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. 2014 Feb;88(4):2056–2070. doi: 10.1128/JVI.03051-13

TABLE 5.

MVEV-specific antibody responsesa

Mouse strain Virus Dose (PFU) Route No. of animals/group Mean log10 antibody titer (SD)b
Mean PRNT50 titer (range)c
First bleed Second bleed First bleed Second bleed
C57BL/6 MVEV.wtd 103 i.m. 2 4.2 (0.4) 4.1 (0.6) 320 (pool) 60 (40–80)
MVEV.C-IRES 105 10 4.0 (0.3) 4.7 (0.3) 40 (pool) 192 (80–320)
MVEV.IFN-β 105 10 2.5 (0.5) 3.7 (0.4) 10 (pool) 50 (<10–80)
MVEV.wte 103 i.v. 4 4.0 (0.2) 4.3 (0.2) 160 (pool) 120 (80–160)
MVEV.IFN-β 103 5 <2.0 2.6 (0.6) <10 (pool) <10 (pool)
MVEV.IFN-β 105 5 4.0 (0.1) 5.3 (0) 10 (pool) 180 (80–320)
BALB/c MVEV.wtf 105 i.m. 6 3.6 (0.3) 4.2 (0.1) 20 (pool) 113 (40–160)
MVEV.C-IRES 105 10 2.8 (0.4) 4.3 (0.4) 10 (pool) 82 (20–160)
MVEV.IFN-β 105 10 2.5 (0.3) 4.2 (0.3) <10 (pool) 15 (<10–40)
MVEV.wt 105 s.c. 10 NTg 3.3 (0.3) NT 20 (pool)
MVEV.C-IRES 105 10 NT 3.7 (0.3) NT 20 (pool)
MVEV.IFN-β 105 10 NT 3.1 (0.1) NT <10 (pool)
a

Groups of 7- to 8-week-old C57B6 or BALB/c mice were immunized with wild-type or recombinant MVEV using the dose and route indicated and were boosted with the same dose and by the same route 3 to 4 weeks later. Sera were collected prior to delivery of the booster dose and at 3 to 4 weeks after the second immunization.

b

ELISA endpoint titers of individual test sera were determined as described in Materials and Methods section.

c

Plaque reduction neutralization by individual or pooled test sera against MVEV were determined as described in Materials and Methods.

d

Three mice succumbed to MVEV.wt infection; the indicated group size represents surviving mice.

e

One mouse succumbed to MVEV.wt infection; the indicated group size represents surviving mice.

f

Four mice succumbed to MVEV.wt infection; the indicated group size represents surviving mice.

g

NT, not tested.