Evidence for clonal propagation in natural isolates of Plasmodium falciparum from Venezuela

We have analyzed 75 isolates of #Plasmodium falciparum$ collected in Venezuela during both the dry (November) and rainy (May-July) seasons, with a range of genetic markers including antigen genes and 14 random amplified polymorphic DNA (RAPD) primers. Thirteen #P. falciparum$ stocks from Kenya and four other #Plasmodium$ species are included in the analysis for comparison. Cross-hybridization shows that the 14 RAPD primers reveal 14 separate regions of the parasite's genome. The #P. falciparum$ isolates are a monophyletic clade significantly different from the other #Plasmodium$ species. We identify three RAPD characters that could be useful as "tags" for rapid species identification. The Venezuelan genotypes fall into two discrete genetic subdivisions associated with either the dry or the rainy season ; the isolates collected in the rainy season exhibit greater genetic diversity. There is significant linkage disequilibrium in each seasonal subsample and in the full sample. In contrast, no linkage disequilibrium is detected in the African sample. These results support the hypothesis that the population structure of #P. falciparum$ in Venezuela, but not in Africa, is predominantly clonal. However, the impact of genetic recombination on Venezuelan #P. falciparum$ seems higher than in parasitic species with long-term clonal evolution like #Trypanosoma cruzi$, the agent of Chagas' disease. The genetic structure of the Venezuelan samples is similar to that of #Escherichia coli$, a bacterium that propagates clonally, with occasional genetic recombination. (Résumé d'auteur