1. Nakayima J, P.P. Abila, L.M. Okedi, M.Akol, V.Alioni and C.P. Otim
Assessment of the prevalence of sleeping sickness in Lango and Teso Sub regions, Uganda
Nakayima J, P.P. Abila, L.M. Okedi, M.Akol, V.Alioni and C.P. Otim
National Livestock Resources Research Institute (NaLIRRI), P.O. Box 96 Tororo, Uganda

2. Introduction
Human African Trypanosomiasis (HAT) - sleeping sickness, is a major cause of mortality and morbidity in sub-Saharan Africa
Sleeping sickness, is a disease caused by infection with protozoan parasite and transmitted by the tsetse fly
Trypanosoma brucei gambiense (West African form)
Trypanosoma brucei rhodesiense (East African form)
Tsetse transmitted trypanosomiasis continues to be a major public health problem in districts bordering the Lake Victoria-River Nile- Lake Kyoga

3. Introduction
In the past decade, rhodesiense sleeping sickness has continued to be reported in:
North and Eastern Uganda in districts of:
Soroti, Kaberamaido and now Lira

4. Objectives
To assess the sleeping sickness status north of Lake Kyoga, Uganda
To establish the risk of gambiense and rhodesiense HAT overlap in Lango and Teso Sub regions

5. Materials and Methods Study Area
Aloi is in lira district North of lat 2ºN
Lira is supplied by the river systems of Aswa and Pager

6. Materials and Methods Methods used were to assess
prevalence of trypanosomiasis in the study areas
also to ascertain the possibility of overlap of T. b. rhodesiense and T. b. gambiense

7. Lymph node aspirate
All patients were systematically screened for enlarged cervical lymph nodes (CLN)
When CLN was enlarged, they were punctured:
The fresh aspirate is expelled onto a slide,
Cover slips were applied to spread the sample aspirate to facilitate the reading
The wet preps were then quickly examined by microscope (M ×40) for the presence of motile trypanosomes

8. CATT
Card agglutination test for trypanosomiasis (CATT) is a specific test for T.b.gambiense
All patients were screened with CATT in order to ascertain the possibility of T. b. gambiense in the known T. b. rhodesiense area

9. Wet film Examination of wet film was done on all suspects
In wet blood films, 5 to 10 μl of finger prick blood was placed on a slide and examined microscopically (M ×40) under a cover slip

10. Heamatocrit Centrifugation Technique (HCT)
HCT was used to screen all the patients given the fact that it concentrates the parasites in one field for easy detection of the parasites
Capillary tubes containing anticoagulant were three-quarters filled with finger prick blood
The dry end sealed with plasticine
By high-speed centrifugation about 13,000 rpm for 6 to 8 min, trypanosomes are concentrated at the buffy coat between the plasma and the erythrocytes
The capillary tubes were mounted in a special holder, and directly examined at low magnification (×10 or ×16) for mobile parasites

11. Animal inoculation
Each isolate was inoculated in both Mastomys natalensis and Swiss mice with a view that:
if infection established in both species, then the infection is T.b. rhodesiense,
but if infection established only in Mastomys rats, then we suspect T.b. gambiense
parasitaemia examined after a period of 3 days

12. DNA analysis
Samples were analyzed using Loop Mediated Isothermal Amplification (LAMP) for Detection of HAT
DNA was extracted from parasites and mammalian cells using “GENE ALL” total DNA extraction kit for blood
LAMP was carried out with the Loopamp DNA amplification kit (Eiken Chemical Co. Ltd, Japan)
LAMP reaction mixture (25ul) contained template DNA, 40 pmol each of FIP and BIP (inner primers), 5 pmol each of F3 and B3 (outer primers), 8U of Bst DNA polymerase large fragment (New England Biolabs Inc.)
1.4 mM deoxynucleoside triphosphates, 0.8 M betaine, 20 mM Tris-HCL (pH 8.8), 10 mM KCL, 10 mM (NH4)2SO4, 8 mM MgSO4, and 0.1% Tween 20
A negative control reaction was incorporated by omitting template DNA from one reaction
The reaction mixture was incubated at 65ºC for 1 hr and heated at 80ºC for 2 min to terminate the reaction

13. Results: Microscopy District S/County Sample Positive Lira Aloi 348 6
Dokolo
1158 1
Kaberamaido
Otuboi
784
Soroti
Serere
359
Total
2648 9

14. Results: Rat inoculations
Parasitaemia was established in both Swiss mice and Mastomys sp. rats
No positive agglutination test was revealed by CATT, a test specific for T.b. gambiense

15. Disease stage Eight of the cases taken to Lwala Hospital:
were stage II with WBC count > 5 cells/mm3 and trypanosomes in CSF.
only one was stage I with < 5 cells/mm3 and no CNS involvement.

16. Results: DNA analysis
Six of the 9 HCT detected cases were found positive by LAMP reaction for T. b. rhodesiense detection
Samples were also picked from 8 suspected patients who were HCT negative but had presenting signs like:
lymph node enlargement and
fever and
The suspected cases tested negative with lamp.

17. Discussions
A new sleeping sickness focus north of Lake Kyoga has been revealed in Aloi, Lira district
The trypanosome species isolated from the study area was T. b. rhodesiense
Infections established in both rodent species
No positive agglutination test was revealed by CATT, a test specific for T.b.gambiense. Thus, there is no T.b.gambiense overlap in this area
The exercise rules out the possibility of HAT overlap of
T.b. gambiense and T.b.rhodesiense within the study area so far

18. Discussions

19. Acknowledgements EANETT DDHS: Lira, Soroti, Kaberamaido, Dokolo
Directorates of Production: Lira, Soroti, Kaberamaido, Dokolo
Director, NaLIRRI
Prof. Sugimoto (Hokkaido, Jp)

20. Thank you for your attention