Azadirachtin disrupts ecdysone signaling and alters sand fly immunity
Jazyk angličtina Země Anglie, Velká Británie Médium electronic
Typ dokumentu časopisecké články
Grantová podpora
101067053
HORIZON EUROPE Marie Sklodowska-Curie Actions
2021-1-IT02-KA131-HED-00000-6888
Erasmus+
PE00000007 INFACT
NextGeneration EU-MUR PNRR Extended Partnership initiative on Emerging Infectious Diseases
CePaViP (16_019/0000759)
European Regional Development Fund (ERDF)
PubMed
39707409
PubMed Central
PMC11662615
DOI
10.1186/s13071-024-06589-8
PII: 10.1186/s13071-024-06589-8
Knihovny.cz E-zdroje
- Klíčová slova
- Phlebotomus perniciosus, Antimicrobial peptides, Azadirachtin, Ecdysone,
- MeSH
- antimikrobiální peptidy genetika farmakologie MeSH
- ekdyson * MeSH
- hmyz - vektory účinky léků genetika parazitologie imunologie MeSH
- hmyzí proteiny genetika metabolismus MeSH
- larva * účinky léků imunologie genetika MeSH
- limoniny * farmakologie MeSH
- Phlebotomus * účinky léků genetika parazitologie imunologie MeSH
- shazování tělního pokryvu účinky léků MeSH
- signální transdukce * účinky léků MeSH
- zvířata MeSH
- Check Tag
- ženské pohlaví MeSH
- zvířata MeSH
- Publikační typ
- časopisecké články MeSH
- Názvy látek
- antimikrobiální peptidy MeSH
- azadirachtin MeSH Prohlížeč
- ekdyson * MeSH
- hmyzí proteiny MeSH
- limoniny * MeSH
BACKGROUND: Leishmaniasis is a group of neglected vector-borne diseases transmitted by phlebotomine sand flies. Leishmania parasites must overcome various defenses in the sand fly midgut, including the insects's immune response. Insect immunity is regulated by the ecdysone hormone, which binds to its nuclear receptor (EcR) and activates the transcription of genes involved in insect immunity. However, the role of ecdysone in sand fly immunity has never been studied. Phlebotomus perniciosus is a natural vector of Leishmania infantum; here, we manipulated its neuroendocrine system using azadirachtin (Aza), a natural compound known to affect ecdysone synthesis. METHODS: Phlebotomus perniciosus larvae and adult females were fed on food containing either Aza alone or Aza plus ecdysone, and the effects on mortality and ecdysis were evaluated. Genes related to ecdysone signaling and immunity were identified in P. perniciosus, and the expression of antimicrobial peptides (AMPs), EcR, the ecdysone-induced genes Eip74EF and Eip75B, and the transcription factor serpent were analyzed using quantitative polymerase chain reaction (PCR). RESULTS: Aza treatment inhibited molting of first-instar (L1) larvae to L2, with only 10% of larvae molting compared to 95% in the control group. Serpent and Eip74EF, attacin, defensin 1, and defensin 2 genes were downregulated by Aza treatment in larvae. Similarly, Aza-treated adult females also presented suppression of ecdysone signaling-related genes and the AMPs attacin and defensin 2. Notably, all gene repression caused by Aza was reversed by adding ecdysone concomitantly with Aza to the larval or female food, indicating that these genes are effective markers for ecdysone repression. CONCLUSIONS: These results highlight the critical role of ecdysone in regulating the development and immunity of P. perniciosus, which potentially could interfere with Leishmania infection.
Department of Biology University of Naples Federico 2 Naples Italy
Department of Parasitology Faculty of Science Charles University Prague Czech Republic
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