TABLE 3.
Infection doses for different F. tularensis strains in C57BL micea
Strain | Genotype
|
Phenotype or complementation | No. of CFU (lethal dose)b
|
|||
---|---|---|---|---|---|---|
FTT0918 | pilA | FTT0086 | Subcutaneous | Intraperitoneal | ||
LVS1 | − | − | Δ93 bp | LVS wt | 3 × 107 | 1 × 101 |
LVS2 | − | − | Δ93 bp | LVS wt | 1 × 106 | 5 × 101 |
FSC688 | − | + | Δ93 bp | LVS2, pilA in cis | 5 × 103 | 3 × 101 |
FSC741 | − | − | + | LVS2, FTT0086 in cis | 2 × 106 | NT |
FSC693 | + | − | Δ93 bp | LVS2, FTT0918 in cis | <5c | <5 |
FSC694 | + | + | Δ93 bp | LVS2, pilA and FTT0918 in cis | <5 | <5 |
FSC200 | + | + | + | Type B wt | <5 | <5 |
FSC767 | − | + | + | FSC200, insertion mutation in FTT0918 | 2 × 102 | <5 |
Mice in groups of five were infected subcutaneously. The result is from one single experiment representative of three experiments of similar design. wt, wild type; Δ, deletion; NT, not tested.
The CFU value is a 50% lethal dose (LD50) calculation (26), but this should not be seen as a standard LD50 experiment since mice were sacrificed if they showed severe sickness. A lethal dose indicated as <5 CFU was used for strains where all animals showed lethal symptoms of infection for doses between two and five bacteria.
The infection kinetics was delayed compared to that for the pilA/FTT0918 double complementation (Fig. 5).