CWD is a fatal neurologic disease of cervids (e.g., deer, elk, moose, reindeer). It is caused by a misfolded form of a normal protein, known as a prion. The misfolded proteins build up in tissues, particularly the brain, causing progressive damage.
CWD belongs to a group of human and animal diseases called transmissible spongiform encephalopathies (TSE). Examples of TSEs in animals include bovine spongiform encephalopathy (BSE), also known as “mad cow disease”; and scrapie in sheep and goats. Examples of TSEs in humans include Creutzfeldt-Jakob disease (CJD), a sporadic prion disease arising in 1:1,000,000 people, and variant Creutzfeldt-Jakob disease (vCJD), which has been linked to the consumption of infected cattle during the “mad cow disease” outbreak in Great Britain and Europe in the 1990s.
CWD spreads through direct contact with the infectious, misfolded proteins (i.e., prion), from infected individuals or contaminated environment. Infectious prions can be excreted in urine, feces, and saliva of infected animals before they show any signs of the disease. Prions persist in animal carcasses and tissues, especially in the brain, spinal cord, and lymph nodes. Infected carcasses can contaminate the environment and spread the disease if left out on the landscape, as prions can persist for ten or more years in soils and be taken up by plants.
The progression of CWD in an infected animal is very slow. After infection, an animal may not show clinical signs of CWD for months or even years. Infected animals gradually become skinnier, emaciated, or “wasted” despite continuing to eat. They may show abnormal behaviors such as a wide stance, staggering gait, or inability to keep their head up.
CWD has now been detected in California’s deer/elk populations. If you see a sick or dead deer that could be due to CWD, please use our online mortality reporting form (preferred) or contact the CDFW Wildlife Health Laboratory directly at (916) 358-2790.
The WHL investigates sick or dead wildlife and is particularly interested in deer and elk that are skinny or “wasted,” show abnormal behaviors, or have a staggering gait. While deer could have a different condition that produce similar clinical signs, testing these animals for CWD is an integral part of ongoing CWD surveillance efforts in California. CDFW relies on members of the public to report sick and dead animals.
Limit the Spread: Legislation and regulations enacted since the 1990s reduce the risk of importing the disease. These include restrictions on the importation of captive deer and elk (and other cervids) into California (CCR Title 14, Section 671 (opens in new tab)), what hunters can bring in from out-of-state hunts (no skull, no backbone) (CCR Title 14, Section712 (link opens in new tab)), a ban on the feeding of wildlife to prevent artificially congregating susceptible animals (CCR Title 14, Section 251.3(opens in new tab)), and a ban on the use or possession of cervid-derived biological materials such as scent lures (CCR Title 14, Section 714 (opens in new tab)).
Surveillance: California has been testing deer and elk for CWD since 1999, with most samples coming from hunter-harvested animals and the rest from vehicle-strike and other sources of deer and elk mortalities. Maintaining robust disease testing is needed to understand disease spread dynamics to better inform management decisions.
In 2024, CDFW first confirmed CWD in California. The Fish and Game Commission adopted regulations in response to these detections that defined a CWD management zone and authorized the CDFW director to designate mandatory testing or testing and handling rules for hunter harvested deer within those management zones (CCR Title 14, section 708.5 (opens in new tab)).
Management: CDFW developed a statewide CWD Management Plan outlining surveillance, response, long-term management, and communication strategies. Management actions will be determined by the prevalence and geographic distribution of CWD as determined through CDFW’s CWD surveillance efforts. General management objectives are to use current scientific understanding and management tools to keep prevalence low where CWD occurs and decrease transmission and spread of the disease to naïve populations.
There are no documented cases of CWD affecting humans. Laboratory and population-based studies suggest that people may not be susceptible to CWD. However, other animal prion diseases, like “mad cow” disease, have caused lethal disease in humans so the risk to people may not be zero. The Centers for Disease Control and Prevention (CDC) and the World Health Organization (WHO) recommend that hunters do not eat meat from deer that test positive for CWD or otherwise appear sick. In addition, CDFW recommends that hunters wear latex or nitrile gloves when field-dressing and processing animals, and that hunters wash their hands and disinfect tools after processing.
Currently, the best tests for CWD require lymph node or brainstem samples taken from a deer or elk after death. However, significant work is going towards optimizing more sensitive, rapid and live-animal tests and these tests may be used as they become available and accepted.