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Microbiology

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Creutzfeldt-Jacob disease   rare, degenerative brain disease--fatal--type of spongiform encephalopathy--progressive death of brain nerve cells--build up of abnormal prion proteins--microscope--see tiny holes where whole areas of nerve cells have died--brain spongy  
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Kuru   initial discovery of Creutzfeldt-Jacob--by cannibalistic tribes who prepared and ate human brains in New Guinea--developed shaking--those who ate fully cooked brains not affected  
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Prions   smallest replicating agents known--no DNA, RNA, or nucleic acids--term comes from proteinaceous agents  
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Scrapie   when spongiform encephalopathy occurs in sheep--scratch themselves on trees/fences until wear through their hide.  
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Spongiform encephalopathy   brain develops so many holes it looks like a sponge--brain fills up with useless protein untile brain damage is done--tens of years to become apparent--always fatal  
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Transmissible spongiform encephalopathy   mutational changes in the protein gene/spontaneous incorrect folding--spread from animal to animal and to humans  
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Describe the smallest biological agent that is replicated   prion--a protein that causes itself to be replicated by the way it folds  
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What damage do prions do?   abnormally folded prion proteins accumulate in the brain until the brain tissue is destroyed and the host dies  
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