TABLE 3.
Route of larval tick infection | B. burgdorferi strain genotype | No. of mice infected/total no. exposed |
---|---|---|
SCID mouse blood meal | WT | 2/2 |
ApospC | 2/2 | |
ApospA | 2/2 | |
Immersion | WT | 2/2 |
ApospC | 2/2 | |
ApospA | 2/2 | |
WT mouse blood meal | WT | 4/4 |
ΔospA | 0/2 | |
ApospC | 0/2 | |
ApospA | 2/2 | |
ApospB | 2/2 |
Twenty nymphs per tick cohort were applied to WT mice and were allowed to feed to repletion. Three weeks after the application of ticks, mouse infection was assessed by seroconversion and by isolation from ears, bladders, and joints. Infected animals were seropositive and had at least two tissues positive out of three tissues assessed. Negative animals were seronegative and had no positive tissues.