Two groups of 5-week old male BALB/c mice each were individually challenged with 5×10³ trypomastigotes of T.b. gambiense IL3707 intraperitoneally (ip) in an inoculum of 0.5 ml of PSG(+) (phosphate, sodium, glucose) buffer. This parasite is a highly virulent strain as described earlier by Inoue et al. (1998). The mice were separated into two groups of 5 mice each and labeled as experimental and control groups respectively. At four day post-infection (DPI), mice from the experimental group were started on ip treatment with Melarsoprol (Mel-B) (obtained from WHO, Geneva) at a dose of 10 mg/kg/day (Poltera et al., 1981). The treatment was by 3 series of 3 injections (1 injection per day during 3 consecutive days) separated by 7 days of rest. In the control group, PSG was administered using a similar protocol.

Two methods were used to detect parasites from infected mice. In the first instance, a drop of blood was obtained by tail snip, spread as a thin smear on a microscope slide, and observed under a light microscope at ×400 magnification. Negative samples were further examined by the more sensitive buffy coat technique as described by Murray et al. (1977). Briefly, infected blood was collected into a heparinized hematocrit tube and centrifuged at 15,000 g for 5 min. The buffy coat was collected onto a glass slide and examined through phase contrast microscopy (Inoue et al., 1998). The first series of diagnoses was done at 4 DPI (just before the start of the first schedule of treatment), 7 DPI (one day after the first schedule of treatment), 14 DPI (just before the second schedule of treatment), 17 DPI (a day after the second schedule of treatment), 24 DPI (just before the third and last schedule of treatment), and 27 DPI (a day after the last schedule of treatment). Thereafter, these diagnostic tests were conducted at regular intervals.

About 10 µl of blood from the tail of a mouse was pipetted into 100 µl of lysis buffer containing a final concentration of 10 mM Tris HCl (pH 8.0), 10mM EDTA (pH 8.0), 100 mM NaCl, 0.5% SDS and 300 µg/ml of proteinase K (Promega Biotech., USA). After incubation for 2 hr at 55℃ (Eyela, Dry Thermobath MG-1100, Tokyo, Japan), 100 µl of phenol: chloroform (1:1) was added and then vortex mixed. The samples were then centrifuged at 4,000 g for 5 min at room temperature and the supernatant (containing DNA) was transferred to a new tube. This phenol:chloroform extraction procedure was repeated twice. To the supernatant was added 10 µl of 3 M sodium acetate (pH 5.2) and 250 µl of 100% ethanol, and frozen at -80℃ for 30 min. These samples were subsequently thawed at room temperature. After centrifugation at 4,000 g for 15 min at 4℃, the supernatant was removed and 500 µl of 70% ethanol was added to the DNA pellet. The samples were again centrifuged at 4,000 g for 5 min at 4℃ and the supernatant was removed. The micro-tubes with DNA samples were then air-dried (Eyela, Centrifugal Vaporizer, Tokyo, Japan). Each DNA sample was dissolved in 10 µl of Tris-EDTA buffer and kept frozen at -30℃ until use.

DNA preparations were amplified in a final volume of 30 µl in a Perkin Elmer PCR machine (Gene Amp 2400, CA, USA). In preparation of the master mix, the following volumes were used; 20.4 µl DDW, 3 µl of 10x PCR buffer (Perkin Elmer, PE Applied Biosystems, CA, USA), 3 µl of 2 mM dNTPs (Perkin Elmer), 0.3 µl of VSG 117 primer (Science Tanaka Co. Ltd., Hokkaido, Japan) (Bromidge et al., 1993) (50 pmol/µl each of sense and antisense), 0.3 µl Taq DNA polymerase (Perkin Elmer), and 3 µl of DNA sample was used as template per reaction program. In the PCR reaction program, samples were incubated at 94℃ for 10 min in an initial denaturation step, followed by 40 cycles at 94℃ (30 sec), 51℃ (1 min) and 72℃ (2 min). The PCR reaction products were analysed by agarose gel electrophoresis and detected visually by UV transillumination (Atto Bioinstrument, Tokyo, Japan) of the ethidium bromide-stained gel.

A summary of the results from various diagnostic tests used to detect T.b. gambiense IL3707 in BALB/c mice that were either treated with Mel-B or PSG(+) is shown in Table 1. Trypanosoma brucei gambiense IL3707 is a highly virulent parasite in BALB/c, and because parasites were identifiable in blood as early as 4 DPI, both techniques by parasite examination of tail blood and PCR were positive. All the mice that were treated by Mel-B were positive for parasites by both PCR and parasitological diagnosis at 4 DPI and just before the start of the first schedule of treatment. By 7 DPI, four mice from the control group died of trypanosome infection while the surviving animal was positive for infection by both parasitological diagnosis and PCR. By 14 DPI, all control mice died of trypanosomosis.

After the first dose of Mel-B (7 DPI), all treated mice were parasitologically negative till the end of the experiment at 104 DPI. Three of the five treated mice during the period between 53 and 80 DPI were PCR positive, indicating that they still harbored an infection. Throughout the experimental period, Mel-B treated mice maintained a normal packed cell volume (PCV) and retained a healthy general appearance (Mbati, 1997).

Detection of trypanosomes in the blood of an infected individual is the most ideal method for diagnosis of African trypanosomosis. However, it has very low sensitivity, though its variant the buffy coat technique is more sensitive (Kanmogne et al., 1996) with a sensitivity of about 59% (Desquesnes, 1997). PCR is exquisitely sensitive and can provide specific and direct information regarding the presence of parasites in infected individuals. Amplification of DNA equivalent to that in a single parasite has been achieved, thus permitting identification of parasites at levels far below the detection limit of the standard parasitological techniques (Masake et al., 1997).

Between 53 and 80 DPI some Mel-B treated mice were parasitologically negative but positive by PCR, and thereafter at 88 DPI were PCR negative. It is conceivable that some trypanosomes escape the early treatment by Mel-B, but are rendered non-pathogenic and are occasionally detected by PCR. These parasites are ultimately destroyed by the host immune response, and thereafter are not detected either parasitologically or by PCR. The results obtained from this study point to the difficulty of establishing a golden standard in the development of an appropriate diagnostic regimen that would assist in the treatment follow-up of trypanosomosis. It is imperative that future studies establish a suitable cut-off time frame between treatment and follow-up (during which time PCR and parasitological diagnosis is negative) to declare an individual cured. Such data would be invaluable in designing a diagnostic regimen for shortening the current 2 year period of treatment follow-up in trypanosomosis patients. Although PCR diagnosis is too expensive for routine diagnosis, this study points to the potential of developing a diagnostic regimen for treatment follow-up that combines conventional microscopy and PCR.