Skip to main page content
U.S. flag

An official website of the United States government

Dot gov

The .gov means it’s official.
Federal government websites often end in .gov or .mil. Before sharing sensitive information, make sure you’re on a federal government site.

Https

The site is secure.
The https:// ensures that you are connecting to the official website and that any information you provide is encrypted and transmitted securely.

Access keys NCBI Homepage MyNCBI Homepage Main Content Main Navigation
. 2019 Jul 23;10(4):e01091-19.
doi: 10.1128/mBio.01091-19.

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

Affiliations

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

Michael T Osterholm et al. mBio. .

Abstract

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.

Keywords: chronic wasting disease; infectious disease; prion disease; prions; public health.

PubMed Disclaimer

Figures

FIG 1
FIG 1
The distribution of detected chronic wasting disease cases in North American captive and free-ranging cervids as of June 2019, courtesy of the United States Geological Survey (https://www.usgs.gov/media/images/distribution-chronic-wasting-disease-north-america-0).

Comment in

References

    1. NIH, NINDS. 2018. Creutzfeldt-Jakob disease fact sheet. https://www.ninds.nih.gov/Disorders/Patient-Caregiver-Education/Fact-She....
    1. Bonda DJ, Manjila S, Mehndiratta P, Khan F, Miller BR, Onwuzulike K, Puoti G, Cohen ML, Schonberger LB, Cali I. 2016. Human prion diseases: surgical lessons learned from iatrogenic prion transmission. Neurosurg Focus 41:E10. doi:10.3171/2016.5.FOCUS15126. - DOI - PMC - PubMed
    1. Wadsworth JDF, Joiner S, Linehan JM, Asante EA, Brandner SB, Collinge J. 2008. The origin of the prion agent of kuru: molecular and biological strain typing. Philos Trans R Soc Lond B Biol Sci 363:3747–3753. doi:10.1098/rstb.2008.0069. - DOI - PMC - PubMed
    1. Alpers MP. 2008. The epidemiology of kuru: monitoring the epidemic from its peak to its end. Philos Trans R Soc Lond B Biol Sci 363:3707–3713. doi:10.1098/rstb.2008.0071. - DOI - PMC - PubMed
    1. Whitfield JT, Pako WH, Collinge J, Alpers MP. 2008. Mortuary rites of the South Fore and kuru. Philos Trans R Soc Lond B Biol Sci 363:3721–3724. doi:10.1098/rstb.2008.0074. - DOI - PMC - PubMed

LinkOut - more resources