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Dietary magnesium and copper affect survival time and neuroinflammation in chronic wasting disease

Chronic wasting disease (CWD), the only known wildlife prion disease, affects deer, elk and moose. The disease is an ongoing and expanding problem in both wild and captive North American cervid populations and is difficult to control in part due to the extreme environmental persistence of prions, wh...

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Autores principales: Nichols, Tracy A., Spraker, Terry R., Gidlewski, Thomas, Cummings, Bruce, Hill, Dana, Kong, Qingzhong, Balachandran, Aru, VerCauteren, Kurt C., Zabel, Mark D.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Taylor & Francis 2016
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4981212/
https://www.ncbi.nlm.nih.gov/pubmed/27216881
http://dx.doi.org/10.1080/19336896.2016.1181249
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author Nichols, Tracy A.
Spraker, Terry R.
Gidlewski, Thomas
Cummings, Bruce
Hill, Dana
Kong, Qingzhong
Balachandran, Aru
VerCauteren, Kurt C.
Zabel, Mark D.
author_facet Nichols, Tracy A.
Spraker, Terry R.
Gidlewski, Thomas
Cummings, Bruce
Hill, Dana
Kong, Qingzhong
Balachandran, Aru
VerCauteren, Kurt C.
Zabel, Mark D.
author_sort Nichols, Tracy A.
collection PubMed
description Chronic wasting disease (CWD), the only known wildlife prion disease, affects deer, elk and moose. The disease is an ongoing and expanding problem in both wild and captive North American cervid populations and is difficult to control in part due to the extreme environmental persistence of prions, which can transmit disease years after initial contamination. The role of exogenous factors in CWD transmission and progression is largely unexplored. In an effort to understand the influence of environmental and dietary constituents on CWD, we collected and analyzed water and soil samples from CWD-negative and positive captive cervid facilities, as well as from wild CWD-endozootic areas. Our analysis revealed that, when compared with CWD-positive sites, CWD-negative sites had a significantly higher concentration of magnesium, and a higher magnesium/copper (Mg/Cu) ratio in the water than that from CWD-positive sites. When cevidized transgenic mice were fed a custom diet devoid of Mg and Cu and drinking water with varied Mg/Cu ratios, we found that higher Mg/Cu ratio resulted in significantly longer survival times after intracerebral CWD inoculation. We also detected reduced levels of inflammatory cytokine gene expression in mice fed a modified diet with a higher Mg/Cu ratio compared to those on a standard rodent diet. These findings indicate a role for dietary Mg and Cu in CWD pathogenesis through modulating inflammation in the brain.
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spelling pubmed-49812122016-08-25 Dietary magnesium and copper affect survival time and neuroinflammation in chronic wasting disease Nichols, Tracy A. Spraker, Terry R. Gidlewski, Thomas Cummings, Bruce Hill, Dana Kong, Qingzhong Balachandran, Aru VerCauteren, Kurt C. Zabel, Mark D. Prion Research Papers Chronic wasting disease (CWD), the only known wildlife prion disease, affects deer, elk and moose. The disease is an ongoing and expanding problem in both wild and captive North American cervid populations and is difficult to control in part due to the extreme environmental persistence of prions, which can transmit disease years after initial contamination. The role of exogenous factors in CWD transmission and progression is largely unexplored. In an effort to understand the influence of environmental and dietary constituents on CWD, we collected and analyzed water and soil samples from CWD-negative and positive captive cervid facilities, as well as from wild CWD-endozootic areas. Our analysis revealed that, when compared with CWD-positive sites, CWD-negative sites had a significantly higher concentration of magnesium, and a higher magnesium/copper (Mg/Cu) ratio in the water than that from CWD-positive sites. When cevidized transgenic mice were fed a custom diet devoid of Mg and Cu and drinking water with varied Mg/Cu ratios, we found that higher Mg/Cu ratio resulted in significantly longer survival times after intracerebral CWD inoculation. We also detected reduced levels of inflammatory cytokine gene expression in mice fed a modified diet with a higher Mg/Cu ratio compared to those on a standard rodent diet. These findings indicate a role for dietary Mg and Cu in CWD pathogenesis through modulating inflammation in the brain. Taylor & Francis 2016-05-24 /pmc/articles/PMC4981212/ /pubmed/27216881 http://dx.doi.org/10.1080/19336896.2016.1181249 Text en © 2016 The Author(s). Published with license by Taylor & Francis http://creativecommons.org/licenses/by-nc/3.0/ This is an Open Access article distributed under the terms of the Creative Commons Attribution-Non-Commercial License http://creativecommons.org/licenses/by-nc/3.0/, which permits unrestricted non-commercial use, distribution, and reproduction in any medium, provided the original work is properly cited. The moral rights of the named author(s) have been asserted.
spellingShingle Research Papers
Nichols, Tracy A.
Spraker, Terry R.
Gidlewski, Thomas
Cummings, Bruce
Hill, Dana
Kong, Qingzhong
Balachandran, Aru
VerCauteren, Kurt C.
Zabel, Mark D.
Dietary magnesium and copper affect survival time and neuroinflammation in chronic wasting disease
title Dietary magnesium and copper affect survival time and neuroinflammation in chronic wasting disease
title_full Dietary magnesium and copper affect survival time and neuroinflammation in chronic wasting disease
title_fullStr Dietary magnesium and copper affect survival time and neuroinflammation in chronic wasting disease
title_full_unstemmed Dietary magnesium and copper affect survival time and neuroinflammation in chronic wasting disease
title_short Dietary magnesium and copper affect survival time and neuroinflammation in chronic wasting disease
title_sort dietary magnesium and copper affect survival time and neuroinflammation in chronic wasting disease
topic Research Papers
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4981212/
https://www.ncbi.nlm.nih.gov/pubmed/27216881
http://dx.doi.org/10.1080/19336896.2016.1181249
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