Eicosanoid Actions in Insect Immunology

Insect Immunology

Volumn , Issue , 2008, Pages 49,i-68,ii

  Stanley, David W ^a   Miller, Jon S ^b  

^a AGRICULTURAL RESEARCH SERVICE   (United States)

^b NORTHERN ILLINOIS UNIVERSITY   (United States)

Author keywords

[No Author keywords available]

Indexed keywords

EID: 59649111632     PISSN: None     EISSN: None     Source Type: Book    
DOI: 10.1016/B978-012373976-6.50005-7     Document Type: Chapter

References (75)

1. J.C. Bedick, H. Tunaz, A.R. Nor Aliza, S.M. Putnam, M.D. Ellis and D.W. Stanley (2001) Eicosanoids act in nodulation reactions to bacterial infections in newly emerged adult honey bees, Apis mellifera, but not in older foragers. Comp. Biochem. Physiol. Part C 130 107-117.
2. S. Bergstrom, R. Ryhage, B. Samuelsson and J. Sjovall (1962) The structure of prostaglandin E, F1 and F2. Acta Chemica Scandinavica 16 501-502.
3. M. Bhattacharya, D.R. Varma and S. Chemtob (1999) Nuclear prostaglandin receptors. Gene Ther. Mol. Biol. 4 323-338.
4. W. Blenau and A. Baumann (2001) Molecular and pharmacological properties of insect biogenic amine receptors: Lessons, from Drosophila melanogaster and Apis mellifera. Arch. Insect Biochem. Physiol. 48 13-38.
5. S. Boyden (1962) The chemotactic effect of mixtures of antibody and antigen on polymorphonuclear leucocytes. J. Exp. Med. 115 453-466.
6. R.M. Breyer, C.K. Bagdassarian, S.A. Myers and M.D. Breyer (2001) Prostanoid receptors: Subtypes and signaling. Annu. Rev. Pharmacol. Toxicol. 41 661-690.
7. K. Büyükgüzel, H. Tunaz, S.M. Putnam and D.W. Stanley (2002) Prostaglandin biosynthesis by midgut tissue isolated from the tobacco hornworm, Manduca sexta. Insect Biochem. Mol. Biol. 32 435-443.
8. E. Büyükgüzel, H. Tunaz, D. Stanley and K. Büyükgüzel (2007) Eicosanoids mediate Gaileria mellonella cellular immune response to viral infection. J. Insect Physiol. 53 99-105.
9. Y. Carton, F. Frey, D.W. Stanley, E. Vass and A.J. Nappi (2002) Dexamethasone inhibition of the cellular immune response of Drosophila melanogaster against a parasitoid. J. Parasitol. 288 405-407.
10. R.J. Clem (2005) The role of apoptosis in defense against baculovirus infection in insects. Curr. Top. Microbiol. 289 113-130.
11. P. Dean, J.C. Gadsden, E.H. Richards, J.P. Edwards, A.K. Charnley and S.E. Reynolds (2002) Modulation by eicosanoids of immune responses by the insect Manduca sexta to the pathogenic fungus Mearhizium anisopliae. J. Invertebr. Pathol. 79 93-101.
12. F. de la Cruz Hernandez-Hernandez, F. Garcia-Gil de Munoz, A. Rojas-Martinez, S. Hernandez-Martinez and H. Lanz-Mandoza (2003) Carminic acid dye from the homopteran Dactylopius coccus hemolymph is consumed during treatment with different microbial elicitors. Arch. Insect Biochem. Physiol. 4 37-45.
13. P.E. Dunn and D.R. Drake (1983) Fate of bacteria injected in naive and immunized larvae of the tobacco hornworm Manduca sexta. J. Invertebr. Pathol. 41 77-85.
14. Y. Durmus, E. Büyükgüzel, B. Terzi, H. Tunaz, D. Stanley and K. Büyükgüzel (2007) Eicosanoids mediate melantoic nodulation reactions to viral infection in larvae of the parasitic wasp. Pimpla turioinellae. J. Insect Physiol. (in press) (March 2007)
15. V. Franssens, G. Simonet, A. Bronckaers, I. Claeys, A. De Loof and J. Vanden Broeck (2005) Eicosanoids mediate the laminarin induced nodulation response in larvae of the flesh fly, Neobellieria bullata. Arch. Insect Biochem. Physiol. 59 32-41.
16. G.G. Gadelhak and D.W. Stanley-Samuelson (1994) Incorporation of polyunsaturated fatty acids into phospholipids of hemocytes from the tobacco hornworm Manduca sexta. Insect Biochem. Mol. Biol. 24 775-785.
17. G.G. Gadelhak, V.K. Pedibhotla and D.W. Stanley-Samuelson (1995) Eicosanoid biosynthesis by hemocytes from the tobacco hornworm, Manduca sexta. Insect Biochem. Mol. Biol. 25 743-749.
18. E.S. Garcia, E.M.M. Machado and P. Azambuja (2004) Effects of eicosanoid biosynthesis inhibitors on the prophenoloxidase-activating system and microaggregation reactions in the hemolymph of Rhodnius prolixus infected with Trypanosoma rangeli. J. Insect Physiol. 50 157-165.
19. G. Goldsworthy, L. Mullen, K. Opoku-Ware and S. Chandrakant (2003) Interactions between the endocrine and immune systems in locusts. Physiol. Entomol. 28 54-61.
20. N. Hatae, Y. Sugimoto and A. Ichikawa (2002) Prostaglandin receptors: Advances in the study of EP3 receptor signaling. J. Biochem. (Tokyo) 131 781-784.
21. R.W. Howard and D.W. Stanley (1999) The tie that binds: Eicosanoids in invertebrate biology. Ann. Entomol. Soc. Am. (Special Issue Honoring Carl Schaefer) 92 880-890.
22. R.A. Jurenka, J.S. Miller, V.K. Pedibhotla, R.L. Rana and D.W. Stanley-Samuelson (1997) Eicosanoids mediate microaggregation and nodulation responses to bacterial infections in black cutworms, Agrotis ipsilon, and true armyworms, Pseudaletia unipuncta. J. Insect Physiol. 43 125-133.
23. R.A. Jurenka, V.K. Pedibhotla and D.W. Stanley (1999) Prostaglandin production in response to bacterial infection in true armyworm larvae. Arch. Insect Biochem. Physiol. 41 225-232.
24. H.S. Kwon, D.W. Stanley and J.S. Miller (2007) Bacterial challenge and eicosanoids act in plasmatocyte spreading. Entomol. Exp. Appl. (in press) (March 2007)
25. J.C. Lord, S. Anderson and D.W. Stanley (2002) Eicosanoids mediate Manduca sexta cellular response to the fungal pathogen Beauveria bassiana: A role for the lipoxygenase pathway. Arch. Insect Biochem. Physiol. 51 46-54.
26. C.A. Mandato, W.L. Diehl-Jones, S.J. Moore and R.G.H. Downer (1997) The effects of eicosanoid biosynthesis inhibitors on prophenoloxidase activation, phagocytosis and cell spreading in Galleria mellonella. J. Insect Physiol. 43 1-8.
27. J.S. Miller (2005) Eicosanoids influence in vitro elongation of plasmatocytes from the tobacco hornworm, Manduca sexta. Arch. Insect Biochem. Physiol. 59 42-51.
28. J.S. Miller and D.W. Stanley (1998) The nodule formation reaction to bacterial infection: Assessing the role of eicosanoids. A. Wiesner (Eds) Techniques in Insect Immunology Fair Haven: SOS Publications 265-270.
29. J.S. Miller and D.W. Stanley (2001) Eicosanoids mediate microaggregation reactions to bacterial challenge in isolated insect hemocyte preparations. J. Insect Physiol. 47 61-69.
30. J.S. Miller and D.W. Stanley (2004) Lipopolysaccharide evokes microaggregation reactions in hemocytes isolated from tobacco hornworms, Manduca sexta. Comp. Biochem. Physiol. Part A 137 285-295.
31. J.S. Miller, T. Nguyen and D.W. Stanley-Samuelson (1994) Eicosanoids mediate insect nodulation responses to bacterial infections. Proc. Natl. Acad. Sci. USA 91 12418-12422.
32. J.S. Miller, R.W. Howard, T. Nguyen, A. Nguyen, R.M.T. Rosario and D.W. Stanley-Samuelson (1996) Eicosanoids mediate nodulation responses to bacterial infections in larvae of the tenebrionid beetle Zophobas atratus. J. Insect Physiol. 42 3-12.
33. J.S. Miller, R.W. Howard, R.L. Rana, H. Tunaz and D.W. Stanley (1999) Eicosanoids mediate nodulation reactions to bacterial infections in adults of the cricket, Gryllus assimulis. J. Insect Physiol. 45 75-83.
34. C.L. Ogg and D.W. Stanley-Samuelson (1992) Phospholipid and triacylglycerol fatty acid compositions of the major life stages and selected tissues of the tobacco hornworm Manduca sexta. Comp. Biochem. Physiol. 101B 345-351.
35. C.L. Ogg, R.W. Howard and D.W. Stanley-Samuelson (1991) Fatty acid composition and incorporation of arachidonic acid into phospholipids of hemocytes from the tobacco hornworm Manduca sexta. Insect Biochem. 21 809-814.
36. Y. Park and Y. Kim (2000) Eicosanoids rescue Spodoptera exigua infected with Xenorhabdus nematophilus, the symbiotic bacteria to the entomopathogenic nematode Steinernema carpocapsae. J. Insect Physiol. 46 1469-1476.
37. Y. Park and D. Stanley (2006) The entomopathogenic bacterium, Xenorhabdus nematophila, impairs insect immunity by inhibition of eicosanoid biosynthesis in adult crickets, Gryllus firmus. Biol. Control 38 247-253.
38. Y. Park, A.R. Nor Aliza and D.W. Stanley (2005) A secretory PLA2 associated with tobacco hornworm hemocytes membrane preparations acts in cellular immune reactions. Arch. Insect Biochem. Physiol. 60 105-115.
39. P.K. Phelps, J.S. Miller and D.W. Stanley (2003) Prostaglandins, not lipoxygenase products, mediate insect microaggregation reactions to bacterial challenge in isolated hemocyte preparations. Comp. Biochem. Physiol. 136 409-416.
40. K.M. Ponnuvel, H. Nakazawa, S. Furukawa, A. Asaoka, J. Ishibashi, H. Tanaka and M. Yamakawa (2003) A lipase isolated from the silkworm Bombyx mori shows antiviral activity against nucleopolyhedrovirus. J. Virol. 77 10725-10729.
41. H.J.R. Popham, K.S. Shelby, S.L. Brandt and T.A. Coudron (2004) Potent virucidal activity in larval Heliothis virescens plasma against Helicoverpa zea single capsid nucleopolyhedrovirus. Virol. 85 2255-2261.
42. Y. Qian, R.C. Essenberg, J.W. Dillwith, A.S. Bowman and J.R. Sauer (1997) A specific prostaglandin E2 receptor and its role in modulating salivary secretion in the female tick, Amblyomma americanum (L.). Insect Biochem. and Molec. Biol. 27 387-395.
43. A.F. Rowley, C.L. Vogan, G.W. Taylor and A.S. Clare (2005) Prostaglandins in non-insectan invertebrates: Recent insights and unsolved problems. J. Exp. Biol. 208 3-14.
44. A. Saumet and C.-H. Lecellier (2006) Anti-viral RNA silencing: Do we look like plants? Retrovirol. 3 http://www.retrovirology.com/content/3/1/3 3. Available at
45. R.H. Schaloske and E.A. Dennis (2006) The phospholiopase A2, superfamily and its group numbering system. Biochem Biophys Acta 1761 1246-1259.
46. D.R. Schleusener and D.W. Stanley-Samuelson (1996) Phospholipase A2 in hemocytes of the tobacco hornworm, Manduca sexta. Arch. Insect Biochem. Physiol. 33 63-74.
47. D.W. Stanley (2000) Eicosanoids in Invertebrate Signal Transduction Systems Princeton: Princeton University Press
48. D.W. Stanley (2005) Eicosanoids. L.I. Gilbert, K. Iatrou, S. Gill (Eds) Comprehensive Molecular Insect Science Vol. 4 Oxford: Elsevier 307-339.
49. D.W. Stanley (2006) Prostaglandins and other eicosanoids in insects: Biological significance. Annu. Rev. Entomol. 51 25-44.
50. D.W. Stanley (2006) The non-venom insect phospholipases A2. Biochem. Biophys. Acta 1761 1383-1390.
51. D.W. Stanley and R.W. Howard (1998) The biology of prostaglandins and related eicosanoids in invertebrates: Cellular, organismal and ecological actions. Am. Zool. 38 369-381.
52. D.W. Stanley and J.S. Miller (2006) Eicosanoid actions in insect cellular immune functions. Entomol. Exp. Appl. 119 1-13.
53. D. Stanley and M. Shapiro (2007) Eicosanoid biosynthesis inhibitors increase the susceptibility of Lymantria dispar to nucleopolyhedrovirus LdMNPV. J. Invertebr. Pathol. 95 119-124.
54. D.W. Stanley, W.W. Hoback, J.C. Bedick, H. Tunaz, R.L. Rana, A.R. Nor Aliza and J.S. Miller (1999) Eicosanoids mediate nodulation reactions to bacterial infections in larvae of the butterfly, Colias eurytheme. Comp. Biochem. Physiol. 41 225-232.
55. D.W. Stanley-Samuelson (1991) Comparative eicosanoid physiology in invertebrate animals. Am. J. Physiol. 260 R849-R853. (Reg. Integ. Comp. Physiol. 29)
56. D.W. Stanley-Samuelson (1994) Assessing the physiological significance of prostaglandins and other eicosanoids in insect physiology. J. Insect Physiol. 40 3-11.
57. D.W. Stanley-Samuelson (1994) Prostaglandins and related eicosanoids in insects. Adv. Insect Physiol. 24 115-212.
58. D.W. Stanley-Samuelson (1994) The biological significance of prostaglandins and other eicosanoids in invertebrates. Am. Zool. 34 589-598.
59. D.W. Stanley-Samuelson and R.H. Dadd (1983) Long-chain polyunsaturated fatty acids: Patterns of occurrence in insects. Insect Biochem. 13 549-558.
60. D.W. Stanley-Samuelson and W. Loher (1986) Prostaglandins in insect reproduction. Ann. Entomol. Soc. Am. 79 841-853.
61. D.W. Stanley-Samuelson and V.K. Pedibhotla (1996) What can we learn from prostaglandins and other eicosanoids in insects? Insect Biochem. Mol. Biol. 26 223-234.
62. D.W. Stanley-Samuelson, E. Jensen, K.W. Nickerson, K. Tiebel, C.L. Ogg and R.W. Howard (1991) Insect immune response to bacterial infection is mediated by eicosanoids. Proc. Natl. Acad. Sci. USA 88 1064-1068.
63. D.W. Stanley-Samuelson, R.A. Jurenka, G.J. Blomquist and W. Loher (1987) Sexual transfer of prostaglandin precursor in the field cricket, Teleogryllus commodus. Physiol. Entomol. 12 347-354.
64. D.W. Stanley-Samuelson and C.L. Ogg (1994) Prostaglandin biosynthesis by fat body from the tobacco hornworm, Manduca sexta. Insect Biochem. Mol. Biol. 24 481-491.
65. D.W. Stanley-Samuelson, V.K. Pedibhotla, R.L. Rana, A.R. Nor Aliza, W.W. Hoback and J.S. Miller (1997) Eicosanoids mediate nodulation responses to bacterial infections in larvae of the silkmoth, Bombyx mori. Comp. Biochem. Physiol. 118A 93-100.
66. Y. Sugimoto and S. Narumiya (2007) Prostaglandin E receptors. J. Biol. Chem. 282 11613-11617.
67. H. Tunaz and D.W. Stanley (2000) Eicosanoids mediate nodulation reactions to bacterial infections in adults of the American cockroach, Periplaneta americana (L.). Proc. Entomol. Soc. Ont. 130 97-108.
68. H. Tunaz, J.C. Bedick, J.S. Miller, W.W. Hoback, R.L. Rana and D.W. Stanley (1999) Eicosanoids mediate nodulation reactions to bacterial infections in adults of two 17-year periodical cicadas, Magicicada septendecim and M. cassini. J. Insect Physiol. 45 923-931.
69. T. Tunaz, S.M. Putnam and D.W. Stanley (2002) Prostaglandin biosynthesis by fat body from larvae of the beetle Zophobas atratus. Arch. Insect Biochem. Physiol. 49 80-93.
70. H. Tunaz, A.A. Isikber and M.K. Er (2003) The role of eicosanoids on nodulation reactions to bacterium Serratia marcescens in larvae of Ostrinia nubilalis. Turk. J. Agric. Forest. 27 269-275.
71. H. Tunaz, Y. Park, K. Büyükgüzel, J.C. Bedick, A.R. Nor Aliza and D.W. Stanley (2003) Eicosanoids in insect immunity: Bacterial infection stimulates hemocytic phospholipase A2 activity in tobacco hornworms. Arch. Insect Biochem. Physiol. 52 1-6.
72. J.M. Uscian and D.W. Stanley-Samuelson (1993) Phospholipase A2 activity in the fat body of the tobacco hornworm Manduca sexta. Arch. Insect Biochem. Physiol. 24 187-201.
73. J. Vanden Broeck (2001) Insect G protein-coupled receptors and signal transduction. Arch. Insect Biochem. Physiol. 48 1-12.
74. U.S. von Euler (1936) On the specific vasodilating and plain muscle stimulating substances from accessory gential glands in men and certain animals (prostaglandin and vestiglandin). J. Physiol. (London) 88 213-234.
75. J.O. Washburn, B.A. Kirkpatrick and L.E. Volkman (1996) Insect protection against viruses. Nature 383 767-768.