Eur. J. Entomol. 103 (2): 355-360, 2006 | DOI: 10.14411/eje.2006.047

The mechanism of the emergence of Cotesia kariyai (Hymenoptera: Braconidae) larvae from the host

Yutaka NAKAMATSU1, Toshiharu TANAKA1, Jeffrey A. HARVEY2
1 Applied Entomology, Graduate School of Bio-Agricultural Sciences, Nagoya University, Chikusa, Nagoya 464-8601, Japan; e-mail: nakamatu@nuagr1.agr.nagoya-u.ac.jp
2 NIOO-KNAW, Centre for Terrestrial Ecology, Boterhoeksestraat 48, P.O. Box 40, 6666 ZG Heteren, Netherlands

At maturity, the endoparasitoid larvae of several subfamilies of the Braconidae have to emerge from inside of the host to pupate. Although the hosts hormonal milieu and the timing of larval parasitoid emergence have been studied, no report has yet focused on the physiological state of the host in connection with the emergence behavior of endoparasitoids. We investigated the mechanism of larval emergence behavior in a gregarious endoparasitoid, Cotesia kariyai. The parasitoid larvae inserted their mandibles into the host cuticle and perforated the integument by moving their head-capsule backwards and forwards. The emerging parasitoid larva must have a physical support (an "anchor") with the terminal appendages in order to exert the necessary pressure to cut the host integument. Morphological observations revealed that each parasitoid larva was enveloped in a capsule just before emerging from their host. Eight and nine day-old parasitoid larvae secreted material around their bodies to form these capsules. This material consisted of acid-glycoproteins which coated the exuvium of the 2nd instar larvae. The haemolymph volume of the parasitised host also decreased in later stages and was dramatically reduced immediatly prior to parasitoid emergence. This final reduction of the host haemolymph volume is the result of absorption by parasitoid larvae. This mechanism allows the parasitoid larvae to create an anchor more easily. The parasitoid larvae could also adhere to each other with the glycoprotein. In addition, these capsules prevent the leaking of host haemolymph through the emergence hole; these holes on the host integument were plugged by the capsules after parasitoid emergence. Although the pressure acquired by the anchor was lost once the head of the parasitoid larvae emerges from the host integument, the parasitoid larvae crawls out of the host cavity using backward pointing spines which enable the parasitoid to grip the capsule and move forward via peristaltic contractions.

Keywords: Braconidae, Cotesia kariyai, Noctuidae, Pseudaletia separata, emergence, emergence behavior, haemolymph volume, parasitoid, anchor

Received: July 8, 2005; Revised: October 25, 2005; Accepted: October 25, 2005; Published: April 6, 2006  Show citation

ACS AIP APA ASA Harvard Chicago Chicago Notes IEEE ISO690 MLA NLM Turabian Vancouver
NAKAMATSU, Y., TANAKA, T., & HARVEY, J.A. (2006). The mechanism of the emergence of Cotesia kariyai (Hymenoptera: Braconidae) larvae from the host. EJE103(2), 355-360. doi: 10.14411/eje.2006.047
Download citation

References

  1. ADAMO S.A., LINN C.E. & BECKAGE N.E. 1997: Correlation between changes in host behaviour and octopamine levels in the tobacco hornworm, Manduca sexta parasitised by the gregarious braconid parasitoid wasp Cotesia congregata. J. Exp. Biol. 200: 117-127 Go to original source...
  2. ALLEYNE M. & BECKAGE N.E. 1997: Parasitism-induced effects on host growth and metabolic efficiency in tobacco hornworm larvae parasitised by Cotesia congregata. J. Insect Physiol. 43: 407-424 Go to original source...
  3. ASKEW R.R. 1971: Parasitic Insect. Heinemann Educational Books, London, 316 pp
  4. BECKAGE N.E. 1997: The parasitic wasps secret weapon. Sci. Am. 277: 82-87 Go to original source...
  5. BECKAGE N.E., FOREMAN R.C., PALMATIER C.M. & TAN F.F. 2002: Inhibition of the larval ecdysis and emergence behavior of the parasitoid Cotesia congregata by methoprene. J. Insect Physiol. 48: 725-732 Go to original source...
  6. EASTHAM L.E.S. 1929: The post-embryonic development of Phaenoserphus viator Hal. (Proctotrupoidea), a parasite of the larva of Pterostichus niger (Carabidae), with notes on the anatomy of the larva. Parasitology 21: 1-21 Go to original source...
  7. FULTON B.B. 1940: The hornworm parasite Apanteles congregatus Say and the hyperparasite, Hypopteromalus tabacum (Fiych). Ann. Entomol. Soc. Am. 33: 231-244 Go to original source...
  8. GODFRAY H.C.J. 1994: Parasitoids-Behavioral and Evolutionary Ecology. Princeton University Press, New Jersey, 473 pp Go to original source...
  9. HARVEY J.A., KADASH K. & STRAND M.R. 2000: Differences in larval feeding behavior correlate with altered developmental strategies in two species of parasitic wasps: implications for the size-fitness hypothesis. Oikos 88: 621-629 Go to original source...
  10. HORTON D.R. & MOORE J. 1993: Behavioral effects of parasite and pathogens of insects. In Beckage N.E., Thompson S.N. & Federici B.A. (eds): Parasites and Pathogens of Insects. Vol. 1: Parasites. Academic Press, New York, pp. 107-124 Go to original source...
  11. NAGATA M., SEONG S. & YOSHITAKE N. 1980: Variation of the haemolymph volume with larval development of the silkworm, Bombyx mori. J. Sericult. Sci. Japan 49: 453-454
  12. NAKAMATSU Y., GYOTOKU Y. & TANAKA T. 2001: The endoparasitoid Cotesia kariyai (Ck) regulates the growth and metabolic efficiency of Pseudaletia separata larvae by venom and Ck polydnavirus. J. Insect Physiol. 47: 573-584 Go to original source...
  13. POULIN R. 1995: Adaptive changes in the behaviour of parasitised animals: a critical review. Int. J. Parasitol. 25: 1371-1383 Go to original source...
  14. TANAKA T., YAGI S. & NAKAMATSU Y. 1992: Regulation of parasitoid sex allocation and host growth by Cotesia (Apanteles) kariyai (Hymenoptera: Braconidae). Ann. Entomol. Soc. Am. 85: 310-316 Go to original source...
  15. SANO Y. 1965: Histological Technics. Nanzando Company, Tokyo
  16. WEINBERG H.L. 1980: Hemolymph volume determination in the tomato fruitworm, Heliothis zea. Experientia 36: 548-549 Go to original source...
  17. WIGGLESWORTH V.B. 1972: The Principles of Insect Physiology. Chapman and Hall, London, 827 pp Go to original source...

This is an open access article distributed under the terms of the Creative Commons Attribution 4.0 International License (CC BY 4.0), which permits use, distribution, and reproduction in any medium, provided the original publication is properly cited. No use, distribution or reproduction is permitted which does not comply with these terms.