The interpretation of disease phenotypes to identify TSE strains in mice: characterisation of BSE using PrP<sup>Sc</sup> distribution patterns in the brain

<p>Abstract</p> <p>In individual animals affected by transmissible spongiform encephalopathies, different disease phenotypes can be identified which are attributed to different strains of the agent. In the absence of reliable technology to fully characterise the agent, classificati...

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Main Authors: Corda Erica, Beck Katy E, Sallis Rosemary E, Vickery Christopher M, Denyer Margaret, Webb Paul R, Bellworthy Susan J, Spencer Yvonne I, Simmons Marion M, Spiropoulos John
Format: Article
Language:English
Published: BMC 2012-12-01
Series:Veterinary Research
Online Access:http://www.veterinaryresearch.org/content/43/1/86
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spelling doaj-ad2d8217e0ae40f9b97faf1bc0f998d52020-11-24T23:51:18ZengBMCVeterinary Research0928-42491297-97162012-12-014318610.1186/1297-9716-43-86The interpretation of disease phenotypes to identify TSE strains in mice: characterisation of BSE using PrP<sup>Sc</sup> distribution patterns in the brainCorda EricaBeck Katy ESallis Rosemary EVickery Christopher MDenyer MargaretWebb Paul RBellworthy Susan JSpencer Yvonne ISimmons Marion MSpiropoulos John<p>Abstract</p> <p>In individual animals affected by transmissible spongiform encephalopathies, different disease phenotypes can be identified which are attributed to different strains of the agent. In the absence of reliable technology to fully characterise the agent, classification of disease phenotype has been used as a strain typing tool which can be applied in any host. This approach uses standardised data on biological parameters, established for a single host, to allow comparison of different prion sources. Traditionally prion strain characterisation in wild type mice is based on incubation periods and lesion profiles after the stabilisation of the agent into the new host which requires serial passages. Such analysis can take many years, due to prolonged incubation periods. The current study demonstrates that the PrP<sup>Sc</sup> patterns produced by one serial passage in wild type mice of bovine or ovine BSE were consistent, stable and showed minimal and predictable differences from mouse-stabilised reference strains. This biological property makes PrP<sup>Sc</sup> deposition pattern mapping a powerful tool in the identification and definition of TSE strains on primary isolation, making the process of characterisation faster and cheaper than a serial passage protocol. It can be applied to individual mice and therefore it is better suited to identify strain diversity within single inocula in case of co-infections or identify strains in cases where insufficient mice succumb to disease for robust lesion profiles to be constructed. The detailed description presented in this study provides a reference document for identifying BSE in wild type mice.</p> http://www.veterinaryresearch.org/content/43/1/86
collection DOAJ
language English
format Article
sources DOAJ
author Corda Erica
Beck Katy E
Sallis Rosemary E
Vickery Christopher M
Denyer Margaret
Webb Paul R
Bellworthy Susan J
Spencer Yvonne I
Simmons Marion M
Spiropoulos John
spellingShingle Corda Erica
Beck Katy E
Sallis Rosemary E
Vickery Christopher M
Denyer Margaret
Webb Paul R
Bellworthy Susan J
Spencer Yvonne I
Simmons Marion M
Spiropoulos John
The interpretation of disease phenotypes to identify TSE strains in mice: characterisation of BSE using PrP<sup>Sc</sup> distribution patterns in the brain
Veterinary Research
author_facet Corda Erica
Beck Katy E
Sallis Rosemary E
Vickery Christopher M
Denyer Margaret
Webb Paul R
Bellworthy Susan J
Spencer Yvonne I
Simmons Marion M
Spiropoulos John
author_sort Corda Erica
title The interpretation of disease phenotypes to identify TSE strains in mice: characterisation of BSE using PrP<sup>Sc</sup> distribution patterns in the brain
title_short The interpretation of disease phenotypes to identify TSE strains in mice: characterisation of BSE using PrP<sup>Sc</sup> distribution patterns in the brain
title_full The interpretation of disease phenotypes to identify TSE strains in mice: characterisation of BSE using PrP<sup>Sc</sup> distribution patterns in the brain
title_fullStr The interpretation of disease phenotypes to identify TSE strains in mice: characterisation of BSE using PrP<sup>Sc</sup> distribution patterns in the brain
title_full_unstemmed The interpretation of disease phenotypes to identify TSE strains in mice: characterisation of BSE using PrP<sup>Sc</sup> distribution patterns in the brain
title_sort interpretation of disease phenotypes to identify tse strains in mice: characterisation of bse using prp<sup>sc</sup> distribution patterns in the brain
publisher BMC
series Veterinary Research
issn 0928-4249
1297-9716
publishDate 2012-12-01
description <p>Abstract</p> <p>In individual animals affected by transmissible spongiform encephalopathies, different disease phenotypes can be identified which are attributed to different strains of the agent. In the absence of reliable technology to fully characterise the agent, classification of disease phenotype has been used as a strain typing tool which can be applied in any host. This approach uses standardised data on biological parameters, established for a single host, to allow comparison of different prion sources. Traditionally prion strain characterisation in wild type mice is based on incubation periods and lesion profiles after the stabilisation of the agent into the new host which requires serial passages. Such analysis can take many years, due to prolonged incubation periods. The current study demonstrates that the PrP<sup>Sc</sup> patterns produced by one serial passage in wild type mice of bovine or ovine BSE were consistent, stable and showed minimal and predictable differences from mouse-stabilised reference strains. This biological property makes PrP<sup>Sc</sup> deposition pattern mapping a powerful tool in the identification and definition of TSE strains on primary isolation, making the process of characterisation faster and cheaper than a serial passage protocol. It can be applied to individual mice and therefore it is better suited to identify strain diversity within single inocula in case of co-infections or identify strains in cases where insufficient mice succumb to disease for robust lesion profiles to be constructed. The detailed description presented in this study provides a reference document for identifying BSE in wild type mice.</p>
url http://www.veterinaryresearch.org/content/43/1/86
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