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In vitro amplification of H-type atypical bovine spongiform encephalopathy by protein misfolding cyclic amplification

The in vitro amplification of prions by serial protein misfolding cyclic amplification has been shown to detect PrP(Sc) to levels at least as sensitive as rodent bioassay but in a fraction of the time. Bovine spongiform encephalopathy is a zoonotic prion disease in cattle and has been shown to occur...

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Detalles Bibliográficos
Autores principales: O‘Connor, Matthew J., Bishop, Keith, Workman, Robert G., Maddison, Ben C., Gough, Kevin C.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Taylor & Francis 2017
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5360153/
https://www.ncbi.nlm.nih.gov/pubmed/28281929
http://dx.doi.org/10.1080/19336896.2016.1259051
Descripción
Sumario:The in vitro amplification of prions by serial protein misfolding cyclic amplification has been shown to detect PrP(Sc) to levels at least as sensitive as rodent bioassay but in a fraction of the time. Bovine spongiform encephalopathy is a zoonotic prion disease in cattle and has been shown to occur in 3 distinct forms, classical BSE (C-BSE) and 2 atypical BSE forms (L-BSE and H-BSE). Atypical forms are usually detected in asymptomatic, older cattle and are suggested to be spontaneous forms of the disease. Here, we show the development of a serial protein misfolding cyclic amplification method for the detection of H-BSE. The assay could detect PrP(Sc) from 3 distinct experimental isolates of H-BSE, could detect PrP(Sc) in as little as 1×10(−12) g of brain material and was highly specific. Additionally, the product of serial protein misfolding cyclic amplification at all dilutions of seed analyzed could be readily distinguished from L-BSE, which did not amplify, and C-BSE, which had PrP(Sc) with distinct protease K-resistance and protease K-resistant PrP(Sc) molecular weights.