Table 1. Composition of the 5 sheep whole blood pools used for preparation of labile blood products.
Collection date | Donor | PrPSc | |||
ID | Incubationperiod | CNS | LRS | ||
Pool 1 | 161 dpi | D1 | 228 dpi | + | + |
D2 | 234 dpi | + | + | ||
D3 | 249 dpi | + | + | ||
Pool 2 | 163 dpi | D4 | 225 dpi | + | + |
D5 | 217 dpi | + | + | ||
D6 | 221 dpi | + | + | ||
Pool 3 | 168 dpi | D7 | 209 dpi | + | + |
D8 | 228 dpi | + | + | ||
D9 | 248 dpi | + | + | ||
Pool 4 | 169 dpi | D10 | 209 dpi | + | + |
D11 | 256 dpi | + | + | ||
D12 | 226 dpi | + | + | ||
Pool 5 | 170 dpi | D13 | 222 dpi | + | + |
D14 | 250 dpi | + | + | ||
D15 | 244 dpi | + | + |
Each pool was obtained by mixing 600–700 mL of whole blood collected in 3 VRQ/VRQ sheep orally inoculated with PG127 classical scrapie isolate. After blood collection (collection date) each donor was monitored till the occurrence of clinical signs. Donors were culled when displaying locomotor difficulties that could impair their abilities to feed (incubation period). TSE was confirmed by detection of abnormal PrP in lymphoid tissues (LRS) and central nervous system (CNS) using immunohistochemistry and Western Blot.