Thursday, December 25, 2008

Lions and Prions and Deer Demise

Lions and Prions and Deer Demise

Michael W. Miller1*, Heather M. Swanson2, Lisa L. Wolfe1, Fred G. Quartarone1, Sherri L. Huwer1, Charles H. Southwick3, Paul M. Lukacs1

1 Colorado Division of Wildlife, Wildlife Research Center, Fort Collins, Colorado, United States of America, 2 City of Boulder Open Space and Mountain Parks, Boulder, Colorado, United States of America, 3 Department of Ecology and Evolutionary Biology, University of Colorado at Boulder, Boulder, Colorado, United States of America

Abstract Background Contagious prion diseases – scrapie of sheep and chronic wasting disease of several species in the deer family – give rise to epidemics that seem capable of compromising host population viability. Despite this prospect, the ecological consequences of prion disease epidemics in natural populations have received little consideration.

Methodology/Principal Findings Using a cohort study design, we found that prion infection dramatically lowered survival of free-ranging adult (>2-year-old) mule deer (Odocoileus hemionus): estimated average life expectancy was 5.2 additional years for uninfected deer but only 1.6 additional years for infected deer. Prion infection also increased nearly fourfold the rate of mountain lions (Puma concolor) preying on deer, suggesting that epidemics may alter predator–prey dynamics by facilitating hunting success. Despite selective predation, about one fourth of the adult deer we sampled were infected. High prevalence and low survival of infected deer provided a plausible explanation for the marked decline in this deer population since the 1980s.

Conclusion Remarkably high infection rates sustained in the face of intense predation show that even seemingly complete ecosystems may offer little resistance to the spread and persistence of contagious prion diseases. Moreover, the depression of infected populations may lead to local imbalances in food webs and nutrient cycling in ecosystems in which deer are important herbivores.

Citation: Miller MW, Swanson HM, Wolfe LL, Quartarone FG, Huwer SL, et al. (2008) Lions and Prions and Deer Demise. PLoS ONE 3(12): e4019. doi:10.1371/journal.pone.0004019

Editor: Matthew Baylis, University of Liverpool, United Kingdom

Received: November 3, 2008; Accepted: November 25, 2008; Published: December 24, 2008

Copyright: © 2008 Miller et al. This is an open-access article distributed under the terms of the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are credited.

Funding: Our funding came from the Colorado Division of Wildlife, the City of Boulder, and the US Department of Agriculture, Animal&Plant Health Inspection Service, Veterinary Services. The funders had no role in study design, data collection and analysis, decision to publish, or preparation of the manuscript.

Competing interests: The authors have declared that no competing interests exist.

* E-mail: mhtml:%7B33B38F65-8D2E-434D-8F9B-8BDCD77D3066%7Dmid://00000094/!x-usc:mailto:mike.miller@state.co.us



http://www.plosone.org/article/info%3Adoi%2F10.1371%2Fjournal.pone.0004019




Greetings,

A disturbing study indeed, but even more disturbing, the fact that this very study shows the potential for transmission of the TSE agent into the wild of yet another species in the USA. Science has shown that the feline is most susceptible to the TSE agent. Will CWD be the demise of the mountain lions, cougars and such in the USA? How many have ever been tested in the USA? I recall there is a study taking place ;

Review A prion disease of cervids: Chronic wasting disease Christina J. Sigurdson et al ;

Mountain lion (Puma concolor) susceptibility to experimental feeding of CWD prions is currently under investigation (M. Miller and L. Wolfe, personal communication).



WHAT about multiple strains of CWD ?



0C7.04

North American Cervids Harbor Two Distinct CWD Strains

Authors

Angers, R. Seward, T, Napier, D., Browning, S., Miller, M., Balachandran A., McKenzie, D., Hoover, E., Telling, G. 'University of Kentucky; Colorado Division of Wildlife, Canadian Food Inspection Agency; University Of Wisconsin; Colorado State University.

Content

Despite the increasing geographic distribution and host range of CWD, little is known about the prion strain(s) responsible for distinct outbreaks of the disease. To address this we inoculated CWD-susceptible Tg(CerPrP)1536+/· mice with 29 individual prion samples from various geographic locations in North America. Upon serial passage, intrastudy incubation periods consistently diverged and clustered into two main groups with means around 210 and 290 days, with corresponding differences in neuropathology. Prion strain designations were utilized to distinguish between the two groups: Type I CWD mice succumbed to disease in the 200 day range and displayed a symmetrical pattern of vacuolation and PrPSc deposition, whereas Type II CWD mice succumbed to disease near 300 days and displayed a strikingly different pattern characterized by large local accumulations of florid plaques distributed asymmetrically. Type II CWD bears a striking resemblance to unstable parental scrapie strains such as 87A which give rise to stable, short incubation period strains such as ME7 under certain passage conditions. In agreement, the only groups of CWD-inoculated mice with unwavering incubation periods were those with Type I CWD. Additionally, following endpoint titration of a CWD sample, Type I CWD could be recovered only at the lowest dilution tested (10-1), whereas Type II CWD was detected in mice inoculated with all dilutions resulting in disease. Although strain properties are believed to be encoded in the tertiary structure of the infectious prion protein, we found no biochemical differences between Type I and Type II CWD. Our data confirm the co·existence of two distinct prion strains in CWD-infected cervids and suggest that Type II CWD is the parent strain of Type I CWD.

see page 29, and see other CWD studies ;



http://www.neuroprion.org/resources/pdf_docs/conferences/prion2008/abstract-book-prion2008.pdf



Sunday, November 23, 2008

PRION October 8th - 10th 2008 Book of Abstracts



http://bse-atypical.blogspot.com/2008/11/prion-october-8th-10th-2008-book-of.html



Biochim Biophys Acta. Author manuscript; available in PMC 2008 December 9. Published in final edited form as: Biochim Biophys Acta. 2007 June; 1772(6): 681-691. Published online 2006 December 15. doi: 10.1016/j.bbadis.2006.12.006. PMCID: PMC2597801 NIHMSID: NIHMS25810

Copyright notice and Disclaimer

The prion strain phenomenon: Molecular basis and unprecedented features

Rodrigo Morales,1,2 Karim Abid,1 and Claudio Soto1# 1 Protein Misfolding Disorders Laboratory, George and Cynthia Mitchell Center for Neurodegenerative diseases, Departments of Neurology, Neuroscience & Cell Biology and Biochemistry & Molecular Biology, University of Texas Medical Branch, 301 University Boulevard, Galveston, Texas, 77555-0646, USA 2 Facultad de Ciencias, Universidad de Chile, Santiago, Chile #To whom correspondence should be addressed at Email: mhtml:%7B33B38F65-8D2E-434D-8F9B-8BDCD77D3066%7Dmid://00000094/!x-usc:mailto:clsoto@utmb.edu The publisher's final edited version of this article is available at Biochim Biophys Acta. See other articles in PMC that cite the published article.

Abstract

Prions are unconventional infectious agents responsible for transmissible spongiform encephalopathies. Compelling evidences indicate that prions are composed exclusively by a misfolded form of the prion protein (PrPSc) that replicates in the absence of nucleic acids. One of the most challenging problems for the prion hypothesis is the existence of different strains of the infectious agent. Prion strains have been characterized in most of the species. Biochemical characteristics of PrPSc used to identify each strain include glycosylation profile, electrophoretic mobility, protease resistance, and sedimentation. In vivo, prion strains can be differentiated by the clinical signs, incubation period after inoculation and the vacuolation lesion profiles in the brain of affected animals. Sources of prion strain diversity are the inherent conformational flexibility of the prion protein, the presence of PrP polymorphisms and inter-species transmissibility. The existence of the strain phenomenon is not only a scientific challenge, but it also represents a serious risk for public health. The dynamic nature and inter-relations between strains and the potential for the generation of a very large number of new prion strains is the perfect recipe for the emergence of extremely dangerous new infectious agents.

snip...

BSE has not only been transmitted to humans. The extensive use of cow-derived material for feeding other animals led to the generation of new diseases in exotic felines such as tiger and cheetah, non human primates, and domestic cats [52,57-60]. As it was mentioned before, the transmission of BSE into these different species could create many new prion strains, each one of them with particular biological and biochemical characteristics and thus a potentially new hazard for human health. Successful transmission of BSE in pigs has been described [61,62] and also in transgenic mice expressing pig PrP (PoPrP) [63]. Porcine derivates are widely consumed and the hypothetic case of "mad pigs" could increase the events of zoonotic transmission of prions to humans. Fortunately, transmission of BSE to pigs is possible only in very drastic conditions, not likely to be occurring naturally [62,63]. More frightening is perhaps the possibility that BSE has been passed into sheep and goats. Studies have already shown that this transmission is possible and actually relatively easy and worrisomely produces a disease clinically similar to scrapie [64]. The cattle origin of this new scrapie makes possible that the new strain may be transmissible to humans. Transmission experiments of BSE infected sheep brain homogenate into human transgenic animal models are currently ongoing in several laboratories. It is very important to note that all materials generated by transmission of BSE in experimental and natural cases show similar biochemical behavior compared to the original inoculum [65], suggesting that all these new generated infectious agents could potentially be hazardous for humans. The origin of BSE is still a mystery. Abundant evidence supports the hypothesis that BSE was produced by cattle feeding with scrapie derivated material [66,67], indicating that bovine PrPSc might be a "conformational intermediary" between ovine PrPSc and human PrPC.

There is currently no mean to predict which will be the conformation of a newly generated strain and how this new PrPSc conformation could affect other species. One interesting new prion disease is CWD, a disease affecting farm and wild species of cervids [68,69]. The origin of CWD and its potential to transmit to humans are currently unknown. This is worrisome, considering that CWD has became endemic in some parts of USA and the number of cases continues to increase [69]. It is presumed that a large number of hunters in the US have been in contact or consumed CWD-infected meat [70]. CWD transmissibility studies have been performed in many species in order to predict how this disease could be spread by consumption of CWD meat [71-73]. In these studies, a special attention has been done to scavenging animals [74], which are presumed to be exposed to high concentration of cervid prions, resulting in the putative generation of many new forms of TSEs. Fortunately negative results were obtained in one experiment done in raccoons infected with CWD [74]. Transmission of CWD to humans cannot be ruled out at present and a similar infective episode to BSE involving CWD could result in catastrophic events, spreading the disease in a very dangerous way through the human population. No clinical evidence linking CWD exposed humans and CJD patients have been found [70], but experimental inoculation of CWD prions into squirrel monkeys propagated the disease [71]. It is important to mention that the species barrier between humans and cervids appears to be greater than with cattle, as judged by experiments with transgenic mice models [75]. Finally, it is important to be aware about CWD transmissibility to other species in which a "conformational intermediary" could be formed, facilitating human infection.

SNIP...

VI. Unique features of prion strains

The biological and infectious characteristics of prions are dramatically different to the conventional infectious agents. These differences are manifested in the prion strains phenomenon in unique and unprecedented features, such as for example strain adaptation and memory, the coexistence and competition of prion strains, among others. In this section, some of these interesting phenomena will be briefly described.

Adaptation of Prion strains

Interspecies transmission of prions could result in the emergence of more than one variety of infectious material. All new collected infectious agents could present particular strain characteristics. That is the case of DY and HY prion strains generation [13,16]. When interspecies transmission of prions occurs, serial passages in the new host are needed in order to stabilize the characteristics of new generated infectious material. In the case of TME transmission in hamsters, at least four serial passages in the new species were required for stabilization [13]. The first passage was characterized by long incubation periods and a dominance of a 19 KDa fragment when newly obtained PrPSc was analyzed after PK digestion. In the three first passages, clinical symptoms were not characteristic of the hamster-adapted HY or DY TME strains. This phenotype was attributed to the combination effects of both strains replicating simultaneously. Thereafter, each of the strains was stabilized in some of the animals and once they are adapted and stabilized, they can be serially propagated in vivo and the characteristics are maintained. It is accepted that both strains present differential conversion kinetics in vitro, with DY being the slowest and HY the fastest [124]. For this reason, in order to select efficiently this prion strain, limit dilutions must be performed [13]. In that way, the most abundant and less convertible DY is favored against the less abundant but fastest HY strain.

Co-existence of prion strains

Related to the above, it has been shown that two or more prion strains can co-exist in natural cases of TSE. Co-existence of prion strains has been found in sporadic cases of CJD [113, 125]. Analyses of several sCJD tissue showed that different biochemical profiles of PrPSc could be found in different brain areas from the same patient [113]. Co-existence of prion strains was mainly observed in patient heterozygous for codon 129 [113]. As many as 50% of these patients present different types of PrPSc in their brains, whereas 9% of MM patients were positive for co-existence of strains. On the other hand, more than one PrPSc type was not observed in VV patients [113].

The biochemical and structural properties of the protein seem to be the major cause of this differential distribution. This observation may explain why sCJD is so heterogeneous in terms of clinical manifestation [34,126,127]. In a recent publication by Bishop et al. [107], vCJD infected transgenic mice expressing human PrPC, present changes in their PrPSc and vacuolation patterns in the brain according to their polymorphic classification for codon 129.

Competition of prion strains

In particular experimental conditions, some prion strains can extend their specific incubation period when co-infected with another strain. Long incubation period prions increase the incubation period of "faster" prions. This phenomenon of "competition of prion strains" has been observed in mice and hamster. In mice, competition between 22A and 22C strains was reported in 1975 by Dickinson et al. [128]. In this study, RIII mice (homozygous for sincs7 allele) were used. 22A and 22C showed long and short incubation period (550 and 230 days), respectively. When 22C strain was intraperitoneally inoculated 100, 200 and 300 days after intraperitoneal administration of the 22A agent, all three experimental groups resulted in Morales et al. Page 8 Biochim Biophys Acta. Author manuscript; available in PMC 2008 December 9. NIH-PA Author Manuscript NIH-PA Author Manuscript NIH-PA Author Manuscript incubation periods and lesion patterns matching 22A prions, suggesting that 22C prions were degraded or excreted, in animals previously infected by 22A. Similar results were obtained by Kimberlin and Walker in 1985 [129] using a different strain of sincs7 mice. These authors treated mice using 22A and 22C prion strain. Before inoculation, 22A was treated with different chemical and physical agents in order to see if the "competitor" or "blocking" characteristics of 22A were maintained. From all treatments, 12M urea was shown to almost abolish the blocking properties of 22A agent. This information suggests that infective properties of long incubation period agent are strictly necessary in order to increase the incubation period of faster prions.

In hamster, similar observations were reported using DY and HY [130]. DY prion strain was inoculated 30 and 60 days prior intraperitoneal inoculation of HY at three different doses. When incubation periods of HY inoculated control group were compared with the animals inoculated at 60 days with DY, significant differences in the incubation periods were found, especially when HY prions were administrated in a higher dose [130]. On the other hand no differences were observed in the case of intranerve inoculation, revealing that competition phenomenon occurs only when peripheral inoculation is performed. These results are surprising considering the fact that DY was reported not to be infectious when intraperitoneally inoculated in hamsters [130]. This data suggest that replication of DY is occurring in peripheral tissues but is not able to reach the central nervous system.

In general, the principal variables that need to be observed for a successful competition are the route of infection, the interval between injections and the particular strains and doses of agent used. Prolongation of incubation periods in TSE are therapeutically beneficial and several strategies are under development to reach this aim, including antibodies, beta-sheet breakers, and other chemical agents [131-133]. The experimental evidence described above suggests that prions could be potentially useful for this purpose. In order to prevent spread of prion disease in cattle or humans, prion strains with incubation periods longer than species' lifespan could be used to slowdown the replication of BSE or vCJD prions.

VII. Concluding Remarks

The existence of different strains of an infectious agent composed exclusively of a protein has been one of the most puzzling issues in the prion field. If is already difficult to understand how a protein can adopt two stable and different folded structures and that one of them can transform the other one into itself, it is unthinkable that the misfolded form can in turn adopt multiple conformations with distinct properties. Yet, compelling scientific evidence support the idea that PrP can adopt numerous folding patterns that can faithfully replicate and produce different diseases. The existence of the strain phenomenon is not only a scientific challenge, but it also represents a serious risk for public health. The dynamic nature and inter-relations between strains and the potential for the generation of many new prion strains depending on the polymorphisms and the crossing of species barrier is the perfect recipe for the emergence of extremely dangerous new infectious agents. Although, substantial progress has been made in understanding the prion strains phenomenon, there are many open questions that need urgent answers, including: what are the structural basis of prion strains?; how are the phenomena of strain adaptation and memory enciphered in the conformation of the prion agent?; to what species can a given prion strain be transmissible?; what other cellular factors control the origin and properties of prion strains?.

...SNIP...END



http://www.pubmedcentral.nih.gov/articlerender.fcgi?tool=pmcentrez&artid=2597801&rendertype=abstract



http://www.pubmedcentral.nih.gov/picrender.fcgi?artid=2597801&blobtype=pdf



Friday, December 12, 2008

The prion strain phenomenon: Molecular basis and unprecedented features



http://bse-atypical.blogspot.com/2008/12/prion-strain-phenomenon-molecular-basis.html



TSS

Wednesday, December 17, 2008 ONE-THIRD OF BOULDER'S DEER INFECTED WITH CWD



http://chronic-wasting-disease.blogspot.com/2008/12/one-third-of-boulders-deer-infected.html



How to cite this article: Vet. Res. (2008) 39:41 DOI: 10.1051/vetres:2008018

Review A prion disease of cervids: Chronic wasting disease Christina J. Sigurdson

Department of Pathology, University of California, San Diego, 9500 Gilman Dr., La Jolla, CA 92093-0612, USA

Received 1 November 2007; accepted 31 March 2008; published online 3 April 2008

Abstract - Chronic wasting disease (CWD) is a prion disease of deer, elk, and moose, initially recognized in Colorado mule deer. The discovery of CWD beyond the borders of Colorado and Wyoming, in Canada and as far east as New York, has led to its emergence as a prion disease of international importance. Epidemiological studies indicate that CWD is horizontally transmitted among free-ranging animals, potentially indirectly by prion-containing secreta or excreta contaminating the environment. Experimental CWD transmission attempts to other wild and domestic mammals and to transgenic mice expressing the prion protein of cattle, sheep, and humans have shed light on CWD species barriers. Transgenic mice expressing the cervid prion protein have proven useful for assessing the genetic influences of Prnp polymorphisms on CWD susceptibility. Accumulating evidence of CWD pathogenesis indicates that the misfolded prion protein or prion infectivity seems to be widely disseminated in many nonneural organs and in blood. This review highlights contemporary research findings in this prion disease of free-ranging wildlife.

Key words: CWD / prion / TSE / cervid / amyloid

Corresponding author: mhtml:%7B33B38F65-8D2E-434D-8F9B-8BDCD77D3066%7Dmid://00000094/!x-usc:mailto:csigurdson@ucsd.edu

© INRA, EDP Sciences 2008

snip...

7. Interspecies CWD transmission

Wild predators and scavengers are presumably feeding on CWD-infected carcasses.

Skeletal muscle has been shown to harbor CWD prion infectivity [2], underscoring that other species will almost certainly be exposed to CWD through feeding. However, CWD has not been successfully transmitted by oral inoculation to species outside of the cervid family, suggestive of a strong species barrier for heterologous PrP conversion. Ferrets (family Mustelidae) can be infected with deer CWD after intracerebral (ic) but not oral exposure [5, 80]. Raccoons resisted even ic infection for up to 2 years thus far [24]. Mountain lion (Puma concolor) susceptibility to experimental feeding of CWD prions is currently under investigation (M. Miller and L. Wolfe, personal communication).

Could wild rodents colonizing CWD- or scrapie-infected pastures serve as an environmental reservoir of prion infectivity? Interestingly, bank voles (Clethrionomys glareolus), are readily infected with CWD and sheep scrapie by intracerebral inoculation ([64]; U. Agrimi, unpublished data) and are considered as a potential reservoir for sheep scrapie [64]. Many vole species occur in North America [65, 83] and further research may determine whether voles enhance CWD or scrapie spread through environmental contamination.

Given that environmental contamination with CWD prions likely occurs [55], domestic

ruminants may be exposed to CWD through common grazing areas. However, sheep and

cattle appear to be poorly susceptible to mule deer CWD: ic inoculation with mule deer CWD succeeded to infect only 2 of 8 sheep [28]; likewise cattle have not been infected after cograzing with CWD-infected mule deer, or after a direct oral exposure (over 6 years) (M. Miller, personal communication). Even direct ic inoculation led to CWD infection in only 5 of 13 cattle (38%) after 2-5 years [26]. In contrast, cattle are highly susceptible to white-tailed deer CWD with 12 of 14 animals developing neurologic disease and PrPSc by only 22 months post-ic inoculation (+/-0.5 months) [29]. Further studies are planned to determine whether

cattle are susceptible to white-tailed deer prions after an oral exposure (J. Richt, personal communication). The differential susceptibility of cattle to CWD from mule deer versus whitetailed deer suggests that CWD strains exist, and that CWD may differentially cross species barriers depending on the strain. Nevertheless, to date, natural CWD infections have been detected only in cervids.

Is the converse true, are cervids susceptible to sheep scrapie? Only one study has been performed on cervid susceptibility to sheep scrapie by the ic route, and showed that 3 of 6 elk developed neurologic signs, spongiform encephalopathy and PrPSc in brain [25]. Further experiments to address this question may be interesting since sheep scrapie is considered a possible source for CWD in North America [89, 91].

8. Human susceptibility to CWD

Millions of North Americans hunt deer and elk (U.S. Department of the Interior, Census Bureau), and there is no doubt that people have been exposed to CWD through venison consumption, particularly in light of recent data showing CWD prions in muscle [2]. Human susceptibility to CWD or to other newly emerging animal TSE [9, 14] is still unclear, although we can be somewhat reassured in that there have been no large scale outbreaks of human TSE cases in Colorado and Wyoming, where CWD has existed for decades [51]. Up until approximately 10 years ago, autopsies were not performed on suspect human TSE cases in many states due to biosafety concerns, therefore the diagnosis of potential new TSE strains has been hampered. This indicates that clinical TSE diagnoses in humans were not confirmed, nor was any strain typing done to look for the appearance of potentially subtle or unusual pathological or biochemical phenotypes of a new TSE strain. Fortunately, the

autopsy rate for suspect cases is improving. At the National Prion Disease Pathology

Surveillance Center at Case Western Reserve University (Cleveland, Ohio), Creutzfeldt-Jakob disease (CJD) suspect cases are studied and classified by CJD subtype. Thus far,

8

*** twenty-seven CJD patients who regularly consumed venison were reported to the

Surveillance Center***,

however there have been no unusual or novel prion subtypes that might indicate the appearance of a new prion strain [7, 41]. Other indirect studies of human susceptibility to CWD also suggest that the risk is low. In biochemical conversion studies, Raymond et al. [68] showed that the efficiency of CWD to

convert recombinant human PrP into amyloid fibrils was low, but similar to that of both BSE and scrapie fibrils to do the same. These results suggest that there is a molecular incompatibility in the conversion of human PrPC by CWD, sheep scrapie, or BSE, and that cross species infections in humans may be rare events.

To determine whether common PrPSc strain features may link CWD and CJD, histopathology and the PrPSc biochemical characteristics from deer and elk were compared with that of humans with sporadic CJD (sCJD) cases that are methionine homozygous at codon 129 of the Prnp gene by Xie et al. [96], although strain features including histologic profile, target organs, and glycoform patterns will not necessarily remain the same upon crossing species barriers [6, 5, 8, 57]. The PrPSc form is cleaved by proteinase-K (PK) at different sites depending on the conformation of the protein and may aid determination of whether the PrPSc conformation is similar. By western blot (SDS-PAGE) of elk CWD, the unglycosylated

PK-resistant PrPSc migrated at 21 kDa, similar to sCJD (MM1 subtype) and the PK cleavage site was the same, occurring at residues 78 and 82 as assessed by N-terminal sequencing. Conformational stability was evaluated by measuring the PrPSc stability under partially denaturing conditions and also showed no significant difference between elk CWD and sCJD MM1 PrPSc. However, elk CWD and human sCJD MM1 strains exhibited distinct glycoform patterns by two dimensional gel electrophoresis, suggesting that the strains differed. Future studies may utilize luminescent conjugated polymers, which were recently shown to distinguish naturally- and experimentally-derived prion strains [79].

To study elk-human prion species barriers, Kong et al. inoculated elk CWD into transgenic mice expressing either human PrP or elk PrP. Whereas the elk PrP expressing mice developed disease after only 118-142 days post-inoculation, human PrP expressing mice (129M) did not develop any features of TSE after more than 657 or more than 756 days [41].

In accordance with these results, Tamgüney et al. also reported that human PrP

overexpressing mice were not susceptible to 9 CWD isolates from mule deer, white-tailed deer, and elk [84]. However, mice have a limited lifespan and further passages may be necessary to detect low levels of prion infectivity that may be present subclinically. Although indirect evidence is accumulating that there may be a robust species barrier for CWD transmission to humans, one report indicates nonhuman primate susceptibility to CWD. Intracerebral inoculation of squirrel monkeys (Saimiri sciureus) demonstrated a positive CWD transmission [49]. Among non-human primates, however, the Prnp sequence of the new world monkeys are the most distant from humans [72], and therefore may not indicate that human prion conversion would occur by CWD.

snip...



http://www.sciencedirect.com/science?_ob=ArticleURL&_udi=B6T1Y-4M4ST6N-5&_user=10&_rdoc=1&_fmt=&_orig=search&_sort=d&view=c&_acct=C000050221&_version=1&_urlVersion=0&_userid=10&md5=7d278ee7dc237b467fa474c66647e0f3




http://www.vetres.org/index.php?option=article&access=standard&Itemid=129&url=/articles/vetres/pdf/2008/04/v08092.pdf



http://stanford.wellsphere.com/cjd-article/a-prion-disease-of-cervids:-chronic-wasting-disease-2008/13819



HOWEVER, why ignore the old science and transmission studies to date ???

Species Born Onset/Died

Ocelot May 1987 Mar 1994
Ocelot Jul 1980 Oct 1995
Puma 1986 May 1991
Puma 1980 May 1995
Puma 1978 May 1995
Lion Nov 1986 Dec 1998
Tiger 1981 Dec 1995
Tiger Feb 1983 Oct 1998
Ankole 1987 May 1995
Ankole 1986 Feb 1991
Bison 1989/90 Oct 1996

Maff data on 15 May 99

kudu 6
gemsbok 1
nyala 1
oryx 2
eland 6
cheetah 9
puma 3
tiger 2
ocelot 2
bison 1
ankole 2
lion 1



http://www.mad-cow.org/zoo_cites_annotated.html



Feline Spongiform Encephalopathy (FSE) FSE was first identified in the UK in 1990. Most cases have been reported in the UK, where the epidemic has been consistent with that of the BSE epidemic. Some other countries (e.g. Norway, Liechtenstein and France) have also reported cases.

Most cases have been reported in domestic cats but there have also been cases in captive exotic cats (e.g. Cheetah, Lion, Asian leopard cat, Ocelot, Puma and Tiger). The disease is characterised by progressive nervous signs, including ataxia, hyper-reactivity and behavioural changes and is fatal.

The chemical and biological properties of the infectious agent are identical to those of the BSE and vCJD agents. These findings support the hypothesis that the FSE epidemic resulted from the consumption of food contaminated with the BSE agent.

The FSE epidemic has declined as a result of tight controls on the disposal of specified risk material and other animal by-products.

References: Leggett, M.M. et al.(1990) A spongiform encephalopathy in a cat. Veterinary Record. 127. 586-588

Synge, B.A. et al. (1991) Spongiform encephalopathy in a Scottish cat. Veterinary Record. 129. 320

Wyatt, J. M. et al. (1991) Naturally occurring scrapie-like spongiform encephalopathy in five domestic cats. Veterinary Record. 129. 233.

Gruffydd-Jones, T. J.et al.. (1991) Feline spongiform encephalopathy. J. Small Animal Practice. 33. 471-476.

Pearson, G. R. et al. (1992) Feline spongiform encephalopathy: fibril and PrP studies. Veterinary Record. 131. 307-310.

Willoughby, K. et al. (1992) Spongiform encephalopathy in a captive puma (Felis concolor). Veterinary Record. 131. 431-434.

Fraser, H. et al. (1994) Transmission of feline spongiform encephalopathy to mice. Veterinary Record 134. 449.

Bratberg, B. et al. (1995) Feline spongiform encephalopathy in a cat in Norway. Veterinary Record 136. 444

Baron, T. et al. (1997) Spongiform encephalopathy in an imported cheetah in France. Veterinary Record 141. 270-271

Zanusso, G et al. (1998) Simultaneous occurrence of spongiform encephalopathy in a man and his cat in Italy. Lancet, V352, N9134, OCT 3, Pp 1116-1117.

Ryder, S.J. et al. (2001) Inconsistent detection of PrP in extraneural tissues of cats with feline spongiform encephalopathy. Veterinary Record 146. 437-441

Kelly, D.F. et al. (2005) Neuropathological findings in cats with clinically suspect but histologically unconfirmed feline spongiform encephalopathy. Veterinary Record 156. 472-477.

TSEs in Exotic Ruminants TSEs have been detected in exotic ruminants in UK zoos since 1986. These include antelopes (Eland, Gemsbok, Arabian and Scimitar oryx, Nyala and Kudu), Ankole cattle and Bison. With hindsight the 1986 case in a Nyala was diagnosed before the first case of BSE was identified. The TSE cases in exotic ruminants had a younger onset age and a shorter clinical duration compared to that in cattle with BSE. All the cases appear to be linked to the BSE epidemic via the consumption of feed contaminated with the BSE agent. The epidemic has declined as a result of tight controls on feeding mammalian meat and bone meal to susceptible animals, particularly from August 1996.

References: Jeffrey, M. and Wells, G.A.H, (1988) Spongiform encephalopathy in a nyala (Tragelaphus angasi). Vet.Path. 25. 398-399

Kirkwood, J.K. et al (1990) Spongiform encephalopathy in an Arabian oryx (Oryx leucoryx) and a Greater kudu (Tragelaphus strepsiceros) Veterinary Record 127. 418-429.

Kirkwood, J.K. (1993) Spongiform encephalopathy in a herd of Greater kudu (Tragelaphus strepsiceros): epidemiological observations. Veterinary Record 133. 360-364

Kirkwood, J. K. and Cunningham, A.A. (1994) Epidemiological observations on spongiform encephalopathies in captive wild animals in the British Isles. Veterinary Record. 135. 296-303.

Food and Agriculture Organisation (1998) Manual on Bovine Spongiform Encephalopathy.



http://www.defra.gov.uk/animalh/bse/othertses/index.html#fse




Subject: FSE: FIRST CONFIRMED CASE REPORTED IN PORTUGAL AND POTENTIAL MAD CAT ESCAPES LAB IN USA Date: August 9, 2007 at 2:27 pm PST

DIA-45 FELINE SPONGIFORM ENCEPHALOPATHY: FIRST CONFIRMED CASE REPORTED IN PORTUGAL

J.F. Silva1, J.J. Correia, 1 J. Ribeiro2, S. Carmo2 and L.Orge3

1 Faculdade de Medicina Veterinária (UTL), Lisbon, Portugal 2 Clínica Veterinária Ani+, Queluz, Portugal 3 Laboratório Nacional de Investigação Veterinária, Unidade de BSE, Lisbon, Portugal

Feline spongiform encephalopathy (FSE), affecting domestic and captive feline species, is a prion disease considered to be related to bovine spongiform encephalopathy (BSE). Here we report the first case diagnosed in Portugal, highlighting the neuroapthological findings. In 2004 a 9-year old intact female Siamese cat was referred with chronic progressive behavioural changes, polydipsia, gait abnormalities and episodes of hypersalivation. Clinical signs progressed to tetraparesis and dementia and euthanasia was performed. At necropsy, brain and spinal cord had no significative changes. Tissue samples from brain, cerebellum, brainstem and spinal cord were collected for histopathology and immunohistochemistry for detection of PrPres. Histology revealed neuropil and neuronal perikarion vacuolation in several areas of the central nervous system together with gliosis and cell rarefaction at the granular layer of the cerebellum. Immunohistochemical detection of PrPres showed a strong and widespread PrPres accumulation as granular and linear deposits as well as associated with some neurons. These findings are supportive of FSE. To the authors knowledge this is the first confirmed case of FSE reported in Portugal.




http://www.neuroprion.com/pdf_docs/conferences/prion2006/abstract_book.pdf




http://www.lniv.min-agricultura.pt/ResourcesUser/I_D/Feline%20Spongiform%20Encephalopathy.pdf





HOUND STUDY

AS implied in the Inset 25 we must not _ASSUME_ that transmission of BSE to other species will invariably present pathology typical of a scrapie-like disease.

snip…



http://www.bseinquiry.gov.uk/files/yb/1991/01/04004001.pdf



2005 DEFRA Department for Environment, Food & Rural Affairs

Area 307, London, SW1P 4PQ Telephone: 0207 904 6000 Direct line: 0207 904 6287 E-mail: h.mcdonagh.defra.gsi.gov.uk

GTN: FAX:

Mr T S Singeltary P.O. Box 42 Bacliff Texas USA 77518

21 November 2001

Dear Mr Singeltary

TSE IN HOUNDS

Thank you for e-mail regarding the hounds survey. I am sorry for the long delay in responding.

As you note, the hound survey remains unpublished. However the Spongiform Encephalopathy Advisory Committee (SEAC), the UK Government’s independent Advisory Committee on all aspects related to BSE-like disease, gave the hound study detailed consideration at their meeting in January 1994. As a summary of this meeting published in the BSE inquiry noted, the Committee were clearly concerned about the work that had been carried out, concluding that there had clearly been problems with it, particularly the control on the histology, and that it was more or less inconclusive. However was agreed that there should be a re-evaluation of the pathological material in the study.

Later, at their meeting in June 95, The Committee re-evaluated the hound study to see if any useful results could be gained from it. The Chairman concluded that there were varying opinions within the Committee on further work. It did not suggest any further transmission studies and thought that the lack of clinical data was a major weakness.

Overall, it is clear that SEAC had major concerns about the survey as conducted. As a result it is likely that the authors felt that it would not stand up to r~eer review and hence it was never published. As noted above, and in the detailed minutes of the SEAC meeting in June 95, SEAC considered whether additional work should be performed to examine dogs for evidence of TSE infection. Although the Committee had mixed views about the merits of conducting further work, the Chairman noted that when the Southwood Committee made their recommendation to complete an assessment of possible spongiform disease in dogs, no TSEs had been identified in other species and hence dogs were perceived as a high risk population and worthy of study. However subsequent to the original recommendation, made in 1990, a number of other species had been identified with TSE ( e.g. cats) so a study in hounds was less

critical. For more details see- http://www.bseinquiry, gov.uk/files/yb/1995/06/21005001 .pdf

As this study remains unpublished, my understanding is that the ownership of the data essentially remains with the original researchers. Thus unfortunately, I am unable to help with your request to supply information on the hound survey directly. My only suggestion is that you contact one of the researchers originally involved in the project, such as Gerald Wells. He can be contacted at the following address.

Dr Gerald Wells, Veterinary Laboratories Agency, New Haw, Addlestone, Surrey, KT 15 3NB, UK

You may also wish to be aware that since November 1994 all suspected cases of spongiform encephalopathy in animals and poultry were made notifiable. Hence since that date there has been a requirement for vets to report any suspect SE in dogs for further investigation. To date there has never been positive identification of a TSE in a dog.

I hope this is helpful

Yours sincerely 4

HUGH MCDONAGH BSE CORRESPONDENCE SECTION

IN CONFIDENCE

CONCEPT NOT FOR FURTHER STUDY OF MATERIAL OBTAINED IN A SURVEY OF HOUNDS FOR EVIDENCE OF A SCRAPIE-LIKE SPONGIFORM ENCEPHALOPATHY (SE)

snip…

b) Fibrillar material closely similar to SAF, found in BSE/Scrapie, was observed in 19 (4.3%) cases, all of which were hounds > 7 years of age. 14/19 of these suspected SAF results correlated with cases in the unresolveable histopathological category.

snip…

The following proposals address the hypothesis that the hound survey observations represent a PrP related or scrapie-like disease of dogs in which the pathological response, and possible the spread of infectivity, is neuroanatomically localized. By inference this could also mean that the disorder is clinically silent and non-progressive.



http://www.bseinquiry.gov.uk/files/yb/1995/02/09001001.pdf



http://www.mad-cow.org/00/aug00_late_news.html#ggg



http://www.kxnet.com/getForumPost.asp?ArticleId=113652



http://www.keeneequinox.com/home/index.cfm?event=displayArticleComments&ustory_id=4d8de1c2-fa09-42dc-958a-7e94e16e22db



PET FOODS MAD CATS AND MAD DOGS BSE/TSEs

worse still, there is serious risk the media could get to hear of such a meeting…

snip…

Crushed heads (which inevitably involve brain and spinal cord material) are used to a limited extent but will also form one of the constituent raw materials of meat and bone meal, which is used extensively in pet food manufacturer…



http://www.bseinquiry.gov.uk/files/yb/1989/03/17004001.pdf



2. The Parliamentary Secretary said that he was concerned about the possibility that countries in which BSE had not yet been detected could be exporting raw meat materials (in particular crushed heads) contaminated with the disease to the UK for use in petfood manufacture…

snip…

YOU explained that imported crushed heads were extensively used in the petfood industry…



http://www.bseinquiry.gov.uk/files/yb/1989/04/14001001.pdf



In particular I do not believe one can say that the levels of the scrapie agent in pet food are so low that domestic animals are not exposed…



http://www.bseinquiry.gov.uk/files/yb/1989/04/24003001.pdf





40. When Sir Richard Southwood gave oral evidence to the Agriculture Select Committee, he said:

‘The case of the cat is the first case of spongiform encephalopathy ever in a cat. Well, it appears to be - but if poor moggie got a bit of the staggers, you took it along to the vet and said it was not very happy, it would be put to sleep in the past and no one would have paid £300 to have a post mortem undertaken. So it is just possible that these were occurring before and were in fact caught from moggie being fed scrapie offal from sheep. I cannot say.’[46]

NEXT, ask yourself how many cats and dogs have ever been tested for TSE in the USA ???

DOGS AND CATS are not tested for TSE. THEY ARE RENDERED UP INTO LITTLE PELLETS, WITH ALL THE OTHER ROAD KILL, and fed back to animals for human and animal consumption. it’s an endless cycle of greed,
and disease. ...TSS


Subject: FELINE ALZHEIMER'S OR MAD CAT DISEASE I.E. FSE ???Date: December 6, 2006 at 9:24 am PST



http://lists.ifas.ufl.edu/cgi-bin/wa.exe?A2=ind0612&L=sanet-mg&P=8385





Friday, December 12, 2008

The prion strain phenomenon: Molecular basis and unprecedented features



http://bse-atypical.blogspot.com/2008/12/prion-strain-phenomenon-molecular-basis.html






TSS

Labels: , , , ,

Elk meat recalled due to CWD Boulder County Health Department and Colorado Department of Public Health and Environment

Warning out on elk meat sold at Boulder farmer's market

By Kevin Vaughan, Rocky Mountain News (Contact) Published December 25, 2008 at 12:05 a.m.

State health officials issued a warning Wednesday after learning that unsuspecting consumers bought hundreds of pounds of elk meat this month from an animal infected with chronic wasting disease.

The elk was sold Dec. 13 at a farmer's market at the Boulder County Fairgrounds.

Although research has found no risk to humans who eat infected elk, officials at the state and Boulder County health departments recommended that the meat not be consumed.

"There's been now 10 years- plus of research looking at whether CWD poses a human health risk, and the evidence to date suggests it does not," said John Pape, epidemiologist at the Colorado Department of Health and Environment.

Still, he said, the research is not definitive.

In all, 15 animals purchased at a commercial Colorado elk ranch were processed in early December at a USDA-licensed plant. All those animals were tested for the disease.

Test results obtained Tuesday indicated that one of the animals was infected with CWD, one of several diseases thought to be caused by misshaped proteins that inflict damage to nerve cells in the brain. It is a cousin to both crapie in sheep and mad cow disease.

Label information

On infected elk meat:

* Seller: High Wire Ranch

* Cuts: chuck roast, arm roast, flat iron, ribeye steak, New York steak, tenderloin, sirloin tip roast, medallions and ground meat.

* Processor: Cedaredge Processing

* USDA triangle number: 34645

For more information, contact John Pape, Colorado Department of Health and Environment, 303-692-2628.


http://www.rockymountainnews.com/news/2008/dec/25/warning-out-on-elk-meat-sold-at-boulder-farmers/



Elk meat recalled due to wasting disease

Publish Date: 12/24/2008

Longmont Times-Call

LONGMONT — Meat from an elk with chronic wasting disease was sold Dec. 13 at the Boulder County Fairgrounds, according to the Colorado Department of Public Health and Environment. The meat is being recalled.

State health officials said the animal was one of 15 elk purchased from High Wire Ranch and processed in early December before being sold at a farmers market at the fairgrounds. The disease was found during a routine preliminary test for CWD; none of the other 14 elk were deemed to be infected.

CWD is not known to be dangerous to humans, health officials said, but the state advises against eating meat from animals with the disease.

The labeling on the meat would include:

• Seller: High Wire Ranch • The type of cut, listed as either “chuck roast,” “arm roast,” “flat iron,” “ribeye steak,” “New York steak,” “tenderloin,” “sirloin tip roast,” “medallions” or “ground meat.”

• Processor: Ceaderedge Processing • A USDA triangle with the number 34645. Final testing is still being conducted. State officials said the meat should be discarded if it matches the packaging label and was bought on the fairgrounds on Dec. 13.

CWD is a disease believed to be caused by prions, misshapen proteins that cause brain damage. The disease affects elk, deer and moose. Other prion diseases include scrapie in sheep and bovine spongiform encephalopathy or “mad cow disease” in cattle.

People with questions about the meat can contact John Pape of the state health department at 303-692-2628.


http://www.timescall.com/news_story.aspID=13382



COLORADO: Farmer's market meat recalled after testing positive for CWD

24.dec.08 9News.com Jeffrey Wolf

Elk meat that was sold at a farmer's market is being recalled because tests show it was infected with chronic wasting disease. The Boulder County Health Department and Colorado Department of Public Health and Environment issued the recall Wednesday after the meat was sold at the Boulder County Fairgrounds on Dec. 13. Although there isn't any human health risk connected with CWD, the recalled was issued as a precaution. About 15 elk were bought from a commercial ranch in Colorado in early December and processed at a licensed plant. All 15 were tested for CWD and one came up positive. The labeling on the product would have the following information: *Seller: High Wire Ranch *The type of cut: "chuck roast," "arm roast," "flat iron," "ribeye steak," "New York steak," "tenderloin," "sirloin tip roast," "medallions" or "ground meat." *Processor: Cedaredge Processing *The USDA triangle containing the number "34645" People with questions about this meat can contact John Pape, epidemiologist at the Colorado Department of Public Health and Environment at 303-692-2628.


http://www.9news.com/money/consumer/article.aspx?storyid=106536&catid=103




COULD NOT FIND any warning or recalls on these two sites confirming their recall of CWD infected meat. ...TSS



http://www.bouldercounty.org/health/environ/foodsafety/index.htm



http://www.cdphe.state.co.us/




0C7.04

North American Cervids Harbor Two Distinct CWD Strains

Authors

Angers, R. Seward, T, Napier, D., Browning, S., Miller, M., Balachandran A., McKenzie, D., Hoover, E., Telling, G. 'University of Kentucky; Colorado Division of Wildlife, Canadian Food Inspection Agency; University Of Wisconsin; Colorado State University.

Content

Despite the increasing geographic distribution and host range of CWD, little is known about the prion strain(s) responsible for distinct outbreaks of the disease. To address this we inoculated CWD-susceptible Tg(CerPrP)1536+/· mice with 29 individual prion samples from various geographic locations in North America. Upon serial passage, intrastudy incubation periods consistently diverged and clustered into two main groups with means around 210 and 290 days, with corresponding differences in neuropathology. Prion strain designations were utilized to distinguish between the two groups: Type I CWD mice succumbed to disease in the 200 day range and displayed a symmetrical pattern of vacuolation and PrPSc deposition, whereas Type II CWD mice succumbed to disease near 300 days and displayed a strikingly different pattern characterized by large local accumulations of florid plaques distributed asymmetrically. Type II CWD bears a striking resemblance to unstable parental scrapie strains such as 87A which give rise to stable, short incubation period strains such as ME7 under certain passage conditions. In agreement, the only groups of CWD-inoculated mice with unwavering incubation periods were those with Type I CWD. Additionally, following endpoint titration of a CWD sample, Type I CWD could be recovered only at the lowest dilution tested (10-1), whereas Type II CWD was detected in mice inoculated with all dilutions resulting in disease. Although strain properties are believed to be encoded in the tertiary structure of the infectious prion protein, we found no biochemical differences between Type I and Type II CWD. Our data confirm the co·existence of two distinct prion strains in CWD-infected cervids and suggest that Type II CWD is the parent strain of Type I CWD.

see page 29, and see other CWD studies ;


http://www.neuroprion.org/resources/pdf_docs/conferences/prion2008/abstract-book-prion2008.pdf



Sunday, November 23, 2008

PRION October 8th - 10th 2008 Book of Abstracts


http://bse-atypical.blogspot.com/2008/11/prion-october-8th-10th-2008-book-of.html



Saturday, September 06, 2008


Chronic wasting disease in a Wisconsin white-tailed deer farm 79% INFECTION RATE Contents: September 1 2008, Volume 20, Issue 5

snip...see full text ;


http://chronic-wasting-disease.blogspot.com/2008/11/commentary-crimes-hurt-essence-of.html



Wednesday, December 17, 2008

White-tailed Deer in Portage County Tests Positive for CWD


http://chronic-wasting-disease.blogspot.com/2008/12/white-tailed-deer-in-portage-county.html



Monday, December 22, 2008

CWD DETECTED IN ELK HUNT AREA 117 SOUTH OF SUNDANCE WYOMING


http://chronic-wasting-disease.blogspot.com/2008/12/cwd-detected-in-elk-hunt-area-117-south.html



CHRONIC WASTING DISEASE


http://chronic-wasting-disease.blogspot.com/



P01.47

Quantifying the Species Barrier in Chronic Wasting Disease by a Novel in vitro Conversion Assay

Li, L1; Coulthart, MB2; Balachandran, A3; Chakrabartty, A4; Cashman, NR1 1University of British Columbia, Brain Research Centre, Canada; 2Public Health Agency of Canada, National Microbiology Laboratory, Canada; 3Animal Diseases Research Institute, Canada Food Inspection Agency, National Reference Laboratory for Scrapie and CWD, Canada; 4Ontario Cancer Institute and Department of Medical Biophysics, University of Toronto, Canada

Background: Chronic wasting disease (CWD) is a transmissible spongiform encephalopathy that can affect North American cervids (deer, elk, and moose). Although the risk of CWD crossing the species barrier and causing human disease is still unknown, however, definite bovine spongiform encephalopathy (BSE) transmission to humans as variant CJD (vCJD), it would seem prudent to limit the exposure of humans to CWD.

Aim: In view of the fact that BSE can be readily transmitted to non-bovid species, it is important to establish the species susceptibility range of CWD.

Methods: In vitro conversion system was performed by incubation of prions with normal brain homogenates as described before, and protease K (PK) resistant PrP was determined by immunoblotting with 6H4 monoclonal prion antibody.

Results: Our results demonstrate that PrPC from cervids (including moose) can be efficiently converted to a protease-resistant form by incubation with elk CWD prions, presumably due to sequence and structural similarities between these species. Interestingly, hamster shows a high conversion ratio by PrPCWD. Moreover, partial denaturation of substrate PrPC can apparently overcome the structural barriers between more distant species.

Conclusions: Our work correctly predicted the transmission of CWD to a wild moose. We find a species barrier for prion protein conversion between cervids and other species, however, this barrier might be overcome if the PrPC substrate has been partially denatured in a cellular environment. Such an environment might also promote CWD transmission to non-cervid species, *** including humans. Acid/GdnHCl-treated brain PrPC was a superior substrate for the in vitro conversion than PrPC treated at physiological pH. This has implications for the process by which the prion protein is converted in disease.


http://www.prion2007.com/pdf/Prion%20Book%20of%20Abstracts.pdf



Subject: DOCKET-- 03D-0186 -- FDA Issues Draft Guidance on Use of Material From Deer and Elk in Animal Feed; Availability Date: Fri, 16 May 2003 11:47:37 -0500 From: "Terry S. Singeltary Sr." To: mhtml:%7B33B38F65-8D2E-434D-8F9B-8BDCD77D3066%7Dmid://00000046/!x-usc:mailto:fdadockets@oc.fda.gov



http://madcowfeed.blogspot.com/2008/07/docket-03d-0186-fda-issues-draft.html




Thursday, April 03, 2008

A prion disease of cervids: Chronic wasting disease

2008 1: Vet Res. 2008 Apr 3;39(4):41

A prion disease of cervids: Chronic wasting disease

Sigurdson CJ.

snip...

*** twenty-seven CJD patients who regularly consumed venison were reported to the Surveillance Center***,

snip...

full text ;


http://chronic-wasting-disease.blogspot.com/2008/04/prion-disease-of-cervids-chronic.html



Wednesday, December 17, 2008

ONE-THIRD OF BOULDER'S DEER INFECTED WITH CWD


http://chronic-wasting-disease.blogspot.com/2008/12/one-third-of-boulders-deer-infected.html




The prion strain phenomenon: Molecular basis and unprecedented features


http://bse-atypical.blogspot.com/2008/12/prion-strain-phenomenon-molecular-basis.html



From: TSS (216-119-163-189.ipset45.wt.net)

Subject: CWD aka MAD DEER/ELK TO HUMANS ???

Date: September 30, 2002 at 7:06 am PST

From: "Belay, Ermias"

To:

Cc: "Race, Richard (NIH)" ; ; "Belay,

Ermias"

Sent: Monday, September 30, 2002 9:22 AM

Subject: RE: TO CDC AND NIH - PUB MED- 3 MORE DEATHS - CWD - YOUNG HUNTERS

Dear Sir/Madam,

In the Archives of Neurology you quoted (the abstract of which was

attached to your email), we did not say CWD in humans will present like

variant CJD.

That assumption would be wrong. I encourage you to read the whole

article and call me if you have questions or need more clarification

(phone: 404-639-3091). Also, we do not claim that "no-one has ever been

infected with prion disease from eating venison." Our conclusion stating

that we found no strong evidence of CWD transmission to humans in the

article you quoted or in any other forum is limited to the patients we

investigated.

Ermias Belay, M.D.

Centers for Disease Control and Prevention

-----Original Message-----

From:

Sent: Sunday, September 29, 2002 10:15 AM

To: mhtml:%7B33B38F65-8D2E-434D-8F9B-8BDCD77D3066%7Dmid://00000046/!x-usc:mailto:rr26k@nih.gov; mhtml:%7B33B38F65-8D2E-434D-8F9B-8BDCD77D3066%7Dmid://00000046/!x-usc:mailto:rrace@niaid.nih.gov; mhtml:%7B33B38F65-8D2E-434D-8F9B-8BDCD77D3066%7Dmid://00000046/!x-usc:mailto:ebb8@CDC.GOV

Subject: TO CDC AND NIH - PUB MED- 3 MORE DEATHS - CWD - YOUNG

HUNTERS

Sunday, November 10, 2002 6:26 PM ......snip........end..............TSS

also,

A. Aguzzi - Chronic Wasting Disease (CWD) also needs to be addressed. Most

serious because of rapid horizontal spread and higher prevalence than BSE in

UK, up to 15% in some populations. Also may be a risk to humans - evidence

that it is not dangerous to humans is thin.


http://www.tseandfoodsafety.org/activities/bse_conference_basel_april_02/2summar



Chronic Wasting Disease and Potential Transmission to Humans

Ermias D. Belay,* Ryan A. Maddox,* Elizabeth S. Williams,† Michael W. Miller,‡ Pierluigi Gambetti,§ and Lawrence B. Schonberger*

*Centers for Disease Control and Prevention, Atlanta, Georgia, USA; †University of Wyoming, Laramie, Wyoming, USA; ‡Colorado Division of Wildlife, Fort Collins, Colorado, USA; and §Case Western Reserve University, Cleveland, Ohio, USA

Suggested citation for this article: Belay ED, Maddox RA, Williams ES, Miller MW, Gambetti P, Schonberger LB. Chronic wasting disease and potential transmission to humans. Emerg Infect Dis [serial on the Internet]. 2004 Jun [date cited]. Available from:http://www.cdc.gov/ncidod/EID/vol10no6/03-1082.htm

--------------------------------------------------------------------------------

Chronic wasting disease (CWD) of deer and elk is endemic in a tri-corner area of Colorado, Wyoming, and Nebraska, and new foci of CWD have been detected in other parts of the United States. Although detection in some areas may be related to increased surveillance, introduction of CWD due to translocation or natural migration of animals may account for some new foci of infection. Increasing spread of CWD has raised concerns about the potential for increasing human exposure to the CWD agent. The foodborne transmission of bovine spongiform encephalopathy to humans indicates that the species barrier may not completely protect humans from animal prion diseases. Conversion of human prion protein by CWD-associated prions has been demonstrated in an in vitro cell-free experiment, but limited investigations have not identified strong evidence for CWD transmission to humans. More epidemiologic and laboratory studies are needed to monitor the possibility of such transmissions.

snip...full text ;


http://www.cdc.gov/ncidod/EID/vol10no6/03-1082.htm




Volume 12, Number 10–October 2006

Research

Human Prion Disease and Relative Risk Associated with Chronic Wasting Disease

Samantha MaWhinney,* W. John Pape,† Jeri E. Forster,* C. Alan Anderson,‡§ Patrick Bosque,‡¶ and Michael W. Miller#

*University of Colorado at Denver and Health Sciences Center, Denver, Colorado, USA; †Colorado Department of Public Health and Environment, Denver, Colorado, USA; ‡University of Colorado School of Medicine, Denver, Colorado, USA; §Denver Veteran's Affairs Medical Center, Denver, Colorado, USA; ¶Denver Health Medical Center, Denver, Colorado, USA; and #Colorado Division of Wildlife, Fort Collins, Colorado, USA

Suggested citation for this article

The transmission of the prion disease bovine spongiform encephalopathy (BSE) to humans raises concern about chronic wasting disease (CWD), a prion disease of deer and elk. In 7 Colorado counties with high CWD prevalence, 75% of state hunting licenses are issued locally, which suggests that residents consume most regionally harvested game. We used Colorado death certificate data from 1979 through 2001 to evaluate rates of death from the human prion disease Creutzfeldt-Jakob disease (CJD). The relative risk (RR) of CJD for CWD-endemic county residents was not significantly increased (RR 0.81, 95% confidence interval [CI] 0.40–1.63), and the rate of CJD did not increase over time (5-year RR 0.92, 95% CI 0.73–1.16). In Colorado, human prion disease resulting from CWD exposure is rare or nonexistent. However, given uncertainties about the incubation period, exposure, and clinical presentation, the possibility that the CWD agent might cause human disease cannot be eliminated.

snip... full text ;


http://0-www.cdc.gov.mill1.sjlibrary.org/ncidod/EID/vol12no10/06-0019.htm



full text ;


http://chronic-wasting-disease.blogspot.com/2006_12_01_archive.html



The statistical incidence of CJD cases in the United States has been revised to reflect that there is one case per 9000 in adults age 55 and older. Eighty-five percent of the cases are sporadic, meaning there is no known cause at present.


http://www.cjdfoundation.org/fact.html



CHRONIC WASTING DISEASE BLOG


http://chronic-wasting-disease.blogspot.com/



http://stanford.wellsphere.com/healing---recovery-article/a-prion-disease-of-cervids:-chronic-wasting-disease-2008/13819



Terry S. Singeltary Sr. P.O. Box 42 Bacliff, Texas USA 77518

Labels: , , ,

Monday, December 22, 2008

CWD DETECTED IN ELK HUNT AREA 117 SOUTH OF SUNDANCE WYOMING

CWD DETECTED IN ELK HUNT AREA 117 SOUTH OF SUNDANCE

12/2/2008

CASPER-- Chronic Wasting Disease (CWD) has been discovered for the first time in elk hunt area 117 south of Sundance.

The Wyoming Game and Fish Department Laboratory analyzed a sample from a targeted cow elk from hunt area 117 and the sample tested positive for CWD. The elk was found at Solider Creek, just east of Highway 85 about 5 miles west of the South Dakota border. Elk hunt area 117 has been considered part of the endemic area for deer (hunt area 6) since 2003. "This area has long been positive for deer and we just now found a positive elk in this area," said Hank Edwards, wildlife disease specialist for the Wyoming Game and Fish Department.

The department recommends that hunters taking elk or deer in this area transport only the following items: cut and wrapped meat, boned meat, animal quarters or other pieces with no portion of the spinal column or head attached, hides without the head, cleaned skull plates (no meat or nervous tissue attached), antlers with no meat or other tissue attached. The head, spine, and other nervous tissue should be left at the site of the kill or disposed of in an approved landfill. Rubber or latex gloves should be worn when field dressing any animal and during butchering.

CWD has been diagnosed in some wild deer, elk, and moose in 10 states and two Canadian provinces. After a review of available scientific data, the World Health Organization in December 1999 stated, "There is currently no evidence that CWD in cervidae (deer and elk) is transmitted to humans." In 2004, Dr. Ermias Belay of the Center for Disease Control said, "The lack of evidence of a link between CWD transmission and unusual cases of CJD, (Creutzfeldt-Jakob disease, a human prion disease) despite several epidemiological investigations, suggest that the risk, if any, of transmission of CWD to humans is low." Nonetheless to avoid risk, both organizations say parts or products from any animal that looks sick and/or tests positive for CWD should not be eaten.

For more information on chronic wasting disease visit the Game and Fish Web site at: .

-WGFD-

http://gf.state.wy.us/services/news/pressreleases/08/12/02/081202_1.asp


0C7.04

North American Cervids Harbor Two Distinct CWD Strains

Authors

Angers, R. Seward, T, Napier, D., Browning, S., Miller, M., Balachandran A., McKenzie, D., Hoover, E., Telling, G. 'University of Kentucky; Colorado Division of Wildlife, Canadian Food Inspection Agency; University Of Wisconsin; Colorado State University.

Content

Despite the increasing geographic distribution and host range of CWD, little is known about the prion strain(s) responsible for distinct outbreaks of the disease. To address this we inoculated CWD-susceptible Tg(CerPrP)1536+/· mice with 29 individual prion samples from various geographic locations in North America. Upon serial passage, intrastudy incubation periods consistently diverged and clustered into two main groups with means around 210 and 290 days, with corresponding differences in neuropathology. Prion strain designations were utilized to distinguish between the two groups: Type I CWD mice succumbed to disease in the 200 day range and displayed a symmetrical pattern of vacuolation and PrPSc deposition, whereas Type II CWD mice succumbed to disease near 300 days and displayed a strikingly different pattern characterized by large local accumulations of florid plaques distributed asymmetrically. Type II CWD bears a striking resemblance to unstable parental scrapie strains such as 87A which give rise to stable, short incubation period strains such as ME7 under certain passage conditions. In agreement, the only groups of CWD-inoculated mice with unwavering incubation periods were those with Type I CWD. Additionally, following endpoint titration of a CWD sample, Type I CWD could be recovered only at the lowest dilution tested (10-1), whereas Type II CWD was detected in mice inoculated with all dilutions resulting in disease. Although strain properties are believed to be encoded in the tertiary structure of the infectious prion protein, we found no biochemical differences between Type I and Type II CWD. Our data confirm the co·existence of two distinct prion strains in CWD-infected cervids and suggest that Type II CWD is the parent strain of Type I CWD.

see page 29, and see other CWD studies ;

http://www.neuroprion.org/resources/pdf_docs/conferences/prion2008/abstract-book-prion2008.pdf


Sunday, November 23, 2008

PRION October 8th - 10th 2008 Book of Abstracts

http://bse-atypical.blogspot.com/2008/11/prion-october-8th-10th-2008-book-of.html


Saturday, September 06, 2008

Chronic wasting disease in a Wisconsin white-tailed deer farm 79% INFECTION RATE

Contents: September 1 2008, Volume 20, Issue 5

snip...see full text ;

http://chronic-wasting-disease.blogspot.com/2008/11/commentary-crimes-hurt-essence-of.html


Wednesday, December 17, 2008 White-tailed Deer in Portage County Tests Positive for CWD

http://chronic-wasting-disease.blogspot.com/2008/12/white-tailed-deer-in-portage-county.html


TSS

Labels: , ,

Wednesday, December 17, 2008

White-tailed Deer in Portage County Tests Positive for CWD

White-tailed Deer in Portage County Tests Positive for CWD

Posted: Dec 17, 2008 06:48 PM CST

MADISON - A second white-tailed deer has tested positive for chronic wasting disease, from a herd of deer that were euthanized in November on a Portage County hunting preserve.

The first CWD-positive deer, a 7½-year-old doe, was discovered during routine testing after it was shot in September. That discovery led to destroying the herd so the rest of the deer could be tested. The second positive deer is a 3½-year-old doe.

Wildlife specialists from the U.S. Department of Agriculture Wildlife Services shot 64 deer at Alligator Creek Whitetails LLC near Junction City, beginning Wednesday, Nov. 12, and finishing Tuesday, Nov. 18. Because the hunting preserve is made up of 119 acres of open, wooded, and tall-grass marsh lands, the shooters returned after snow fell to check for tracks to see whether any deer remained. At that time, they shot two more deer. Those CWD test results are not available yet.

The National Veterinary Services Laboratory in Ames, Iowa, confirmed the positive result after initial screening tests at the Wisconsin Veterinary Diagnostic Laboratory in Madison.

The CWD-positive deer had been born on the property and did not have ties to any other deer farm. The preserve was placed under quarantine immediately when the first positive test result was reported Oct. 9 to the state veterinarian's office. A quarantine means that no live deer could be moved onto or off the premises.

Areas of heavy deer traffic on the preserve will have the top soil removed and replaced to reduce the risk of contamination. Stocking deer or elk on the property is prohibited for five years, and fences must be maintained during that time to prevent free-ranging deer from entering. The herd owner will receive state and federal indemnities that pay a portion of the appraised value of the deer.

This was the first new CWD-infected herd on a Wisconsin farm since January 2005. To date, 98 farm-raised animals in Wisconsin have tested positive for CWD, including 82 on a separate Portage County operation. One of the infected animals was an elk; the rest have been white-tailed deer. More than 22,500 farm-raised deer in Wisconsin have been tested for CWD.

Chronic wasting disease is a disease that is known to affect deer, elk and moose. Prions - a particular type of protein in the brain - become malformed and create microscopic holes in the brain. The disease is always fatal. Scientists have not determined exactly what causes the malformed prions or how the disease is transmitted, but one means of transmission may be ingestion of prion-contaminated soil. When CWD was first reported in free-ranging white-tailed deer in Wisconsin in February 2002, it was the first appearance of the disease east of the Mississippi River. CWD was first found in a Wisconsin farm-raised deer in September 2002.


http://www.nbc26.com/Global/story.asp?S=9541420



THEY need to get a handle on these deer farms, or just shut them down altogether. they seem to be nothing more than a petri dish of deadly pathogens, especially CWD. i know there are folks that make a living out there in this industry, but at what expense to the wild are we willing to let money and greed go, and how far $

a few findings to ponder ;

0C7.04

North American Cervids Harbor Two Distinct CWD Strains

Authors

Angers, R. Seward, T, Napier, D., Browning, S., Miller, M., Balachandran A., McKenzie, D., Hoover, E., Telling, G. 'University of Kentucky; Colorado Division of Wildlife, Canadian Food Inspection Agency; University Of Wisconsin; Colorado State University.

Content

Despite the increasing geographic distribution and host range of CWD, little is known about the prion strain(s) responsible for distinct outbreaks of the disease. To address this we inoculated CWD-susceptible Tg(CerPrP)1536+/· mice with 29 individual prion samples from various geographic locations in North America. Upon serial passage, intrastudy incubation periods consistently diverged and clustered into two main groups with means around 210 and 290 days, with corresponding differences in neuropathology. Prion strain designations were utilized to distinguish between the two groups: Type I CWD mice succumbed to disease in the 200 day range and displayed a symmetrical pattern of vacuolation and PrPSc deposition, whereas Type II CWD mice succumbed to disease near 300 days and displayed a strikingly different pattern characterized by large local accumulations of florid plaques distributed asymmetrically. Type II CWD bears a striking resemblance to unstable parental scrapie strains such as 87A which give rise to stable, short incubation period strains such as ME7 under certain passage conditions. In agreement, the only groups of CWD-inoculated mice with unwavering incubation periods were those with Type I CWD. Additionally, following endpoint titration of a CWD sample, Type I CWD could be recovered only at the lowest dilution tested (10-1), whereas Type II CWD was detected in mice inoculated with all dilutions resulting in disease. Although strain properties are believed to be encoded in the tertiary structure of the infectious prion protein, we found no biochemical differences between Type I and Type II CWD. Our data confirm the co·existence of two distinct prion strains in CWD-infected cervids and suggest that Type II CWD is the parent strain of Type I CWD.

see page 29, and see other CWD studies ;


http://www.neuroprion.org/resources/pdf_docs/conferences/prion2008/abstract-book-prion2008.pdf



Sunday, November 23, 2008

PRION October 8th - 10th 2008 Book of Abstracts


http://bse-atypical.blogspot.com/2008/11/prion-october-8th-10th-2008-book-of.html



Saturday, September 06, 2008

Chronic wasting disease in a Wisconsin white-tailed deer farm 79% INFECTION RATE Contents: September 1 2008, Volume 20, Issue 5

snip...see full text ;


http://chronic-wasting-disease.blogspot.com/2008/11/commentary-crimes-hurt-essence-of.html




kind regards, terry

Labels: , , ,

ONE-THIRD OF BOULDER'S DEER INFECTED WITH CWD

CITY OF BOULDER

OPEN SPACE BOARD OF TRUSTEES AGENDA ITEM

MEETING DATE: December 10, 2008 AGENDA

TITLE: Chronic Wasting Disease Study Results

PRESENTERS: Open Space and Mountain Parks Michael D. Patton, Director Heather M. Swanson, Wildlife Ecologist Colorado Division of Wildlife Michael W. Miller, Senior Wildlife Veterinarian

EXECUTIVE SUMMARY:

Chronic wasting disease (CWD) is a fatal prion disease occurring in mule deer inhabiting Open Space and Mountain Parks (OSMP) properties. Beginning in 2005, OSMP and the Colorado Division of Wildlife (CDOW) undertook a 3 year research project to examine CWD on OSMP and private property in the Table Mesa area to increase the understanding ofCWD and possibly CWD management. During the course of the study, 131 mule deer were captured and collared and 115 adult deer were monitored. Each deer was tested for CWD status once per year using either tonsil or rectal mucosa biopsy (both techniques developed for testing live animals). In addition, a mark-resight census was performed (visual counts of collared and un-collared deer within the study area are analyzed using a population census model to estimate overall population size) annually to estimate the population of mule deer residing in the study area.

OSMP and CDOW staff participants found CWD prevalence within the study area (south Boulder between Baseline, Eldorado Springs Drive, Broadway and the Flatirons mountain front) to be surprisingly high - overall approximately 29 percent of the deer sampled were infected. Staff also found that average survival time for infected deer was significantly lower than for uninfected deer. Cause of death varied somewhat between years, but the most common mortality causes were mountain lion predation, clinical CWD and vehicle collisions. Mark-resight inventory estimations of the deer population within the study area showed a decrease in local deer numbers over estimates derived from census efforts in the late 1980s. The high prevalence, low survivorship, and decreasing population numbers suggest that CWD is having a measurable effect on the mule deer herd living in south Boulder. High prevalence makes previously discussed management actions such as test­and-cull control unlikely to be feasible.

AGENDA ITEM # 5 PAGE 1

STAFF RECOMMENDATION:

This is an information item only. No action is requested from the Board at this time.

COMMUNITY SUST AINABILITY ASSESSMENTS AND IMPACTS:

Economic: The Open Space and Mountain Parks program contributes to the economic vitality of the city because it provides the setting and services that help to attract a diversity of businesses and to recruit and retain employees. As a result, understanding of wildlife health issues on OSMP properties is crucial.

Environmental: The extent of CWD infection and associated deer population declines are likely to have some impact on the environment due to the importance of mule deer as large herbivores on OSMP properties. The overall impact of this is presently unknown.

Social: Wildlife on OSMP support a quality visitor experience and so understanding of disease impacts on wildlife populations is important to maintain a quality visitor experience. Declines in deer populations may diminish the visitor experience by reducing opportunities to view and enjoy mule deer. Because no human health threat has been identified for CWD, direct impacts to the citizens of Boulder are unlikely.

OTHER IMPACTS:

Fiscal: OMSP funded the study in conjunction with the CDOW. Overall expenditures over 3 years totaled approximately $60,000 in non-staff expenses. CDOW contributed significant funding well beyond that provided by OSMP. Field work was supplemented by funds from the US Department of Agriculture, Animal and Plant Health Inspection Service, Veterinary Services.

Staff time: Staff time included time spent as part ofthe normal work plan of the wildlife ecologist and rangers. Approximately 1.5 seasonal employees were hired specifically to work on the CWD study including capture and monitoring of deer. CDOW provided staffing similar to or in excess of what OSMP contributed.

PUBLIC FEEDBACK:

At the beginning of the study, several members ofthe public spoke in favor of the study before the Open Space Board of Trustees (OSBT). At that time, the study also received significant media attention including two stories on 9News and one in the Daily Camera. Since the initial start-up phase, no formal public comment has been received; however, numerous informal individual public contacts have been made in the course of conducting field work over the last 3 years. This presentation, as well as a presentation to the Colorado Wildlife Commission, will provide the public with a summary of the results of the study. The primary results of the study recently have been accepted for publication, and additional publications featuring other aspects of the data are likely in the future. Dr. Charles Southwick, professor emeritus at CD Boulder has been involved in consultation throughout the study and appears as a co-author on the submitted study results paper.

ANALYSIS: Chronic wasting disease is a prion disease occurring in several members of the cervid family including mule deer, white-tailed deer, elk and moose. Presence of CWD in Boulder mule deer was first detected in 1997, but local prevalence had not been estimated prior to our study. In an effort to understand prevalence and the possible impact of CWD on Boulder and other Front Range deer populations as well as contribute to the broader understanding of CWD in wild cervids, the CDOW proposed a study to examine CWD in mule deer found on OMSP lands and surrounding residential areas in south Boulder.

In summer 2005, OSBT approved the study of CWD on OSMP properties in conjunction with the CDOW. The original memo and study plan are attached (Attachments A and B). Since that time, the OSMP and CDOW staff participants have completed 3 full years ofthe study including capturing 131 deer. Captured deer were tested for CWD and fitted with a radio collars for monitoring. Age was estimated from tooth wear and blood samples were collected for additional analysis. Deer were monitored throughout the year to determine location, condition and cause of death for individuals that died. Beginning the week of December 8, 2008, the staffs will begin to recapture the 24 remaining, test-negative deer to remove their collars as the batteries begin to malfunction. The 4 positive deer will continue to be monitored as long as their collars function.

During each year of the study, a mark-resight inventory of deer residing within the study area during late November and early December was also completed. These data were analyzed to provide overall population estimates within the study area and were compared between years and to earlier data (1987-2001.) collected in this same area using similar methods.

Results:

Prevalence among the male deer sampled was 41 percent, about twice the prevalence among the adult females (20 percent). Life expectancy for uninfected deer was approximately 3 times longer than for infected deer. Main causes of death for infected deer were death from "chronic wasting" syndrome and predation by mountain lions. Mountain lions were more likely to kill infected animals than uninfected animals although this effect varied over years and seemed to be impacted by management of mountain lions in the area. The combination of high infection rates and relatively low survival of infected deer would be expected to cause a decline in deer abundance over time, and the observed trends in deer abundance around Table Mesa appear consistent with these predictions: the occurrence of chronic wasting disease in this population over the last two decades (based on historical field records and observations) has coincided with a measurable decline in estimated deer abundance in this area since the late 1980s.

Next Steps:

Based on the information collected as part of this study, the deer population in south Boulder is predicted, based on population-disease models, to continue to remain low or possibly decline further. However, lack of complete understanding of prion diseases makes this future uncertain. Based on the high prevalence detected, previously discussed management actions such as test and cull are not recommended. Under the circumstances, this situation may best serve as an opportunity to watch and learn how prion disease affects

AGENDA ITEM # 5 PAGE 3

wild populations over the long term. Follow-up studies looking at population and prevalence trends would be of value in refining predictive models of CWD and its potential control. Although current options for management of the disease are limited, experimental examination of potential management actions still could be considered. Future cooperation between OSMP and CD OW to study the population or experimental management actions will depend on interest and funding availability for both agencies.

Because CWD appears to be negatively impacting this deer population, minimizing additional adverse effects will be important to help maintain the overall viability ofthis population. Residential development within deer habitat already has been minimized by the presence of OSMP lands, but possible improvement of available habitat quality may merit consideration. Increased disturbance/stress from humans, including disturbance from recreational use (on OSMP, deer have been shown to be sensitive to recreational use­Miller et al. 2001 and Germaine, et al. unpublished data) also may influence habitat use and deer behavior, and these influences also may merit consideration in the context of CWD and overall deer population management.

Although the implications of our findings for the deer population are disconcerting, the study was a success from a scientific and agency cooperation standpoint. No free-ranging mule deer population with CWD has previously been studied in this way, making these data quite valuable in improving the overall understanding of CWD in wild deer populations. The Table Mesa deer population may provide an important opportunity to examine the long-term effects of CWD infection in a wild population. The study logistics went well and cooperation between OSMP and CDOW proved to be extremely beneficial; many strong collaborative relationships were built through the study; including those that led to the current mountain lion study occurring on OSMP properties, making future cooperation likely.

Submitted by:

Michael D. Patton, Director

Heather M. Swanson, Wildlife Ecologist

ATTACHMENTS:

A. Original OSBT memo dated July 27,2005

B. Original study plan



http://www.bouldercolorado.gov/files/openspace/pdf_osbtmemos/memo.pdf



One-third of Boulder’s deer infected

Depth of chronic wasting disease means culling no longer an option, experts say

By Ryan Morgan (Contact)
Originally published 08:40 p.m., December 16, 2008
Updated 08:40 p.m., December 16, 2008


A new study shows one out of three mule deer in south Boulder suffers from chronic wasting disease — and those results mean the traditional approach of killing infected animals to fight the disease probably won’t work, researchers say.

“Everything that’s been tried to control chronic wasting disease really fails in the face of that kind of infection rate,” said Heather Swanson, a wildlife ecologist for Boulder’s Open Space and Mountain Parks Department.

In a memo to city leaders, Boulder’s open space officials said they no longer favor killing to deal with chronic wasting disease. The Boulder City Council, which can also set land-management policies for the city’s open space properties, hasn’t yet weighed in on the matter.

Researchers from the Colorado Division of Wildlife and the city teamed up starting in 2005 to study the mule deer population — the first study of its kind to take place in Boulder, Swanson said. The study focused on deer in an area bordered by Baseline Road on the north, Eldorado Springs Drive on the south, Broadway on the east and the Flatirons on the west.

During the study, ecologists tranquilized 115 mule deer, affixed them with radio collars and tested them for chronic wasting disease, an affliction similar to “mad cow disease,” in which misfolded proteins riddle an animal’s brain with holes, eventually killing it.

They found that overall, 29 percent of the deer tested had the disease. Those animals on average died much sooner than non-infected deer, and they often fell prey to mountain lions. Swanson said many of the infected deer preyed upon by cougars didn’t show symptoms that were obvious to human researchers.

“The mountain lions seem to be much better at detecting it,” she said.

Forty-one percent of male mule deer were infected, compared with 20 percent of females, because males cover more territory, which puts them at higher risk of being exposed to the disease, Swanson said.

Scientists still don’t know exactly how chronic wasting disease is transmitted, although researchers suspect it’s passed on from the urine, feces or saliva of infected animals. Swanson said some research suggests that the prions may stick to clay soils as well.

For the past several years, land managers have consistently said the best way to curb the spread of chronic wasting disease is to find infected animals and kill them. But killing one-third of any deer population isn’t a realistic approach, Swanson said, and could do more harm than good.

Diseased animals can still reproduce, thereby contributing to the health of the population, she said — something they wouldn’t be able to do if they were killed as soon as they were shown to be infected.

“With a population that’s in a precipitous decline, removing that large of a number of animals probably isn’t a good idea,” she said. “They may still be contributing to the population” before dying of the disease.

In the memo to the Boulder City Council, open space scientists said the disease has resulted in fewer deer in and around Boulder.

“The occurrence of chronic wasting disease in this population over the last two decades ... has coincided with a measurable decline in estimated deer abundance in this area since the late 1980s,” according to the memo.

Swanson said scientists are hoping ever-increasing numbers of deer don’t get infected, and she said some models of the disease predict the infection rate should level off soon. That’s because chronic wasting disease is thought to require a certain level of deer density to spread quickly — once sufficient numbers of deer die, that density is depleted and the rate of infection slows.

That’s the hope, anyway. Swanson said there’s really only one way to know for sure.

“At this point, we’re just recommending that we watch the population and see what happens,” she said.


http://www.coloradodaily.com/news/2008/dec/16/one-third-boulders-deer-infected/


DISTURBING to me is the fact no one seems to be concerned with the mountain lions or cougars and the potential for transmission of CWD to those species in the wild, which we know is very possible, if not already happened. ...



Species Born Onset/Died
Ocelot May 1987 Mar 1994
Ocelot Jul 1980 Oct 1995
Puma 1986 May 1991
Puma 1980 May 1995
Puma 1978 May 1995
Lion Nov 1986 Dec 1998
Tiger 1981 Dec 1995
Tiger Feb 1983 Oct 1998
Ankole 1987 May 1995
Ankole 1986 Feb 1991
Bison 1989/90 Oct 1996


Maff data on 15 May 99
kudu 6
gemsbok 1
nyala 1
oryx 2
eland 6
cheetah 9
puma 3
tiger 2
ocelot 2
bison 1
ankole 2
lion 1




http://www.mad-cow.org/zoo_cites_annotated.html



0C7.04

North American Cervids Harbor Two Distinct CWD Strains

Authors

Angers, R. Seward, T, Napier, D., Browning, S., Miller, M., Balachandran A., McKenzie, D., Hoover, E., Telling, G. 'University of Kentucky; Colorado Division of Wildlife, Canadian Food Inspection Agency; University Of Wisconsin; Colorado State University.

Content

Despite the increasing geographic distribution and host range of CWD, little is known about the prion strain(s) responsible for distinct outbreaks of the disease. To address this we inoculated CWD-susceptible Tg(CerPrP)1536+/· mice with 29 individual prion samples from various geographic locations in North America. Upon serial passage, intrastudy incubation periods consistently diverged and clustered into two main groups with means around 210 and 290 days, with corresponding differences in neuropathology. Prion strain designations were utilized to distinguish between the two groups: Type I CWD mice succumbed to disease in the 200 day range and displayed a symmetrical pattern of vacuolation and PrPSc deposition, whereas Type II CWD mice succumbed to disease near 300 days and displayed a strikingly different pattern characterized by large local accumulations of florid plaques distributed asymmetrically. Type II CWD bears a striking resemblance to unstable parental scrapie strains such as 87A which give rise to stable, short incubation period strains such as ME7 under certain passage conditions. In agreement, the only groups of CWD-inoculated mice with unwavering incubation periods were those with Type I CWD. Additionally, following endpoint titration of a CWD sample, Type I CWD could be recovered only at the lowest dilution tested (10-1), whereas Type II CWD was detected in mice inoculated with all dilutions resulting in disease. Although strain properties are believed to be encoded in the tertiary structure of the infectious prion protein, we found no biochemical differences between Type I and Type II CWD. Our data confirm the co·existence of two distinct prion strains in CWD-infected cervids and suggest that Type II CWD is the parent strain of Type I CWD.

see page 29, and see other CWD studies ;

http://www.neuroprion.org/resources/pdf_docs/conferences/prion2008/abstract-book-prion2008.pdf



Sunday, November 23, 2008

PRION October 8th - 10th 2008 Book of Abstracts

http://bse-atypical.blogspot.com/2008/11/prion-october-8th-10th-2008-book-of.html



Biochim Biophys Acta. Author manuscript; available in PMC 2008 December 9. Published in final edited form as: Biochim Biophys Acta. 2007 June; 1772(6): 681-691. Published online 2006 December 15. doi: 10.1016/j.bbadis.2006.12.006. PMCID: PMC2597801 NIHMSID: NIHMS25810

Copyright notice and Disclaimer


The prion strain phenomenon: Molecular basis and unprecedented features


Rodrigo Morales,1,2 Karim Abid,1 and Claudio Soto1# 1 Protein Misfolding Disorders Laboratory, George and Cynthia Mitchell Center for Neurodegenerative diseases, Departments of Neurology, Neuroscience & Cell Biology and Biochemistry & Molecular Biology, University of Texas Medical Branch, 301 University Boulevard, Galveston, Texas, 77555-0646, USA 2 Facultad de Ciencias, Universidad de Chile, Santiago, Chile #To whom correspondence should be addressed at Email: clsoto@utmb.edu The publisher's final edited version of this article is available at Biochim Biophys Acta. See other articles in PMC that cite the published article.


Abstract


Prions are unconventional infectious agents responsible for transmissible spongiform encephalopathies. Compelling evidences indicate that prions are composed exclusively by a misfolded form of the prion protein (PrPSc) that replicates in the absence of nucleic acids. One of the most challenging problems for the prion hypothesis is the existence of different strains of the infectious agent. Prion strains have been characterized in most of the species. Biochemical characteristics of PrPSc used to identify each strain include glycosylation profile, electrophoretic mobility, protease resistance, and sedimentation. In vivo, prion strains can be differentiated by the clinical signs, incubation period after inoculation and the vacuolation lesion profiles in the brain of affected animals. Sources of prion strain diversity are the inherent conformational flexibility of the prion protein, the presence of PrP polymorphisms and inter-species transmissibility. The existence of the strain phenomenon is not only a scientific challenge, but it also represents a serious risk for public health. The dynamic nature and inter-relations between strains and the potential for the generation of a very large number of new prion strains is the perfect recipe for the emergence of extremely dangerous new infectious agents.


snip...


BSE has not only been transmitted to humans. The extensive use of cow-derived material for feeding other animals led to the generation of new diseases in exotic felines such as tiger and cheetah, non human primates, and domestic cats [52,57-60]. As it was mentioned before, the transmission of BSE into these different species could create many new prion strains, each one of them with particular biological and biochemical characteristics and thus a potentially new hazard for human health. Successful transmission of BSE in pigs has been described [61,62] and also in transgenic mice expressing pig PrP (PoPrP) [63]. Porcine derivates are widely consumed and the hypothetic case of "mad pigs" could increase the events of zoonotic transmission of prions to humans. Fortunately, transmission of BSE to pigs is possible only in very drastic conditions, not likely to be occurring naturally [62,63]. More frightening is perhaps the possibility that BSE has been passed into sheep and goats. Studies have already shown that this transmission is possible and actually relatively easy and worrisomely produces a disease clinically similar to scrapie [64]. The cattle origin of this new scrapie makes possible that the new strain may be transmissible to humans. Transmission experiments of BSE infected sheep brain homogenate into human transgenic animal models are currently ongoing in several laboratories. It is very important to note that all materials generated by transmission of BSE in experimental and natural cases show similar biochemical behavior compared to the original inoculum [65], suggesting that all these new generated infectious agents could potentially be hazardous for humans. The origin of BSE is still a mystery. Abundant evidence supports the hypothesis that BSE was produced by cattle feeding with scrapie derivated material [66,67], indicating that bovine PrPSc might be a "conformational intermediary" between ovine PrPSc and human PrPC.


There is currently no mean to predict which will be the conformation of a newly generated strain and how this new PrPSc conformation could affect other species. One interesting new prion disease is CWD, a disease affecting farm and wild species of cervids [68,69]. The origin of CWD and its potential to transmit to humans are currently unknown. This is worrisome, considering that CWD has became endemic in some parts of USA and the number of cases continues to increase [69]. It is presumed that a large number of hunters in the US have been in contact or consumed CWD-infected meat [70]. CWD transmissibility studies have been performed in many species in order to predict how this disease could be spread by consumption of CWD meat [71-73]. In these studies, a special attention has been done to scavenging animals [74], which are presumed to be exposed to high concentration of cervid prions, resulting in the putative generation of many new forms of TSEs. Fortunately negative results were obtained in one experiment done in raccoons infected with CWD [74]. Transmission of CWD to humans cannot be ruled out at present and a similar infective episode to BSE involving CWD could result in catastrophic events, spreading the disease in a very dangerous way through the human population. No clinical evidence linking CWD exposed humans and CJD patients have been found [70], but experimental inoculation of CWD prions into squirrel monkeys propagated the disease [71]. It is important to mention that the species barrier between humans and cervids appears to be greater than with cattle, as judged by experiments with transgenic mice models [75]. Finally, it is important to be aware about CWD transmissibility to other species in which a "conformational intermediary" could be formed, facilitating human infection.


SNIP...


VI. Unique features of prion strains

The biological and infectious characteristics of prions are dramatically different to the conventional infectious agents. These differences are manifested in the prion strains phenomenon in unique and unprecedented features, such as for example strain adaptation and memory, the coexistence and competition of prion strains, among others. In this section, some of these interesting phenomena will be briefly described.

Adaptation of Prion strains

Interspecies transmission of prions could result in the emergence of more than one variety of infectious material. All new collected infectious agents could present particular strain characteristics. That is the case of DY and HY prion strains generation [13,16]. When interspecies transmission of prions occurs, serial passages in the new host are needed in order to stabilize the characteristics of new generated infectious material. In the case of TME transmission in hamsters, at least four serial passages in the new species were required for stabilization [13]. The first passage was characterized by long incubation periods and a dominance of a 19 KDa fragment when newly obtained PrPSc was analyzed after PK digestion. In the three first passages, clinical symptoms were not characteristic of the hamster-adapted HY or DY TME strains. This phenotype was attributed to the combination effects of both strains replicating simultaneously. Thereafter, each of the strains was stabilized in some of the animals and once they are adapted and stabilized, they can be serially propagated in vivo and the characteristics are maintained. It is accepted that both strains present differential conversion kinetics in vitro, with DY being the slowest and HY the fastest [124]. For this reason, in order to select efficiently this prion strain, limit dilutions must be performed [13]. In that way, the most abundant and less convertible DY is favored against the less abundant but fastest HY strain.


Co-existence of prion strains


Related to the above, it has been shown that two or more prion strains can co-exist in natural cases of TSE. Co-existence of prion strains has been found in sporadic cases of CJD [113, 125]. Analyses of several sCJD tissue showed that different biochemical profiles of PrPSc could be found in different brain areas from the same patient [113]. Co-existence of prion strains was mainly observed in patient heterozygous for codon 129 [113]. As many as 50% of these patients present different types of PrPSc in their brains, whereas 9% of MM patients were positive for co-existence of strains. On the other hand, more than one PrPSc type was not observed in VV patients [113].


The biochemical and structural properties of the protein seem to be the major cause of this differential distribution. This observation may explain why sCJD is so heterogeneous in terms of clinical manifestation [34,126,127]. In a recent publication by Bishop et al. [107], vCJD infected transgenic mice expressing human PrPC, present changes in their PrPSc and vacuolation patterns in the brain according to their polymorphic classification for codon 129.


Competition of prion strains


In particular experimental conditions, some prion strains can extend their specific incubation period when co-infected with another strain. Long incubation period prions increase the incubation period of "faster" prions. This phenomenon of "competition of prion strains" has been observed in mice and hamster. In mice, competition between 22A and 22C strains was reported in 1975 by Dickinson et al. [128]. In this study, RIII mice (homozygous for sincs7 allele) were used. 22A and 22C showed long and short incubation period (550 and 230 days), respectively. When 22C strain was intraperitoneally inoculated 100, 200 and 300 days after intraperitoneal administration of the 22A agent, all three experimental groups resulted in Morales et al. Page 8 Biochim Biophys Acta. Author manuscript; available in PMC 2008 December 9. NIH-PA Author Manuscript NIH-PA Author Manuscript NIH-PA Author Manuscript incubation periods and lesion patterns matching 22A prions, suggesting that 22C prions were degraded or excreted, in animals previously infected by 22A. Similar results were obtained by Kimberlin and Walker in 1985 [129] using a different strain of sincs7 mice. These authors treated mice using 22A and 22C prion strain. Before inoculation, 22A was treated with different chemical and physical agents in order to see if the "competitor" or "blocking" characteristics of 22A were maintained. From all treatments, 12M urea was shown to almost abolish the blocking properties of 22A agent. This information suggests that infective properties of long incubation period agent are strictly necessary in order to increase the incubation period of faster prions.


In hamster, similar observations were reported using DY and HY [130]. DY prion strain was inoculated 30 and 60 days prior intraperitoneal inoculation of HY at three different doses. When incubation periods of HY inoculated control group were compared with the animals inoculated at 60 days with DY, significant differences in the incubation periods were found, especially when HY prions were administrated in a higher dose [130]. On the other hand no differences were observed in the case of intranerve inoculation, revealing that competition phenomenon occurs only when peripheral inoculation is performed. These results are surprising considering the fact that DY was reported not to be infectious when intraperitoneally inoculated in hamsters [130]. This data suggest that replication of DY is occurring in peripheral tissues but is not able to reach the central nervous system.


In general, the principal variables that need to be observed for a successful competition are the route of infection, the interval between injections and the particular strains and doses of agent used. Prolongation of incubation periods in TSE are therapeutically beneficial and several strategies are under development to reach this aim, including antibodies, beta-sheet breakers, and other chemical agents [131-133]. The experimental evidence described above suggests that prions could be potentially useful for this purpose. In order to prevent spread of prion disease in cattle or humans, prion strains with incubation periods longer than species' lifespan could be used to slowdown the replication of BSE or vCJD prions.


VII. Concluding Remarks


The existence of different strains of an infectious agent composed exclusively of a protein has been one of the most puzzling issues in the prion field. If is already difficult to understand how a protein can adopt two stable and different folded structures and that one of them can transform the other one into itself, it is unthinkable that the misfolded form can in turn adopt multiple conformations with distinct properties. Yet, compelling scientific evidence support the idea that PrP can adopt numerous folding patterns that can faithfully replicate and produce different diseases. The existence of the strain phenomenon is not only a scientific challenge, but it also represents a serious risk for public health. The dynamic nature and inter-relations between strains and the potential for the generation of many new prion strains depending on the polymorphisms and the crossing of species barrier is the perfect recipe for the emergence of extremely dangerous new infectious agents. Although, substantial progress has been made in understanding the prion strains phenomenon, there are many open questions that need urgent answers, including: what are the structural basis of prion strains?; how are the phenomena of strain adaptation and memory enciphered in the conformation of the prion agent?; to what species can a given prion strain be transmissible?; what other cellular factors control the origin and properties of prion strains?. ...SNIP...END


http://www.pubmedcentral.nih.gov/articlerender.fcgi?tool=pmcentrez&artid=2597801&rendertype=abstract



http://www.pubmedcentral.nih.gov/picrender.fcgi?artid=2597801&blobtype=pdf





Friday, December 12, 2008


The prion strain phenomenon: Molecular basis and unprecedented features

http://bse-atypical.blogspot.com/2008/12/prion-strain-phenomenon-molecular-basis.html




TSS

Labels: ,