Following the BSE epidemic in cattle and the emergence of a variant form of
Creutzfeldt-Jakob disease in humans, the question was raised whether BSE h
as been transmitted to small ruminants by the inadvertent feeding of infect
ious meat and bone meal. Such infections could easily be conceiled in count
ries where scrapie is endemic. To address this issue by immune-chemically a
nalyzing the PrPSc fragments, we have developed two lines of research. Firs
tly we have focused on the development of criteria for the differential cha
racterization of experimental BSE and scrapie strains/isolates in rodents.
To date, three criteria have been identified: quantification of the relativ
e banding intensities of PrPSc glycotypes using a photoimaging technique; t
he non-uniform kinetic of proteinase K degradation of PrPSc; and difference
s in the molecular masses of their nonglycosylated PrPSc fragments after PK
cleavage in immunoblot. The second line of research focused on the impleme
ntation of the criteria described above to representative samples from scra
pie diseased Irish sheep. Using these three criteria, no evidence was found
for the presence of a BSE infection in these animals. However, the final c
onclusion must take into account the results of mouse incubation lime and m
ouse lesion profile data which are currently being generated.