Emergence of a novel bovine spongiform encephalopathy (BSE) prion from an atypical H-type BSE

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Emergence of a novel bovine spongiform encephalopathy (BSE) prion from an atypical H-type BSE

The H-type of atypical bovine spongiform encephalopathy (H-BSE) was serially passaged in bovinized transgenic (TgBoPrP) mice. At the fourth passage, most challenged mice showed a typical H-BSE phenotype with incubation periods of 223 ± 7.8 days. However, a different phenotype of BSE prion with shorter incubation periods of 109 ± 4 days emerged in a minor subset of the inoculated mice. The latte...

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Human prion diseases and bovine spongiform encephalopathy (BSE).

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Epidemiological Analysis of Bovine Spongiform Encephalopathy (bse)

Bovine spongiform encephalopathy (BSE) in cattle, scrapie in sheep and goats, chronic wasting disease (CWD) in cervids, and Creutzfeldt-Jakob disease (CJD) in humans are known as prion diseases or transmissible spongiform encephalopathies (TSE), which cause neurodegenerative disorders. BSE was first reported in the United Kingdom (UK) in 1987, following which over 180,000 cases have been report...

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BSE--bovine spongiform encephalopathy ('mad cow disease').

About BSE BSE (bovine spongiform encephalopathy) is a progressive neurological disorder of cattle that results from infection by an unusual transmissible agent called a prion. The nature of the transmissible agent is not well understood. Currently, the most accepted theory is that the agent is a modified form of a normal protein known as prion protein. For reasons that are not yet understood, t...

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ژورنال

عنوان ژورنال: Scientific Reports

سال: 2016

ISSN: 2045-2322

DOI: 10.1038/srep22753