#1908041 - 05/02/10 02:37 AM
Chronic Wasting disease (CWD)
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Locksley
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Chronic Wasting disease (CWD) Occurrence By the mid-1990s, CWD had been diagnosed among free-ranging deer and elk in a contiguous area in northeastern Colorado and southeastern Wyoming, where the disease is now endemic. In recent years, CWD has been found in areas outside of this disease-endemic zone, including areas east of the Mississippi River in Illinois, New York, West Virginia, and Wisconsin. The geographic range of diseased animals currently includes 13 U.S. states and two Canadian provinces and is likely to continue to grow. Surveillance studies of hunter-harvested animals indicate the overall prevalence of the disease in northeastern Colorado and southeastern Wyoming from 1996 to 1999 was estimated to be approximately 5% in mule deer, 2% in white-tailed deer, and <1% in elk.
Chronic Wasting Disease Among Free-Ranging Cervids by County, United States, March 2010 Chronic wasting disease and potential transmission to humans. Belay E, Maddox R, Williams E, et al. EID. June 2004;10(6):977-84. Overview of what is currently known about CWD in both captive and wild deer and elk in the United States. The article discusses transmission of CWD to other animals, as well at the epidemiologic and laboratory studies assessing the risk of CWD transmission to humans.
Fatal degenerative neurologic illnesses in men who participated in wild game feasts - Wisconsin, 2002. Centers for Disease Control and Prevention. MMWR Morb Mortal Wkly Rep. 2003;52:125-7. Epidemiologic investigation to assess risk of possible CWD transmission to men who participated in wild game feasts from 1993-1999 in Wisconsin.
Creutzfeldt-Jakob disease in unusually young patients who consumed venison. Belay ED, Gambetti P, Schonberger LB, et al. Arch Neurol. 2001;58:1673-8. This report examines the possible transmission of CWD to humans.
Chronic wasting disease of elk: transmissibility to humans examined by transgenic mouse models. Kong Q, Huang S, Zou W, et al. Neurobiol Dis. 2005;25(35)7944-9. This article indicates that there is a substantial species barrier for transmission of CWD from elks to humans.
http://www.cdc.gov/ncidod/dvrd/cwd/index.htm BSE (Bovine Spongiform Encephalopathy, or Mad Cow Disease) Additional Case of BSE Detected in Canada: On May 15, 2009, the Canadian Food, Inspection Agency (CFIA) announced the confirmation of bovine spongiform encephalopathy (BSE) in an 80-month-old dairy cow from Alberta. http://www.cdc.gov/ncidod/dvrd/bse/
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#1908474 - 05/02/10 12:48 PM
Re: Chronic Wasting disease (CWD)
[Re: ]
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Diehard Hunter
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CWD was found last year in Virginia.
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#1909509 - 05/03/10 07:21 AM
Re: Chronic Wasting disease (CWD)
[Re: Diehard Hunter]
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BigWes50
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I hope it never makes it here but the probability of it happening is very high!
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#1910963 - 05/04/10 03:15 AM
Re: Chronic Wasting disease (CWD)
[Re: Buck Nekkid]
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bowriter
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I'll bet dollars to doughnuts we have had it here for years and in every state with cervids.
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#1911468 - 05/04/10 01:40 PM
Re: Chronic Wasting disease (CWD)
[Re: Diehard Hunter]
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TC4ever
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CWD was found last year in Virginia.
It has been 'found" the past couple of years in Virginia in at least one N.W. county bordering W.Va. The VDGIF checks many deer from this county for CWD.It is fairly common in that portion of W.Va.
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#1913156 - 05/05/10 08:06 PM
Re: Chronic Wasting disease (CWD)
[Re: TC4ever]
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tickweed
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Probably a matter of time, if not already here.
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#1914206 - 05/06/10 01:18 PM
Re: Chronic Wasting disease (CWD)
[Re: tickweed]
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BSK
Jerkasourous of the non-typical kind
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Probably just a matter of time. But just like other new diseases, Nature will "clense" itself. Some deer will be naturally immune to the disease (just like some elk are) and eventually we will have a population of deer that are all immune. Although it could get ugly while the disease is being weeded out through Natural Selection.
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#1915519 - 05/07/10 07:51 AM
Re: Chronic Wasting disease (CWD)
[Re: bowriter]
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BSK
Jerkasourous of the non-typical kind
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BSK-Explain what you mean by new disease? What time span defines "new disease"? I personally have known about it for over 40 years. I am convinced it has been around for well over 100 years. Does that make me "new"?
CWD-like diseases have been around, especially in sheep and possibly in cattle, for much of recorded history. However, the disease jumping the species barrier to deer and elk makes it a "new" disease for those species (like avian flu jumping the species barrier to humans, as it did in 1918-19).
"New" diseases to a particular species occur fairly regularly on a biological time-frame (once or twice per century), but often these are current diseases that mutate to something new or are a disease in another species--sometime even a fairly benign disease--that jumps the species barrier and is highly dangerous to the new species (i.e. AIDS).
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#1915568 - 05/07/10 08:22 AM
Re: Chronic Wasting disease (CWD)
[Re: BSK]
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bowriter
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When Elizabeth first discivered the disease, she was convinced it had present in the wild for many years. It wasn't until we began penning elk and studying them that we became aware of it. There was no question the elk we were studying brought it in with them from the mountain.
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#1915683 - 05/07/10 09:42 AM
Re: Chronic Wasting disease (CWD)
[Re: bowriter]
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BSK
Jerkasourous of the non-typical kind
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When Elizabeth first discivered the disease, she was convinced it had present in the wild for many years. It wasn't until we began penning elk and studying them that we became aware of it. There was no question the elk we were studying brought it in with them from the mountain.
I used to believe CWD was probably a naturally occurring disease in cervids. However, the massive testing of wild populations, the documented spread of the disease, and the sudden cross-species development of CWD in mule deer in a penned facility that had held scrapie infected sheep makes it much more likely a "new" disease to elk and deer that is being spread across the country by the translocation of infected animals.
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"Know where you stand, and stand there" --Jesuit Father Daniel Berrigan
"There is no reasoning someone out of a position he has not reasoned himself into." --Clive James
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#1916319 - 05/07/10 06:30 PM
Re: Chronic Wasting disease (CWD)
[Re: BSK]
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bowriter
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No question that is how it id being spread. But how did it spread to moose and caribou? And when did they decide it was jumping a species barrier? I quit worrying about it a couple years ago and haven't really kept up with recent developments.
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#1916649 - 05/07/10 09:50 PM
Re: Chronic Wasting disease (CWD)
[Re: bowriter]
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spitndrum
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Bad Stuff
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#1916801 - 05/08/10 01:16 AM
Re: Chronic Wasting disease (CWD)
[Re: spitndrum]
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Locksley
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Infectious Prions in the Saliva and Blood of Deer with Chronic Wasting Disease Candace K. Mathiason,1 Jenny G. Powers,3 Sallie J. Dahmes,4 David A. Osborn,5 Karl V. Miller,5 Robert J. Warren,5 Gary L. Mason,1 Sheila A. Hays,1 Jeanette Hayes-Klug,1 Davis M. Seelig,1 Margaret A. Wild,3 Lisa L. Wolfe,6 Terry R. Spraker,1,2 Michael W. Miller,6 Christina J. Sigurdson,1 Glenn C. Telling,7 Edward A. Hoover1*
A critical concern in the transmission of prion diseases, including chronic wasting disease (CWD) of cervids, is the potential presence of prions in body fluids. To address this issue directly, we exposed cohorts of CWD-naïve deer to saliva, blood, or urine and feces from CWD-positive deer. We found infectious prions capable of transmitting CWD in saliva (by the oral route) and in blood (by transfusion). The results help to explain the facile transmission of CWD among cervids and prompt caution concerning contact with body fluids in prion infections. http://www.sciencemag.org/cgi/content/abstract/sci;314/5796/133 The Host Range of Chronic Wasting Disease Is Altered on Passage in Ferrets Jason C. Bartza, Richard F. Marsha, Debbie I. McKenziea and Judd M. Aiken1, a
a Department of Animal Health and Biomedical Sciences, University of Wisconsin, 1655 Linden Drive, Madison, Wisconsin, 53706
Received 5 June 1998; revised 17 July 1998; accepted 15 September 1998. Available online 6 April 2002.
Abstract Chronic wasting disease (CWD), a member of the transmissible spongiform encephalopathies (TSEs), was first identified in captive mule and black-tail deer in 1967. Due to the failure to transmit CWD to rodents, we investigated the use of ferrets (Mustela putorius furo) as a small animal model of CWD. The inoculation of CWD into ferrets resulted in an incubation period of 17–21 months on primary passage that shortened to 5 months by the third ferret passage. The brain tissue of animals inoculated with ferret-passaged CWD exhibited spongiform degeneration and reactive astrocytosis. Western blot analysis of ferret-passaged CWD demonstrated the presence of PrP-res. Unlike mule deer CWD, ferret-passaged CWD was transmissible to Syrian golden hamsters (Mesocricetus auratus). Increasing the passage number of CWD in ferrets increased the pathogenicity of the agent for hamsters. This increase in host range of a field isolate on interspecies transmission emphasizes the need for caution when assessing the potential risk of transmission of TSEs, such as bovine spongiform encephalopathy, to new host species.
C. Gibbs http://www.sciencedirect.com/science?_ob...c962a8f2eb6fab8 Prions in Skeletal Muscles of Deer with Chronic Wasting Disease Rachel C. Angers,1* Shawn R. Browning,1*† Tanya S. Seward,2 Christina J. Sigurdson,4‡ Michael W. Miller,5 Edward A. Hoover,4 Glenn C. Telling1,2,3§ Prions are transmissible proteinaceous agents of mammals that cause fatal neurodegenerative diseases of the central nervous system (CNS). The presence of infectivity in skeletal muscle of experimentally infected mice raised the possibility that dietary exposure to prions might occur through meat consumption (1). Chronic wasting disease (CWD), an enigmatic and contagious prion disease of North American cervids, is of particular concern. The emergence of CWD in an increasingly wide geographic area and the interspecies transmission of bovine spongiform encephalopathy (BSE) to humans as variant Creutzfeldt Jakob disease (vCJD) have raised concerns about zoonotic transmission of CWD. To test whether skeletal muscle of diseased cervids contained prion infectivity, Tg(CerPrP) mice (2) expressing cervid prion protein (CerPrP) were inoculated intracerebrally with extracts prepared from the semitendinosus/semimembranosus muscle group of CWD-affected mule deer or from CWD-negative deer. The availability of CNS materials also allowed for direct comparisons of prion infectivity in skeletal muscle and brain. All skeletal muscle extracts from CWDaffected deer induced progressive neurological dysfunction in Tg(CerPrP) mice, with mean incubation times ranging between 360 and È490 days, whereas the incubation times of prions from the CNS ranged from È230 to 280 days (Table 1). For each inoculation group, the diagnosis of prion disease was confirmed by the presence of disease-associated, protease-resistant PrP (PrPSc) in the brains of multiple infected Tg(CerPrP) mice Esee (3) for examples^. In contrast, skeletal muscle and brain material from CWD-negative deer failed to induce disease in Tg(CerPrP) mice (Table 1), and PrPSc was not detected in the brains of asymptomatic mice as late as 523 days after inoculation (3). http://www.cst.cmich.edu/users/gehri1tm/...0al.%202009.pdf Chronic wasting disease (CWD) is perhaps the most enigmatic of the naturally occurring prion diseases. Although recognized as a transmissible spongiform encephalopathy (TSE) since the late 1970s (Williams and Young 1980, 1982), interest in and concern about CWD has only recently emerged. CWD most closely resembles scrapie in sheep in most respects, but recent media and public reaction to CWD has been more reminiscent of that afforded to bovine spongiform encephalopathy (BSE) less than a decade ago. Yet, with the exception of transmissible mink encephalopathy (TME), CWD is the rarest of the known animal TSEs: fewer than 1,000 cases have been diagnosed worldwide, and all but two of these occurred in North America. CWD is unique among the TSEs in that it affects free-living species (Spraker et al. 1997; Miller et al. 2000). The three natural host species for CWD, mule deer (Odocoileus hemionus), white-tailed deer (O. virginianus), and Rocky Mountain elk (Cervus elaphus nelsoni), are all in the family Cervidae and native to North America. Like scrapie, CWD is contagious: epidemics are self-sustaining in both captive and free-ranging cervid populations (Miller et al. 1998, 2000). The geographic extent of endemic CWD in free-ranging wildlife was initially thought to be quite limited and its natural rate of expansion slow; however, recent investigations have revealed that CWD has been inadvertently spread much more widely via market-driven movements of infected, farmed elk and deer. Both the ecological and economic consequences of CWD and its spread remain to be determined; moreover, public health implications remain a question of intense interest. Here, we review current understanding of CWD, its implications, and its management. http://www.ncbi.nlm.nih.gov/pubmed/15148993 Introduction The apparent transmission of bovine spongiform encephalopathy (BSE) to humans (Bruce et al., 1997; Hill et al., 1997) and other mammalian species emphasizes the importance of considering the potential for cross-species transmission of other animal transmissible spongiform encephalopathy (TSE) diseases. A high percentage (up to 15%) of free-ranging deer and elk in parts of north-eastern Colorado and south-eastern Wyoming are infected with chronic wasting disease (CWD) (Miller et al., 2000). CWD-infected cervids have also been identified in game farms in several other western US states. Although it appears that natural transmission of CWD between cervids is important in the maintenance of the CWD epidemic, the origin of CWD and the mode of transmission between wild animals are not understood. Furthermore, it is not clear whether the disease can be transmitted to humans who hunt and eat these animals or to domestic livestock whose range may overlap with infected cervids. The transmissibility of CWD to animals should be tested experimentally in vivo, but such tests will take years to complete because of the long incubation periods commonly encountered in interspecies TSE transmissions. Because of these problems, and the fact that CWD transmissibility cannot be tested directly in humans, we have sought alternative clues to the potential interspecies transmissibility of CWD. http://www.ncbi.nlm.nih.gov/pmc/articles/PMC302048/ The PrP gene encodes the putative causative agent of the transmissible spongiform encephalopathies (TSEs), a heterogeneous group of fatal, neurodegenerative disorders including human Creutzfeldt–Jakob disease, bovine spongiform encephalopathy, ovine scrapie and chronic wasting disease (CWD) of North American deer and elk. Polymorphisms in the PrP gene are associated with variations in relative susceptibility, pathological lesion patterns, incubation times and clinical course of TSEs of humans, mice and sheep. Sequence analysis of the PrP gene from Rocky Mountain elk showed only one amino acid change (Met to Leu at cervid codon 132). Homozygosity for Met at the corresponding polymorphic site (Met to Val) in humans (human codon 129) predisposes exposed individuals to some forms of Creutzfeldt–Jakob disease. In this study, Rocky Mountain elk homozygous for PrP codon 132 Met were over-represented in both free- ranging and farm-raised CWD-affected elk when compared to unaffected control groups. http://jgv.sgmjournals.org/cgi/content/abstract/80/10/2765
Edited by Locksley (05/08/10 02:04 AM)
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