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.

• 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

CHR3 (nhr-23, NF1F4), the homologue of Drosophila DHR3 and mammalian ROR/RZR/RevErbA nuclear hormone receptors, is important for proper epidermal development and molting in the nematode Caenorhabditis elegans. Disruption of CHR3 (nhr-23) function leads to developmental changes, including incomplete molting and a short, fat (dumpy) phenotype. Here, we studied the role of CHR3 during larval development by using expression assays and RNA-mediated interference. We show that the levels of expression of CHR3 (nhr-23) cycle during larval development and reduction of CHR3 function during each intermolt period result in defects at all subsequent molts. Assaying candidate gene expression in populations of animals treated with CHR3 (nhr-23) RNA-mediated interference has identified dpy-7 as a potential gene acting downstream of CHR3. These results define CHR3 as a critical regulator of all C. elegans molts and begin to define the molecular pathway for its function.

• MeSH
• Caenorhabditis elegans růst a vývoj   fyziologie   MeSH
• DNA vazebné proteiny * MeSH
• hmyzí proteiny * MeSH
• larva MeSH
• polymerázová řetězová reakce s reverzní transkripcí MeSH
• receptory peptidů bezobratlých genetika   fyziologie   MeSH
• shazování tělního pokryvu * MeSH
• teplota MeSH
• trans-aktivátory * MeSH
• vývojová regulace genové exprese * MeSH
• zvířata MeSH
• Check Tag
• zvířata MeSH
• Publikační typ
• časopisecké články MeSH
• práce podpořená grantem MeSH
• Názvy látek
• CHR3 protein, Choristoneura fumiferana MeSH Prohlížeč
• DNA vazebné proteiny * MeSH
• hmyzí proteiny * MeSH
• receptory peptidů bezobratlých MeSH
• trans-aktivátory * MeSH