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Detection of Pseudomonas syringae pv. aptata in Irrigation Water Retention Basins by Immunofluorescence Colony-staining

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Abstract

Bacterial blight of cantaloupe (Cucumis melo) caused by Pseudomonas syringae pv. aptata was first observed in south-western France and has since spread to all cantaloupe-growing areas of this country. Use of pesticides registered for this disease has proved ineffective and no commercial cultivars of cantaloupe are resistant to this blight. To develop control strategies for this disease, the principal sources of inoculum were investigated. Among the different sources of inoculum studied, we report the isolation of P. syringae pv. aptata from irrigation water retention basins in south-western France using the immunofluorescence colony-staining (IFC) method. In this study, the pathogen was detected at a low concentration (12 and 70cful−1) in two different retention basins. These results suggest that P. syringae pv. aptata can survive in water used to irrigate cantaloupe crops and could be a source of inoculum for epidemics of bacterial blight. To develop control strategies for this bacterial disease, the importance of water retention basins as sources of inoculum for bacterial blight of cantaloupe needs to be evaluated relative to other potential sources such as seeds, plants from nurseries and plant debris in the soil.

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References

  • Audy P, Braat CE, Saindon G, Huang HC and Laroche A (1996) A rapid and sensitive PCR-based assay for concurrent detection of bacteria causing common and halo blights in bean seed. Phytopathology 86: 361–366

    Google Scholar 

  • Cazorla FM, Tores JA, Olalla L, Perez-Garcia A, Farre JM and de Vincente A (1998) Bacterial apical necrosis of mango in southern Spain: A disease caused by Pseudomonas syringae pv. syringae. Phytopathology 88: 614–620

    Google Scholar 

  • Cother EJ and Gilbert RL (1990) Presence of Erwinia chrysanthemi in two major river systems and their alpine sources in Australia. Journal of Applied Bacteriology 69: 729–738

    Google Scholar 

  • Elphinstone JG, Stanford H and Stead DE (1998) Survival and transmission of Ralstonia solanacearum in aquatic plants of Solanum ducamara and associated surface water in England. Bulletin OEPP/EPPO Bulletin 28: 93–94

    Google Scholar 

  • Farag N, Stead, DE and Janse JD (1999) Ralstonia (Pseudomonas) solanacearum race 3, biovar 2, detected in surface (irrigation)water in Egypt. Journal of Phytopathology 147: 485–487

    Google Scholar 

  • Franken AAJM, Kamminga GC, Snijders W, Van der Zouwen PS and Birnbaum YE (1993) Detection of Clavibacter michiganensis ssp. michiganensis in tomato seeds by immunofluorescence microscopy and dilution plating. Netherlands Journal of Plant Pathology 99: 125–137

    Google Scholar 

  • Guillorit-Randeau C, Maladrin L and Samson R (1996) Identification of two serological flagellar types (H1 and H2) in Pseudomonas syringae pathovars. European Journal of Plant Pathology 102: 99–104

    Google Scholar 

  • Harrison MD, Franc GD, Maddox DA and Michaud JE (1987) Presence of Erwinia carotovora in surface water in North America. Journal of Applied Bacteriology 62: 565–570

    Google Scholar 

  • Hirano SS, Rouse DI, Clayton MK and Upper CD (1995) Pseudomonas syringae pv. syringae and bacterial brown spot of snap bean: A study of epiphytic phytopathogenic bacteria and associated disease. Plant Disease 79: 1085–1093

    Google Scholar 

  • King EO, Ward MK and Raney DE (1954) Two simple media for the demonstration of pyocianin and fluorescin. Journal of Laboratory Clinical and Medical 44: 301–307

    Google Scholar 

  • Knoche KK, Clayton MK and Fulton RW (1987) Comparison of resistance in tobacco to Pseudomonas syringae pv. tabaci races 0 and 1 by infectivity titrations and bacterial multiplications. Phytopathology 77: 1364–1368

    Google Scholar 

  • Lindemann J, Arny DC and Upper CD (1985) Aerial dispersal of epiphytic bacteria over bean plants. Applied and Environmental Microbiology 50: 1229–1232

    Google Scholar 

  • Mannulis S, Kogan N, Valinsky L, Dror O and Kleitman F (1998) Detection of Erwinia herbicola pv. gypsophilae in gypsophila plants by PCR. European Journal of Plant Pathology 104: 85–91

    Google Scholar 

  • McCarter SM, Jones JB, Gitaitis RD and Smithley DR (1983) Survival of Pseudomonas syringae pv. tomato in association with tomato seed, soil, host tissue, and epiphytic weed hosts in Georgia. Phytopathology 73: 1393–1398

    Google Scholar 

  • McCarter-Zorner NJ, Franc GD, Harrison MD, Michaud JE, Quinn CE, Ann Sells I and Graham DC (1984) Soft rot Erwinia bacteria in surface and undergroundwaters in southern Scotland and in Colorado, United States. Journal of Applied Bacteriology 57: 95–105

    Google Scholar 

  • McDonald JG (1995) Disease control through crop certification: herbaceous crops. Canadian Journal of Plant Pathology 17: 267–273

    Google Scholar 

  • Mohan SK and Schaad NW (1987) An improved agar plating assay for detecting Pseudomonas syringae pv. syringae and P.s. pv. phaseolicola in contaminated been seed. Phytopathology 77: 1390–1395

    Google Scholar 

  • Morris CE, Glaux C, Latour X, Gardan L, Samson R and Pitrat M (2000) The relationship of host range, physiology, and genotype to virulence on cantaloupe in Pseudomonas syringae from cantaloupe blight epidemics in France. Phytopathology 90: 636–646

    Google Scholar 

  • Ojeda S and Verdier V (2000) Detecting Xanthomonas axonopodis pv. manihotis in cassava true seeds by nested polymerase chain reaction assay. Canadian Journal of Plant Pathology 22: 241–247

    Google Scholar 

  • Prosen D, Hatziloukas E, Schaad NW and Panopoulos NJ (1993) Specific detection of Pseudomonas syringae pv. phaseolicola DNA in bean seed by polymerase chain reaction-based amplification of a phaseolotoxin gene region. Phytopathology 83: 965–970

    Google Scholar 

  • Saunier M, Maladrin L and Samson R (1996) Distribution of Pseudomonas syringae pathovars into twenty-three O serogroups. Applied Environmental Microbiology 62: 2360–2374

    Google Scholar 

  • Schaad NW (1988) Laboratory Guide for Identification of Plant Pathogenic Bacteria, 2nd edn. The American Phytopathological Society, APS Press, St. Paul

    Google Scholar 

  • Schaad NW, Cheong SS, Tamaki S, Hatziloukas E and Panopoulos NJ (1995) A combined biological and enzymatic amplification (BIO-PCR) technique to detect Pseudomonas syringae pv. phaseolicola in bean seed extracts. Phytopathology 85: 243–248

    Google Scholar 

  • Van der Wolf JM, Van Bekkum PJ, Van Elsas JD, Nijhuis EH, Vriend SGC and Ruissen MA (1998) Immunofluorescence colony staining and selective enrichment in liquid medium for studying the population dynamics of Ralstonia solanacearum (race 3) in soil. Bulletin OEPP/EPPO Bulletin 28: 71–79

    Google Scholar 

  • Van Vuurde JWL, Van den Bovenkamp GW and Bimbaum Y (1983) Immunofluorescence microscopy and enzyme-linked immunosorbent assay as potential routine tests for the detection of Pseudomonas syringae pv. phaseolicola and Xanthomonas campestris pv. phaseoli in bean seed. Seed Science and Technology 11: 547–559

    Google Scholar 

  • Van Vuurde JWL (1987) New approach in detecting phytopathogenic bacteria by combined immunoisolation and immunoidentification assays. Bulletin OEPP/EPPO Bulletin 17: 139–148

    Google Scholar 

  • Van Vuurde JWL, Kastelein P and Van der Wolf JM (1995) Immunofluorescence colony-staining (IFC) as a concept for bacterial detection in quality testing of plant materials ad ecological research. Bulletin OEPP/EPPO Bulletin 25: 157–162

    Google Scholar 

  • Wenneker M, Verdel MSW, Groeneveld RMW, Kempenaar C, Van Beuningen AR and Janse JD (1999) Ralstonia (Pseudomonas) solanacearum race 3 (biovar 2) in surfacewater and natural weed hosts: First report on stinging nettle (Urtica dioica). European Journal of Plant Pathology 105: 307–315

    Google Scholar 

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Riffaud, CH., Morris, C. Detection of Pseudomonas syringae pv. aptata in Irrigation Water Retention Basins by Immunofluorescence Colony-staining. European Journal of Plant Pathology 108, 539–545 (2002). https://doi.org/10.1023/A:1019919627886

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