The Toll pathway mediates Drosophila resilience to Aspergillus mycotoxins through specific Bomanins

Rui Xu1,2,3, Yanyan Lou1,2,3, Antonin Tidu2,4

  • 1Sino-French Hoffmann Institute, Guangzhou Medical University, Guangzhou, China.

EMBO Reports
|November 2, 2022
PubMed

Insights

Host defense involves resistance and resilience. Drosophila Toll pathway and Bomanins protect against Aspergillus fumigatus toxins, enhancing host resilience to infection.

Area of Science:

  • Immunology
  • Infectious Diseases
  • Toxicology

Background:

  • Host defense mechanisms include resistance and resilience.
  • The Toll signaling pathway in Drosophila is linked to antimicrobial peptide secretion and fungal resistance.
  • Aspergillus fumigatus poses a threat through both infection and mycotoxin production.

Purpose of the Study:

  • To investigate the role of the Drosophila Toll pathway and Bomanins in host defense against Aspergillus fumigatus.
  • To determine if Toll pathway and Bomanins confer resilience against fungal mycotoxins.
  • To elucidate the mechanism by which Bomanins provide protection against mycotoxins.

Main Methods:

  • Utilizing Drosophila mutants in the Toll pathway and Bomanin locus.
  • Challenging flies with Aspergillus fumigatus and its mycotoxins (restrictocin, verruculogen).
  • Assessing survival rates and employing genetic manipulation (overexpression) to study rescue effects.

Main Results:

  • Toll pathway mutants exhibit susceptibility to mycotoxins, independent of fungal invasion.
  • Bomanin locus mutants are vulnerable to restrictocin and verruculogen.
  • Overexpression of specific Bomanins rescues mycotoxin susceptibility.
  • BomS6 expression in the nervous system enhances recovery and survival from verruculogen exposure.

Conclusions:

  • The Toll pathway and Bomanins contribute to host resilience by neutralizing mycotoxins.
  • Innate immunity provides protection against microbial toxins, increasing host tolerance to infection.
  • Secreted peptides play a crucial role in mitigating toxin-induced damage and enhancing host survival.

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