Table 1.
Summary of treatments performed in the BALB/c mice
Groups |
Route of administration |
Treatments
a
|
Mice number |
||
---|---|---|---|---|---|
Total mice | In HI b and CMI c | In challenge d | |||
I |
Intramuscular vaccination |
100 μl PBS |
10 |
3 |
7 |
|
|
100 μg pVAX1 |
10 |
3 |
7 |
|
|
100 μg pVAX1-MEG-CTXA2/B |
10 |
3 |
7 |
II |
Intranasal vaccination |
200 μl BRD509 |
10 |
3 |
7 |
|
|
200 μl BRD509/pVAX1 |
10 |
3 |
7 |
|
|
200 μl BRD509/pVAX1-MEG-CTXA2/B |
10 |
3 |
7 |
III |
Intraoral vaccination |
50 μl BRD509 |
10 |
3 |
7 |
|
|
50 μl BRD509/pVAX1 |
10 |
3 |
7 |
50 μl BRD509/pVAX1-MEG-CTXA2/B | 10 | 3 | 7 |
aThe mice were randomly divided into intramuscular, intranasal and intraoral immunization groups (30 mice per group). For the intramuscular group, the mice were injected 100 μl 1 μg/μl recombinant plasmid or empty plasmid in the quadriceps muscle; For the nasal group, each mouse was given a nasal drip of 50 μl 109 cfu/ml Salmonella bacteria with recombinant plasmid or empty plasmid; The oral group was administrated 200 μl 109 cfu / ml Salmonella bacteria with recombinant plasmid or empty plasmid orally; Each group also had 10 mice which were treated with Salmonella without plasmid or saline as negative control. Mice were vaccinated three times at 2 week intervals.
bHumoral immunity (HI) was tested by collecting sera from three immunized mice in each group.
cCellular immunity (CMI) was evaluated by splenocytes from three immunized mice per group 2 weeks after the last immunization.
dFour weeks after the last immunization, immunized mice were challenged intraperitoneally with 1 × 103 tachyzoites of T. gondii RH strain.