Dergiler / Turkish Journal of Zoology / 2018 / Cilt: 42 - Sayı: 4

The role of a novel Wo l b a c h i a (Rickettsiales: Anaplasmataceae) synthetic peptide, WolFar, in regulating prostaglandin levels in the hemolymph of Acheta domesticus (Orthoptera: Gryllidae)

Sayfa
422–431
Yayın Tarihi
2018-07-26
DOI
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⚡ TL;DR(1 Cümlede Hızlı Çıkarım)

This indicates that WolFar is able to stimulate the immune system of insects and can be further developed as a potential biopesticide.

📌 3 Maddede Bu Makale

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Amaç & Hipotez:Prostaglandins and other eicosanoids are known as regulating agents for cellular immune responses to pathogen threats in an insect?s hemolymph.
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Temel Bulgular & Veri:Three concentrations of peptides, 0.83 mmol/L (100%), 0.63 mmol/L (75%), and 0.42 mmol/L (50%), were injected and observed for 72 h.
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Sonuç & Katkı:This indicates that WolFar is able to stimulate the immune system of insects and can be further developed as a potential biopesticide.
🔬Tür:Araştırma Makalesi
📍Kapsam:Genişletilmiş Akademik Örneklem
⚙️Değişkenler:Prostaglandin · hemolymph · Acheta domesticus

Abstract

Prostaglandins and other eicosanoids are known as regulating agents for cellular immune responses to pathogen threats in an insect?s hemolymph. A novel synthetic peptide, WolFar, was customized from a conserved region of the Wolbachia surface protein (WSP), isolated from an economically important endoparasitoid species, Fopius arisanus. WolFar consists of nine amino acids (SYY VRL QYN) and was tested on the house cricket, Acheta domesticus. Three concentrations of peptides, 0.83 mmol/L (100%), 0.63 mmol/L (75%), and 0.42 mmol/L (50%), were injected and observed for 72 h. The regulation of prostaglandin E2 (PGE2) in the hemolymph of A. domesticus was determined using ELISA and by observation of nodules in the internal system of A. domesticus. The results showed that there were significant increases in PGE2 in response to peptide injection at 24, 48, and 72 h after treatment. Furthermore, higher concentrations of peptide were directly proportional to the level of PGE2 activity. These findings were supported by the abundance of nodules that formed in the internal system and fat body of A. domesticus, detectable at 72 h into the treatment. This indicates that WolFar is able to stimulate the immune system of insects and can be further developed as a potential biopesticide.

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Bu Makaleye Atıf Yap

MOHAMMED, M. A., AMAN-ZUKI, A., WAHIDA, N. O., TAGAMI, Y., YAAKOP, S. (2018). The role of a novel Wo l b a c h i a (Rickettsiales: Anaplasmataceae) synthetic peptide, WolFar, in regulating prostaglandin levels in the hemolymph of Acheta domesticus (Orthoptera: Gryllidae). Turkish Journal of Zoology, Cilt: 42 - Sayı: 4, 422–431. https://ajindex.com/articles/176714

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Kaynakça (9)

  1. Adamo SA (1999). Evidence for adaptive changes in egg laying in crickets exposed to bacteria and parasites. Anim Behav 57: 117-124.
  2. Asgharian H, Chang PL, Mazzoglio PJ, Negri I (2014). Wolbachia is not all about sex: male-feminizing Wolbachia alters the leafhopper Zyginidia pullula transcriptome in a mainly sex- independent manner. Front Microbiol 5: 430. Azad AF, Beard CB (1998). Rickettsial pathogens and their arthropod vectors. Emerg Infect Diseases 4: 179. Bali GK, Kaur S (2013). Phenoloxidase activity in haemolymph of Spodoptera litura (Fabricius) mediating immune responses challenge with entomopathogenic fungus, Beauveria bassiana (Balsamo) Vuillmin. J Entomol Zool Stud 1: 118-123.
  3. Baldo L, Lo N, Werren JH (2005). Mosaic nature of the Wolbachia surface protein. J Bacteriol 187: 5406-5418.
  4. Bazzocchi C, Ceciliani F, McCall JW, Ricci I, Genchi C, Bandi C (2000). Antigenic role of the endosymbionts of filarial nematodes: IgG response against the Wolbachia surface protein in cats infected with Dirofilaria immitis. Proc R Soc Lond B Biol Sci 267: 2511- 2516. Billingsley PF, Lehane MJ (1996). Structure and ultrastructure of the insect midgut. In: Billingsley P, Lehane MJ, editors. Biology of the Insect Midgut. Berlin, Germany: Springer, pp. 3-30.
  5. Bordenstein SR, Werren JH (2007). Bidirectional incompatibility among divergent Wolbachia and incompatibility level differences among closely related Wolbachia in Nasonia. Heredity 99: 278. Braig HR, Zhou W, Dobson SL, O’Neill SL (1998). Cloning and characterization of a gene encoding the major surface protein of the bacterial endosymbiont Wolbachia pipientis. J Bacteriol 180: 2373-2378.
  6. Brattig NW, Bazzocchi C, Kirschning CJ, Reiling N, Büttner DW, Ceciliani F, Geisinger F, Hochrein H, Ernst M, Wagner H et al. (2004). The major surface protein of Wolbachia endosymbionts in filarial nematodes elicits immune responses through TLR2 and TLR4. J Immunol 173:437-445.
  7. Brattig NW, Rathjens U, Ernst M, Geisinger F, Renz A, Tischendorf FW (2000). Lipopolysaccharide-like molecules derived from Wolbachia endobacteria of the filaria Onchocerca volvulus are candidate mediators in the sequence of inflammatory and antiinflammatory responses of human monocytes. Microbes Infect 2: 1147-1157.
  8. Brelsfoard CL, Dobson SL (2009). Wolbachia -based strategies to control insect pests and disease vectors. Asia Pac J Mol Biol Biotechnol 17: 55-63.
  9. Bulet P, Cociancich S, Dimarcq JL, Lambert J, Reichhart JM, Hoffmann D, Hetru C, Hoffmann JA