Abstract

BackgroundRelease of gene-drive mutants to suppress Anopheles mosquito reproduction is a promising method of malaria control. However, many scientific, regulatory and ethical questions remain before transgenic mosquitoes can be utilised in the field. At a behavioural level, gene-drive carrying mutants should be at least as sexually attractive as the wildtype populations they compete against, with a key element of Anopheles copulation being acoustic courtship. We analysed sound emissions and acoustic preference in a doublesex mutant previously used to collapse Anopheles gambiae (s.l.) cages.MethodsAnopheles rely on flight tones produced by the beating of their wings for acoustic mating communication. We assessed the impact of disrupting a female-specific isoform of the doublesex gene (dsxF) on the wing beat frequency (WBF; measured as flight tone) of males (XY) and females (XX) in homozygous dsxF− mutants (dsxF−/−), heterozygous dsxF− carriers (dsxF+/−) and G3 dsxF+ controls (dsxF+/+). To exclude non-genetic influences, we controlled for temperature and wing length. We used a phonotaxis assay to test the acoustic preferences of mutant and control mosquitoes.ResultsA previous study showed an altered phenotype only for dsxF−/− females, who appear intersex, suggesting that the female-specific dsxF allele is haplosufficient. We identified significant, dose-dependent increases in the WBF of both dsxF−/− and dsxF+/− females compared to dsxF+/+ females. All female WBFs remained significantly lower than male equivalents, though. Males showed stronger phonotactic responses to the WBFs of control dsxF+/+ females than to those of dsxF+/− and dsxF−/− females. We found no evidence of phonotaxis in any female genotype. No male genotypes displayed any deviations from controls.ConclusionsA prerequisite for anopheline copulation is the phonotactic attraction of males towards female flight tones within mating swarms. Reductions in mutant acoustic attractiveness diminish their mating efficiency and thus the efficacy of population control efforts. Caged population assessments may not successfully reproduce natural mating scenarios. We propose to amend existing testing protocols to better reflect competition between mutants and target populations. Our findings confirm that dsxF disruption has no effect on males; for some phenotypic traits, such as female WBFs, the effects of dsxF appear dose-dependent rather than haplosufficient.

Highlights

  • Release of gene-drive mutants to suppress Anopheles mosquito reproduction is a promising method of malaria control

  • We found that whilst male (XY) mutant flight tones were not significantly different to male controls, female (XX) mutant flight tones had significantly higher frequencies than those of their respective controls, with both showing an increase towards the male flight tone in a seemingly dose-response fashion

  • All male flight tones were found to be greater than all female flight tones (ANOVA: F(1, 114) = 336.471, P < 0.0001), but we found no differences between males (ANOVA: F(2, 57) = 0.51354, P = 0.6011)

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Summary

Introduction

Release of gene-drive mutants to suppress Anopheles mosquito reproduction is a promising method of malaria control. Malaria remains a major cause of mortality and morbidity worldwide despite significant advances made in disease control since the turn of the century [2, 3]. This is in part due to the reduced efficacy of current control tools such as insecticidal nets and indoor residual spraying, as well as the emergence of secondary disease vectors [4,5,6]. Laboratory cage trials have demonstrated that the introduction of dsxF mutants into cages of wildtype mosquitoes was sufficient to lead to eventual population collapse [10]

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