrapie to humans.Nature. 1997 Jul 17;388(6639):285-8. doi: 10.1038/40876. Nature. 1997. PMID: 9230438
-
[Consequences of BSE/TSE for the clinical diagnostic in cattle and sheep].Dtsch Tierarztl Wochenschr. 2002 Aug;109(8):342-4. Dtsch Tierarztl Wochenschr. 2002. PMID: 12224461 Review. German.
-
[Bovine spongiform encephalopathy: a new entity caused by a non-conventional transmissible agent].Bull Acad Natl Med. 1990 Jun-Jul;174(6):731-9; discussion 740-1. Bull Acad Natl Med. 1990. PMID: 2271982 Review. French.
Cited by
-
Treatment of Prion Disease with Heterologous Prion Proteins.PLoS One. 2015 Jul 2;10(7):e0131993. doi: 10.1371/journal.pone.0131993. eCollection 2015. PLoS One. 2015. PMID: 26134409 Free PMC article.
-
Crossing the species barrier--viruses and the origins of AIDS in perspective.J R Soc Med. 1989 Sep;82(9):519-23. doi: 10.1177/014107688908200904. J R Soc Med. 1989. PMID: 2677368 Free PMC article. Review. No abstract available.
-
Prion Strain Diversity.Cold Spring Harb Perspect Med. 2016 Dec 1;6(12):a024349. doi: 10.1101/cshperspect.a024349. Cold Spring Harb Perspect Med. 2016. PMID: 27908925 Free PMC article. Review.
-
Conformation-Dependent Influences of Hydrophobic Amino Acids in Two In-Register Parallel β-Sheet Amyloids, an α-Synuclein Amyloid and a Local Structural Model of PrPSc.ACS Omega. 2022 Aug 24;7(35):31271-31288. doi: 10.1021/acsomega.2c03523. eCollection 2022 Sep 6. ACS Omega. 2022. PMID: 36092583 Free PMC article.
-
Metal imbalance and compromised antioxidant function are early changes in prion disease.Biochem J. 2002 Feb 15;362(Pt 1):253-8. doi: 10.1042/0264-6021:3620253. Biochem J. 2002. PMID: 11829763 Free PMC article.
Publication types
MeSH terms
Substances
LinkOut - more resources
Full Text Sources
Other Literature Sources
Medical
Molecular Biology Databases
Research Materials
Miscellaneous