Abstract

Zika virus infection and dengue and chikungunya fevers are emerging viral diseases that have become public health threats. Their aetiologic agents are transmitted by the bite of genus Aedes mosquitoes. Without effective therapies or vaccines, vector control is the main strategy for preventing the spread of these diseases. Increased insecticide resistance calls for biorational actions focused on control of the target vector population. The chitin required for larval survival structures is a good target for biorational control. Chitin synthases A and B (CHS) are enzymes in the chitin synthesis pathway. Double-stranded RNA (dsRNA)-mediated gene silencing (RNAi) achieves specific knockdown of target proteins. Our goal in this work, a new proposed RNAi-based bioinsecticide, was developed as a potential strategy for mosquito population control. DsRNA molecules that target five different regions in the CHSA and B transcript sequences were produced in vitro and in vivo through expression in E. coli HT115 and tested by direct addition to larval breeding water. Mature and immature larvae treated with dsRNA targeting CHS catalytic sites showed significantly decreased viability associated with a reduction in CHS transcript levels. The few larval and adult survivors displayed an altered morphology and chitin content. In association with diflubenzuron, this bioinsecticide exhibited insecticidal adjuvant properties.

Highlights

  • Arboviruses, such as Yellow fever virus, Dengue virus serotypes 1–41,2, Zika virus and Chikungunya virus[3], are responsible for significant human morbidity and mortality in affected regions

  • Blast analysis of the Ae. aegypti protein database allowed the identification of two proteins with high identity to the Tribolium castaneum CHS genes AAEL002718-RA (CHSA) (NP_0010394021) query sequence: AAEL002718-PA, CHSA, and AAEL005618-PA, CHSB

  • In the chitin synthase protein (CHS) nucleotide alignment, the regions chosen as targets for gene silencing were highlighted: CHSA 2718_1 (1550–1750 nt), 2718_2 (1064–1291 nt), 2718_3 (1928–2014 nt), CHSB 5618_1 (1205–1384 nt) and 5618_2 (693–940 nt) (Table 1)

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Summary

Introduction

Arboviruses, such as Yellow fever virus, Dengue virus serotypes 1–41,2, Zika virus and Chikungunya virus[3], are responsible for significant human morbidity and mortality in affected regions. These diseases are transmitted by mosquito bites and have an enormous impact on public health. The specificity of RNAi makes these approaches environmentally safer than other methods currently in use, minimizing toxicity to non-target species and reducing the possibility of resistance in insect populations[33,34,35]

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