A secondary metabolite acting as a signalling molecule controls Pseudomonas entomophila virulence
Isabelle Vallet-Gely1, Onya Opota, Audrey Boniface
1Centre de Génétique Moléculaire, CNRS, 91198 Gif-sur-Yvette, France. vallet@cgm.cnrs-gif.fr
Abstract:
Pseudomonas entomophila is an entomopathogenic bacterium that is lethal to Drosophila melanogaster within 1-2 days of ingestion of high doses. Flies orally infected with P. entomophila rapidly succumb despite the induction of both local and systemic immune responses. Recent studies suggest that its virulence relies on its ability to cause irreversible damages to the intestinal epithelium, in contrast to what is observed with milder pathogenic bacteria such as Erwinia carotovora carotovora Ecc15 or Pseudomonas aeruginosa PA14. The GacS/GacA two-component system plays a key role in P. entomophila pathogenicity. Here, we report the identification of the pvf genes, whose products are involved in production of a secondary metabolite involved in P. entomophila virulence. A pvf mutant is impaired in its ability to persist within the gut, to trigger the fly immune responses and to inflict gut damages. The expression of several genes is affected in a pvf mutant, independently of the Gac system. Moreover, growing a pvf mutant in medium supplemented with supernatant extracts from either the wild-type strain or a gacA mutant restore its pathogenicity. Collectively, our results indicate that we identified genes involved in the synthesis of a signalling molecule that controls P. entomophila virulence independently from the Gac system.
Insights
Pseudomonas entomophila virulence relies on a novel signaling molecule, independent of the Gac system. This molecule is crucial for bacterial gut persistence, immune response triggering, and host damage in Drosophila melanogaster.
Area of Science:
- Microbiology
- Molecular Biology
- Insect Pathology
Background:
- Pseudomonas entomophila is an entomopathogenic bacterium lethal to Drosophila melanogaster.
- Its virulence involves irreversible intestinal epithelium damage, unlike milder pathogens.
- The GacS/GacA two-component system is critical for P. entomophila pathogenicity.
Purpose of the Study:
- Identify genes and molecules controlling P. entomophila virulence.
- Investigate the role of these factors independently of the Gac system.
- Characterize the function of the pvf genes in bacterial pathogenesis.
Main Methods:
- Genetic analysis to identify virulence factor (pvf) genes.
- Construction and characterization of a pvf mutant.
- Assessment of bacterial persistence, immune response, and gut damage in infected flies.
- Gene expression analysis in wild-type and mutant strains.
- Complementation experiments using supernatant extracts.
Main Results:
- The pvf genes are identified as crucial for producing a secondary metabolite involved in virulence.
- A pvf mutant shows impaired gut persistence, reduced immune response induction, and diminished gut damage.
- Gene expression changes in the pvf mutant are independent of the Gac system.
- Restoration of pathogenicity in the pvf mutant by wild-type or gacA mutant supernatant extracts.
Conclusions:
- The study identifies pvf genes involved in synthesizing a signaling molecule controlling P. entomophila virulence.
- This virulence mechanism operates independently of the Gac system.
- The findings reveal a novel pathway for bacterial pathogenesis in insects.
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