Skip to main content
. 2014 Mar 31;7:145. doi: 10.1186/1756-3305-7-145

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.

HHS Vulnerability Disclosure