Chronic Wasting Disease
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Chronic wasting disease (CWD) is a transmissible spongiform encephalopathy (TSE) of deer and elk. To date, this disease has been found only in cervids (members of the deer family). First recognized as a clinical "wasting" syndrome in 1967 in mule deer in a wildlife research facility in northern Colorado, it was identified as a TSE in 1978. CWD is typified by chronic weight loss leading to death. There is no known relationship between CWD and any other TSE of animals or people.
In the mid-1980s, CWD was detected in free-ranging deer and elk in contiguous portions of northeastern Colorado and southeastern Wyoming. In May 2001, CWD was also found in free-ranging deer in the southwestern corner of Nebraska (adjacent to Colorado and Wyoming) and later in additional areas in western Nebraska. The limited area of northern Colorado, southern Wyoming, and western Nebraska in which free-ranging deer and/or elk positive for CWD have been found is referred to as the endemic area. Soon after diagnosis of the disease as a TSE, Colorado and Wyoming wildlife management agencies stopped the movement of deer and elk from their research facilities; wild cervids have not been translocated from the endemic area. In 2002, CWD also has been detected in wild deer in south-central Wisconsin, southwestern South Dakota, the western slope of Colorado, southern New Mexico, and northern Illinois.
CWD also has been diagnosed in farmed elk and deer herds in a number of States and in two Canadian provinces. The first positive farmed elk herd in the United States was detected in 1997 in South Dakota.
Chronic_wasting_disease_dec_2004.jpg
Since then, 25 additional positive elk herds and three positive farmed deer herds have been found: South Dakota (7), Nebraska (4), Colorado (10), Oklahoma (1), Kansas (1), Minnesota (1), Montana (1), Wisconsin (2) and New York (1). As of October 2002, three of these 27 positive herds remain under State quarantine. Twenty-three of the herds have been depopulated or have been slaughtered and tested, and the quarantine has been lifted from one herd that underwent rigorous surveillance with no further evidence of disease. CWD also has been found in farmed elk in the Canadian provinces of Saskatchewan and Alberta and in free-ranging mule deer in Saskatchewan. For more information on CWD in Canada, visit the Canadian Food Inspection Agency Web site at [1] (http:www.inspection.gc.ca/english/anima/heasan/disemala/cwdmdce.shtml).
Species that have been affected with CWD include Rocky Mountain elk, mule deer, white-tailed deer, and black-tailed deer. Other ruminant species, including wild ruminants and domestic cattle, sheep, and goats, have been housed in wildlife facilities in direct or indirect contact with CWD-affected deer and elk with no evidence of disease transmission. There is ongoing research to further explore the possibility of transmission of CWD to other species.
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Causative agent
The agent responsible for CWD (and other TSEs, such as scrapie and bovine spongiform encephalopathy) has not been completely characterized. There are three main theories on the nature of the agent that causes CWD: (1) the agent is a prion, an abnormal form of a normal protein, known as cellular prion protein, most commonly found in the central nervous system. The abnormal prion protein infects the host animal by promoting conversion of normal cellular prion protein to the abnormal form; (2) the agent is an unconventional virus; (3) the agent is a virino, or incomplete virus composed of nucleic acids protected by host proteins. The CWD agent is smaller than most viral particles and does not evoke any detectable immune response or inflammatory reaction in the host animal. Based on experience with other TSE agents, the CWD agent is assumed to be resistant to enzymes and chemicals that normally break down proteins, as well as resistant to heat and normal disinfection procedures.
Clinical signs
Most cases of CWD occur in adult animals. The disease is progressive and always fatal. The most obvious and consistent clinical sign of CWD is weight loss over time. Behavioral changes also occur in the majority of cases, including decreased interactions with other animals, listlessness, lowering of the head, blank facial expression, and repetitive walking in set patterns. In elk, behavioral changes may also include hyperexcitability and nervousness. Affected animals continue to eat grain but may show decreased interest in hay. Excessive salivation and grinding of the teeth also are observed. Most deer show increased drinking and urination.
Diagnosis
Research is being conducted to develop live-animal diagnostic tests for CWD. Currently, definitive diagnosis is based on postmortem examination (necropsy) and testing. Gross lesions seen at necropsy reflect the clinical signs of CWD, primarily emaciation. Aspiration pneumonia, which may be the actual cause of death, also is a common finding in animals affected with CWD. On microscopic examination, lesions of CWD in the central nervous system resemble those of other TSEs. In addition, scientists use a technique called immunohistochemistry to test brain tissue for the presence of the abnormal prion protein to diagnose CWD.
Epidemiology
The origin and mode of transmission of CWD is unknown. Animals born in captivity and those born in the wild have been affected with the disease. Based on epidemiology, transmission of CWD is thought to be lateral or from animal to animal; although maternal transmission may occur, it appears to be relatively unimportant in maintaining epidemics.