Chronic Wasting Disease discovered on game farm Saskatchewan Wednesday Dec. 21, 2011

Chronic Wasting Disease discovered on game farm

CTV Saskatoon

Date: Wednesday Dec. 21, 2011 5:55 PM CST

Chronic wasting disease has been discovered on another game farm in Saskatchewan. It is the fourth case in the province so far this year.

The latest case involves a white tail deer from a farm in the Prince Albert area. The animal was discovered to be carrying the disease through a mandatory testing program for all animals over the age of 12 months that die on farms.

Canada Food Inspection Agency scientists say the disease poses very little risk to humans.

However, they say to prevent the spread of CWD to other animals or farms it is necessary to slaughter the entire herd.

Alex McIsaac, from CIFA, says slaughter is the only way to do an accurate test. "Unfortunately we don't have a live animal test at this time so that's the only way we can determine how far it has spread, unfortunately it's by destroying animals and using this post-mortem sample."

http://saskatoon.ctv.ca/servlet/an/local/CTVNews/20111221/sas-cwd-111221/20111221/?hub=Saskatoon



Saskatchewan deer tests positive for fatal disorder

CWD case doesn't raise concern with CFIA

Reported by Brent Bosker First Posted: Dec 20, 2011 8:46am

Chronic Wasting Disease (CWD) has resurfaced in Saskatchewan.

According to the Canadian Food Inspection Agency (CFIA), a white tail deer tested positive for the fatal disorder last month on a farm in the Prince Albert district.

The farm where the deer tested positive has been quarantined and the remainder of the herd will be destroyed.

The case isn’t raising any concern with the CFIA who monitors and investigates cases.

“Basically this is about what we would expect to see,” said Alex McIsaac, veterinarian disease control specialist with CFIA.

“We find these cases through surveillance … it’s a mandatory requirement for cervid producers in Saskatchewan to submit heads from animals over 12 months of age that die unexpectedly,” McIssac said.

CWD is a degenerative disease that affects the central nervous system of cervids such as elk, moose and deer.

The disease is a spongy type of legion on the brain that McIssac said causes a number of symptoms.

“We would see a lack of coordination, difficulty walking, separation from herd (so now they don’t feel they’re a part of the herd they’re a little nervous about where they are), excess of salivation (so they drool a lot), depression … and unusual behavior.”

This case comes six months after the last case was reported and is the fourth one this year.

Since surveillance began in 1996 there have been 66 cases across Canada, predominantly in Saskatchewan.

Saskatchewan had five cases in 2010 and two in 2009.

Edited by News Talk Radio's Karin Yeske.

http://cjme.com/story/saskatchewan-deer-tests-positive-fatal-disorder/37094




Herds infected with Chronic Wasting Disease in Canada in 2011

The CFIA works with provincial governments and industry to conduct regular CWD surveillance. Ongoing provincial surveillance for CWD varies with each particular province's perceived threat and infection status. Testing is mandatory in Manitoba, Saskatchewan, Alberta and the Yukon; it is voluntary elsewhere.

In addition, CWD is a reportable disease under the Health of Animals Regulations. This means that all suspected cases must be reported to the CFIA.

The following table lists domestic cervid herds confirmed to be infected with CWD in Canada in 2011.

Current as of: 2011-11-30

Date confirmed Location Animal type infected

November 22 Saskatchewan Deer

May 15 Saskatchewan Elk

January 19 Saskatchewan Deer

January 4 Saskatchewan Deer

http://www.inspection.gc.ca/english/anima/disemala/rep/2011cwdmdce.shtml




CWD ALBERTA CANADA STATISTICS 2011

http://www.srd.alberta.ca/FishWildlife/WildlifeDiseases/ChronicWastingDisease/CWDUpdates/documents/CWD-PositiveStats-WildDeerAlberta-Dec2011.pdf



http://www.environment.gov.sk.ca/cwd



http://www.environment.gov.sk.ca/Default.aspx?DN=2634b531-ef3e-43da-9dc4-2c7e9cb36cf5



http://www.agriculture.gov.sk.ca/Default.aspx?DN=4aa45d0a-145a-44ad-b970-0e749381af14



http://www.inspection.gc.ca/english/anima/disemala/cwdmdc/cwdmdce.shtml




ALBERTA

http://www1.agric.gov.ab.ca/$department/deptdocs.nsf/all/rsb7193





YUKON

http://www.emr.gov.yk.ca/agriculture/disease_monitoring.html





Wednesday, June 01, 2011

Management of CWD in Canada: Past Practices, Current Conditions, Current Science, Future Risks and Options

http://chronic-wasting-disease.blogspot.com/2011/06/management-of-cwd-in-canada-past.html



see the incredible infection rate from cwd at this game farm in Wisconsin ;



Tuesday, December 20, 2011

CHRONIC WASTING DISEASE CWD WISCONSIN Almond Deer (Buckhorn Flats) Farm Update DECEMBER 2011

http://chronic-wasting-disease.blogspot.com/2011/12/chronic-wasting-disease-cwd-wisconsin.html



Monday, January 05, 2009

CWD, GAME FARMS, BAITING, AND POLITICS

http://chronic-wasting-disease.blogspot.com/2009/01/cwd-game-farms-baiting-and-politics.html


http://chronic-wasting-disease.blogspot.com/2008/08/cwd-feeding-and-baiting-piles.html



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




http://transmissiblespongiformencephalopathy.blogspot.com/



Saturday, November 12, 2011

Human Prion Disease and Relative Risk Associated with Chronic Wasting Disease

Fri, 22 Sep 2006 09:05:59 –0500

http://chronic-wasting-disease.blogspot.com/2011/11/human-prion-disease-and-relative-risk.html




Monday, June 27, 2011

Zoonotic Potential of CWD: Experimental Transmissions to Non-Human Primates

http://chronic-wasting-disease.blogspot.com/2011/06/zoonotic-potential-of-cwd-experimental.html




Friday, March 4, 2011

Alberta dairy cow found with mad cow disease

http://transmissiblespongiformencephalopathy.blogspot.com/2011/03/alberta-dairy-cow-found-with-mad-cow.html




Wednesday, August 11, 2010

REPORT ON THE INVESTIGATION OF THE SIXTEENTH CASE OF BOVINE SPONGIFORM ENCEPHALOPATHY (BSE) IN CANADA

http://bse-atypical.blogspot.com/2010/08/report-on-investigation-of-sixteenth.html




Thursday, August 19, 2010

REPORT ON THE INVESTIGATION OF THE SEVENTEENTH CASE OF BOVINE SPONGIFORM ENCEPHALOPATHY (BSE) IN CANADA

http://bseusa.blogspot.com/2010/08/report-on-investigation-of-seventeenth.html




Thursday, February 10, 2011

TRANSMISSIBLE SPONGIFORM ENCEPHALOPATHY REPORT UPDATE CANADA FEBRUARY 2011 a nd how to hide mad cow disease in Canada Current as of: 2011-01-31

http://madcowtesting.blogspot.com/2011/02/transmissible-spongiform-encephalopathy.html



Thursday, August 19, 2010


SCRAPIE CANADA UPDATE Current as of 2010-07-31

The following table lists sheep flocks and/or goat herds confirmed to be infected with scrapie in Canada in 2010.

Current as of: 2010-07-31

http://nor-98.blogspot.com/2010/08/scrapie-canada-update-current-as-of.html



Increased Atypical Scrapie Detections

Press reports indicate that increased surveillance is catching what otherwise would have been unreported findings of atypical scrapie in sheep. In 2009, five new cases have been reported in Quebec, Ontario, Alberta, and Saskatchewan. With the exception of Quebec, all cases have been diagnosed as being the atypical form found in older animals. Canada encourages producers to join its voluntary surveillance program in order to gain scrapie-free status. The World Animal Health will not classify Canada as scrapie-free until no new cases are reported for seven years. The Canadian Sheep Federation is calling on the government to fund a wider surveillance program in order to establish the level of prevalence prior to setting an eradication date. Besides long-term testing, industry is calling for a compensation program for farmers who report unusual deaths in their flocks.

http://gain.fas.usda.gov/Recent%20GAIN%20Publications/This%20Week%20in%20Canadian%20Agriculture%20%20%20%20%20Issue%2028_Ottawa_Canada_11-6-2009.pdf


The most recent assessments (and reassessments) were published in June 2005 (Table I; 18), and included the categorisation of Canada, the USA, and Mexico as GBR III. Although only Canada and the USA have reported cases, the historically open system of trade in North America suggests that it is likely that BSE is present also in Mexico.



http://www.oie.int/boutique/extrait/06heim937950.pdf



http://nor-98.blogspot.com/2011/06/usda-scrapie-report-for-april-2011-new.html




Wednesday, February 16, 2011

IN CONFIDENCE

SCRAPIE TRANSMISSION TO CHIMPANZEES

IN CONFIDENCE

http://scrapie-usa.blogspot.com/2011/02/in-confidence-scrapie-transmission-to.html



Sunday, April 18, 2010

SCRAPIE AND ATYPICAL SCRAPIE TRANSMISSION STUDIES A REVIEW 2010

http://scrapie-usa.blogspot.com/2010/04/scrapie-and-atypical-scrapie.html




Monday, April 25, 2011

Experimental Oral Transmission of Atypical Scrapie to Sheep

Volume 17, Number 5-May 2011

http://nor-98.blogspot.com/2011/04/experimental-oral-transmission-of.html



Monday, November 30, 2009

USDA AND OIE COLLABORATE TO EXCLUDE ATYPICAL SCRAPIE NOR-98 ANIMAL HEALTH CODE

http://nor-98.blogspot.com/2009/11/usda-and-oie-collaborate-to-exclude.html



I strenuously urge the USDA and the OIE et al to revoke the exemption of the legal global trading of atypical Nor-98 scrapie TSE. ...TSS


Friday, February 11, 2011

Atypical/Nor98 Scrapie Infectivity in Sheep Peripheral Tissues

http://nor-98.blogspot.com/2011/02/atypicalnor98-scrapie-infectivity-in.html

PRICE OF MAD COW TSE PRION POKER GOES UP $$$

NATURAL FIELD CASE OF BSE TO A GOAT ;

Saturday, December 3, 2011

Isolation of Prion with BSE Properties from Farmed Goat Volume 17, Number 12—December 2011

http://transmissiblespongiformencephalopathy.blogspot.com/2011/12/isolation-of-prion-with-bse-properties.html

Wednesday, August 18, 2010

Incidence of CJD Deaths Reported by CJD-SS in Canada as of July 31, 2010

http://creutzfeldt-jakob-disease.blogspot.com/2010/08/incidence-of-cjd-deaths-reported-by-cjd.html



Thursday, August 4, 2011

Terry Singeltary Sr. on the Creutzfeldt-Jakob Disease Public Health Crisis, Date aired: 27 Jun 2011 (SEE VIDEO)

http://transmissiblespongiformencephalopathy.blogspot.com/2011/08/terry-singeltary-sr-on-creutzfeldt.html



Sunday, August 21, 2011

The British disease, or a disease gone global, The TSE Prion Disease (SEE VIDEO)

http://transmissiblespongiformencephalopathy.blogspot.com/2011/08/british-disease-or-disease-gone-global.html


Saturday, March 5, 2011

MAD COW ATYPICAL CJD PRION TSE CASES WITH CLASSIFICATIONS PENDING ON THE RISE IN NORTH AMERICA

http://transmissiblespongiformencephalopathy.blogspot.com/2011/03/mad-cow-atypical-cjd-prion-tse-cases.html




TSS

CWD Update 102 October 20, 2011

CWD Update 102 October 20, 2011

State and Provincial Updates

The following press release was issued on October 20, 2011 by the Missouri Department of Agriculture

(http://mda.mo.gov/news/2011/Chronic_Wasting_Disease_Found_in_Captive_Deer):



Chronic Wasting Disease Found in Captive Deer

The Missouri departments of Agriculture, Conservation and Health and Senior Services and the U.S. Department of Agriculture announced that a captive white-tailed deer in Macon County, Missouri has tested positive for Chronic Wasting Disease (CWD). CWD is a neurological disease found in deer, elk and moose.

"We have a plan in place and our team is actively working to ensure that this situation is addressed quickly and effectively," said State Veterinarian Dr. Linda Hickam. "Fortunately there is no evidence that CWD poses a risk to humans, non cervid livestock, household pets or food safety."

The animal that tested positive for CWD was a captive white-tailed deer inspected as part of the State's CWD surveillance and testing program. Preliminary tests were conducted by the USDA National Veterinary Services Laboratory in Ames, Iowa.

Upon receiving the confirmed CWD positive, Missouri's departments of Agriculture, Conservation and Health and Senior Services initiated their CWD Contingency Plan. The plan was developed in 2002 by the Cervid Health Committee, a task force comprised of veterinarians, animal health officers and conservation officers from USDA, MDA, MDC and DHSS working together to mitigate challenges associated with CWD.

In February 2010 a case of CWD was confirmed in Linn County on a captive hunting preserve operated by the same entity, Heartland Wildlife Ranches, LLC. The Linn County facility was depopulated and no further infection was identified at that facility. The current case was identified through increased surveillance required by the management plan implemented from the previous CWD incident.

CWD is transmitted by live animal to animal contact or soil to animal contact. The disease was first recognized in 1967 in captive mule deer in the Colorado Division of Wildlife captive wildlife research facility in Fort Collins, Colorado. CWD has been documented in deer and/or elk in Colorado, Illinois, Kansas, Maryland, Michigan, Minnesota, Montana, Nebraska, New Mexico, New York, North Dakota, Oklahoma, South Dakota, Utah, Virginia, West Virginia, Wisconsin, and the Canadian Provinces of Alberta and Saskatchewan. There has been no evidence that the disease can be transmitted to humans.

"Missouri's proactive steps to put a testing protocol in place and create a contingency plan years ago is proving beneficial. We are in a solid position to follow pre-established steps to ensure Missouri's valuable whitetail deer resource remains healthy and strong," said Jason Sumners Missouri's Deer Biologist, Missouri Department of Conservation.

For more information regarding CWD, please contact Missouri's State Veterinarian Dr. Linda Hickam at (573) 751-3377.

Federal Budget Update - USDA

The following excerpt regarding FY2012 USDA CWD funding was copied from the "2012 USDA Budget Explanatory Notes for Committee on Appropriations,"

http://www.obpa.usda.gov/budsum



http://www.obpa.usda.gov/18aphis2011notes.pdf:




Federal role in Chronic Wasting Disease surveillance activities (-$13.926 million)

Chronic wasting disease (CWD) is a degenerative neurological illness affecting elk and deer (cervids) in North America. APHIS' activities related to this disease include: surveillance and management in both farmed and wild populations; assistance to State agencies for quarantine of affected animals and premises; humane euthanasia and testing affected and exposed animals; and, establishment of a voluntary Herd Certification Program (HCP) in coordination with States, the farmed cervid industry, and the U.S. Animal Health Associations.

The success of the voluntary HCP is based upon cooperation and shared responsibility between the Federal government and State and local interests. Since these are local or regional disease spread issues, State and local governments should assume a more active role and better anticipate and plan for future needs. The reduction will eliminate funding provided to States and Tribes through cooperative agreements and indemnity payments for CWD affected herds. APHIS plans to use $1.826 million in FY 2012 to provide a Federal level of coordination for the voluntary Herd Certification Program.

Federal Budget Update – DHHS-CDC

The following excerpt regarding FY2012 CDC prion funding was copied from the Department of Health and Human Services Fiscal Year 2012 "Justification of Estimates for Appropriation Committees,"

http://www.cdc.gov/fmo/topic/Budget%20Information/appropriations_budget_form_pdf/FY2012_CDC_CJ_Final.pdf:



Prion Disease (-$5.473 million)

The FY 2012 budget request reflects an elimination of the Prion Disease line ($5.473 million). This program takes a disease-specific approach rather than a broad public health approach to infectious and zoonotic diseases. In addition, CDC is not able to demonstrate significant public health impact within this program at the current funding level.

Recent Publications

Detection of Chronic Wasting Disease Prions in Salivary, Urinary, and Intestinal Tissues of Deer: Potential Mechanisms of Prion Shedding and Transmission

Nicholas J. Haley, Candace K. Mathiason, Scott Carver, Mark Zabel, Glenn C. Telling, and Edward A. Hoover

Journal of Virology, July 2011, p. 6309-6318, Vol. 85, No. 13

Abstract:

Efficient horizontal transmission is a signature trait of chronic wasting disease (CWD) in cervids. Infectious prions shed into excreta appear to play a key role in this facile transmission, as has been demonstrated by bioassays of cervid and transgenic species and serial protein misfolding cyclic amplification (sPMCA). However, the source(s) of infectious prions in these body fluids has yet to be identified. In the present study, we analyzed tissues proximate to saliva, urine, and fecal production by sPMCA in an attempt to elucidate this unique aspect of CWD pathogenesis. Oropharyngeal, urogenital, and gastrointestinal tissues along with blood and obex from CWD-exposed cervids (comprising 27 animals and >350 individual samples) were analyzed and scored based on the apparent relative CWD burden. PrPCWD-generating activity was detected in a range of tissues and was highest in the salivary gland, urinary bladder, and distal intestinal tract. In the same assays, blood from the same animals and unseeded normal brain homogenate controls (n = 116 of 117) remained negative. The PrP-converting activity in peripheral tissues varied from 10–11- to 100-fold of that found in brain of the same animal. Deer with highest levels of PrPCWD amplification in the brain had higher and more widely disseminated prion amplification in excretory tissues. Interestingly, PrPCWD was not demonstrable in these excretory tissues by conventional Western blotting, suggesting a low prion burden or the presence of protease-sensitive infectious prions destroyed by harsh proteolytic treatments. These findings offer unique insights into the transmission of CWD in particular and prion infection and trafficking overall.

http://jvi.asm.org/cgi/content/abstract/85/13/6309



Minor Oral Lesions Facilitate Transmission of Chronic Wasting Disease

Nathaniel D. Denkers, Glenn C. Telling, and Edward A. Hoover

Journal of Virology, February 2011, p. 1396-1399, Vol. 85, No. 3

Abstract:

While chronic wasting disease (CWD) prion transmission, entry, and trafficking remain incompletely elucidated, natural exposure of the oral and/or nasal mucous membranes seems certain. Cervids commonly sustain minor lesions on oral mucous membranes that could have an impact on susceptibility to prion infection. To explore this potential cofactor, we studied cohorts of cervid PrP transgenic mice with or without superficial abrasions on the lingual mucosa to determine whether minor oral mucosa lesions may enhance susceptibility to CWD infections. Results demonstrated that minor lingual abrasions substantially facilitate CWD transmission, revealing a cofactor that may be significant in cervids and perhaps other species.

http://jvi.asm.org/cgi/content/abstract/85/3/1396



There Is No Safe Dose of Prions

Helen R. Fryer, Angela R. McLean

PLoS ONE 6(8): e23664. doi:10.1371/journal.pone.0023664

Abstract:

Understanding the circumstances under which exposure to transmissible spongiform encephalopathies (TSEs) leads to infection is important for managing risks to public health. Based upon ideas in toxicology and radiology, it is plausible that exposure to harmful agents, including TSEs, is completely safe if the dose is low enough. However, the existence of a threshold, below which infection probability is zero has never been demonstrated experimentally. Here we explore this question by combining data and mathematical models that describe scrapie infections in mice following experimental challenge over a broad range of doses. We analyse data from 4338 mice inoculated at doses ranging over ten orders of magnitude. These data are compared to results from a within-host model in which prions accumulate according to a stochastic birth-death process. Crucially, this model assumes no threshold on the dose required for infection. Our data reveal that infection is possible at the very low dose of a 1000 fold dilution of the dose that infects half the challenged animals (ID50). Furthermore, the dose response curve closely matches that predicted by the model. These findings imply that there is no safe dose of prions and that assessments of the risk from low dose exposure are right to assume a linear relationship between dose and probability of infection. We also refine two common perceptions about TSE incubation periods: that their mean values decrease linearly with logarithmic decreases in dose and that they are highly reproducible between hosts. The model and data both show that the linear decrease in incubation period holds only for doses above the ID50. Furthermore, variability in incubation periods is greater than predicted by the model, not smaller. This result poses new questions about the sources of variability in prion incubation periods. It also provides insight into the limitations of the incubation period assay.

http://www.plosone.org/article/info%3Adoi%2F10.1371%2Fjournal.pone.0023664



White-tailed deer are susceptible to the agent of sheep scrapie by intracerebral inoculation

Justin J Greenlee, Jodi D Smith and Robert A Kunkle

Veterinary Research 2011, 42:107 doi:10.1186/1297-9716-42-107

Abstract:

Interspecies transmission studies afford the opportunity to better understand the potential host range and origins of prion diseases. The purpose of this experiment was to determine susceptibility of white-tailed deer to the agent of scrapie after intracerebral inoculation and to compare clinical signs and lesions to those reported for chronic wasting disease (CWD). Deer (n = 5) were inoculated with 1 mL of a 10% (wt/vol) brain homogenate derived from a sheep clinically affected with scrapie. A non-inoculated deer was maintained as a negative control. Deer were observed daily for clinical signs of disease and euthanized and necropsied when unequivocal signs of scrapie were noted. One animal died 7 months post inoculation (pi) due to intercurrent disease. Examinations of brain tissue for the presence of the disease-associated abnormal prion protein (PrPSc) by western blot (WB) and immunohistochemistry (IHC) were

negative whereas IHC of lymphoid tissues was positive. Deer necropsied at 15-22 months pi were positive for scrapie by IHC and WB. Deer necropsied after 20 months pi had clinical signs of depression and progressive weight loss. Tissues with PrPSc immunoreactivity included brain (at levels of cerebrum, hippocampus, colliculus, cerebellum, and brainstem), trigeminal ganglion, neurohypophysis, retina, spinal cord, and various lymphoid tissues including tonsil, retropharyngeal and mesenteric lymph nodes, Peyer's patches, and spleen. This work demonstrates for the first time that white-tailed deer are susceptible to sheep scrapie by intracerebral inoculation. To further test the susceptibility of white-tailed deer to scrapie these experiments will be repeated with a more natural route of inoculation.

http://www.veterinaryresearch.org/content/42/1/107/abstract



Modeling Routes of Chronic Wasting Disease Transmission: Environmental Prion Persistence Promotes Deer Population Decline and Extinction

Emily S. Almberg, Paul C. Cross, Christopher J. Johnson, Dennis M. Heisey, Bryan J. Richards

PLoS ONE 6(5): e19896. doi:10.1371/journal.pone.0019896

Abstract:

Chronic wasting disease (CWD) is a fatal disease of deer, elk, and moose transmitted through direct, animal-to-animal contact, and indirectly, via environmental contamination. Considerable attention has been paid to modeling direct transmission, but despite the fact that CWD prions can remain infectious in the environment for years, relatively little information exists about the potential effects of indirect transmission on CWD dynamics. In the present study, we use simulation models to demonstrate how indirect transmission and the duration of environmental prion persistence may affect epidemics of CWD and populations of North American deer. Existing data from Colorado, Wyoming, and Wisconsin's CWD epidemics were used to define plausible short-term outcomes and associated parameter spaces. Resulting long-term outcomes range from relatively low disease prevalence and limited host-population decline to host-population collapse and extinction. Our models suggest that disease prevalence and the severity of population decline is driven by the duration that prions remain infectious in the environment. Despite relatively low epidemic growth rates, the basic reproductive number, R0, may be much larger than expected under the direct-transmission paradigm because the infectious period can vastly exceed the host's life span. High prion persistence is expected to lead to an increasing environmental pool of prions during the early phases (i.e. approximately during the first 50 years) of the epidemic. As a consequence, over this period of time, disease dynamics will become more heavily influenced by indirect transmission, which may explain some of the observed regional differences in age and sex-specific disease patterns. This suggests management interventions, such as culling or vaccination, will become increasingly less effective as CWD epidemics progress.

http://www.plosone.org/article/info%3Adoi%2F10.1371%2Fjournal.pone.0019896



Broad and fine-scale genetic analysis of white-tailed deer populations: estimating the relative risk of chronic wasting disease spread

Catherine I. Cullingham, Evelyn H. Merrill, Margo J. Pybus, Trent K. Bollinger, Gregory A. Wilson, David W. Coltman

Evolutionary Applications. Volume 4, Issue 1, pages 116–131, January 2011

Abstract:

Chronic wasting disease is a transmissible spongiform encephalopathy of cervids, similar to sheep scrapie that has only recently been detected in wild populations of white-tailed deer (Odocoileus virginianus) and mule deer (Odocoileus hemionus hemionus) in western Canada. Relatively little is known about local transmission dynamics of the disease or the potential for long-distance spread. We analysed the population genetic structure of over 2000 white-tailed deer sampled from Alberta, British Columbia, and Saskatchewan using microsatellite profiles and mtDNA sequencing to assess the relative risk of disease spread. There was very little differentiation among subpopulations and a weak trend of increasing differentiation with geographic distance. This suggests that the potential for long-distance disease spread through the dispersal of infected individuals is possible, yet the risk of spread should gradually diminish with distance from infection foci. Within subpopulations, females were more related than expected by chance (R > 0) within a radius of approximately 500 m. Sex-biased philopatry and social interactions among related females may facilitate local disease transmission within social groups. Local herd reduction may therefore be an effective tool for reducing the disease prevalence when implemented at the appropriate spatial scale.

http://onlinelibrary.wiley.com/doi/10.1111/j.1752-4571.2010.00142.x/abstract



http://www.cwd-info.org/pdf/UD102.pdf





===========================end...TSS======================




Friday, October 21, 2011

Chronic Wasting Disease Found in Captive Deer Missouri

http://chronic-wasting-disease.blogspot.com/2011/10/chronic-wasting-disease-found-in.html



Wednesday, October 12, 2011

White-tailed deer are susceptible to the agent of sheep scrapie by intracerebral inoculation

http://chronic-wasting-disease.blogspot.com/2011/10/white-tailed-deer-are-susceptible-to.html



Thursday, June 09, 2011

Detection of CWD prions in salivary, urinary, and intestinal tissues of deer: potential mechanisms of prion shedding and transmission

http://chronic-wasting-disease.blogspot.com/2011/06/detection-of-cwd-prions-in-salivary.html



Saturday, May 14, 2011

Modeling Routes of Chronic Wasting Disease Transmission: Environmental Prion Persistence Promotes Deer Population Decline and Extinction

http://chronic-wasting-disease.blogspot.com/2011/05/modeling-routes-of-chronic-wasting.html



Oral.26: Minor Oral Lesions Facilitate CWD Infection

Nathaniel D. Denkers,1,† Glenn C. Telling2 and Edward A. Hoover1 1Colorado State University; Fort Collins, CO USA; 2University of Kentuckty; Lexington, KY USA †Presenting author; Email: nddenk@colostate.edu

Purpose: While the exact mechanisms of chronic wasting disease (CWD) prion transmission, entry, and trafficking remain incompletely elucidated, transmission by exposure of the oral and/or nasal mucous membranes seems certain. As part of foraging, cervids likely experience minor lesions in the oral mucous membranes; these could have impact on susceptibility to prion entry and subsequent infection. To explore this potential co-factor, we used cervid PrP transgenic mice to assess whether or not micro-abrasions to the tongue may enhance susceptibility to oral CWD infection and whether or not infectious CWD PrPCWD could be detected immediately after exposure.

Methods: Two sets of FVB mice transgenically expressing the normal cervid PrPC protein [Tg(CerPrP-E226)5037+/-], with or without abrasions on the lingual mucosa, were inoculated orally with 10µl of a 10% w/v brain homogenate from either CWD-positive or negative deer. Abrasions were created by lightly scratching the dorsal lingual epithelium with a 27g needle. Cohorts were sacrificed at either early [0, 1, and 4 h post inoculation (pi)] or late [3, 12, and 24 months pi] time points or when signs of neurologic disease were observed. Tongue, lymphoid tissue, and the brain were assessed by western blotting and tyramide signal amplification (TSA) immunohistochemistry to detect the CWD abnormal prion protein (PrPCWD).

Results: Between 296 and 515 dpi, 9 of the 9 CWD-inoculated mice with lingual lesions developed clinical signs of neurologic dysfunction mandating euthanasia. Only the brain in all nine mice was positive for PrPCWD by western blot and TSA immunohistochemistry. Conversely, all mice without oral lesions remained asymptomatic for >700 dpi and no evidence of PrPCWD was detected in these mice terminally. Moreover, no evidence of PrPCWD could be detected when the micro-abrasion sites were examined at 0, 1, or 4 h after oral exposure or at any pre-terminal time point thereafter.

Conclusions: Micro-abrasions to the lingual surface substantially facilitated CWD transmission, suggesting that minor oral mucosal lesions may be a significant co-factor facilitating infection in foraging cervids or other species.

http://www.prion2011.ca/files/PRION_2011_-_Posters_(May_5-11).pdf



more on CWD from the PRION2011 ;


FELINE SPONGIFORM ENCEPHALOPATHY FSE

http://felinespongiformencephalopathyfse.blogspot.com/



Monday, May 23, 2011

Atypical Prion Diseases in Humans and Animals 2011

Top Curr Chem (2011)

DOI: 10.1007/128_2011_161

# Springer-Verlag Berlin Heidelberg 2011

http://bse-atypical.blogspot.com/2011/05/atypical-prion-diseases-in-humans-and.html



Tuesday, May 31, 2011

Chronic Wasting Disease DOI: 10.1007/128_2011_159 # Springer-Verlag Berlin Heidelberg 2011

http://chronic-wasting-disease.blogspot.com/2011/05/chronic-wasting-disease-doi.html



Wednesday, September 21, 2011

Evidence for distinct CWD strains in experimental CWD in ferrets

http://chronic-wasting-disease.blogspot.com/2011/09/evidence-for-distinct-cwd-strains-in.html



UPDATED DATA ON 2ND CWD STRAIN

Wednesday, September 08, 2010

CWD PRION CONGRESS SEPTEMBER 8-11 2010

http://chronic-wasting-disease.blogspot.com/2010/09/cwd-prion-2010.html



Wednesday, August 24, 2011

There Is No Safe Dose of Prions

http://transmissiblespongiformencephalopathy.blogspot.com/2011/08/there-is-no-safe-dose-of-prions.html



Wednesday, August 24, 2011

All Clinically-Relevant Blood Components Transmit Prion Disease following a Single Blood Transfusion: A Sheep Model of vCJD

http://transmissiblespongiformencephalopathy.blogspot.com/2011/08/all-clinically-relevant-blood.html



Sunday, June 5, 2011

PRION TSE FUNDING, WHAT ARE THE PRIORITIES of APHCA, ASEAN, OIE, Korea, and USA ?

http://transmissiblespongiformencephalopathy.blogspot.com/2011/06/prion-tse-funding-what-are-priorities.html



Friday, April 15, 2011

PRION TRANSMISSIBLE SPONGIFORM ENCEPHALOPATHY PROJECTS, RESEARCH FUNDING, BSE VOLUNTARY TESTING UPDATE IN NORTH AMERICA 2011

http://prionunitusaupdate2008.blogspot.com/2011/04/prion-transmissible-spongiform.html



Editorial: The European Response to BSE: A Success Story

EFSA Journal 2011; 9(9):e991 [3 pp.]. doi:10.2903/j.efsa.2011.e991 Author Herbert Budka, Member and Vice-Chair of EFSA's Panel on Biological Hazards (BIOHAZ)Contact

editor-in-chief.efsajournal@efsa.europa.eu

Type: Editorial Published: 02 September 2011 Affiliation: European Food Safety Authority (EFSA), Parma, Italy Article

snip...

Moreover, transmission experiments to non-human primates suggest that some TSE agents in addition to Classical BSE prions in cattle (namely L-type Atypical BSE, Classical BSE in sheep, transmissible mink encephalopathy (TME) and chronic wasting disease (CWD) agents) might have zoonotic potential.

snip...

http://www.efsa.europa.eu/en/efsajournal/pub/e991.htm?emt=1




http://www.efsa.europa.eu/en/efsajournal/doc/e991.pdf



see full text and more here ;


Monday, October 10, 2011

EFSA Journal 2011 The European Response to BSE: A Success Story

http://transmissiblespongiformencephalopathy.blogspot.com/2011/10/efsa-journal-2011-european-response-to.html



Thursday, August 4, 2011

Terry Singeltary Sr. on the Creutzfeldt-Jakob Disease Public Health Crisis, Date aired: 27 Jun 2011

http://transmissiblespongiformencephalopathy.blogspot.com/2011/08/terry-singeltary-sr-on-creutzfeldt.html




layperson

TSS

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