Insect pathogenic fungus interacts with the gut microbiota to accelerate mosquito mortality

Ge Wei1,2, Yiling Lai1, Guandong Wang1,2

  • 1Key Laboratory of Insect Developmental and Evolutionary Biology, Institute of Plant Physiology and Ecology, Shanghai Institutes for Biological Sciences, Chinese Academy of Sciences, Shanghai 200032, China.

Insights

The insect gut microbiota accelerates mosquito death from fungal infections. The pathogenic fungus Beauveria bassiana interacts with gut bacteria, promoting pathogen growth and mosquito mortality.

Area of Science:

  • Insect pathology
  • Microbial ecology
  • Host-pathogen interactions

Background:

  • The insect gut microbiota influences host interactions with pathogens.
  • Entomopathogenic fungi infect insects via the cuticle, unlike ingested pathogens.
  • The role of gut microbiota in fungal pathogenesis is largely unknown.

Purpose of the Study:

  • To investigate the interaction between the gut microbiota and entomopathogenic fungi in mosquitoes.
  • To elucidate the mechanisms by which gut microbiota affects fungal pathogenesis.

Main Methods:

  • Topical infection of mosquitoes with Beauveria bassiana.
  • Comparison of mortality rates between mosquitoes with and without gut microbiota.
  • Analysis of gut microbiota composition and bacterial load post-infection.
  • Gene expression analysis of antimicrobial peptides and dual oxidase (Duox).

Main Results:

  • Mosquitoes with gut microbiota exhibited significantly faster mortality after B. bassiana infection.
  • Fungal infection induced gut dysbiosis, increasing bacterial load and decreasing diversity.
  • Serratia marcescens overgrowth in the midgut and translocation to hemocoel enhanced fungal killing.
  • B. bassiana toxin oosporein down-regulated Duox expression in the mosquito midgut.

Conclusions:

  • The gut microbiota significantly contributes to B. bassiana-induced mosquito mortality.
  • Fungal infection disrupts gut homeostasis, favoring opportunistic bacterial pathogens.
  • Oosporein-mediated Duox suppression is a key mechanism in fungal pathogenesis.