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Insecticide Resistance Status of the Anopheles Funestus Population in Central African Republic: a Challenge in the War

Overview
Journal Parasit Vectors
Publisher Biomed Central
Date 2016 Apr 27
PMID 27113956
Citations 17
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Abstract

Background: In the Central African Republic, malaria is a major public health problem and the leading cause of death among children. This disease appears to be hyperendemic but no substantial entomological data, including data on Anopheles spp. susceptibility to insecticides, is available. This study evaluates, for the first time in the CAR, the status of insecticide resistance in the Anopheles funestus population, the second major vector of malaria in Africa.

Methods: WHO standard bioassay susceptibility tests were performed on the An. funestus population using F1 generation from gravid females mosquitoes (F0) collected by manual aspirator sampling of households in Gbanikola, Bangui in October 2014 to assess: (i) An. funestus susceptibility to bendiocarb, malathion, permethrin, lamda-cyhalothrin, deltamethrin and DDT, and (ii) the effect of pre-exposure to the piperonyl butoxide (PBO) synergist on insecticide susceptibility. Additional tests were conducted to investigate metabolic resistance status (cytochrome P450 monooxygenases, glutathione S-transferases, and esterases).

Results: A high phenotypic resistance of An. funestus population to malathion, DDT and pyrethroids was observed with a mortality rate ranging from 23 to 74%. For the pyrethroid groups, the mortality rate was 35, 31 and 23% for lambda-cyhalothrin, deltamethrin, and permethrin, respectively. In contrast a 100% mortality rate to bendiocarb was recorded. Knockdown time (KDT) was long for all pyrethroids, DDT and malathion with KDT50 higher than 50 min. Pre-exposure of An. funestus to PBO synergist significantly restored susceptibility to all pyrethroids (Fisher's exact test P <0.0001) but not in DDT (Fisher's exact test P = 0.724). Data from biochemical tests suggest the involvement of cytochrome P450 monooxygenases, esterases and glutatione S-transferases in the resistance of An. funestus population from Gbanikola (Wilcoxon test P <0.05).

Conclusion: Evidence of biochemical resistance to insecticide was detected in An. funestus population from the district of Gbanikola, Bangui. This study suggests that detoxifying enzymes are involved in insecticide resistance of An. funestus. However, despite disruptive violence, further research is urgently needed to assess the insecticide susceptibility status of An. funestus population in all CAR regions; insecticide resistance could rapidly compromise the success of malaria control programs.

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References
1.
Casimiro S, Coleman M, Mohloai P, Hemingway J, Sharp B . Insecticide resistance in Anopheles funestus (Diptera: Culicidae) from Mozambique. J Med Entomol. 2006; 43(2):267-75. DOI: 10.1603/0022-2585(2006)043[0267:iriafd]2.0.co;2. View

2.
Feachem R, Sabot O . Global malaria control in the 21st century: a historic but fleeting opportunity. JAMA. 2007; 297(20):2281-4. DOI: 10.1001/jama.297.20.2281. View

3.
Feachem R, Sabot O . A new global malaria eradication strategy. Lancet. 2008; 371(9624):1633-5. DOI: 10.1016/S0140-6736(08)60424-9. View

4.
Okoye P, Brooke B, Koekemoer L, Hunt R, Coetzee M . Characterisation of DDT, pyrethroid and carbamate resistance in Anopheles funestus from Obuasi, Ghana. Trans R Soc Trop Med Hyg. 2008; 102(6):591-8. DOI: 10.1016/j.trstmh.2008.02.022. View

5.
Czeher C, Labbo R, Arzika I, Duchemin J . Evidence of increasing Leu-Phe knockdown resistance mutation in Anopheles gambiae from Niger following a nationwide long-lasting insecticide-treated nets implementation. Malar J. 2008; 7:189. PMC: 2562389. DOI: 10.1186/1475-2875-7-189. View