Abstract

BackgroundIn the Guadeloupe and Saint Martin islands, Aedes aegypti mosquitoes are the only recognized vectors of dengue, chikungunya, and Zika viruses. For around 40 years, malathion was used as a mosquito adulticide and temephos as a larvicide. Since the European Union banned the use of these two insecticide molecules in the first decade of the 21st century, deltamethrin and Bacillus thuringiensis var. israelensis are the remaining adulticide and larvicide, respectively, used in Guadeloupe. In order to improve the management of vector control activities in Guadeloupe and Saint Martin, we investigated Ae. aegypti resistance to and mechanisms associated with deltamethrin, malathion, and temephos.MethodsAe. aegypti mosquitoes were collected from six different localities of Guadeloupe and Saint Martin. Larvae were used for malathion and temephos bioassays, and adult mosquitoes for deltamethrin bioassays, following World Health Organization recommendations. Knockdown resistance (Kdr) genotyping for V1016I and F1534C mutations, and expression levels of eight enzymes involved in detoxification mechanisms were examined in comparison with the susceptible reference Bora Bora strain.ResultsResistance ratios (RR50) calculated for Ae. aegypti larvae showed high resistance levels to temephos (from 8.9 to 33.1-fold) and low resistance levels to malathion (from 1.7 to 4.4-fold). Adult females displayed moderate resistance levels to deltamethrin regarding the time necessary to affect 50% of individuals, varying from 8.0 to 28.1-fold. Molecular investigations on adult mosquitoes showed high resistant allele frequencies for V1016I and F1534C (from 85 to 96% and from 90 to 98%, respectively), as well as an overexpression of the glutathione S-transferase gene, GSTe2, the carboxylesterase CCEae3a, and the cytochrome genes 014614, CYP6BB2, CYP6M11, and CYP9J23.ConclusionsAe. aegypti populations from Guadeloupe and Saint Martin exhibit multiple resistance to organophosphates (temephos and malathion), and pyrethroids (deltamethrin). The mechanisms associated with these resistance patterns show strong frequencies of F1534C and V1016I Kdr mutations, and an over-expression of CCEae3a, GSTe2, and four cytochrome P450 genes (014614, CYP9J23, CYP6M11, CYP6BB2). These results will form the baseline for a deeper understanding of the insecticide resistance levels and associated mechanisms of Ae. aegypti populations and will be used to improve vector control strategies in Guadeloupe and Saint Martin.

Highlights

  • In the Guadeloupe and Saint Martin islands, Aedes aegypti mosquitoes are the only recognized vectors of dengue, chikungunya, and Zika viruses

  • The mechanisms associated with these resistance patterns show strong frequencies of F1534C and V1016I Knockdown resistance (Kdr) mutations, and an over-expression of CCEae3a, glutathione S-transferase 2 (GSTe2), and four cytochrome P450 genes (014614, CYP9J23, CYP6M11, CYP6BB2)

  • These results will form the baseline for a deeper understanding of the insecticide resistance levels and associated mechanisms of Ae. aegypti populations and will be used to improve vector control strategies in Guadeloupe and Saint Martin

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Summary

Introduction

In the Guadeloupe and Saint Martin islands, Aedes aegypti mosquitoes are the only recognized vectors of dengue, chikungunya, and Zika viruses. Most of the Latin American countries and Caribbean islands were still reporting CHIKV outbreaks when a new threat was reported from Brazil—the arrival of the Zika virus (ZIKV) [3]. This arbovirus, new for the American region, was first considered as a mild disease until the discovery of Guillain-Barré and microcephaly syndromes associated with ZIKV infections [4]. In the French West Indies, both CHIKV and ZIKV are transmitted by the mosquito species Aedes aegypti, the vector of the dengue viruses that cause epidemics in the region every 2 to 3 years [6]. Since no specific treatment and/or vaccines are commonly available against CHIKV and ZIKV, and since the dengue vaccine has been deployed only very recently in a small number of experimental areas [7], the control of vectors and personal protection against mosquito bites remain the only available tools for preventing and controlling these emerging arboviral diseases [8, 9]

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