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. 2007 Feb 21;81(9):4615–4624. doi: 10.1128/JVI.02628-06

TABLE 2.

Scrapie incubation period in murine neuroblastoma (N2A) and C2C12 myoblast and myotube cell lysates

Samplea Trial 1b
Trial 2
Incubation period, days (mean ± SD)c No. affected/no. inoculated No. of times cultures were passed after scrapie infection Incubation period, days (mean ± SD) No. affected/no. inoculated No. of times cultures were passed after scrapie infection
22L scrapie-infected brain 137 ± 7d 5/5 NAe NDf NA NA
22L scrapie-infected N2A cells 125 ± 7.6* 5/5 19 138 ± 2.2 5/5 15
22L scrapie-infected C2C12 myoblasts 138 ± 6.2* 6/6 17 145 ± 4.3 6/6 14
22L scrapie-infected C2C12 myotubes 132 ± 2.2 5/5 17 137 ± 1.7 4/4 14
22L A3 scrapie-infected C2C12 myoblasts ND NA NA 139 ± 6.4 4/4 18
22L A3 scrapie-infected C2C12 myotubes ND NA NA 133 ± 0.6 3/3 18
C2C12 myoblasts >250 0/5 17 >205 0/3 14
C2C12 myotubes ND NA NA >205 0/3 14
a

For the brain sample, a 1% (wt/vol) homogenate was used. For all other samples, a 56-cm2 tissue culture at ∼90% to 100% confluence was trypsinized and resuspended in phosphate-buffered saline, and the total cell lysate was inoculated into each group of mice.

b

Trials represent C2C12 muscle cells and N2A cells from independent scrapie infection experiments.

c

Brain homogenates or tissue lysates were intracerebrally inoculated into C57Bl/6 mice and the time to onset of clinical disease was measured. *, Tukey's Studentized range test, P < 0.05.

d

The presence of PrPSc in the brains of all clinically ill mice was confirmed by Western blotting.

e

NA, not applicable.

f

ND, not done.