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

Prion

a School of Veterinary Medicine and Science, The University of Nottingham, Sutton Bonington Campus , College Road, Sutton Bonington , Leicestershire , UK.

Published: January 2017

AI Article Synopsis

  • The study demonstrates that serial protein misfolding cyclic amplification (PMCA) can effectively detect prions at levels comparable to traditional rodent bioassays, but in a much shorter time frame.
  • Atypical forms of bovine spongiform encephalopathy (BSE), specifically H-BSE, were analyzed using this method, showing that it could identify prion proteins (PrP) from various experimental isolates with high sensitivity.
  • The PMCA method distinctly differentiates H-BSE from other BSE forms, L-BSE and C-BSE, based on specific molecular characteristics and resistance to protease K.

Article Abstract

The in vitro amplification of prions by serial protein misfolding cyclic amplification has been shown to detect PrP 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 from 3 distinct experimental isolates of H-BSE, could detect PrP in as little as 1×10 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 with distinct protease K-resistance and protease K-resistant PrP molecular weights.

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Source
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC5360153PMC
http://dx.doi.org/10.1080/19336896.2016.1259051DOI Listing

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