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. 2018 Apr 23;86(5):e00088-18. doi: 10.1128/IAI.00088-18

TABLE 1.

Attenuation of gene knockout P. yoelii preerythrocytic stages in BALB/c mice

Parasite name or genotype No. of sporozoites used for inoculationa Mouse No. of mice patentb No. of days to patencyc
1971cl1d 1,000 BALB/cJ 3/3 3 (3)
1971cl1d 10,000 BALB/cJ 3/3 3 (3)
lisp2 1,000 BALB/cJ 6/8 5 (4)
7 (2)
lisp2 10,000 BALB/cJ 7/7 4 (2)
5 (4)
6 (1)
plasmei2 50,000 BALB/cByJ 0/10
200,000 BALB/cByJ 3/30 5 (2)
6 (1)
500,000 BALB/cByJ 4/30 5 (2)
6 (1)
7 (1)
plasmei2 lisp2 50,000 BALB/cJ 0/30
50,000 BALB/cByJ 0/10
200,000 BALB/cByJ 0/29
500,000 BALB/cByJ 0/26
fabb/f 500,000 BALB/cJ 0/10
500,000 BALB/cByJ 0/20
a

Salivary gland sporozoites were isolated from infected Anopheles stephensi mosquitoes, and mice were i.v. challenged with the listed number of sporozoites.

b

The number of patent mice per number of mice challenged is indicated. Detection of blood stage patent parasitemia was carried out by Giemsa-stained thin blood smear. Attenuation was considered complete if mice remained blood stage negative for 21 days.

c

If mice became blood stage patent, the day to patency is listed, with the number of mice that became patent in parentheses.

d

The marker-free GFP-luciferase-expressing 1971cl1 parasite has a wild-type phenotype in all aspects of the life cycle, including sporozoite infectivity, and was used for the creation of all of the gene knockouts.