Originally posted by LVPharm
Prior to the "prion", I think the common theory was that diseases such as "kuru" were caused by something called a "slow virus" (perhaps because of a long incubation period following administration of infective material into test subjects?)
Wasn't Kuru also called "laughing sickness" because of the uncontrollable laughing associated with this affliction?
As far as visualization of prions, I'm sure they've attempted crystallography in an attempt to view the structures, but I haven't seen anything.
Yes, what I carried away from those lectures in the early eighties was retrovirus and slow virus. Prion never entered my vocabulary until recently. It was exciting research because, remember, at the time HIV was a newly emerging phenomena and attempts were being made to link the slow virus concept to a wide spectrum of diseases from cancers to ALS/parkinsons/MS.
Read this from Patricia Doyle PhD and her emerging diseases message board:
Coincidence, Edmonton to mass slaughter deer in futile attempt to stop CWD
PB ? 01/30/2003,
'THEY' do love the dramatic spectacle of mass slaughter of animals don't they - is it to convince us or themselves that they are doing 'something'??
When will they learn that the spongiform encephalopathies are not a 'catchable' disease - it is something the animal/human develops if given the right environment.
Of the heavy metals, manganese is the worst culprit - even then most animals might resist that if all else is normal - but manganese is in the 'salt' licks and is being spewed out by every passing car - plus goodness knows what is in the feed now!
Add to that, the animals are probably being sprayed by organophosphates, which have been proved to deform the prion protein without the other factors - and really the animals don't stand a chance.
But along comes a well meaning 'scientist' who declares that one animal must have 'caught' it from another, and hey presto the whole herd gets wiped out.
Given that WE ALL HAVE PRIONS - there is not a disease called prion - each body makes them as part of its defence against free radical damage - the prions are normally re-absorbed in the normal course of events - but if they become malformed because of the above factors, then the body no longer recognises them and has no means of dealing with what is now a foreign agent.
End of spiel - Pat
Then in this article Patricia states that it is spread by blood transfusion
http://rense.com/general46/prion.htm