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. 2008 Mar 14;4(3):e1000017. doi: 10.1371/journal.ppat.1000017

Table 2. Mouse infections with RNA viruses.

Virus Route Mouse strain Mouse Age (weeks) Infected Mice (n = ) Days p.i. Organs Figure
LDV i.p. C57BL/6 3–4 9 1a Brain-Liver 2 A.
MHV-A59 i.c. C57BL/6 3–4 10 3b Brain-Liver 2 B.
TMEV-DA1 i.c. 129/Sv 3–4 2 5c Brain 2 C.
LACVdelNSse i.p. B6.A2G-Mx1 6 2 7b Brain 2 D.
TMEV-GDVIIe i.c. FVB/N 3–4 2 5b Brain 2 E.
TMEV-GDVII i.c. C57BL/6 3–4 6 4b Brain 2 F.
MHV-A59 i.p. C57BL/6 3–4 7 2d Liver 2 G.
MHV-A59 i.p. 129/Sv 5 3 2d Liver 2 H.
a

1 day post-infection was reported to correspond to the peak of LDV replication and of IFN expression in vivo.

b

Mice infected with highly neurovirulent viruses were sampled when signs of encephalitis were prominent (generally less than 24 hours before death).

c

The DA1 strain of TMEV produces a transient encephalitis lasting about 1 or 2 weeks. In mice with the H-2 b haplotype, the virus is then rapidly cleared by the cytolytic T lymphocyte response [40],[41]. Mice were sampled at 5 days post-infection, a time-point representative of the acute phase of infection.

d

Preliminary RT-PCR experiments failed to reveal a clear difference in IFN expression and viral load between 129/Sv mice infected i.p. for 2 days and for 7 days. Only mice with amounts of MHV-A59 detectable by conventional RT-PCR were taken into account.

e

These samples from TMEV (GDVII strain) and LACVdelNSs infected brains were from a previous work [33].