Skip to main content
Log in

Role of the Lipoxygenase/lyase Pathway of Host-food Plants in the Host Searching Behavior of Two Parasitoid Species, Cotesia glomerata and Cotesia plutellae

  • Published:
Journal of Chemical Ecology Aims and scope Submit manuscript

Abstract

To elucidate the role of the plant lipoxygenase (LOX)/lyase pathway for host search behavior of two parasitic wasps attacking herbivorous larvae, an Arabidopsis mutant (all84) was isolated with a mutation somewhere in the LOX/lyase pathway. Detached leaves of the mutant were shown to release less (Z)-3-hexenal, a first green leaf volatile (GLV) product of the LOX/lyase pathway. The braconid larval parasitoids studied, Cotesia glomerata and Cotesia plutella, differ in their ability to discriminate among plant volatiles induced by feeding of lepidopteran hosts and nonhosts: C. plutella only responds to plant volatiles induced by hosts (Plutella larvae), whereas the response by the more generalist C. glomerata is not host specific. The Arabidopsis mutant all84 infested by Pieris larvae was less attractive to C. glomerata than Arabidopsis wild type (wt) infested by the host larvae. C. glomerata was attracted by two of the GLV biosynthesized through the LOX/lyase pathway, (E)-2-hexenal and (Z)-3-hexenyl acetate. However, attraction of C. plutellae to volatiles from Plutella-infested all84 plants did not differ from attraction to host-infested wt Arabidopsis. Both wasp species were arrested to the respective host-infested edge of the wt leaf by showing characteristic antennal searching behavior on the edge. In C. glomerata, the duration of this searching behavior at the infested leaf edge was significantly shorter on all84 plants than on wt plants. By contrast, the duration of the searching behavior of C. plutellae on the host-infested leaf edge of all84 was not significantly different from that on the wt leaf. These data suggest that the LOX/lyase pathway is directly involved in the production of attractants and arrestants important for host search behavior of the more generalist C. glomerata, but not for the specialist C. plutellae.

This is a preview of subscription content, log in via an institution to check access.

Access this article

Price excludes VAT (USA)
Tax calculation will be finalised during checkout.

Instant access to the full article PDF.

Fig. 1
Fig. 2
Fig. 3
Fig. 4

Similar content being viewed by others

References

  • Bate, N. J. and Rothstein, S. J. 1998. C6-volatiles derived from the lipoxygenase pathway induce a subset of defense-related genes. Plant J. 16:561–569.

    Article  PubMed  CAS  Google Scholar 

  • Birkett, M. A., Chamberlain, K., Guerrieri, E., Pickett, J. A., Wadhams, L. J., and Yasuda, T. 2003. Volatiles from whitefly-infested plants elicit a host-locating response in the parasitoid, Encarsia formosa. J. Chem. Ecol. 29:1589–1600.

    Article  CAS  Google Scholar 

  • Dicke, M. and van Loon, J. J. A. 2000. Multitrophic effects of herbivore-induced plant volatiles in an evolutionary context. Entomol. Exp. Appl. 97:237–249.

    Article  CAS  Google Scholar 

  • Dicke, M. and Vet, L. E. M. 1999. Plant-carnivore interactions: Evolutionary and ecological consequences for plant, herbivore and carnivore, pp. 483–520, in H. Olff, V. K. Brown, and R. H. Drent (eds.). Herbivores: Between Plants and Predators. Blackwell Science Ltd., Oxford.

    Google Scholar 

  • Dicke, M., Gols, R., Ludeking, D., and Posthumus, M. A. 1999. Jasmonic acid and herbivory differentially induce carnivore-attracting plant volatiles in lima bean plants. J. Chem. Ecol. 25:1907–1922.

    Article  CAS  Google Scholar 

  • Gouinguené, S., Pickett, J. A., Wadhams, L. J., Birkett, M. A., and Turlings, T. C. J. 2005. Antennal electrophysiological responses of three parasitic wasps to caterpillar-induced volatiles from maize (Zea mays mays), cotton (Gossypium herbaceum), and cowpea (Vigna unguiculata). J. Chem. Ecol. 31:1023–1038.

    Article  PubMed  CAS  Google Scholar 

  • Hatanaka, A. 1993. The biogeneration of green odour by green leaves. Phytochemistry 34:1201–1218.

    Article  CAS  Google Scholar 

  • Hopke, J., Donath, J., Blechert, S., and Boland, W. 1994. Herbivore-induced volatiles: The emission of acyclic homoterpenes from leaves of Phaseolus lunatus and Zea mays can be triggered by a β-glucosidase and jasmonic acid. FEBS Lett. 352:146–150.

    Article  PubMed  CAS  Google Scholar 

  • Horikoshi, M., Takabayashi, J., Yamaoka, R., Yano, S., Ohsaki, N., and Sato, Y. 1997. Cotesia glomerata female wasps use fatty acids from plant–herbivore complex in host searching. J. Chem. Ecol. 23:1505–1515.

    Article  CAS  Google Scholar 

  • Horiuchi, J., Arimura, G., Ozawa, R., Shimoda, T., Takabayashi, J., and Nishioka, T. 2001. Exogenous ACC enhances volatiles production mediated by jasmonic acid in Lima bean leaves. FEBS Lett. 509:332–336.

    Article  PubMed  CAS  Google Scholar 

  • Karban, R. and Baldwin, I. 1997. Induced Response to Herbivory. The University of Chicago Press, Chicago.

    Google Scholar 

  • Kessler, A. and Baldwin, I. T. 2002. Plant responses to insect herbivory: The emerging molecular analysis. Annu. Rev. Plant Biol. 53:299–328.

    Article  PubMed  CAS  Google Scholar 

  • Kishimoto, K., Matsui, K., Ozawa, R., and Takabayashi, J. 2005. Volatile C6-aldehydes and allo-ocimene activate defense genes and induce resistance against Botrytis cinerea in Arabidopsis thaliana. Plant Cell Physiol. 6:1093–1102.

    Article  CAS  Google Scholar 

  • Matsui, K., Kurishita, S., Hisamitsu, A., and Kajiwara, T. 2000. A lipid-hydrolysing activity involved in hexenal formation. Biochem. Soc. Trans. 28:857–860.

    Article  PubMed  CAS  Google Scholar 

  • Ozawa, R., Arimura, G., Takabayashi, J., Shimoda, T., and Nishioka, T. 2000. Involvement of jasmonate- and salicylate-related signaling pathways for the production of specific herbivore-induced volatiles in plants. Plant Cell Physiol. 41:391–398.

    PubMed  CAS  Google Scholar 

  • Sato, Y. 1979. Experimental studies on parasitization by Apanteles glomeratus. IV. Factors leading a female to the host. Physiol. Entomol. 4:63–70.

    Article  Google Scholar 

  • Schmelz, E. A., Alborn, H. T., Banchio, E., and Tumlinson, J. H. 2003. Quantitative relationships between induced jasmonic acid levels and volatile emission in Zea mays during Spodoptera exigua herbivory. Planta 216:665–673.

    PubMed  CAS  Google Scholar 

  • Shiojiri, K., Takabayashi, J., Yano, S., and Takafuji, A. 2000a. Flight response of parasitoid toward plant–herbivore complexes: A comparative study of two parasitoid–herbivore systems on cabbage plants. Appl. Entomol. Zool. 35:87–92.

    Article  Google Scholar 

  • Shiojiri, K., Takabayashi, J., Yano, S., and Takafuji, A. 2000b. Herbivore-species-specific interactions between crucifer plants and parasitic wasps (Hymenoptera: Braconidae) that are mediated by infochemicals present in areas damaged by herbivores. Appl. Entomol. Zool. 35:519–524.

    Article  Google Scholar 

  • Takabayashi, J. and Dicke, M. 1996. Plant–carnivore mutualism through herbivore-induced carnivore attractants. Trends Plant Sci. 1:109–113.

    Article  Google Scholar 

  • Takabayashi, J., Noda, T., and Takahashi, S. 1991. Plants produce attractants for Apanteles kariyai, a parasitoid of Pseudaletia separata: Cases of “communication” and “misunderstanding” in parasitoid–plant interactions. Appl. Entomol. Zool. 26:237–243.

    Google Scholar 

  • Takabayashi, J., Sato, Y., Horikoshi, M., Yamaoka, R., Yano, S., Ohsaki, N., and Dicke, M. 1998. Plant effects on parasitoid foraging: Differences among two tritrophic systems. Biol. Control 11:97–103.

    Article  Google Scholar 

  • Van Poecke, R. M. P. and Dicke, M. 2002. Induced parasitoid attraction by Arabidopsis thaliana: Involvement of the octadecanoid and the salicylic acid pathway. J. Exp. Bot. 53:1793–1799.

    Article  PubMed  CAS  Google Scholar 

  • Whitman, D. W. and Eller, F. J. 1992. Orientation of Microplitis croceipes (Hymenoptera, Braconidae) to green leaf volatiles—Dose–response curves. J. Chem. Ecol. 18:1743–1753.

    Article  CAS  Google Scholar 

Download references

Acknowledgment

This study was supported by CREST of Japan Science and Technology Corporation (JST).

Author information

Authors and Affiliations

Authors

Corresponding author

Correspondence to Junji Takabayashi.

Rights and permissions

Reprints and permissions

About this article

Cite this article

Shiojiri, K., Ozawa, R., Matsui, K. et al. Role of the Lipoxygenase/lyase Pathway of Host-food Plants in the Host Searching Behavior of Two Parasitoid Species, Cotesia glomerata and Cotesia plutellae . J Chem Ecol 32, 969–979 (2006). https://doi.org/10.1007/s10886-006-9047-6

Download citation

  • Received:

  • Revised:

  • Accepted:

  • Published:

  • Issue Date:

  • DOI: https://doi.org/10.1007/s10886-006-9047-6

Keywords

Navigation