Abstract

Mosquito larvae continuously encounter microbes in their aquatic environment, which serve as food and play a critical role in successful development. In previous work, we isolated a Chromobacterium sp. (C.sp_P) with larvicidal activity from the midgut of dengue vector Aedes mosquitoes in Panama. In this study, we found a positive correlation between initial concentrations of C.sp_P and larval mortality rates, and that C.sp_P is more efficient at inducing larval mortality in a high nutrient environment. Multiple Chromobacterium species induce larval mortality with similar efficacy to C.sp_P except for C. subtsugae. We also found that a non-lethal dose of C.sp_P lengthens development time and increases mortality over multiple developmental stages, suggesting persistent effects of exposure. Additionally, we showed that larvicidal activity persists in the larval breeding water after removal of live bacteria, and that the larvicidal factor in C.sp_P-treated water is smaller than 3 kDa, heat resistant to 90 °C, and lost after vacuum centrifugation. We showed that C.sp_P produces hydrogen cyanide in culture and in larval water at concentrations sufficient to kill An. gambiae larvae, and treatment of the larval water with a cyanide antidote eliminated larvicidal activity. We conclude that a potential mechanism by which C.sp_P can induce larval mortality is via production of hydrogen cyanide.

Highlights

  • Bacteria in larvae can be transstadially transmitted to adult midguts[5], though the mechanism of this transmission is unclear

  • We showed that larval mortality is not induced by treatment with another bacterium isolated from the mosquito midgut, Comamonas sp., when added to larval breeding water at similar concentrations as C.sp_P (Fig. S1)

  • We found that larvicidal activity is retained after removal of live C.sp_P from breeding water, indicating that the bacteria are producing a factor or factors that act(s) independently of live bacteria

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Summary

Introduction

Bacteria in larvae can be transstadially transmitted to adult midguts[5], though the mechanism of this transmission is unclear. This has implications for vector borne disease prevention, as the midgut microbiota of adult female mosquitoes has been shown to influence vector competence for Plasmodium falciparum (the etiological agent of malaria) and dengue virus[8,9]. Multiple bacteria prevent infection by P. falciparum when present in the midgut of adult female An. gambiae, a primary mosquito vector of this parasite[10–12]. This and other species from this genus are ingested by mosquito larvae and release toxins in the larval digestive tract[16]. We aimed to further characterize the larvicidal activity of C.sp_P and to better understand the mechanism of larval killing by the bacteria

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