DsFoxO knockout affects development and fecundity of Drosophila suzukii

Shan Zhao1,2,3, Ruijuan Wang1,2,3, Yan Liu1,2,3

  • 1Institute of Plant Protection, Shandong Academy of Agricultural Sciences, Jinan, China.

Frontiers in Physiology
|December 11, 2023
PubMed

Insights

Knocking out the Forkhead box O (FoxO) gene in Drosophila suzukii significantly reduced survival and fecundity. Transcriptome analysis revealed altered metabolic and signaling pathways, highlighting FoxO's crucial role in fly development and reproduction.

Area of Science:

  • Genetics and Molecular Biology
  • Developmental Biology
  • Entomology

Background:

  • Forkhead box O (FoxO) transcription factors regulate vital cellular processes across species.
  • Understanding FoxO's function is crucial for various physiological and pathological mechanisms.
  • Drosophila suzukii poses significant challenges as an agricultural pest.

Purpose of the Study:

  • To investigate the impact of Forkhead box O (FoxO) gene knockout on the development and fecundity of Drosophila suzukii.
  • To elucidate the molecular mechanisms underlying these effects using transcriptome analysis.

Main Methods:

  • Established a Drosophila suzukii FoxO knockout (DsFoxO-KO) strain utilizing CRISPR/Cas9 gene editing.
  • Evaluated developmental parameters including survival rates and stage durations.
  • Assessed fecundity (egg-laying capacity) in the mutant and control strains.
  • Performed transcriptome sequencing to identify differentially expressed genes (DEGs) and analyze associated pathways.

Main Results:

  • DsFoxO-KO flies exhibited significantly lower survival rates across larval, pupal, and adult stages.
  • Developmental durations for egg, larva, and adult preoviposition periods were significantly extended in the DsFoxO-KO strain.
  • Fecundity was drastically reduced in DsFoxO-KO flies (20.31 eggs/female) compared to controls (430.47 eggs/female).
  • Transcriptome analysis identified 612 DEGs, primarily linked to metabolic processes.
  • Key signaling pathways (mTOR, MAPK, Wnt, Toll/Imd), insect hormone biosynthesis, autophagy, and apoptosis were altered in DsFoxO-KO flies.

Conclusions:

  • The knockout of DsFoxO profoundly affects Drosophila suzukii development and reproductive capacity.
  • Transcriptome data provides critical insights into the molecular pathways regulated by DsFoxO.
  • FoxO plays an essential role in Drosophila suzukii, suggesting potential targets for pest management strategies.