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Manganese Enhances Prion Protein Survival in Model Soils and Increases Prion Infectivity to Cells

Prion diseases are considered to be transmissible. The existence of sporadic forms of prion diseases such as scrapie implies an environmental source for the infectious agent. This would suggest that under certain conditions the prion protein, the accepted agent of transmission, can survive in the en...

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Detalles Bibliográficos
Autores principales: Davies, Paul, Brown, David R.
Formato: Texto
Lenguaje:English
Publicado: Public Library of Science 2009
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2760146/
https://www.ncbi.nlm.nih.gov/pubmed/19844576
http://dx.doi.org/10.1371/journal.pone.0007518
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author Davies, Paul
Brown, David R.
author_facet Davies, Paul
Brown, David R.
author_sort Davies, Paul
collection PubMed
description Prion diseases are considered to be transmissible. The existence of sporadic forms of prion diseases such as scrapie implies an environmental source for the infectious agent. This would suggest that under certain conditions the prion protein, the accepted agent of transmission, can survive in the environment. We have developed a novel technique to extract the prion protein from soil matrices. Previous studies have suggested that environmental manganese is a possible risk factor for prion diseases. We have shown that exposure to manganese is a soil matrix causes a dramatic increase in prion protein survival (∼10 fold) over a two year period. We have also shown that manganese increases infectivity of mouse passaged scrapie to culture cells by 2 logs. These results clearly verify that manganese is a risk factor for both the survival of the infectious agent in the environment and its transmissibility.
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spelling pubmed-27601462009-10-21 Manganese Enhances Prion Protein Survival in Model Soils and Increases Prion Infectivity to Cells Davies, Paul Brown, David R. PLoS One Research Article Prion diseases are considered to be transmissible. The existence of sporadic forms of prion diseases such as scrapie implies an environmental source for the infectious agent. This would suggest that under certain conditions the prion protein, the accepted agent of transmission, can survive in the environment. We have developed a novel technique to extract the prion protein from soil matrices. Previous studies have suggested that environmental manganese is a possible risk factor for prion diseases. We have shown that exposure to manganese is a soil matrix causes a dramatic increase in prion protein survival (∼10 fold) over a two year period. We have also shown that manganese increases infectivity of mouse passaged scrapie to culture cells by 2 logs. These results clearly verify that manganese is a risk factor for both the survival of the infectious agent in the environment and its transmissibility. Public Library of Science 2009-10-21 /pmc/articles/PMC2760146/ /pubmed/19844576 http://dx.doi.org/10.1371/journal.pone.0007518 Text en Davies, Brown. http://creativecommons.org/licenses/by/4.0/ This is an open-access article distributed under the terms of the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are properly credited.
spellingShingle Research Article
Davies, Paul
Brown, David R.
Manganese Enhances Prion Protein Survival in Model Soils and Increases Prion Infectivity to Cells
title Manganese Enhances Prion Protein Survival in Model Soils and Increases Prion Infectivity to Cells
title_full Manganese Enhances Prion Protein Survival in Model Soils and Increases Prion Infectivity to Cells
title_fullStr Manganese Enhances Prion Protein Survival in Model Soils and Increases Prion Infectivity to Cells
title_full_unstemmed Manganese Enhances Prion Protein Survival in Model Soils and Increases Prion Infectivity to Cells
title_short Manganese Enhances Prion Protein Survival in Model Soils and Increases Prion Infectivity to Cells
title_sort manganese enhances prion protein survival in model soils and increases prion infectivity to cells
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2760146/
https://www.ncbi.nlm.nih.gov/pubmed/19844576
http://dx.doi.org/10.1371/journal.pone.0007518
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