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Mem. Inst. Oswaldo Cruz ; 102(3): 293-298, June 2007. tab
Article in English | LILACS | ID: lil-452504

ABSTRACT

In Western Amazon areas with perennial malaria transmission, long term residents frequently develop partial immunity to malarial infection caused either by Plasmodium falciparum or P. vivax, resulting in a considerable number of non-symptomatically infected individuals. For yet unknown reasons, these individuals sporadically develop symptomatic malaria. In order to identify if determined parasite genotypes, defined by a combination of eleven microsatellite markers, were associated to different outcomes - symptomatic or asymptomatic malaria - we analyzed infecting P. falciparum parasites in a suburban riverine population. Despite of detecting a high degree of diversity in the analyzed samples, several microsatellite marker alleles appeared accumulated in parasites from non-symptomatic infections. This result may be interpreted that a number of microsatellites, which are not directly related to antigenic features, could be associated to the outcome of malarial infection. The result may also point to a low frequency of recombinatorial events which otherwise would dissociate genes under strong immune pressure from the relatively neutral microsatellite loci.


Subject(s)
Humans , Animals , DNA, Protozoan/genetics , Malaria, Falciparum/parasitology , Microsatellite Repeats/genetics , Plasmodium falciparum/genetics , Alleles , Brazil , Genetic Markers , Genotype , Polymerase Chain Reaction , Risk Factors
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