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. Author manuscript; available in PMC: 2022 Sep 7.
Published in final edited form as: Exp Parasitol. 2021 Jul 17;228:108135. doi: 10.1016/j.exppara.2021.108135

Table 2. Parasitological and clinical effects of Trypanosoma brucei rhodesiense strains on mouse.

Parasitological and Clinical Parameters Control KETRI
3801
KETRI
2636
EATRO
1762
KETRI
3928
Median pre-patent period (IQR) N/A 3(3–3) 4(3–5) 3(3–4) 4.5(4–8)a
✣First peak parasitaemia (dpi) N/A 4 6 6 20
†Clinical signs (days) N/A 7 8 9 33
% PCV change at day 14 dpi −2.42 −26.51 −25.48 −20.70 −3.68
% PCV change before extremis −4.09 (56) −26.51 (14) −23.95 (28) −17.58 (35) −22.43 (56)
% Weight change 16.21 −24.12 −19.75 −17.79 13.84
⨤Median survival time (days) N/A 20 33 35 -

IQR: interquartile range.

dpi: days post infection.

✣

First peak parasitaemia considered at level of ≥ antilog 7, and more often followed by reduction in parasite numbers.

†

Clinical signs observed include rough or poor coat condition and pallor of skin, reduced activity, hunched appearance, laboured breathing and crowding.

⨤

The values are estimated from Fig. 3.

a

Of the 10 mice, the pre-patent period of one animal was 17 days, and clearly an outlier.