Medium-term
and long-term in vitro conservation and safe international exchange
of yam (Dioscorea spp.) germplasm
Bernard Malaurie*
GeneTrop - Unité de Génétique
et d'Amélioration des Plantes - Centre ORSTOM** - 911 avenue
Agropolis - BP. 5045 -F. 34032. Montpellier Cedex 1, France.
Tel: Bureau (33)-- 4 67 41 62 44.Standard
(33)-- 4 67 41 61 00
Fax: (33)-- 4 67 54 78 00
E-mail : Bernard.Malaurie@mpl.orstom.fr
Marie-France Trouslot
GeneTrop - Unité de Génétique
et d'Amélioration des Plantes - Centre ORSTOM **- 911 avenue
Agropolis - BP. 5045 -F. 34032. Montpellier Cedex 1, France.
Julien Berthaud
GeneTrop - Unité de Génétique
et d'Amélioration des Plantes - Centre ORSTOM** - 911 avenue
Agropolis - BP. 5045 -F. 34032. Montpellier Cedex 1, France.
Mustapha Bousalem
Laboratoire de Phytovirologie
des Régions Chaudes (LPRC) - CIRAD-ORSTOM** - avenue du val de
Montferrand - BP. 5035 -F. 34032 - Montpellier Cedex 1, France.
Agnès Pinel
Laboratoire de Phytovirologie
des Régions Chaudes (LPRC) - CIRAD-ORSTOM** - avenue du val de
Montferrand - BP. 5035 -F. 34032 - Montpellier Cedex 1, France.
Jean Dubern
Laboratoire de Phytovirologie
des Régions Chaudes (LPRC) - CIRAD-ORSTOM** - avenue du val de
Montferrand - BP. 5035 -F. 34032 - Montpellier Cedex 1, France.
E-mail : dubern@melusine.mpl.orstom.fr
http://www.mpl.orstom.fr
*Corresponding author
**ORSTOM is now called IRD, Institut de Recherche pour le Developpement.
Keywords:
Active and base in vitro genebanks', Chemotherapy, Cryopreservation,
Disease-free techniques, Indexation techniques, Slow growth condition
culture, Virus eradication, Yam viruses.
Yam edible tubers feed
million of peoples in the intertropical area, where they represent 12%
of human feeding. However, as a vegetatively propagated crop, yam is
seriously affected by an accumulation of pathogens. Establishing in
vitro germplasm collection is a process that cleans the plants from
all diseases but viruses. It gives a good control on the preservation
of the yam genetic resources and facilitates international exchanges
of healthy plant material.
Two kinds of in vitro germplasm preservation were considered :
slow growth condition culture for mid-term preservation, and cryopreservation
using the encapsulation/dehydration technique for long-term preservation.
Virus eradication was approached by meristem culture and chemo and thermotherapy.
Production of virus-free plants was controlled by ELISA.
We succeeded in the introduction and maintenance of 20 yam species,
under slow growth conditions. Cryopreservation was applied successfully
on two edible yam species, Dioscorea. alata L and D.
bulbifera L. Virus-free plants were obtained by meristem culture
in D. cayenensis-D. rotundata complex and D. praehensilis.
Indexation allowed the detection of different virus (poty-, potex-,
badna- and cucumovirus), where the most important potyvirus was YMV.
Mid-term conservation of yam germplasm is used routinely, and from these
conditions a direct acclimatization is possible. On the cryopreservation
aspect, experiments are under way to apply the optimized protocol to
genotypes which are more representative of the diversity, to insure
a routinely use. More work can be conducted now on virus eradication,
based on knowledge accumulated on potyvirus diversity, on several tests
available for yam indexing (ELISA, rt/PCR, monoclonal antibodies) and
on new sanitation techniques.
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