© Benaki Phytopathological Institute
        
        
          Abstracts - 16th Hellenic Phytopathological Congress
        
        
          31
        
        
          P.F. S
        
        
          ARRIS
        
        
          1
        
        
          *, E.A. T
        
        
          RANTAS
        
        
          1
        
        
          , D.A. B
        
        
          ALTRUS
        
        
          3
        
        
          , C.T. B
        
        
          ULL
        
        
          4
        
        
          , W.P. W
        
        
          ECHTER
        
        
          5
        
        
          , S. Y
        
        
          AN
        
        
          6
        
        
          , C.D. J
        
        
          ONES
        
        
          7
        
        
          ,
        
        
          J.L. D
        
        
          ANGL
        
        
          7,8
        
        
          , N.J. P
        
        
          ANOPOULOS
        
        
          2,9
        
        
          , F.N. V
        
        
          ERVERIDIS
        
        
          1
        
        
          , B.A. V
        
        
          INATZER
        
        
          6
        
        
          and D.E. G
        
        
          OUMAS
        
        
          1
        
        
          1
        
        
          Department of Plant Sciences, School of Agricultural Technology, Technological
        
        
          Educational Institute of Crete, Greece.
        
        
          2
        
        
          Department of Biology, University of
        
        
          Crete, Heraklion, Greece.
        
        
          3
        
        
          School of Plant Sciences, The University of Arizona,
        
        
          Tucson, Arizona, USA.
        
        
          4
        
        
          United States Department of Agriculture, Agricultural
        
        
          Research Service, Salinas, CA, USA.
        
        
          5
        
        
          United States Department of Agriculture–
        
        
          Agricultural Research Service, Charleston, South Carolina, USA.
        
        
          6
        
        
          Department of
        
        
          Plant Pathology, Physiology, and Weed Science, Virginia Tech, Blacksburg, Virginia,
        
        
          USA.
        
        
          7
        
        
          Department of Biology, University of North Carolina at Chapel Hill, Chapel
        
        
          Hill, North Carolina, USA.
        
        
          8
        
        
          Howard Hughes Medical Institute.
        
        
          9
        
        
          Professor Emeritus,
        
        
          University Crete, Heraklion, Greece and University of California, Berkeley, CA, USA.
        
        
          *Present Address: The Sainsbury Laboratory, John Innes Centre, Norwich Research
        
        
          Park, Norwich NR4 7UH, UK
        
        
          nage
        
        
          pv.
        
        
          maculicola
        
        
          ES4326 as identical to
        
        
          Pcal
        
        
          ES4326, the model pathogen
        
        
          P. syringae
        
        
          pv.
        
        
          tomato
        
        
          DC3000 of
        
        
          Arabidopsis thaliana
        
        
          and
        
        
          tomato, and
        
        
          P. syringae
        
        
          pv.
        
        
          syringae
        
        
          B728a
        
        
          bean pathogen. All
        
        
          Pcal
        
        
          strains harbour two
        
        
          genomic islands containing genetic elements
        
        
          for type VI secretion systems (T6SSs). Surpris-
        
        
          ingly, one of the
        
        
          Pcal
        
        
          T6SS is phylogenetical-
        
        
          ly closer to
        
        
          P. aeruginosa
        
        
          T6SS-I than the
        
        
          P. sy-
        
        
          ringae
        
        
          T6SSs. All
        
        
          Pcal
        
        
          strains also harbour a
        
        
          hrp/hrc
        
        
          gene cluster coding for a type III se-
        
        
          cretion apparatus (T3SS), which in regard to
        
        
          structure and DNA sequence is most similar
        
        
          to
        
        
          Psy
        
        
          B728a, although
        
        
          Pst
        
        
          DC3000 is the clos-
        
        
          er relative, suggesting horizontal gene trans-
        
        
          fer of the
        
        
          hrp/hrc
        
        
          cluster between the strains’
        
        
          ancestors. Although the overall genetic con-
        
        
          tent of each of the four
        
        
          Pcal
        
        
          genomes appears
        
        
          to be highly similar, the repertoire of the type
        
        
          III effector proteins (T3EPs) was found to be
        
        
          significantly divergent between the exam-
        
        
          ined strains, reinforcing previous molecular
        
        
          data suggesting the existence of two distinct
        
        
          lineages within this pathovar of
        
        
          Pseudomonas
        
        
          cannabina
        
        
          .
        
        
          Comparative genomic study of closely re-
        
        
          lated
        
        
          pathogens
        
        
          with different host range
        
        
          provides insights into mechanisms of host-
        
        
          pathogen interaction, differential virulence
        
        
          factors, and pathogen evolution. Moreover,
        
        
          sequencing of various strains of the same
        
        
          pathogen can reveal additional information
        
        
          concerning pathogen diversity and the mo-
        
        
          lecular basis of virulence differences between
        
        
          strains. In the current study we present draft
        
        
          genome sequences and a comparative ge-
        
        
          nomics analysis of four strains of
        
        
          Pseudomo-
        
        
          nas cannabina
        
        
          pv.
        
        
          alisalensis
        
        
          (
        
        
          Pcal
        
        
          ), one of the
        
        
          causative agents of bacterial blight of cruci-
        
        
          fers, isolated from geographically distant ar-
        
        
          eas of Greece and the USA. Since
        
        
          Pcal
        
        
          causes
        
        
          disease in a wide range of plant species and
        
        
          can infect both monocots and dicots, includ-
        
        
          ing the model plants
        
        
          Arabidopsis thaliana
        
        
          and
        
        
          tomato, draft genome sequences of four
        
        
          Pcal
        
        
          strains were obtained to develop hypothe-
        
        
          ses regarding the molecular basis of virulence
        
        
          and host range determinants of this patho-
        
        
          gen. Genomes were also compared to the ge-
        
        
          nome of the recently reclassified strain
        
        
          P. syri-
        
        
          
            Study of the resistance of tomato hybrid CLX3731 transgenic plants
          
        
        
          
            overexpressing the
          
        
        
          
            gmgstu4
          
        
        
          
            gene after infection with the bacterium
          
        
        
          
            P.
          
        
        
          
            syringae
          
        
        
          
            pv.
          
        
        
          
            tomato
          
        
        
          Ν. Τ
        
        
          ZIOUTZIOU
        
        
          1
        
        
          , P. M
        
        
          ADESIS
        
        
          2
        
        
          and I. Ν
        
        
          IANIOU
        
        
          -Ο
        
        
          BEIDAT
        
        
          1
        
        
          1
        
        
          Laboratory of Genetics and Plant Breeding, School of Agriculture, A.U.TH. , GR-541
        
        
          24 Thessaloniki, Greece.
        
        
          2
        
        
          Institute of Agrobiotechnology, C.E.R.TH., 6
        
        
          th
        
        
          km Charilaou-
        
        
          Thermis Road, GR-570 01 Thermi, Thessaloniki, Greece