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Virulence genes are carried by a megaplasmid of the plant pathogen Pseudomonas solanacearum

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Summary

A class of avirulent mutants of the plant pathogenic bacterium Pseudomonas solanacearum, strain GMI1000, resistant to acridine orange (Acrr), harbour a deletion of over 85 kb in their genome. This deletion affects, a≤1,000 kb megaplasmid which has previously been shown to be present in most of the strains of this species. In addition at least 11 out of 13 independent Tn5 insertions, leading to loss of virulence, are located on the megaplasmid. Nine of them are present in the region which is deleted from the Acrr mutants. These results suggest that the majority of virulence genes identified so far are plasmid borne.

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References

  • Banfalvi Z, Kondorosi E, Kondorosi A (1985) Rhizobium meliloti carries two megaplasmids. Plasmid 13:129–138

    Google Scholar 

  • Batut J, Terzaghi B, Ghérardi M, Huguet M, Terzaghi E, Garnerone AM, Boistard P, Huguet T (1985) Localization of a symbiotic fix region on Rhizobium meliloti pSym megaplasmid more than 200 kilobases from the nod-nif region. Mol Gen Genet 199:232–239

    Google Scholar 

  • Boucher C, Message B, Debieu D, Dischek C (1981) Use of P-1 incompatibility group plasmids to introduce transposons into Pseudomonas solanacearum. Phytopathology 71:639–642

    Google Scholar 

  • Boucher CA, Barberis PA, Trigalet AP, Démery DA (1985) Transposon mutagenesis of Pseudomonas solanacearum: isolation of Tn5-induced avirulent mutants. J Gen Microbiol 131:2449–2457

    Google Scholar 

  • Buddenhagen I, Kelman A (1964) Biological and physiological aspects of bacterial wilt caused by Pseudomonas solanacearum. Ann Rev Phytapathol 2:203–230

    Google Scholar 

  • Burkardt E, Burkardt HJ (1984) Visualization and exact molecular weight determination of a Rhizobium meliloti megaplasmid. J Mol Biol 175:213–218

    Google Scholar 

  • Cami B, Kourilsky P (1978) Screening of cloned recombinant DNA in bacteria by in situ colony hybridization. Nucleic Acids Res 5:2381–2390

    Google Scholar 

  • Comai L, Kosuge T (1980) Involvement of plasmid deoxyribonucleic acid in indolacetic acid synthesis in Pseudomonas savastanoi. J Bacteriol 143:950–957

    Google Scholar 

  • Dagert M, Ehrlich SD (1979) Prolonged incubation in calcium chloride improves the competence of Escherichia coli cells. Gene 6:23–28

    Google Scholar 

  • Ditta G, Stanfield S, Corbin D, Helinski D (1980) Broad host range DNA cloning system for gram-negative bacteria: construction of a gene bank of Rhizobium meliloti. Proc Natl Acad Sci USA 77:7347–7351

    Google Scholar 

  • Driguès P, Démery-Lafforgue D, Trigalet A, Dupin P, Samain D, Asselineau J (1985) Comparative studies of lipopolysaccharide and exopolysaccharide from a virulent strain of Pseudomonas solanacearum and from three avirulent mutants. J Bacteriol 162:504–509

    Google Scholar 

  • Friedman AM, Long SR, Brown SE, Buikema WJ, Ausubel FM (1982) Construction of a broad host range cosmid cloning vector and its use in the genetic analysis of Rhizobium mutants. Gene 18:289–296

    Google Scholar 

  • Hendrick CA, Sequeira L (1984) Lipopolysaccharide-defective mutants of the wilt pathogen Pseudomonas solanacearum. Appl Environ Microbiol 48:94–101

    Google Scholar 

  • Hirota Y (1960) The effect of acridine dyes on mating type factors in Escherichia coli. Genetics 46:57

    Google Scholar 

  • Husain A, Kelman A (1958) The role of pectic and celluloytic enzymes in pathogenesis by Pseudomonas solanacearum. Phytopathology 48:377–386

    Google Scholar 

  • Kelman A (1953) The bacterial wilt caused by Pseudomonas solanacearum. North Carolina Agricultural Experiment Station Technical Bulletin 99

  • Kelman A (1954) The relationship of pathogenicity in Pseudomonas solanacearum to colony appearance on a tetrazolium medium. Phytopathology 44:693–695

    Google Scholar 

  • Kerr A, Manigault P, Tempé J (1977) Transfer of virulence in vivo and in vitro in Agrobacterium. Nature 265:560–561

    Google Scholar 

  • Long SR (1984) Genetics of Rhizobium nodulation. In: Kosuge T, Nester E (eds) Plant-microbe interaction. Macmillan Publishing Co, NY, pp 265–306

    Google Scholar 

  • Maniatis T, Fritsch E, Sambrook J (1982) Molecular cloning. A laboratory manual. Cold Spring Harbor Laboratory, Cold Spring Harbor, NY

    Google Scholar 

  • Message B, Boistard P, Pitrat M, Schmit J, Boucher C (1978) A new class of fluidal avirulent mutants of Pseudomonas solanacearum unable to induce a hypersensitive reaction. Proc 4th Interactional Conference on Plant Pathogenic Bacteria. Station de pathologie végétale INRA, 49000 Beaucouzé, France, pp 823–833

  • Murai N, Skoog F, Doyle ME, Hanson R (1980) Relationships between cytokinin production, presence of plasmids, and fasciation caused by strains of Corynebacterium fascians. Proc Natl Acad Sci USA 77:619–623

    Google Scholar 

  • Piwowarski JM, Shaw P (1982) Characterization of plasmids from plant pathogenic Pseudomonads. Plasmid 7:85–94

    Google Scholar 

  • Rosenberg C, Casse-Delbart F, Dusha I, David M, Boucher C (1982) Megaplasmids in the plant associated Rhizobium meliloti and Pseudomonas solanacearum. J Bacteriol 150:402–406

    Google Scholar 

  • Sequeira L, Kelman A (1961) The accumulation of growth substances in plant infected by Pseudomonas solanacearum. Phytopathology 52:439–448

    Google Scholar 

  • Sparks RB, Lacy GH (1980) Purification and characterization of cryptic plasmids pLS1 and pLS2 from Erwinia chrysanthemi. Phytopathology 70:369–372

    Google Scholar 

  • Staskawicz BJ, Dahlbeck D, Miller J, Damm D (1983) Molecular analysis of virulence genes in Pseudomonas solanacearum. In: Pülher A (ed) Molecular genetics of the bacteria-plant interaction. Springer, Berlin Heidelberg New York, pp 345–352

    Google Scholar 

  • Van Gijsegem F, Toussaint A, Schoonejans E (1985) In vivo cloning of the pectate lyase and cellulase genes of Erwinia chrysanthemi. EMBO J 4:787–792

    Google Scholar 

  • Van Larebecke N, Engler G, Holster M, Van den Elsacker S, Zaenen I, Schilperoot RA, Schell J (1974) Large plasmid in Agrobacterium tumefaciens essential for crown-gall inducing ability. Nature 252:169–170

    Google Scholar 

  • White FF, Neser EW (1980) Hairy root: plasmid encodes virulence trait in Agrobacterium rhizogenes. J Bacteriol 141:1134–1141

    Google Scholar 

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Communicated by J. Schell

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Boucher, C., Martinel, A., Barberis, P. et al. Virulence genes are carried by a megaplasmid of the plant pathogen Pseudomonas solanacearum . Molec. Gen. Genet. 205, 270–275 (1986). https://doi.org/10.1007/BF00430438

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  • DOI: https://doi.org/10.1007/BF00430438

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