Abstract
Clinical and pathological characterisation of blood stream (BSF) and cerebrospinal fluid (CSF) forms of
Trypanosoma brucei rhodesiense trypanosome isolated from a sleeping sickness patient were investigated in
rabbits. The study aimed at investigating whether there is any significant difference in clinical and
pathological presentation in rabbits infected by the two forms of trypanosomes. Each form of parasite was
inoculated into five rabbits at 104 trypanosomes/ml while five rabbits were used as un-infected controls.
Parasitaemia development, body temperature, packed cell volume (PCV), body weight, food and water
intake, heartbeat and respiration were monitored daily for 30 days post infection when the experiment was
terminated. Pathological changes were evaluated following euthanasia. All the infected rabbits became
parasitaemic 6 days post infection (dpi) and the parasitaemia levels were significantly higher (p=0.01) for the
BSF than the CSF infected rabbits. No significant difference was observed in heartbeat, respiration, food and
water intake as well as PCV. However, CSF infected rabbits had a significantly (p=0.01) higher body
temperature and weights than BSF infected rabbits. There was no major difference in the clinical
manifestation of the disease caused by the two forms of parasite. However, temporary paralysis was observed
around the left side of the neck in one rabbit infected with CSF trypanosomes whereas mucoid stool with the
presence of amoeba cysts were observed in the rabbits infected with the BSF trypanosomes. The spleen
weights of CSF infected rabbits was heavier (3.59 ± 1.13 grams) than the BSF infected rabbits (2.92± 0.78
grams). The proportions of monocytes were significantly higher (p<0.05) in the CSF infected rabbits while
neutrophils proportions were significantly higher (p<0.05) in the BSF infected rabbits. The rest of the
haematological changes were not significantly different. Results from this study demonstrate that BSF
trypanosomes appeared relatively more virulent than the CSF trypanosomes. It would be important to carry
out similar studies using a higher number of both BSF and CSF trypanosomes isolated from the same patient
and different patients to authenticate this observation.