PxSpätzle3 Regulates the Toll Pathway To Affect Bacillus thuringiensis Susceptibility of Plutella xylostella

J Agric Food Chem. 2025 Mar 5;73(9):5129-5139. doi: 10.1021/acs.jafc.4c11380. Epub 2025 Feb 18.

Abstract

Spätzle is an important messenger in the Toll pathway of the insect innate immune system. However, the function of Spätzle in regulating the Toll pathway in Bacillus thuringiensis (Bt) susceptibility of Plutella xylostella is unclear. In this study, we cloned the Spätzle3 gene of P. xylostella. Molecular docking and yeast two-hybrid experiments indicated that PxSpätzle3 combined with PxToll6 to regulate the Toll pathway. After knocking out PxSpätzle3, the expression of downstream Toll pathway genes and antimicrobial peptides (AMPs) decreased. Antibacterial assays showed that PxGloverin2 could inhibit Bt8010. Further bioassays revealed that the susceptibility of the mutant to Bt8010 was significantly higher than that of the wild type. Intriguingly, the gut bacteria Enterobacter sp. EbPXG5 enhanced the lethality of Bt8010 to the mutant P. xylostella. Our findings clarify that PxSpätzle3 activates the Toll pathway by binding with PxToll6, regulates AMP production, and affects the susceptibility of P. xylostella to Bt8010. Additionally, our study uncovers the role of gut bacteria in this process. These insights provide new ideas for the sustainable control of pests.

Keywords: Bacillus thuringiensis; Plutella xylostella; Spätzle; Toll pathway; antimicrobial peptides; innate immunity.

MeSH terms

  • Animals
  • Antimicrobial Peptides / chemistry
  • Antimicrobial Peptides / genetics
  • Antimicrobial Peptides / metabolism
  • Antimicrobial Peptides / pharmacology
  • Bacillus thuringiensis* / chemistry
  • Bacillus thuringiensis* / genetics
  • Bacterial Proteins / genetics
  • Bacterial Proteins / metabolism
  • Immunity, Innate
  • Insect Proteins* / chemistry
  • Insect Proteins* / genetics
  • Insect Proteins* / metabolism
  • Larva / growth & development
  • Molecular Docking Simulation
  • Moths* / drug effects
  • Moths* / genetics
  • Moths* / immunology
  • Signal Transduction / drug effects
  • Toll-Like Receptors / genetics
  • Toll-Like Receptors / immunology
  • Toll-Like Receptors / metabolism

Substances

  • Insect Proteins
  • Toll-Like Receptors
  • Antimicrobial Peptides
  • Bacterial Proteins