Polypeptides of Acrolepiopsis assectella cocoon (Lepidoptera: Yponomeutoidea): An external host-acceptance kairomone for the parasitoid Diadromus pulchellus (Hymenoptera: Ichneumonidae)

Journal of Insect Physiology

Volumn 45, Issue 4, 1999, Pages 375-384

  Benedet F ^a   Bigot, Y ^a   Renault, S ^a   Pouzat, J ^a   Thibout, E ^a  

^a UNIVERSITÉ DE TOURS   (France)

Author keywords

Cocoon; Contact kairomone; Glycopolypeptides; Host acceptance; Parasitoid; Sericin

Indexed keywords

GLYCOPEPTIDE; KAIROMONE; POLYPEPTIDE; SERICIN; UNCLASSIFIED DRUG;

COCOON; HOST-PARASITE INTERACTION; KAIROMONE; PARASITOID;

ARTICLE; HOST PARASITE INTERACTION; HYMENOPTERA; LEPIDOPTERA; NONHUMAN; PROTEIN GLYCOSYLATION; PROTEIN ISOLATION; WASP;

ACROLEPIOPSIS ASSECTELLA; DIADROMUS PULCHELLUS; ICHNEUMONIDAE; LEPIDOPTERA; YPONOMEUTOIDEA;

EID: 0344492726     PISSN: 00221910     EISSN: None     Source Type: Journal    
DOI: 10.1016/S0022-1910(98)00136-X     Document Type: Article

References (51)

1. Alrouz H., Thibout E. Premières observations sur le comportement alimentaire des larves de la teigne du poireau, Acrolepiopsis assectella, rôle des Allium. Acta Oecologica. Oecologia applicata. 9:1988;261-273.
2. Arnault C. Conséquences de l'alimentation artificielle sur le développement larvaire de la teigne du poireau Acrolepiopsis assectella. Entomologia Experimentalis et Applicata. 32:1982;116-122.
3. Asano Y., Sinohara H. Amino sugars in various silk fibroins. Naturwissenschaften. 55:1968;345.
4. Ausubel, F.M., Brent, R., Kingston, R.E., Moore, D.D., Seidman, J.G., Smith, J.A., Struhl, K., 1990. Current Protocols in Molecular Biology, vol. 1. Greene Publishing and Wiley Intersciences, New York.
5. Auger J., Mellouki F., Vannereau A., Boscher J., Cosson L., Mandon N. Analysis of Allium sulfur amino acids by HPLC after derivatization. Chromatographia. 36:1993;347-350.
6. Bekkaoui A., Thibout E. Rôle de substances cuticulaires non volatiles d'Acrolepiopsis assectella (Lep.: Hyponomeutoïdea) dans la reconnaissance de l'hôte par les parasitoïdes Diadromus pulchellus et D. collaris (Hym.: Ichneumonidae). Entomophaga. 37:1992;627-639.
7. Bekkaoui A., Thibout E. Role of the cocoon of Acrolepiopsis assectella (Lep., Yponomeutoïdea) in host recognition by the parasitoid Diadromus pulchellus (Hym.: Ichneumonidae). Entomophaga. 38:1993;101-113.
8. Bidlingmeyer B.A., Cohen S.A., Tarvin T.L. Rapid analysis of amino acids using pre-column derivatization. Journal of Chromatography. 336:1984;93-104.
9. Bin F., Vinson S.B., Strand M.R., Colazza S., Jones W.A. Source of an egg kairomone for Trissolcus basalis, a parasitoid of Nezara viridula. Physiological Entomology. 18:1993;7-15.
10. Blum H., Beier H., Gross H.J. Improved silver staining of plant proteins RNA and DNA in polyacrylamide gels. Electrophoresis. 8:1987;93-99.
11. Chirgwin J.M., Pzybyla A.E., MacDonald R.J., Rutter W.J. Isolation of biologically active ribonucleic acid from sources enriched in ribonuclease. Biochemistry. 18:1979;5294-5299.
12. Doutt, R.L., 1964. Biological characteristics of entomophagous adults. In: De Bach, P. (Ed.), Biological Control of Insect Pests and Weeds. Chapman and Hall, London, pp. 145-167.
13. Fournier A. Quantitative data on the Bombyx mori L. silkworm: a review. Biochimie. 61:1979;283-320.
14. Freddi G., Bianchi A.S., Ishikawa H., Tsukada M. Chemical composition and physical properties of Gonometa rufobrunnae silk. Journal of Applied Polymer Science. 48:1993;99-106.
15. Garel A., Deleage G., Prudhomme J.-C. Structure and organization of the Bombyx mori sericin 1 gene and of the sericins 1 deduced from the sequence of the ser 1B cDNA. Insect Biochemistry and Molecular Biology. 27:1997;469-477.
16. Handman E., McConville M.J., Goding J.W. Carbohydrate antigens as possible parasite vaccines - A case of the Leishmania glycolipid. Immunology Today. 8:1987;181-185.
17. Hegdekar B.M., Arthur A.P. Host hemolymph chemicals that induce oviposition in the parasite Itoplectis conquisitor (Hymenoptera: Ichneumonidae). Canadian Entomologist. 105:1973;787-793.
18. Henson R.B., Vinson S.B., Barfield C.S. Ovipositional behavior of Bracon mellitor Say, a parasitoid of the boll weevil (Anthonomus grandis Boheman) III Isolation and identification of natural releasers of ovipositor probing. Journal of Chemical Ecology. 3:1977;151-152.
19. Jones R.L., Lewis W.J., Bowman M.C., Beroza M., Bierl B.A. Host-searching stimulant for parasite of corn-earworm: isolation, identification, and synthesis. Science. 173:1971;842-843.
20. Kainoh Y., Tatsuki S., Sugie H., Tamaki Y. Host egg kairomones essential for egg-larval parasitoid, Ascogaster reticulatus Watanabe. (Hymenoptera: Braconidae): II Identification of internal kairomone. Journal of Chemical Ecology. 15:1989;1219-1229.
21. Komatsu K.-I. Chemistry and structure of silk. Japan Agricultural Research Quarterly. 13:1979;64-72.
22. Labeyrie V. Contribution à l'étude de la dynamique des populations d'insectes: I. Influence stimulatrice de l'hôte Acrolepiopsis assectella Z. sur la multiplication d'un hyménoptère Ichneumonidae (Diadromus pulchellus). Entomophaga Hors série. 1:1960;1-193.
23. Laemmli U.K. Cleavage of structural proteins during the assembly of the head of bacteriophage T4. Nature. 227:1970;680-685.
24. Lecomte C., Thibout E. Etude olfactométrique de l'action de diverses substances allélochimiques végétales dans la recherche de l'hôte par Diadromus pulchellus (Hymenoptera, Ichneumonidae). Entomologia Experimentalis et Applicata. 35:1984;295-303.
25. Lecomte C., Thibout E., Thibeaudeau C. Etude en microscopie électronique à balayage, des organes sensoriels de Diadromus pulchellus WSM (Hymenoptera, Ichneumonidae). II. L'ovipositeur et les tarses des femelles. Bulletin de la Société Scientifique de Bretagne. 62:1991;9-24.
26. Mattiacci L., Dicke M. The parasitoid Cotesia glomerata (Hymenoptera: Braconidae) discriminates between first and fifth larval instars of its host Pieris brassicae, on the basis of contact cues from frass, silk, and herbivore-damaged leaf tissue. Journal of Insect Behavior. 8:1995;485-498.
27. Millar J.G., Hare J.D. Identification and synthesis of a kairomone inducing oviposition by parasitoid Aphytis melinus from california red scale covers. Journal of Chemical Ecology. 19:1993;1721-1736.
28. Mudd A., Corbet S.A. Response of the ichneumonid parasite Nemeritis canescens to kairomones from the flour moth, Ephestia kuehniella. Journal of Chemical Ecology. 8:1982;843-850.
29. Neuhoff V., Arold N., Taube D., Ehrhardt W. Improved staining of proteins in polyacrylamide gels including isoelectric focusing gels with clear background at nanogram sensivity using Coomassie brillant blue G250 and R250. Electrophoresis. 9:1988;255-262.
30. Nogushi M., Arai S., Yamashita M., Kato H., Fujimaki M. Isolation and identification of acidic oligopeptides in a flavor potentiating fraction from a fish protein hydrolysate. Journal of Agricultural and Food Chemistry. 23:1975;49-54.
31. Prudhomme, J.-C., Couble, P., Garel, J.-P., Daillie, J., 1985. Silk synthesis. In: Kerkut, G.A. and Gilbert, L.I. (Eds.), Comprehensive Insect Physiology, Biochemistry and Pharmacology. Pergamon Press, Oxford, pp. 571-594.
32. Schmidt J.M. The role of physical factors in tritrophic interactions. Redia. 74 App. 1991;43-93.
33. Sinohara H., Asano Y., Fukui A. Glycopeptides from silk fibroin of Bombyx mori. Biochimica et Biophysica Acta. 237:1971;273-279.
34. Sinohara H. Glycopeptides isolated from sericin of the silkworm, Bombyx mori. Comparative Biochemistry and Physiology. 63B:1979;87-91.
35. Snell T.W., Rico-Martinez R., Kelly L.N., Battle T.E. Identification of a sex pheromone from a rotifer. Marine Biology. 123:1995;347-353.
36. Strand M.R., Vinson S.B. Source and characterization of an egg recognition kairomone of Telenomus heliothidis, a parasitoid of Heliothis virescens. Physiological Entomology. 7:1982;83-90.
37. Strand M.R., Vinson S.B. Analyses of an egg recognition kairomone of Telenomus heliothidis (Hymenoptera: Scelionidae). Isolation and host function. Journal of Chemical Ecology. 9:1983;423-432.
38. Strand M.R., Williams H.J., Vinson S.B., Mudd A. Kairomonal activities of 2-acylcyclohexane-1,3 dione produced by Ephestia kuehniella Zeller in eliciting searching behaviour by the parasitoid Bracon hebetor (Say). Journal of Chemical Ecology. 15:1989;1491-1500.
39. Takabayashi J., Takahashi S. Host selection behavior of Anicetus beneficus Ishii et Yasumatsu (Hymenoptera: Encyrtidae). III. Presence of ovipositional stimulants in the scale wax of the genus Ceroplastes. Applied Entomology and Zoology. 20:1985;173-178.
40. Takabayashi J., Takahashi S. Effects of kairomones in the host searching behaviour of Apanteles kariyai Watanabe (Hymenoptera: Braconidae), a parasitoid of the common armyworm, Pseudaletia separata Walker (Lepidoptera: Noctuidae). II Isolation and identification of arrestants produced by the host larvae. Applied Entomology and Zoology. 21:1986;114-118.
41. Takahashi S., Hajika M., Takabayashi J., Fukui M. Oviposition stimulants in the coccoid cuticular waxes of Aphytis yanonensis De Bach & Rosen. Journal of Chemical Ecology. 16:1990;1657-1665.
42. Tamura T., Inoue H., Suzuki Y. The fibroin genes of Antheraea yamamai and Bombyx mori are different in their core regions but reveal a striking sequence similarity in their 5′ ends and 5′ flanking regions. Molecular and General Genetics. 207:1987;189-195.
43. Thibout E. La spécificité de Diadromus pulchellus (Hyménoptère: Ichneumonidae) vis-à-vis de son hôte Acrolepiopsis assectella, la teigne du poireau. Entomophaga. 33:1988;439-452.
44. Tilden R.L., Ferkovich S.M. Kairomonal stimulation of oviposition into an artificial substrate by the endoparasitoid Microplitis croceipes (Hymenoptera: Braconidae). Annals of the Entomological Society of America. 81:1988;152-156.
45. Vinson S.B. Host selection by insect parasitoids. Annual Review of Entomology. 21:1976;109-133.
46. Vinson, S.B., 1984. Parasitoid-host relationship. In: Bell W.J. and Carde, R.T. (Eds.), Chemical Ecology of Insects. Chapman and Hall, New York, pp. 205-233.
47. Vinson S.B. Chemical signals used by parasitoids. Redia. 74 App. 1991;15-42.
48. Vinson S.B., Piper G.L. Source and characterization of host recognition kairomones of Tetrastichus hagenowii, a parasitoid of cockroach eggs. Physiological Entomology. 11:1986;459-468.
49. Weseloh R.M. Effects on behavior of Apanteles melanoscelus females caused by modifications in extraction, storage, and presentation of gypsy moth silk kairomone. Journal of Chemical Ecology. 3:1977;723-735.
50. Yamasaki Y., Maekawa K. Synthesis of a peptide with a delicious taste. Agricultural and Biological Chemistry. 44:1980;93-97.
51. Zurovec M., Sehnal F., Scheller K., Kumaran A.K. Silk gland specific cDNA from Galleria mellonella L. Insect Biochemistry and Molecular Biology. 22:1992;55-67.