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. 2017 Jun 21;12(6):e0179317. doi: 10.1371/journal.pone.0179317

Table 1. Infection of mice with L- and S-type prions with or without passaging in GT1-7 cells.

Inoculum 1 PrPSc in inoculum 2 Subsequent passages in mice
n/n0 3 Survival days 4 Prion phenotype
Exp. 1 6 Mo1 brain (463 days, L-type) 5 + 8/9 196 ± 31.6 S-type
1/9 289 L-type
GT1-7 exposed to Mo1 brain + 9/9 278 ± 5.7 L-type
Mo2 brain (251 days, S-type) + 10/10 148 ± 8.9 S-type
GT1-7 exposed to Mo2 8/9 288 ± 36.8 S-type
1/9 375 L-type
Mo3 brain (150 days, S-type) + 5/5 143 ± 4.3 S-type
GT1-7 exposed to Mo3 brain 9/9 246 ±17.6 S-type
Exp. 2 Mo1’ brain (469 days, L-type) + 5/10 220 ± 7.2 S-type
5/10 290 ± 6.4 L-type
GT1-7 exposed to Mo1’ brain + 9/9 285 ± 15.4 L-type
Mo2’ brain (295 days, L-type) + 1/11 195 S-type
10/11 273 ±13.8 L-type
GT1-7 exposed to Mo2’ brain + 9/9 277±14.7 L-type
Mo3’ brain (276 days, L-type) + 5/5 191 ± 7.1 S-type
GT1-7 exposed to Mo3’ brain + 10/10 280 ± 13.1 L-type

1 Inoculum (brain or GT1-7 cells) was intracerebrally injected into ICR mice.

2 PrPSc accumulation was confirmed by western blotting: +, PrPSc positive;–, PrPSc negative.

3 Number of diseased mice out of total number of challenged mice.

4 Survival periods were determined as the time from inoculation to the clinical endpoint or death (mean survival days ± standard deviation).

5 Survival periods and prion phenotype of the individual mouse used for the inoculation are indicated.

6 Experiment numbers are the same as in Fig 1.