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. 2004 Jun 30;24(26):5974–5981. doi: 10.1523/JNEUROSCI.0122-04.2004

Table 2.

Prion load in brains and spleens of individual tg640 mice




Transmission of brain to indicator mice

Transmission of spleen to indicator mice
Mouse genotypes
Days after inoculation; route of infection
Brain infectivity (logLD50 per gram)
Attack rate (mean ± SD days)
Spleen infectivity (logLD50 per gram)
Attack rate (mean ± SD days)
MBP-PrP 35 d; intraperitoneal <1.5 0/4 <1.5 0/4
<1.5 0/4 <1.5 3/4 (99,148,150)a
140 d; intraperitoneal <1.5 0/4 <1.5 0/4
<1.5 0/4 <1.5 0/4
210 d; intracerebral <1.5 0/4 <1.5 0/4
<1.5 0/3 <1.5 0/4
Prnp+/+ 35 d; intraperitoneal <1.5 0/4 5.0 4/4 (73 ± 5)
<1.5 0/4 5.1 4/4 (72 ± 4)
140 d; intraperitoneal 5.3 4/4 (68 ± 6) 4.0 3/3 (84 ± 4)
4.9 4/4 (74 ± 7) 5.1 4/4 (72 ± 8)
167 d; intracerebral 6.3 4/4 (58 ± 6) 5.1 4/4 (72 ± 5)
6.1 4/4 (60 ± 7) 5.3 4/4 (70 ± 2)
Prnpo/o 42 d; intraperitoneal <1.5 0/4 <1.5 0/4


<1.5
0/4
<1.5
1/4 (99)

Wild-type (Prnp+/+) and tg640 mice homozygous for the MBP-PrP transgenic cluster were inoculated intraperitoneally and intracerebrally and killed for analysis at the time points indicated.

a

Prion disease in three of four tga20 indicator mice that had received spleen extracts from a 35 dpi-challenged tg640 mouse is most likely a result of prions persisting from the inoculum.