It is misleading to tell the public that there are no health risks from eating meat from an animal infected with Chronic Wasting Disease. To the contrary, scientists have identified a new strain of human prion disease as CWD-huPrPSc
http://www.jbc.org/cgi/doi/10.1074/jbc.M110.198465 January 2011:
Generation of a New Form of Human PrPSc in Vitro by Interspecies Transmission from Cervid Prions*
Marcelo A. Barria, Glenn C. Telling, Pierluigi Gambetti, James A. Mastrianni
and Claudio Soto,*
" . . . the species barrier from cervid to humans is prion strain-dependent and humans can be vulnerable to novel cervid prion strains"
'Our results agree with that prediction and suggest that the newly generated CWD-huPrPSc acquires the
biochemical properties of the cervid infectious material (Fig. 4, A and B)."
Interesting reading from the Centers for Disease Control and Prevention (CDC) is their article on hunters and game eaters infected with various prion diseases:
http://wwwnc.cdc.gov/eid/article/10/6/03-1082_article.htm
Back in 2004, the CDC wrongly concluded that if the disease did not manifest as Creutzfeldt Jakob disease, it was not caused by CWD prions.
However, in JUNE 22, 2012 – Nobel Laureate Stanley Prusiner, UCSF, and colleagues, confirm Alzheimer's is a prion disease, but there are many different strains.
“Now he concludes, they (prions) are actually capable of multiplying what he terms "alternative" shapes, with each shape responsible for different type of dementia. ”
“The brain diseases caused by prions include Alzheimer's, Parkinson's Huntington's, amyotrophic lateral sclerosis, also known as Lou Gehrig's
disease, and other varied disorders known collectively as the frontotemporal dementias, Prusiner said “
http://www.alzheimers-prions.com/pdf/JUNE2012PRUSINER-ETAL-ALZHEIMERSISAPRIONDISEASE.pdf
Human prion disease infections caused by CWD may present as sporadic Creutzfeldt Jakob Disease, Early onset Alzheimer's dementia, classic Alzheimer's Disease or some other neurodegenerative disease.
Helane Shields, Alton, NH hshields@tds.net http://www.alzheimers-prions/com
http://www.jbc.org/cgi/doi/10.1074/jbc.M110.198465 January 2011:
Generation of a New Form of Human PrPSc in Vitro by Interspecies Transmission from Cervid Prions*
Marcelo A. Barria, Glenn C. Telling, Pierluigi Gambetti, James A. Mastrianni
and Claudio Soto,*
" . . . the species barrier from cervid to humans is prion strain-dependent and humans can be vulnerable to novel cervid prion strains"
'Our results agree with that prediction and suggest that the newly generated CWD-huPrPSc acquires the
biochemical properties of the cervid infectious material (Fig. 4, A and B)."
Interesting reading from the Centers for Disease Control and Prevention (CDC) is their article on hunters and game eaters infected with various prion diseases:
http://wwwnc.cdc.gov/eid/article/10/6/03-1082_article.htm
Back in 2004, the CDC wrongly concluded that if the disease did not manifest as Creutzfeldt Jakob disease, it was not caused by CWD prions.
However, in JUNE 22, 2012 – Nobel Laureate Stanley Prusiner, UCSF, and colleagues, confirm Alzheimer's is a prion disease, but there are many different strains.
“Now he concludes, they (prions) are actually capable of multiplying what he terms "alternative" shapes, with each shape responsible for different type of dementia. ”
“The brain diseases caused by prions include Alzheimer's, Parkinson's Huntington's, amyotrophic lateral sclerosis, also known as Lou Gehrig's
disease, and other varied disorders known collectively as the frontotemporal dementias, Prusiner said “
http://www.alzheimers-prions.com/pdf/JUNE2012PRUSINER-ETAL-ALZHEIMERSISAPRIONDISEASE.pdf
Human prion disease infections caused by CWD may present as sporadic Creutzfeldt Jakob Disease, Early onset Alzheimer's dementia, classic Alzheimer's Disease or some other neurodegenerative disease.
Helane Shields, Alton, NH hshields@tds.net http://www.alzheimers-prions/com