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Parasitism of seed of Douglas fir (Pseudotsuga menziesii) by the seed chalcid, Megastigmus spermotrophus, and its influence on seed hormone physiology

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Abstract

Parasitism of Douglas fir (Pseudotsuga menziesii) megagametophytes by the seed chalcid, Megastigmus spermotrophus Wachtl, occurs naturally after pollination but before fertilization. In the absence of fertilization, the presence of insect larvae within the megagametophyte prevents abortion and the storage tissue continues to develop as if the seed had been fertilized. We investigated the effect of parasitism on the metabolism of abscisic acid (ABA), auxins, cytokinins, and gibberellins during early development of Douglas fir seeds. Hormones and hormone metabolites of infested and uninfested megagametophytes with or without pollination were analyzed by HPLC–ESI/MS/MS. At 1 week after Megastigmus introduction, the insect’s presence stimulated ABA accumulation in unpollinated megagametophytes compared to unpollinated, unparasitized megagametophytes. In pollinated material, parasitism did not stimulate ABA accumulation compared to levels present in unparasitized megagametophytes. In all four treatments, the metabolism of ABA occurred primarily through conjugation to the ABA glucose ester (ABAGE), while the 7′-, 8′- and, 9′-hydroxylation pathways were only minor. ABAGE levels declined with time in all treatments and this occurred to a greater extent in pollinated, parasitized megagametophytes, suggesting that the insect’s presence induced the dramatic decrease in ABAGE. Although there were temporal variations in the auxin, cytokinin, and gibberellin profiles of parasitized megagametophytes, the profiles were generally similar to those of unparasitized megagametophytes. Our results suggest that failure of parasitized megagametophytes to abort may be due to the insect inducing similar hormone profiles to those present during normal development of Douglas fir seed.

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References

  • von Aderkas P, Rouault G, Wagner R, Chiwocha S, Roques A (2005a) Multinucleate storage cells in Douglas fir (Pseudotsuga menziesii (Mirbel) Franco) and the effect of seed infestation by the chalcid Megastigmus spermotrophus Wachtl. Heredity 94:616–622

    Article  CAS  Google Scholar 

  • von Aderkas P, Rouault G, Wagner R, Rohr R, Roques A (2005b) Seed parasitism redirects ovule development in Douglas fir. Proc R Soc Lond B Biol Sci 272:1491–1496

    Article  Google Scholar 

  • Chiwocha S, von Aderkas P (2002) Endogenous levels of free and conjugated forms of auxin, cytokinins, and abscisic acid during seed development in Douglas fir. Plant Growth Regul 36:191–200

    Article  CAS  Google Scholar 

  • Chiwocha SDS, Abrams SR, Ambrose SJ, Cutler AJ, Loewen M, Ross ARS, Kermode AR (2003) A method for profiling classes of plant hormones and their metabolites using liquid chromatography-electrospray ionization tandem mass spectrometry: an analysis of hormone regulation of thermodormancy of lettuce (Lactuca sativa L.) seeds. Plant J 35:405–417

    Article  PubMed  CAS  Google Scholar 

  • Chiwocha SDS, Cutler AJ, Abrams SR, Ambrose SJ, Yang J, Ross ARS, Kermode AR (2005) The etr1-2 mutation in Arabidopsis thaliana affects the abscisic acid, auxin, cytokinin and gibberellin metabolic pathways during maintenance of seed dormancy, most-chilling and germination. Plant J 42:35–48

    Article  PubMed  CAS  Google Scholar 

  • Cutler AJ, Krochko JE (1999) Formation and breakdown of ABA. Trends Plant Sci 4:472–478

    Article  PubMed  Google Scholar 

  • Dodeman VL, Ducreux G, Kreis M (1997) Zygotic embryogenesis versus somatic embryogenesis. J Exp Bot 48:1493–1509

    CAS  Google Scholar 

  • Feurtado JA, Ambrose SJ, Cutler AJ, Ross ARS, Abrams SR, Kermode AR (2004) Dormancy termination of western white pine (Pinus monticola Dougl. Ex D. Don) seeds is associated with changes in abscisic acid metabolism. Planta 218:630–639

    Article  PubMed  CAS  Google Scholar 

  • Finkelstein RR, Tenbarge KM, Shumway JE, Crouch ML (1985) Role of ABA in the maturation of rapeseed embryos. Plant Physiol 78:630–636

    Article  PubMed  CAS  Google Scholar 

  • Kapik RH, Dinus RJ, Dean JFD (1995). Abscisic acid and zygotic embryogenesis in Pinus taeda. Tree Physiol 15:485–490

    PubMed  CAS  Google Scholar 

  • Kucera B, Cohn MA, Leubner-Metzger G (2005) Plant hormone interactions during seed dormancy release and germination. Seed Sci Res 15:281–307

    Article  CAS  Google Scholar 

  • Mapes CC, Davies PJ (2001a) Indole-3-acetic acid and ball gall development on Solidago altissima. New Phytol 151:195–202

    Article  CAS  Google Scholar 

  • Mapes CC, Davies PJ (2001b) Cytokinins in the ball gall of Solidago altissima and in the gall forming larvae of Eurosta solidaginis. New Phytol 151:203–212

    Article  CAS  Google Scholar 

  • Nambara E, Marion-Poll A (2005) Abscisic acid biosynthesis and catabolism. Annu Rev Plant Biol 56:165–185

    Article  PubMed  CAS  Google Scholar 

  • Roques A, Skrzypczynska M (2003) Seed-infesting chalcids of the genus Megastigmus Dalman, 1820 (Hymenoptera: Torymidae) native and introduced to the West Palearctic region: taxonomy, host specificity and distribution. J Nat Hist 37:127–238

    Google Scholar 

  • Rouault G, Turgeon J, Candau J-N, Roques A, von Aderkas P (2004) Oviposition strategies of conifer seed chalcids in relation to host phenology. Naturwissenschaften 91:472–480

    Article  PubMed  CAS  Google Scholar 

  • Sandberg G, Ernstsen A, Hamnede M (1987) Dynamics of indole-3-acetic acid and indole-3-ethanol during maturation and germination of Pinus sylvestris seeds. Physiol Plant 71:411–418

    Article  CAS  Google Scholar 

  • Sauter A, Dietz K-J, Hartung W (2002) A possible stress physiological role of abscisic acid conjugates in root-to-shoot signalling. Plant Cell Environ 25:223–228

    Article  PubMed  CAS  Google Scholar 

  • Singh H (1978) Embryology of gymnosperms. Gebrüder Borntraeger, Berlin

    Google Scholar 

  • Weis AE, Walton R, Crego CL (1988) Reactive plant tissue sites and the population biology of gall makers. Annu Rev Entomol 33:467–486

    Article  Google Scholar 

  • Zhou R, Cutler AJ, Ambrose SJ, Galka MM, Nelson KM, Squires TM, Loewen MK, Jadhav AS, Ross ARS, Taylor DC, Abrams SR (2004) A new abscisic acid catabolic pathway. Plant Physiol 134:361–369

    Article  PubMed  CAS  Google Scholar 

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Acknowledgments

We gratefully acknowledge the help of Drs. R. Bennett, Allison R. Kermode, and Andrew R.S. Ross, as well as Andrea Coulter, Chris Dewdney, Jenny Robb, Stephen O’Leary, and Stephen J. Ambrose. The following agencies provided support for this research: Protein Engineering Network of Centres of Excellence, Fonds France-Canada pour la Recherche, Conseil Général de la Région Centre, Canadian Forestry Service, British Columbia Ministry of Forests and the Natural Sciences and Engineering Research Council of Canada.

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Correspondence to S. Chiwocha or P. von Aderkas.

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Communicated by Scott Russell.

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Chiwocha, S., Rouault, G., Abrams, S. et al. Parasitism of seed of Douglas fir (Pseudotsuga menziesii) by the seed chalcid, Megastigmus spermotrophus, and its influence on seed hormone physiology. Sex Plant Reprod 20, 19–25 (2007). https://doi.org/10.1007/s00497-006-0039-z

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