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Pyoluteorin production byPseudomonas fluorescens strain CHA0 is involved in the suppression ofPythium damping-off of cress but not of cucumber

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Abstract

Pseudomonas fluorescens strain CHA0 is an effective biocontrol agent of various soilborne pathogens. It controls damping-off or root rot caused byPythium ultimum on cucumber, wheat and cress. Strain CHA0 synthesizes several antibiotic metabolites such as hydrogen cyanide, 2,4-diacetylphloroglucinol, and pyoluteorin. The role of pyoluteorin in the suppression of damping-off was investigated. Two Tn5 mutants (CHA660 and CHA661) of strain CHA0 were isolated which had lost the capacity to produce pyoluteorin but still produced 2,4-diacteylphloroglucinol and HCN. These mutants still inhibitedP. ultimum on malt agar (which favours the production of 2,4-diacetylphloroglucinol) but had partially lost the ability to inhibit this pathogen on King's B agar (which favours the production of pyoluteorin). The two pyoluteorin-negative mutants showed a reduced capacity to suppress damping-off of cress caused byP. ultimum but were as effective in the protection of cucumber against this pathogen as the wild-type strain.

These results indicate that, depending on the plant, pyoluteorin production plays a role in the suppression of damping-off by strain CHA0 without being a major mechanism in disease suppression. We suggest that the contribution of pyoluteorin to the biocontrol activity of strain CHA0 is determined by the quantity of this antibiotic produced in the rhizosphere, which might depend on the root exudates of the host plant.

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References

  • Bachmann BJ (1972) Pedigree of some mutant strains ofEscherichia coli K-12. Bacteriol Rev 36: 525–557

    Google Scholar 

  • Boulnois GJ, Varley JM, Sharpe GS and Franklin FCH (1985) Transposon donor plasmids, based on Collb-P9, for use inPseudomonas putida and a variety of other gram negative bacteria. Mol Gen Genet 200: 65–67

    Google Scholar 

  • Castric P (1977) Glycine metabolism byPseudomonas aeruginosa: hydrogen cyanide biosynthesis. J Bacteriol 130: 826–831

    Google Scholar 

  • Défago G, Berling C-H, Burger U, Haas D, Kahr G, Keel C, Voisard C, Wirthner P and Wüthrich B (1990) Suppression of black root rot of tobacco and other root diseases by strains ofPseudomonas fluorescens: potential applications and mechanisms. In: Hornby D, Cook RJ, Henis Y, Ko WH, Rovira AD, Schippers B and Scott PR (eds.) Biological Control of Soil-Borne Plant Pathogens. (pp. 93–108) CAB International

  • Gewitz HS, Pistorius EK, Voss H and Vennesland B (1976) Cyanide formation in preparations fromChlorella vulgaris Beijerinck: Effect of sonication and amygdalin addition. Planta (Berl) 131: 145–148

    Google Scholar 

  • Gutterson N (1990) Microbial fungicides: recent approaches to elucidating mechanisms. Crit. Rev. Biotechnol 10: 69–91

    Google Scholar 

  • Homma Y and Suzui T (1989) Role of antibiotic production in suppression of radish damping-off by seed bacterization withPseudomonas cepacia. Ann Phytopath Soc Japan 55: 643–652

    Google Scholar 

  • Howell CR and Stipanovic RD (1979) Control ofRhizoctonia solani on cotton seedlings withPseudomonas fluorescens and with an antibiotic produced by the bacterium. Phytopathology 69: 480–482

    Google Scholar 

  • Howell CR and Stipanovic RD (1980) Suppression ofPythium ultimum-induced damping-off of cotton seedlings byPseudomonas fluorescens and its antibiotic, pyoluteorin. Phytopathology 70: 712–715

    Google Scholar 

  • Howie W and Suslow T (1991) Role of antibiotic biosynthesis in the inhibition ofPythium ultimum in the cotton spermosphere and rhizosphere byPseudomonas fluorescens. Mol Plant-Microbe Interact 4: 393–399

    Google Scholar 

  • James D Jr and Gutterson N (1986). Multiple antibiotics produced byPseudomonas fluorescens Hv37a and their differential regulation by glucose. Appl Environ Microbiol 52: 1183–1189

    Google Scholar 

  • Jayaswal RK, Fernandez MA, Visintin L and Upadhyay RS (1992) Transposson Tn5-259 mutagenesis ofPseudomonas cepacia to isolate mutants deficient in antifungal activity. Can J Microbiol 38: 309–312

    Google Scholar 

  • Keel C, Maurhofer M, Oberhänsli Th, Voisard C, Haas D and Défago G. (1991) Role of 2,4-diacetylphoroglucinol in the suppression of take-all of wheat by a strain ofPseudomonas fluorescens. In: Beemster ABR, Bollen GJ, Gerlagh M, Ruissen MA, Schippers B and Tempel A (eds.) Biotic Interactions and Soil-Borne Diseases. pp. 335–338 Elsevier, Amsterdam, Oxford, New York, Tokyo

    Google Scholar 

  • Keel C, Schnider U, Maurhofer M, Voisard C, Laville J, Burger U, Wirthner P, Haas D and Défago G (1992) Suppression of root diseases byPseudomonas fluorescens CHAO: Importance of the bacterial secondary metabolite 2,4-diacetylphloroglucinol. Mol Plant-Microbe Interact 5: 4–13

    Google Scholar 

  • Keel C, Voisard C, Berling C-H, Kahr G and Défago G (1989) Iron sufficiency, a prerequisite for suppression of tobacco black root rot byPseudomonas fluorescens strain CHAO under gnotobiotic conditions. Phytopathology 79: 584–589

    Google Scholar 

  • Keel C, Wirthner Ph, Oberhänsli Th, Voisard C, Burger U, Haas D and Défago G (1990) Pseudomonads as antagonists of plant pathogens in the rhizosphere: role of the antibiotic 2,4-diacetylphloroglucinol in the supression of black root rot of tobacco. Symbiosis 9: 327–341

    Google Scholar 

  • King EO, Ward MK and Raney DE (1954) Two simple media for the demonstration of pyocyanin and fluorescein. J Lab Clin Med 44: 301–307

    Google Scholar 

  • Kraus J and Loper JE (1991) Biocontrol of Pythium damping-off of cucumber byPseudomonas fluorescens Pf-5: mechanistic studies. In: Keel C, Koller B and Défago G (eds.) Plant Growth Promoting Rhizobacteria-Progress and Prospects. pp. 172–176 IOBC Bulletin 14/8

  • Kraus J and Loper JE (1992) Lack of evidence for a role of antifungal metabolite production byPseudomonas fluorescens Pf-5 in biological control of Pythium damping-off of cucumber. Phytopathology 83: 264–271

    Google Scholar 

  • Maurhofer M, Keel C, Schnider U, Voisard C, Haas D and Défago G (1992) Influence of enhanced antibiotic production inPseudomonas fluorescens strain CHAO on its disease suppressive capacity. Phytopathology 82: 190–195

    Google Scholar 

  • Meyer J-M and Abdallah MA (1978) The fluorescent pigment ofPseudomonas fluorescens: biosynthesis, purification and physicochemical properties. J Gen Microbiol 107: 319–328

    Google Scholar 

  • Ohmori T, Hagiwara S, Ueda A, Minoda Y and Yamada K (1978) Production of pyoluteorin and its derivatives fromn-paraffin byPseudomonas aeruginosa S 10B2. Agric Biol Chem 42: 2031–2036

    Google Scholar 

  • Stanisich VA and Holloway BW (1972) A mutant sex factor ofPseudomonas aeruginosa. Genet Res 19: 91–108

    Google Scholar 

  • Stutz E, Défago G and Kern H (1986) Naturally occurring fluorescent pseudomonads involved in supression of black root rot of tobacco. Phytopathology 76: 181–185.

    Google Scholar 

  • Thomashow LS and Weller DM (1988) Role of a phenazine antibiotic fromPseudomonas fluorescens in biological control ofGaeumannomyces graminis var.tritici. J Bacteriol 170: 3499–3508

    Google Scholar 

  • Thomashow LS, Weller DM, Bonsall RF and Pierson III LS (1990) Production of the antibiotic phenazine-1-carboxylic acid by fluorescentPseudomonas species in the rhizosphere of wheat. Appl Environ Microbiol 56: 908–912

    Google Scholar 

  • Voisard C, Rella M and Haas D (1988) Conjugative transfer of plasmid RP1 to soil isolates ofPseudomonas fluorescens is facilitated by certain large RP1 deletions. FEMS Microbiol Lett 55: 9–14

    Google Scholar 

  • Voisard C, Keel C, Haas D and Défago G (1989) Cyanide production byPseudomonas fluorescens helps suppress black root rot of tobacco under gnotobiotic conditions. EMBO J 8: 361–358

    Google Scholar 

  • Wüthrich B and Défago G (1991) Suppression of wheat take-all and black root rot of tobacco byPseudomonas fluorescens strain CHAO: results of field and pot experiments. In: Keel C, Keller B and Défago G (eds.) Plant Growth Promoting Rhizobacteria-Progress and Prospects (pp. 17–22) IOBC Bulletin 14/8

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Maurhofer, M., Keel, C., Haas, D. et al. Pyoluteorin production byPseudomonas fluorescens strain CHA0 is involved in the suppression ofPythium damping-off of cress but not of cucumber. Eur J Plant Pathol 100, 221–232 (1994). https://doi.org/10.1007/BF01876237

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