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Chronic Wasting Disease -
Adaption To Rodents

From Patricia Doyle, PhD
ProMed Mail
5-15-7

Source - Journal of Virology
 
(The following information is taken from the abstract of a paper entitled "Transmission and Adaptation of Chronic Wasting Disease to Hamsters and Transgenic Mice: Evidence for Strains," by Gregory J. Raymond and 9 others, published in the April 2007 issue of the Journal of Virology p. 4305-4314, Vol. 81, No. 8 http://jvi.asm.org/cgi/content/abstract/81/8/4305.
 
The authors are at the Laboratory of Persistent Viral Diseases, Rocky Mountain Veterinary Branch, NIAID, NIH, Rocky Mountain Laboratories, Hamilton, Montana 59840, Department of Veterinary Sciences, University of Wyoming, Laramie, Wyoming 82070, and the Colorado Division of Wildlife, Wildlife Research Center, Fort Collins, Colorado 80526-20974. - Mod.CP)
 
 
In vitro screening using the cell-free prion protein conversion system [which assays sensitivity to proteinase K digestion] indicated that certain rodents may be susceptible to chronic wasting disease (CWD). Therefore, CWD isolates from mule deer, white-tailed deer, and elk were inoculated intracerebrally into various rodent species to assess the rodents' susceptibility and to develop new rodent models of CWD.
 
The species inoculated were Syrian golden, Djungarian, Chinese, Siberian, and Armenian hamsters, transgenic mice expressing the Syrian golden hamster prion protein, and RML Swiss and C57BL10 wild-type mice.
 
The transgenic mice and the Syrian golden, Chinese, Siberian, and Armenian hamsters had limited susceptibility to certain of the CWD inocula, as evidenced by incomplete attack rates and long incubation periods. For serial passages of CWD isolates in Syrian golden hamsters, incubation periods rapidly stabilized, with isolates having either short (85 to 89 days) or long (408 to 544 days) mean incubation periods and distinct neuropathological patterns. In contrast, wild-type mouse strains and Djungarian hamsters were not susceptible to CWD.
 
These results show that CWD can be transmitted and adapted to some species of rodents and suggest that the cervid-derived CWD inocula may have contained or diverged into at least 2 distinct transmissible spongiform encephalopathy (TSE) strains.
 
These rodent-adapted CWD models may be useful in comparative studies of TSE strains in vivo as well as for testing potential anti-TSE therapeutic agents.
 
http://jvi.asm.org/cgi/content/abstract/81/8/4305
 
Reported by Joseph P. Dudley, Ph.D
 
 
Patricia A. Doyle DVM, PhD
Bus Admin, Tropical Agricultural Economics
Univ of West Indies
 
 
 
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Zhan le Devlesa tai sastimasa
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