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Zoh D. D., Alou L. P. A., Toure M., Pennetier Cédric, Camara S., Traore D. F., Koffi A. A., Adja A. M., Yapi A., Chandre Fabrice. (2018). The current insecticide resistance status of Anopheles gambiae (s.l.) (Culicidae) in rural and urban areas of Bouaké, Cote d'Ivoire. Parasites and Vectors, 11, p. art. 118 [12 p.]. ISSN 1756-3305.

Titre du document
The current insecticide resistance status of Anopheles gambiae (s.l.) (Culicidae) in rural and urban areas of Bouaké, Cote d'Ivoire
Année de publication
2018
Type de document
Article référencé dans le Web of Science WOS:000427131000001
Auteurs
Zoh D. D., Alou L. P. A., Toure M., Pennetier Cédric, Camara S., Traore D. F., Koffi A. A., Adja A. M., Yapi A., Chandre Fabrice
Source
Parasites and Vectors, 2018, 11, p. art. 118 [12 p.] ISSN 1756-3305
Background: Several studies were carried out in experimental hut station in areas surrounding the city of Bouake, after the crisis in Cote d'Ivoire. They reported increasing resistance levels to insecticide for malaria transmiting mosquitoes. The present work aims to evaluate the current resistance level of An. gambiae (s.l.) in rural and urban areas in the city of Bouake. Methods: Larvae of Anopheles gambiae (s.l.) were collected from five different study sites and reared to adult stages. The resistance status was assessed using the WHO bioassay test kits for adult mosquitoes, with eight insecticides belonging to pyrethroids, organochlorines, carbamates and organophosphates classes. Molecular assays were performed to identify the molecular forms of An. gambiae (s.l.), the L1014F kdr and the ace-1R alleles in individual mosquitoes. The synergist PBO was used to investigate the role of enzymes in resistance. Biochemical assays were performed to detect potential increased activities in mixed function oxidase (MFO) levels, non-specific esterases (NSE) and glutathione S-transferases (GST). Results: High resistance levels to pyrethroids, organochlorines, and carbamates were observed in Anopheles gambiae (s.l.) from Bouake. Mortalities ranged between 0 and 73% for the eight tested insecticides. The pre-exposure to PBO restored full or partial susceptibility to pyrethroids in the different sites. The same trend was observed with the carbamates in five sites, but to a lesser extent. With DDT, pre-exposure to PBO did not increase the mortality rate of An. gambiae (s.l.) from the same sites. Tolerance to organophosphates was observed. An increased activity of NSE and higher level of MFO were found compared to the Kisumu susceptible reference strain. Two molecular forms, S form [(An. gambiae (s.s)] and M form (An. coluzzi) were identified. The kdr allele frequencies vary from 85.9 to 99.8% for An. gambiae (s.s.) and from 81.7 to 99.6% for An. coluzzii. The ace-1R frequencies vary between 25.6 and 38.8% for An. gambiae (s.s.) and from 28.6 to 36.7% for An. coluzzii. Conclusion: Resistance to insecticides is widespread within both An. gambiae (s. s.) and An. coluzzii. Two mechanisms of resistance, i.e. metabolic and target-site mutation seemed to largely explain the high resistance level of mosquitoes in Bouake. Pyrethroid resistance was found exclusively due to the metabolic mechanism.
Plan de classement
Sciences fondamentales / Techniques d'analyse et de recherche [020] ; Entomologie médicale / Parasitologie / Virologie [052]
Description Géographique
COTE D'IVOIRE ; BOUAKE
Localisation
Fonds IRD [F B010072487]
Identifiant IRD
fdi:010072487
Contact