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Transmissibility of caprine scrapie in ovine transgenic mice
BACKGROUND: The United States control program for classical ovine scrapie is based in part on the finding that infection is typically spread through exposure to shed placentas from infected ewes. Transmission from goats to sheep is less well described. A suitable rodent model for examining the effec...
Autores principales: | , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
BioMed Central
2012
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3489715/ https://www.ncbi.nlm.nih.gov/pubmed/22472560 http://dx.doi.org/10.1186/1746-6148-8-42 |
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author | O’Rourke, Katherine I Schneider, David A Spraker, Terry R Dassanayake, Rohana P Highland, Margaret A Zhuang, Dongyue Truscott, Thomas C |
author_facet | O’Rourke, Katherine I Schneider, David A Spraker, Terry R Dassanayake, Rohana P Highland, Margaret A Zhuang, Dongyue Truscott, Thomas C |
author_sort | O’Rourke, Katherine I |
collection | PubMed |
description | BACKGROUND: The United States control program for classical ovine scrapie is based in part on the finding that infection is typically spread through exposure to shed placentas from infected ewes. Transmission from goats to sheep is less well described. A suitable rodent model for examining the effect of caprine scrapie isolates in the ovine host will be useful in the ovine scrapie eradication effort. In this study, we describe the incubation time, brain lesion profile, glycoform pattern and PrP(Sc) distribution patterns in a well characterized transgenic mouse line (Tg338) expressing the ovine VRQ prion allele, following inoculation with brain from scrapie infected goats. RESULTS: First passage incubation times of caprine tissue in Tg338 ovinized mice varied widely but second passage intervals were shorter and consistent. Vacuolation profiles, glycoform patterns and paraffin-embedded tissue blots from terminally ill second passage mice derived from sheep or goat inocula were similar. Proteinase K digestion products of murine tissue were slightly smaller than the original ruminant inocula, a finding consistent with passage of several ovine strains in previous reports. CONCLUSIONS: These findings demonstrate that Tg338 mice propagate prions of caprine origin and provide a suitable baseline for examination of samples identified in the expanded US caprine scrapie surveillance program. |
format | Online Article Text |
id | pubmed-3489715 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2012 |
publisher | BioMed Central |
record_format | MEDLINE/PubMed |
spelling | pubmed-34897152012-11-06 Transmissibility of caprine scrapie in ovine transgenic mice O’Rourke, Katherine I Schneider, David A Spraker, Terry R Dassanayake, Rohana P Highland, Margaret A Zhuang, Dongyue Truscott, Thomas C BMC Vet Res Research Article BACKGROUND: The United States control program for classical ovine scrapie is based in part on the finding that infection is typically spread through exposure to shed placentas from infected ewes. Transmission from goats to sheep is less well described. A suitable rodent model for examining the effect of caprine scrapie isolates in the ovine host will be useful in the ovine scrapie eradication effort. In this study, we describe the incubation time, brain lesion profile, glycoform pattern and PrP(Sc) distribution patterns in a well characterized transgenic mouse line (Tg338) expressing the ovine VRQ prion allele, following inoculation with brain from scrapie infected goats. RESULTS: First passage incubation times of caprine tissue in Tg338 ovinized mice varied widely but second passage intervals were shorter and consistent. Vacuolation profiles, glycoform patterns and paraffin-embedded tissue blots from terminally ill second passage mice derived from sheep or goat inocula were similar. Proteinase K digestion products of murine tissue were slightly smaller than the original ruminant inocula, a finding consistent with passage of several ovine strains in previous reports. CONCLUSIONS: These findings demonstrate that Tg338 mice propagate prions of caprine origin and provide a suitable baseline for examination of samples identified in the expanded US caprine scrapie surveillance program. BioMed Central 2012-04-02 /pmc/articles/PMC3489715/ /pubmed/22472560 http://dx.doi.org/10.1186/1746-6148-8-42 Text en Copyright ©2012 O'Rourke et al.; licensee BioMed Central Ltd. http://creativecommons.org/licenses/by/2.0 This is an Open Access article distributed under the terms of the Creative Commons Attribution License ( http://creativecommons.org/licenses/by/2.0), which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited. |
spellingShingle | Research Article O’Rourke, Katherine I Schneider, David A Spraker, Terry R Dassanayake, Rohana P Highland, Margaret A Zhuang, Dongyue Truscott, Thomas C Transmissibility of caprine scrapie in ovine transgenic mice |
title | Transmissibility of caprine scrapie in ovine transgenic mice |
title_full | Transmissibility of caprine scrapie in ovine transgenic mice |
title_fullStr | Transmissibility of caprine scrapie in ovine transgenic mice |
title_full_unstemmed | Transmissibility of caprine scrapie in ovine transgenic mice |
title_short | Transmissibility of caprine scrapie in ovine transgenic mice |
title_sort | transmissibility of caprine scrapie in ovine transgenic mice |
topic | Research Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3489715/ https://www.ncbi.nlm.nih.gov/pubmed/22472560 http://dx.doi.org/10.1186/1746-6148-8-42 |
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