Table 3.
Sample | Treatment | PPP flux | -fold increase | |
A | Trophozoites growing in normal RBCs | nil | 5.28 ± 0.84 n = 4 |
1 |
B | Trophozoites growing in oxidatively stressed normal RBCs | low XO/X b | 37.4 ± 4.5 n = 3 |
7.1 |
C | Trophozoites growing in G6PDdeficient RBCs | nil | 10.1 ± 1.3 n = 4 |
1.9 |
PPP flux was measured in Sendai-virus treated trophozoites growing in normal RBCs (A), oxidatively stressed RBCs (B) and G6PD-deficient RBCs (C). Trophozoite stage parasites were isolated from host RBCs by Sendai-virus treatment and incubated in RPMI 1640 without NaHCO3, but containing 1 μCi/ml D- [1-14C] glucose at 5% haematocrit. After 90 min of preincubation at 37°C, PPP flux was measured by quantifying produced [14C]-CO2 as indicated (see Methods). Production of [14C]-CO2 is expressed as μmol/1010 cells/h at 37°C. Mean values ± SD of n separate experiments as indicated. Significance of experiments: A vs B; A vs C; and B vs C, p < 0.001 bLow XO/X: XO 0.1 mU/ml, see legend to Table 2.