6533b837fe1ef96bd12a1e8f

RESEARCH PRODUCT

A chromosome map of the Flavescence dorée phytoplasma

Sylvie Malembic-maherSylvie Malembic-maherElisabeth Boudon-padieuElisabeth Boudon-padieuElisabeth Boudon-padieuXavier FoissacXavier FoissacFiona ConstableFiona ConstableFiona ConstableGuillaume ArnaudGuillaume ArnaudAgnès CimermanAgnès CimermanPatricia CarlePatricia Carle

subject

DNA BacterialPhytoplasmaBACTERIOLOGIEMolecular Sequence DataCARTOGRAPHIE GENETIQUEMicrobiologyRestriction fragmentFLAVESCENCE DOREEMALADIE DES PLANTES03 medical and health sciencesBacterial ProteinsMOLLICUTEDeoxyribonucleases Type II Site-Specific030304 developmental biologySouthern blotGenetics0303 health sciencesbiology030306 microbiologyChromosomeFabaceaeGenes rRNASequence Analysis DNAGenome projectGENETIQUEPhysical Chromosome Mappingbiology.organism_classificationElectrophoresis Gel Pulsed-FieldBlotting SouthernRestriction site[SDV.MP]Life Sciences [q-bio]/Microbiology and ParasitologyItalyPHYTOPLASME DE LA FLAVESCENCE DOREEPhytoplasmabiology.proteinMollicutesCARTE CHROMOSOMIQUEFranceRRNA Operon

description

International audience; The Flavescence dorée phytoplasma (FD-P), a non-cultivable, plant-pathogenic bacterium of the class Mollicutes, is the causal agent of a quarantine disease affecting vineyards of southern Europe, mainly in southern France and northern Italy. To investigate FD-P diversity and phytoplasma genetic determinants governing the FD-P life cycle, a genome project has been initiated. A physical map of the chromosome of FD-P strain FD92, purified from infected broad beans, was constructed by performing restriction digests of the chromosome and resolving the fragments by PFGE. Single and double digestions of the chromosome with the enzymes SalI, BssHII, MluI and EagI were performed and used to map 13 restriction sites on the FD-P chromosome. The size of the chromosome was calculated to be 671 kbp. Southern blot analyses using cloned phytoplasma probes were carried out to assist in the arrangement of contiguous restriction fragments and to map eight genetic loci, including the two rRNA operons, the tuf, uvrB-degV and secY-map (FD9) genes, the FD2 marker and two orphan sequences (FDDH29 and FDSH05) isolated through subtractive suppression hybridization.

10.1099/mic.0.2007/013888-0https://hal.inrae.fr/hal-02664031