Chronic Wasting Disease of Deer and Elk: A Review with Recommendations for Management

Chronic wasting disease (CWD) has emerged as an important disease of wild and farmed cervids in North America. Of the transmissible spongiform encephalopathies (TSEs), or prion diseases, CWD is the only 1 found in free-ranging species. Because the TSEs include infamous diseases like bovine spongiform encephalopathy (BSE) of cattle and variant Creutzfeldt-Jakob disease of humans, CWD by association has become a disease of interest beyond the parochial concerns where it is found. Consequently, wildlife managers are faced with developing programs for addressing CWD. Mule deer (Odocoileus hemionus), white-tailed deer (O. virginianus), and Rocky Mountain elk (Cervus elaphus nelsoni) are the only species known to be naturally susceptible to CWD. Although implications of CWD are not entirely clear at this time, we know that CWD is a fatal, contagious disease of mature reproductive segments of deer and elk populations. It has been endemic in free-ranging cervids in a core area of contiguous portions of southeastern Wyoming and northeastern Colorado, USA, for a minimum of 20 years and probably longer. The known geographic distribution of endemic CWD is relatively limited at this time, although as results of intensified surveillance become available, this may change. Foci of CWD in free-ranging deer have been identified distant from the core endemic area as far east as Wisconsin. Distribution has greatly expanded in the last decade or more via commerce in infected farmed elk; as a result, CWD recently has been found in multiple jurisdictions of the plains, foothills, and Rocky Mountains of western North America, and in South Korea. Studies of the biology and natural history of CWD over the last few years have resulted in a better understanding of its pathogenesis and epidemiology. Chronic wasting disease is transmitted horizontally from infected to susceptible cervids. Early involvement of alimentary tract-associated lymphoid tissues during incubation suggests plausible routes for transmission via feces or saliva. Residual environmental contamination also appears to be important in sustaining epidemics. Studies of CWD epidemiology led to development of models to help explain the history of CWD as well as forecast its impacts on deer and elk populations. Improved tests allow CWD to be diagnosed early in incubation, long before clinical signs appear. Where CWD is not known to occur, managers should be, and in some cases are, developing surveillance programs and regulations that prevent or reduce the likelihood that CWD will be introduced into their jurisdictions. Where CWD is already endemic, responsible agencies are conducting surveillance to assess status and trends in prevalence and geographic distribution, managing deer and elk populations to limit spread, and developing and evaluating techniques for further controlling and perhaps eradicating CWD. Programs for addressing the challenges of CWD management will require interagency cooperation, commitment of funds and personnel, and applied research.

[1]  N. T. Hobbs,et al.  Evaluation of antemortem sampling to estimate chronic wasting disease prevalence in free-ranging mule deer , 2002 .

[2]  G R Hartsough,et al.  Encephalopathy of mink. I. Epizootiologic and clinical observations. , 1965, The Journal of infectious diseases.

[3]  E. Williams,et al.  CHRONIC WASTING DISEASE OF CAPTIVE MULE DEER: A SPONGIFORM ENCEPHALOPATHY1 , 1980, Journal of wildlife diseases.

[4]  M. Jeffrey,et al.  Spongiform Encephalopathy in a Nyala (Tragelaphus angasi) , 1988, Veterinary pathology.

[5]  L. Schonberger,et al.  Creutzfeldt-Jakob disease in unusually young patients who consumed venison. , 2001, Archives of neurology.

[6]  A. Hofman,et al.  A new variant of Creutzfeldt-Jakob disease in the UK , 1996, The Lancet.

[7]  S. Prusiner Novel proteinaceous infectious particles cause scrapie. , 1982, Science.

[8]  C. Masters,et al.  Transmissible spongiform encephalopathies , 2004, The Lancet.

[9]  M. Miller,et al.  Chronic wasting disease in deer and elk in North America. , 2002, Revue scientifique et technique.

[10]  J. R. Greig Observations on the Transmission of the Disease by Mediate Contact , 1940 .

[11]  D. Gajdusek The Potential Risk to Humans of Amyloids in Animals , 1996 .

[12]  E. Williams,et al.  EPIZOOTIOLOGY OF CHRONIC WASTING DISEASE IN FREE-RANGING CERVIDS IN COLORADO AND WYOMING , 2000, Journal of wildlife diseases.

[13]  J. Miller,et al.  Immunohistochemical Diagnosis of Chronic Wasting Disease in Preclinically Affected Elk from a Captive Herd , 2000, Journal of veterinary diagnostic investigation : official publication of the American Association of Veterinary Laboratory Diagnosticians, Inc.

[14]  F. Cohen,et al.  Quantitative traits of prion strains are enciphered in the conformation of the prion protein. , 2000, Archives of virology. Supplementum.

[15]  M. Miller,et al.  Comparison of Histological Lesions and Immunohistochemical Staining of Proteinase-resistant Prion Protein in a Naturally Occurring Spongiform Encephalopathy of Free-ranging Mule Deer (Odocoileus hemionus) with Those of Chronic Wasting Disease of Captive Mule Deer , 2002, Veterinary pathology.

[16]  N. Hunter,et al.  Natural scrapie in British sheep: breeds, ages and PrP gene polymorphisms , 1992, Veterinary Record.

[17]  J. Grosclaude,et al.  Early accumulation of PrP(Sc) in gut-associated lymphoid and nervous tissues of susceptible sheep from a Romanov flock with natural scrapie. , 2000, The Journal of general virology.

[18]  L. Lund,et al.  The natural occurrence of scrapie in moufflon , 1992, Veterinary Record.

[19]  Hoinville Lj A review of the epidemiology of scrapie in sheep. , 1996 .

[20]  J. Aiken,et al.  The host range of chronic wasting disease is altered on passage in ferrets. , 1998, Virology.

[21]  F. Cohen,et al.  Prion diseases of humans and animals , 1996 .

[22]  D. Taylor Inactivation of transmissible degenerative encephalopathy agents: A review. , 2000, Veterinary journal.

[23]  S. Prusiner,et al.  Prions in skeletal muscle , 2002, Proceedings of the National Academy of Sciences of the United States of America.

[24]  B. Chesebro BSE and Prions: Uncertainties About the Agent , 1998, Science.

[25]  M. Miller,et al.  Validation of Monoclonal Antibody F99/97.6.1 for Immunohistochemical Staining of Brain and Tonsil in Mule Deer (Odocoileus Hemionus) with Chronic Wasting Disease , 2002, Journal of veterinary diagnostic investigation : official publication of the American Association of Veterinary Laboratory Diagnosticians, Inc.

[26]  H. Fraser,et al.  Transmission of bovine spongiform encephalopathy and scrapie to mice. , 1992, The Journal of general virology.

[27]  F. Cohen,et al.  Eight prion strains have PrPSc molecules with different conformations , 1998, Nature Medicine.

[28]  E. Williams,et al.  EPIDEMIOLOGY OF CHRONIC WASTING DISEASE IN CAPTIVE ROCKY MOUNTAIN ELK , 1998, Journal of wildlife diseases.

[29]  R. Somerville,et al.  Straining the prion hypothesis , 1998, Nature.

[30]  M. Miller,et al.  DETECTION OF BIAS IN HARVEST-BASED ESTIMATES OF CHRONIC WASTING DISEASE PREVALENCE IN MULE DEER , 2000, Journal of wildlife diseases.

[31]  J. Mickelson,et al.  PrP genotypes and experimental scrapie in orally inoculated Suffolk sheep in the United States. , 1997, The Journal of general virology.

[32]  R. Race,et al.  Comparative analysis of scrapie agent inactivation methods. , 1993, Journal of virological methods.

[33]  John E. Gross,et al.  Chronic wasting disease in mule deer: disease dynamics and control. , 2001 .

[34]  G. J. Raymond,et al.  Evidence of a molecular barrier limiting susceptibility of humans, cattle and sheep to chronic wasting disease , 2000, The EMBO journal.

[35]  E. Williams,et al.  Detection of PrPCWD in mule deer by immunohistochemistry of lymphoid tissues , 2002, Veterinary Record.

[36]  E. Williams,et al.  PrP genotypes of captive and free-ranging Rocky Mountain elk (Cervus elaphus nelsoni) with chronic wasting disease. , 1999, The Journal of general virology.

[37]  G. D. Hunter,et al.  The physico-chemical nature of the scrapie agent. , 1976, Frontiers of biology.

[38]  S. Cousens,et al.  Transmissions to mice indicate that ‘new variant’ CJD is caused by the BSE agent , 1997, Nature.

[39]  L. Karstad,et al.  Transmissible encephalopathy of mink in Ontario. , 1968, The Canadian veterinary journal = La revue veterinaire canadienne.

[40]  S. Prusiner,et al.  Prion diseases and the BSE crisis. , 1997, Science.

[41]  Christl A. Donnelly,et al.  Predicted vCJD mortality in Great Britain , 2000, Nature.

[42]  M. Miller,et al.  SPONGIFORM ENCEPHALOPATHY IN FREE-RANGING MULE DEER (ODOCOILEUS HEMIONUS), WHITE-TAILED DEER (ODOCOILEUS VIRGINIANUS) AND ROCKY MOUNTAIN ELK (CERVUS ELAPHUS NELSONI) IN NORTHCENTRAL COLORADO , 1997, Journal of wildlife diseases.

[43]  D. Taylor,et al.  Inactivation of the bovine spongiform encephalopathy agent by rendering procedures , 1995, Veterinary Record.

[44]  E A Hoover,et al.  Oral transmission and early lymphoid tropism of chronic wasting disease PrPres in mule deer fawns (Odocoileus hemionus). , 1999, The Journal of general virology.

[45]  D. Oppenheimer,et al.  Scrapie disease in sheep. Historical, clinical, epidemiological, pathological and practical aspects of the natural disease. , 1983 .

[46]  Stanley B. Prusiner,et al.  Slow transmissible diseases of the nervous system , 1979 .

[47]  M. Jeffrey,et al.  A novel progressive spongiform encephalopathy in cattle , 1987, Veterinary Record.

[48]  J. Ryan,et al.  Bovine spongiform encephalopathy: epidemiological studies , 1988, Veterinary Record.

[49]  A. Chong,et al.  Feline spongiform encephalopathy: fibril and PrP studies , 1992, Veterinary Record.

[50]  P. Lansbury,et al.  Molecular assessment of the potential transmissibilities of BSE and scrapie to humans , 1997, Nature.

[51]  R. Race,et al.  Serological evidence for an inflammatory response in murine scrapie. , 2001, The Journal of infectious diseases.

[52]  Y. Charnay,et al.  Spontaneous spongiform encephalopathy in a young adult rhesus monkey , 1996, The Lancet.

[53]  P. Brown,et al.  Survival of scrapie virus after 3 years' interment , 1991, The Lancet.

[54]  E. Williams,et al.  Preliminary Findings on the Experimental Transmission of Chronic Wasting Disease Agent of Mule Deer to Cattle , 2001, Journal of veterinary diagnostic investigation : official publication of the American Association of Veterinary Laboratory Diagnosticians, Inc.