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Molecular analysis of banana streak virus integrants in the nuclear genome of Musa balbisiana

Piffanelli P., Noa-Carrazana J.C., Benabdelmouna A., Matsumoto T., Silva-Rosales L., Lheureux F., Teycheney P.Y., Geering A.D., D'Hont A., Frison E.A., Roux N., Côte F.X., Glaszmann J.C., Sasaki T., Caruana M.L.. 2004. In : Picq Claudine (ed.), Vézina Anne (ed.). First International congress on Musa: harnessing research for improved livelihoods, 6-9 July 2004, Penang, Malaysia. Abstract guide. Montpellier : INIBAP, p. 36-36. International Congress on Musa: Harnessing Research for Improved Livelihoods. 1, 2004-07-06/2004-07-09, Penang (Malaisie).

Recently, it was demonstrated that Banana streak virus (BSV) sequences are integrated into the nuclear genome of Musa balbisiana. There is strong experimental evidence that some of these BSV integrated sequences, called BSV endogenous pararetroviruses (BSV EPRVs), can give rise to infectious episomal BSV genomes upon stress conditions. Such stress include interspecific genetic crosses, therefore this phenomenon represents a serious limitation to the creation of novel Musa hydrids between A and B genomes and to the diffusion of such hybrids. As part of an international effort within the Musa Genomics Consortium aimed at defining the integration patterns of BSV EPRV sequences into the nuclear genome of Musa species and the mechanisms leading to the activation of such BSV EPRV sequences, we have constructed and characterised three BAC libraries from M. acuminata 'Cavendish' (AAA), M. acuminata 'Calcutta 4' (AA) and M. balbisiana PKW (BB) nuclear genomes, respectively. Complete genomes of four different BSV strains (BSV-Ol "Obino L'Ewai", BSV-Gf "Gold Finger", BSV-Im "Imove", BSV-Mys "Mysore") were used as probes to screen the BAC libraries and FISH experiments were carried out to test for the presence of integrated viral sequences within Musa A and B chromosomes. Upon screening we identified 10 BAC clones positive for BSV-Ol, 9 BAC clones positive for BSV-Gf and 24 BAC clones positive for BSV-Im from the M. balbisiana PKW BAC library. On the other hand, screening of either M. acuminata 'Calcutta 4' and M. acuminata 'Cavendish' BAC libraries with the four complete viral sequences revealed that none of these BAC clones contained any BSV sequences. BAC clones found positive upon screening were further characterized by BAC-end sequencing and RFLP-fingerprinting, and selected BACs containing BSV-Ol or BSV-Gf EPRV sequences were completely sequenced. Detailed analysis of the nucleotide sequences and chromosomal organisation of BSV-Ol and BSV-Gf EPRV seq

Mots-clés : musa balbisiana; génétique moléculaire; génome; noyau cellulaire; virus des végétaux; hybride; séquence nucléotidique; musa acuminata; banque de gènes

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