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. 2005 Oct;73(10):6877–6884. doi: 10.1128/IAI.73.10.6877-6884.2005

TABLE 1.

Viable bacteria recovered from mice that were vaccinated with clone pool DNA (trial 1) and challenged with live M. avium subsp. paratuberculosisa

Immunization group Spleen
Mesenteric lymph nodes
CFU/mgb SEM P valuec CFU/mgb SEM P valuec
No DNA, noninfected 0.0 0.0 0.0 0.0
No DNA, infected 2,047.3 478.2 1,240.1 218.0
Microcarrier, infected 1,422.6 264.6 0.2680 1,538.5 298.5 0.4295
Vector DNA, infected 1,604.6 268.0 0.4299 1,246.5 270.2 0.9855
Clone pool 1 27.2 26.3 0.0001 63.5 62.4 0.0001
Clone pool 2 11.4 8.9 0.0001 41.2 33.1 0.0001
Clone pool 3 1,470.0 253.6 0.3004 948.7 231.1 0.3712
Clone pool 4 2,377.7 628.2 0.6804 911.4 270.4 0.3565
Clone pool 5 1,436.7 452.9 0.3662 714.6 201.0 0.0933
Clone pool 6 1,578.9 224.2 0.3869 1,543.7 392.5 0.5075
Clone pool 7 793.6 432.2 0.0679 1,057.2 885.6 0.8433
Clone pool 8 724.4 385.5 0.0451 281.5 162.7 0.0024
Clone pool 9 1,130.3 416.7 0.1655 1,441.9 771.9 0.8024
Clone pool 10 144.2 93.7 0.0010 247.4 174.7 0.0023
Clone pool 11 2,754.2 399.5 0.2714 3,239.0 729.4 0.0171
a

BALB/c mice were immunized with clone pool DNA (2 μg), boosted 3 weeks later, and challenged intraperitoneally with live M. paratuberculosis (strain 6112; 108 CFU). Mice were necropsied after 3 months of infection, and tissues were processed for culture.

b

Mean CFU/mg tissue (n = 10).

c

The values in boldface type are P values for groups that were significantly different than the no-DNA, infected control group (P < 0.05).