Abstract:
A total of 570 samples of both sexes were collected from malaria-suspected patients who
attended Medani Pediatric and adult teaching Hospital during August-December 2005.
That period was the peak of malaria transmission season in the area. Out of these, 155
samples were detected to be positive for malaria and 140 cases (90%) out of the positive
samples were due to Plasmodium falciparum and the rest, which were excluded from the
study, (15 patients) were due to other plasmodium species. Based on the clinical data, the
Plasmodium faciparum patients were classified as asymptomatic (7 patients) and
symptomatic patients (133 patients). Among the symptomatic patients, 106 (75.7%) were
detected as mild anemia, 24 (17.1%) as severe anemia and 10 (7.2%) as subject with
normal hemoglobin level. Among the symptomatic patients also there are 22 cerebral
malaria, 12 pregnant, 8 patient with splenomegally and two with hepatomegally. Patients
are categorized into 4 age groups, group 1 has 71 (50.7%) individuals followed by groups
2,3, and 4 which have 44 (31.4%), 17 (12.1%), and 8 (5.8%) individuals respectively.
One of the goals of this work was molecular characterization of the parasite populations
circulating in Gazira, central part of Sudan. This work investigated the extent of genetic
polymorphism in P. falciparum field isolates from Gazira. Allelic diversity was analyzed
in the highly polymorphic parasite genes encoding the merozoite surface proteins-1
(MSP-1) and -2 (MSP-2) and the glutamate-rich protein (GLURP) by the polymerase
chain reaction. Different size polymorphism was detected in all genes analyzed, with 13
and 8 variants for the MSP-1 and MSP-2 alleles, respectively, and 5 size variants for the
GLURP. Moreover, based on the studied genetic markers, most infections consisted of
more than one genetically distinct parasite clones. These results suggest that the P.
falciparum parasite populations circulating in this region are genetically homogeneous
and point to an association between the extent of parasite genetic diversity and the
intensity of malaria transmission
Different genotypes were found to be associated with severity of disease. In this respect,
association between high parasitemia and anemia on one hand and variants of K1 were
found, MAD20, RO33 and FC allelic families on the other hand. In addition, some
IV
variants of the allelic families were found to be associated with children between 0-10
years of age. Individuals living in malaria endemic areas generally harbor multiple
parasite strains which known by Multiplicity of infection (MOI) and can be used as an
indicator of immune status. One of the goals of this study was to examine the MOI in
Plasmodium faciparum-infected samples and to relate it to severity of the disease. Results
of genotyping reveal that MOI was significantly higher at the end of transmission season
and the majority of PCR positive subjects had multiple infections at that time points
(54%). No association between MOI and severity of disease was observed. MOI did not
vary over age at any time points. There was a significant correlation between MOI and
parasite density, as the higher parasite counts increases the probability of having multiple
infections. One of the major goals of this work was the investigation of the immune
response of glutamate rich protein among the study population as an indicator for
acquisition of protective immunity. This is achieved by estimation of IgG, IgG1, IgG3
and IgM antibodies directed against GLURP-R0, GLURP-R1 and GLURP-R2. The
results indicate comparatively high titres of these antibodies to the three fragments of
GLURP, although R2 and R0 encountered with significantly higher concentrations of the
antibodies. The results also showed that IgG3 was presented with high concentration
followed by IgG1 suggesting their protective role and their major participation in
acquisition of immunity to malaria. The results of association between immune response
and different strain of Plasmodium population isolated in this work reveal that some
strain are encountered with high immune response and severity of malaria. This
association supports the speculation of the presence of strain-specific immunity and
premunition among inhabitants of malaria endemic areas. The results also re-enforce the
ongoing announcement that any future malaria vaccine should include GLURP fragments
notably GLURP-R2 and GLURP-R0.
Ethical clearance for this work has been approved by the ethical committee of the
institute of endemic diseases, faculty of medicine, University of Khartoum.