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  Eur.J.Hortic.Sci. 83 (3) 125-134 | DOI: 10.17660/eJHS.2018/83.3.1
ISSN 1611-4426 print and 1611-4434 online | © ISHS 2018 | European Journal of Horticultural Science | Original article

In vitro shoot multiplication and rooting of wild Paeonia officinalis L., subsp. officinalis

G. Marino, F. Grandi, E. Muzzi and M.E. Giorgioni
Dip. Scienze e Tecnologie Agro-Alimentari (DISTAL), Università di Bologna, 40127 Bologna, Italy

SUMMARY
Paeonia officinalis L., subsp. officinalis, is a herbaceous peony spontaneously growing on rocky slopes, up to 1,800 m of altitude, from Southern France to Albany, that includes Tuscan and Emilian Apennines. Its propagation occurs by rhizome or seeds under natural growing conditions; however, seeds need a couple of years to germinate. The aim of the present research was to set up a protocol for the in vitro propagation of this species, useful for its reintroduction in the natural environment, and suitable at nursery level. The combined effect of 6-benzyladenine (BA) and polyvinylpyrrolidone (PVP) was investigated on shoot multiplication of single shoots and small shoot clusters, in agarized culture media. A two-step rooting procedure was used, providing one-week culture of shoots in complete darkness on media enriched with indole-3-butyric acid (IBA) and their transfer to auxin-free media. Agarized media or perlite soaked in liquid media were used for both root induction and elongation phases.
Complete culture survival was obtained with 1.0 g L-1 PVP and the use of small shoot clusters as explants. BA at 2.0 mg L-1 gave the maximum mean shoot multiplication (2.7) from a single shoot at the 3rd subculture; however, very short shoots were produced by shoot clusters after three further subcultures. BA at 1.0 g L-1 allowed a constant multiplication (about 2:1) of well-elongated shoots regardless of the explant type. The multiplication rates reported here are quite low, but comparable to data available in the literature for in vitro grown shoots of wild herbaceous P. lactiflora. The maximum rooting percentage (50%) was obtained in liquid media, for shoots from 1.0 mg L-1 BA treated with 2.5 mg L-1 IBA, although not different from other IBA treatments (1 and 5 mg L-1). The present results are promising with regard to the in vitro phases. However, they also suggest further research in improving rooting and achieving successful acclimatization of healthy plants. If this goal is reached, micropropagation might represent an alternative vegetative propagation method for the reintroduction in the natural environment of this species, and its release at nursery level as plant for gardens.

Keywords BA, in vitro propagation, micropropagation, PVP, wild herbaceous peony

Significance of this study

What is already known on this subject?

  • The present paper follows our previous results on wild P. officinalis embryo culture and shoot induction. Very poor data are available in the literature on micropropagation of this species.
What are the new findings?
  • BA and PVP combinations strongly influenced shoot multiplication rates and survival. Best rooting of the shoots was in perlite soaked in liquid culture medium.
What is the expected impact on horticulture?
  • Micropropagation might favour plant reintroduction in the natural environment and the use for gardening of wild P. officinalis, naturally propagated by rhizome or seeds.

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E-mail: mariaeva.giorgioni@unibo.it  

References

  • Bouza, L., Jacques, M., Scotta, B., and Miginiac, E. (1994). Relation between auxin and cytokinin contents and in vitro rooting of three Peony (Paeonia suffruticosa Andr.). Plant Growth Reg. 15, 69–73. https://doi.org/10.1007/BF00024678.

  • Buchheim, J.A.T., Burkhart, L.F., and Meyer, M.M. (1994). Effect of exogenous gibberellic acid, abscisic acid, and benzylaminopurine on epicotyls dormancy of cultured herbaceous peony embryos. Plant Cell Tissue Org. Cult. 36, 35–43. https://doi.org/10.1007/BF00048313.

  • George, E.F. (1993). Plant Propagation by Tissue Culture, Part 1, The Technology (Edington, Wilts.: Exegetics Ltd.).

  • George, E.F., Hall, M.A., and De Klerk, G.J. (2007). Plant Propagation by Tissue Culture, Vol. 1, The Background (Springer Science & Business Media).

  • Gabryszewska, E. (1998). The influence of cytokinins, thidiazuron, paclobutrazol and red light on shoot proliferation of herbaceous peony cv. Jadwiga in vitro. J. Fruit Ornam. Plant Res. 6(3–4), 157–169.

  • Gabryszewska, E. (2010). The effects of glucose and growth regulators on the organogenesis of Paeonia lactiflora Pall. in vitro. J. Fruit Ornam. Plant Res. 18(2), 309–320.

  • Gabryszewska, E., and Kawa-Miszczak, L. (2009). Rooting in vitro and acclimatization in the greenhouse of herbaceous peony plantlets. 12th National Conference In vitro Cultures, Poznan, Poland, 9–11 Sept. (poster).

  • Hazarika, B.N. (2006). Morpho-physiological disorders in in vitro culture of plants. Sci. Hortic. 108, 105–120. https://doi.org/10.1016/j.scienta.2006.01.038.

  • Hosoki, T., Ando, M., Kubara, T., Hamada, M., and Itami, M. (1989). In vitro propagation of herbaceous peony (Paeonia lactiflora Pall.) by a longitudinal shoot-split method. Plant Cell Rep. 8, 243–246. https://doi.org/10.1007/BF00778543.

  • Marino, G., Grandi, F., Valente, C., and Giorgioni, M.E. (2014). Primi risultati sulla moltiplicazione in vitro di Paeonia officinalis a partire da embrioni (Preliminary results on in-vitro propagation of Paeonia officinalis through the use of embryos as initial explants). In Atti X Convegno sulla Biodiversità, Roma, 3–5 sept. (Roma: CNR). e-book, ISBN 978-88-97081-76-0, p.106–112.

  • Murashige, T., and Skoog, F. (1962). A revised medium for rapid growth and bioassays with tobacco tissue cultures. Physiol. Plant. 15, 473–497. https://doi.org/10.1111/j.1399-3054.1962.tb08052.x.

  • Rather, Z.A., and Paul, T.M. (2010). Studies on in vitro propagation of peony (Paeonia spp.) in Kashmir. http://dspaces.uok.edu.in/jspui//handle/1/1060.

  • Rogers, A. (2009). Peonies. (UK: Timber Press).

  • Sahrawat, A.K., and Chand, S. (2001). Continuous somatic embryogenesis and plant regeneration from hypocotyl segments of Psoralea corylifolia Linn., an endangered and medicinally important Fabaceae plant. Current Sci. 81(10), 1328–1331.

  • Seyring, M. (2000). Mikrovermehrungbei Paeonien. Ausfallrate ist noch zu hoch.Das TASPO Gartenbaumagazin 10(2), 30–31 (Braunschweig: Thalacker Medien).

  • Seyring, M. (2002). In vitro cloning of Helleborus niger. Plant Cell Rep. 20, 895–900. https://doi.org/10.1007/s00299-001-0420-1.

  • Shen, M., Wang, Q., Yu, X.N., and Teixeira da Silva, J.A. (2012). Micropropagation of herbaceous peony (Paeonia lactiflora Pall.). Sci. Hortic. 148, 30–38. https://doi.org/10.1016/j.scienta.2012.09.017.

  • Tian, D., Tilt, K.M., Dane, F., Woods, F.M., and Sibley, J.L. (2010). Comparison of shoot induction ability of different explants in herbaceous peony (Paeonia lactiflora Pall.). Sci. Hortic. 123, 385–389. https://doi.org/10.1016/j.scienta.2009.10.007.

  • Yu, X.N., Wu, H.J., Teixeira da Silva, J.A., and Shen, M.M. (2012). Multiple shoot induction and rooting of Paeonia lactiflora ‘Da Fu Gui’. African J. Biotech. 11(41), 9776–9781.

  • Zar, J.H. (1984). Biostatistical Analysis (Englewood Cliffs, NJ: Prentice-Hall Inc.).

Received: 19 September 2017 | Accepted: 6 March 2018 | Published: 26 June 2018 | Available online: 26 June 2018

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