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Chronic Wasting Disease in Cervids: Implications for Prion Transmission to Humans and Other Animal Species

Chronic wasting disease (CWD) is a prion-related transmissible spongiform encephalopathy of cervids, including deer, elk, reindeer, sika deer, and moose. CWD has been confirmed in at least 26 U.S. states, three Canadian provinces, South Korea, Finland, Norway, and Sweden, with a notable increase in...

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Autores principales: Osterholm, Michael T., Anderson, Cory J., Zabel, Mark D., Scheftel, Joni M., Moore, Kristine A., Appleby, Brian S.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: American Society for Microbiology 2019
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6650550/
https://www.ncbi.nlm.nih.gov/pubmed/31337719
http://dx.doi.org/10.1128/mBio.01091-19
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author Osterholm, Michael T.
Anderson, Cory J.
Zabel, Mark D.
Scheftel, Joni M.
Moore, Kristine A.
Appleby, Brian S.
author_facet Osterholm, Michael T.
Anderson, Cory J.
Zabel, Mark D.
Scheftel, Joni M.
Moore, Kristine A.
Appleby, Brian S.
author_sort Osterholm, Michael T.
collection PubMed
description Chronic wasting disease (CWD) is a prion-related transmissible spongiform encephalopathy of cervids, including deer, elk, reindeer, sika deer, and moose. CWD has been confirmed in at least 26 U.S. states, three Canadian provinces, South Korea, Finland, Norway, and Sweden, with a notable increase in the past 5 years. The continued geographic spread of this disease increases the frequency of exposure to CWD prions among cervids, humans, and other animal species. Since CWD is now an established wildlife disease in North America, proactive steps, where possible, should be taken to limit transmission of CWD among animals and reduce the potential for human exposure.
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spelling pubmed-66505502019-08-06 Chronic Wasting Disease in Cervids: Implications for Prion Transmission to Humans and Other Animal Species Osterholm, Michael T. Anderson, Cory J. Zabel, Mark D. Scheftel, Joni M. Moore, Kristine A. Appleby, Brian S. mBio Opinion/Hypothesis Chronic wasting disease (CWD) is a prion-related transmissible spongiform encephalopathy of cervids, including deer, elk, reindeer, sika deer, and moose. CWD has been confirmed in at least 26 U.S. states, three Canadian provinces, South Korea, Finland, Norway, and Sweden, with a notable increase in the past 5 years. The continued geographic spread of this disease increases the frequency of exposure to CWD prions among cervids, humans, and other animal species. Since CWD is now an established wildlife disease in North America, proactive steps, where possible, should be taken to limit transmission of CWD among animals and reduce the potential for human exposure. American Society for Microbiology 2019-07-23 /pmc/articles/PMC6650550/ /pubmed/31337719 http://dx.doi.org/10.1128/mBio.01091-19 Text en Copyright © 2019 Osterholm et al. https://creativecommons.org/licenses/by/4.0/ This is an open-access article distributed under the terms of the Creative Commons Attribution 4.0 International license (https://creativecommons.org/licenses/by/4.0/) .
spellingShingle Opinion/Hypothesis
Osterholm, Michael T.
Anderson, Cory J.
Zabel, Mark D.
Scheftel, Joni M.
Moore, Kristine A.
Appleby, Brian S.
Chronic Wasting Disease in Cervids: Implications for Prion Transmission to Humans and Other Animal Species
title Chronic Wasting Disease in Cervids: Implications for Prion Transmission to Humans and Other Animal Species
title_full Chronic Wasting Disease in Cervids: Implications for Prion Transmission to Humans and Other Animal Species
title_fullStr Chronic Wasting Disease in Cervids: Implications for Prion Transmission to Humans and Other Animal Species
title_full_unstemmed Chronic Wasting Disease in Cervids: Implications for Prion Transmission to Humans and Other Animal Species
title_short Chronic Wasting Disease in Cervids: Implications for Prion Transmission to Humans and Other Animal Species
title_sort chronic wasting disease in cervids: implications for prion transmission to humans and other animal species
topic Opinion/Hypothesis
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6650550/
https://www.ncbi.nlm.nih.gov/pubmed/31337719
http://dx.doi.org/10.1128/mBio.01091-19
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