Figure 1.
Figure 1. Increased resistance to CM in CCR5-deficient mice infected with PbA. (A-B) CM incidence occurring between day 7 and day 10 (A) and survival time (B) of WT (n = 13), F1 (n = 7), and KO (n = 10) mice infected with PbA (106 PEs). Neurologic signs first appear late on days 7 through 10 (B, shaded area), with death occurring in less than 24 hours after their onset. On day 10, as calculated by Fisher exact test, P < .05 between WT (or F1) and KO mice. This experiment is representative of 3 experiments. (C-D) Parasitemia (C) and hemoglobin levels (D) of PbA-infected WT (n = 5) and KO (n = 5) mice. Mortality is indicated on the first graph at the top (WT mice) and at the bottom (KO mice) as the number of dead mice (d) on that day. F1 mice have parasitemia and hemoglobin level profiles similar to these observed for the WT mice. Error bars represent mean (SE) of 5 mice.

Increased resistance to CM in CCR5-deficient mice infected with PbA. (A-B) CM incidence occurring between day 7 and day 10 (A) and survival time (B) of WT (n = 13), F1 (n = 7), and KO (n = 10) mice infected with PbA (106 PEs). Neurologic signs first appear late on days 7 through 10 (B, shaded area), with death occurring in less than 24 hours after their onset. On day 10, as calculated by Fisher exact test, P < .05 between WT (or F1) and KO mice. This experiment is representative of 3 experiments. (C-D) Parasitemia (C) and hemoglobin levels (D) of PbA-infected WT (n = 5) and KO (n = 5) mice. Mortality is indicated on the first graph at the top (WT mice) and at the bottom (KO mice) as the number of dead mice (d) on that day. F1 mice have parasitemia and hemoglobin level profiles similar to these observed for the WT mice. Error bars represent mean (SE) of 5 mice.

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