Table 1. Analysis of apoptosis in thymus.
Groupsa | 3 days p.i.b | 5 days p.i.b | ||
Annexin V+PI-±SE (%) | Annexin V+PI+±SE (%) | Annexin V+PI-±SE (%) | Annexin V+PI+±SE (%) | |
VK627 | 19.59±1.83c | 1.16±0.12 | 16.82±1.37 c | 2.87±0.32 |
rVK627E | 9.43±1.52 | 1.21±0.17 | 10.36±1.01 | 1.84±0.12 |
TsE627 | 10.21±1.45d | 1.12±0.28 | 11.01±1.13 d | 1.13±0.23 |
rTsE627K | 20.58±3.03 | 1.31±0.34 | 19.19±1.21 | 2.11±0.07 |
Mock | 11.88±1.84 | 0.96±0.07 | 12.11±1.45 | 0.87±0.06 |
Mice (n = 6/group) were i.n. infected with 104 PFU of VK627, rVK627E, TsE627, rTsE627K.
Mice were euthanized on 3 day p.i. and 5 day p.i., and three thymuses per group per time point were prepared for single cell suspension. Following staining with AnnexinV and PI, apoptotic cells were analyzed by flow cytometry. The early apoptotic cells were determined by annexin V+/PI− and late apoptotic cells were determined by annexin V+/PI+. The data shown represents mean ± SD for three independent experiments.
p<0.05 compared to rVK627E;
p<0.05 compared to rTsE627K.