Chronic Wasting Disease
Research at
the USGS-Wisconsin Cooperative Wildlife Research Unit
Chronic
wasting disease (CWD) is a fatal neurodegenerative disease of mule deer
(Odocoileus
hemionus), white-tailed deer (O. virginianus), and elk (Cervus
elaphus) associated with the presence of transmissible protease
resistant
prion proteins (or prions). Although the transmission route of
CWD is
unknown, it may be transmitted among deer and elk by direct contact or
indirectly through the environment. Maternal transmission does not
appear to be
an important component of CWD epidemiology. Appearance of clinical
signs is
usually delayed, but symptoms typically appear within 18-24 months
after
experimental infections, and include weight loss, anorexia, repetitive
behaviors, hyperesthesia and intractability with progression to severe
emaciation, severe behavioral changes, excessive salivation, tremors,
and mild
ataxia. Pre-clinical disease can be detected in animal lymph node and
brain
tissues using a variety of diagnostic methods.
Historically,
CWD was believed occur only in the western
CWD was discovered in south-central
An integrated research and management program has developed from this
collaboration including the USGS-NWHC, the Wisconsin
Department of Natural Resources (WDNR), and the
USGS-WCWRU. Research
studies at WCWRU have focused on understanding the epidemiology and
transmission of CWD in white-tailed deer, the landscape patterns
associated
with CWD distribution and spread, potential CWD transmission into other
wildlife species, and evaluation of CWD surveillance and management
actions.