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Academic literature on the topic 'Paludisme – Afrique occidentale'
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Dissertations / Theses on the topic "Paludisme – Afrique occidentale"
Gay, Frédérick. ""Chimiorésistance de "Plasmodium falciparum" : études sur les populations impaludées et sur les populations plasmodiales"." Montpellier 2, 1992. http://www.theses.fr/1992MON20277.
Full textRoustant, Frédérique. "Le paludisme en zone de savane africaine : étude épidémiologique en mileu rural et péri-urbain." Aix-Marseille 1, 1994. http://www.theses.fr/1994AIX11077.
Full textBenoît-Vical, Françoise. "Evaluation de l'activité antimalarique in vitro de divers extraits végétaux bruts et purifiés sur Plasmodium falsiparum." Montpellier 1, 1997. http://www.theses.fr/1997MON13511.
Full textLouvet, Samuel. "MODULATIONS INTRASAISONNIÈRES DE LA MOUSSON D'AFRIQUE DE L'OUEST ET IMPACTS SUR LES VECTEURS DU PALUDISME À NDIOP (SÉNÉGAL) : DIAGNOSTICS ET PRÉVISIBILITÉ." Phd thesis, Université de Bourgogne, 2008. http://tel.archives-ouvertes.fr/tel-00333234.
Full textDjogbenou, Luc Salako. "Dynamique des mécanismes de résistance aux insecticides liés à la modification de cibles dans les populations naturelles d’Anopheles gambiae s. L. D’Afrique de l’Ouest." Montpellier 2, 2008. http://www.theses.fr/2008MON20085.
Full textVector control is one of the most effective methods of malaria prevention in sub-Saharan Africa. Resistance to pyrethroid insecticides (kdr mutation) has appeared in vectors of malaria, especially in An. Gambiae s. L. The effectiveness of pyrethroid-treated nets seems to be threatened by this resistance and the search for alternative insecticides is a priority. In the laboratory, as in field studies, the presence of an acetylcholinesterase mutation (ace-1R), which confers resistance to carbamates and organophosphates (insecticides proposed as alternatives to pyrethroids), provides an advantage to An. Gambiae s. S. In contact with the insecticide. This advantage is shown in heterozygotes by measuring the partial dominance of the gene. In the absence of insecticides, a genetic cost affects some life history traits of resistant mosquitoes, reducing their chances of reproduction. This genetic cost is probably due to the important reduction of enzymes activity coded by ace-1R. The ace-1R mutation is already present in high frequencies in natural populations of West Africa. This distribution results from a single mutation event that has been spread across our study sites by migration. Its presence in M and S forms of Anopheles gambiae s. S. Is due to a introgression phenomenon. The mutation is present in the two alleles : one ace-1R resistant allele made of a copy of the ace-1 gene carrying the G119S mutation, and one duplicated allele, Ag-ace-1D, that carries one susceptible and one resistant G119S copy linked on the same chromosome. This duplication might reduce the cost associated with the resistance and impair vector control strategies based on alternating insecticides. These alleles are in competition in natural populations of Anopheles gambiae, the primary vector of malaria in West Africa. In Benin, two species of the An. Gambiae complex (An. Gambiae s. S. And An. Arabiensis) were found either alone or in sympatry. In An. Gambiae s. S. , the S molecular form is present in almost all localities, whereas the M form was found in high proportions only in the south and the north. The study of resistance mechanisms due to target site modification in Anopheles gambiae s. L. And Culex quinquefasciatus reveal that many populations are resistant to DDT and permethrin. In Anopheles gambiae, the comparison of mortality with DDT and permethrin indicates that the resistance is due in large part to the kdr mutation. However, the distribution of this mutation is variable between sites. Our study showed a strong link between the frequency of the kdr mutation and agricultural use of insecticide against cotton pests. In all cases, very few samples of the two species (An. Gambiae and Cx. Quinquefasciatus) were found to be resistant to the carbamates and organophosphates used. The frequency of the ace-1R mutation was also small. This indicates that the use of carbamates and organophosphates might still be used in a resistance management strategy. These studies offer interesting perspectives on the possibilities of vector control for prevention of malaria. In fact, they allow improving our understanding of the biology and ecology of the vector and on the resistance mechanisms. In the pursuit of a better vector control strategy, it would be interesting for scientists in developed countries studying genomic to work in collaboration with scientists in areas where malaria is present and with local institutions