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Structure and colonization dynamics of epiphytic bacterial communities and of selected component strains on tomato (Lycopersicon esculentum) leaves

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Abstract

The sizes and compositions of bacterial populations found on leaves of greenhouse and field grown tomato plants were studied by dilution plating, fatty acid methyl ester analysis (FAME), and BIOLOG plates of isolates in pure cultures. In the greenhouse, overhead-irrigated plants sustained higher microbial populations (up to 105 cfu g−1) than soil-irrigated plants (103 cfu g−1). Strains isolated from overhead-irrigated plants grown in a vegetable garden (n=216) and from greenhouse-grown plants (n=114) were subjected to FAME analysis. Similarly, strains from soil-irrigated field-grown plants (n=83) were identified using BIOLOG plates. In each case, populations were dominated by a few genera. When concentrated phyllosphere washes (CPW) were sprayed on greenhouse-grown, soil-irrigated plants, leaf bacterial populations of more than 105 CFU g−1 were sustained for 4 days; sterile buffer-sprayed leaves sustained less than 104 CFU g−1. No significant enrichment of any strain isolated from the sprayed leaves could be detected by FAME identification of randomly selected colonies. However, when recurring leaf saprophytic species (both Gram-positive and Gram-negative) isolated from these experiments and from plants grown outdoors were tested for epiphytic colonization under stressful conditions, all could still be detected at various levels up to 4 days after inoculation, indicating differential epiphytic fitness. The non-epiphytic bacteriaEscherichia coli andAzospirillum brasilense disappeared from the leaf surface within the same experimental period.

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References

  1. Austin B, Goodfellow M, Dickinson CH (1978) Numerical taxonomy of phylloplane bacteria isolated fromLolium perenne. J Gen Microbiol 104:139–155

    Google Scholar 

  2. Beattie AG, Lindow SE (1995) The secret life of foliar bacterial pathogens on leaves. Annu Rev Phytopathol 33:145–172

    Article  CAS  PubMed  Google Scholar 

  3. Blakeman JP (1991) Foliar bacterial pathogens: Epiphytic growth and interactions on leaves. J Appl Bacteriol 70 (Suppl):49S-59S

    Google Scholar 

  4. Butchmann C, Kies U, Deckwer WD, Hecht V (1997) Performance of three phase fluidized bed reactor for quinoline degradation on various supports at steady state and dynamic conditions. Biotech Bioeng 56:295–303

    Article  Google Scholar 

  5. Butterworth J, McCartney HA (1991) The dispersal of bacteria from leaf surfaces by water splash. J Appl Bacteriol 71:484–496

    Google Scholar 

  6. Chernin L, Ismailov Z, Khmel I, Perebityuk A, Chet I Development of new preparations for biological control of crop diseases as a joint Israel-CIS venture. Sci Isr Tech Adv (in press)

  7. Doyle MP (1990) Fruit and vegetable safety—microbiological considerations. Hort Sci 25:1478–1481

    Google Scholar 

  8. Dunlap PV (1997)N-Acyl-l-homoserine lactone autoinducers in bacteria: Unity and diversity. In: Shapiro JA, Dworkin M (eds) Bacteria as Multicellular Organisms. Oxford University Press, New York, pp 69–106

    Google Scholar 

  9. Ercolani GL (1978)Pseudomonas savastonoi and other bacteria colonizing the surface of olive leaves in the field. J Gen Microbiol 109:245–257

    Google Scholar 

  10. Ercolani GL (1991) Distribution of epiphytic bacteria on olive leaves and the influence of leaf age and sampling time. Microb Ecol 21:25–48

    Article  Google Scholar 

  11. Hirano SS, Nordheim EV, Arny DE, Upper CD (1982) Lognormal distribution of epiphytic bacterial populations on leaf surfaces. Appl Environ Microbiol 44:695–700

    PubMed  Google Scholar 

  12. Hirano SS, Upper CD (1992) Population dynamics ofPseudomonas syringae in the phyllosphere. In: Galli E, Silver S, Withold B (eds)Pseudomonas: Molecular Biology and Biotechnology. ASM, Washington DC, pp 21–29

    Google Scholar 

  13. Jacques MA (1996) The effect of leaf age and position on the dynamics of microbial populations on aerial plant surfaces. In: Morris CE, Nicot PC, Nguyen-The C (eds) Aerial Plant Surface Microbiology. Plenum Press, New York, pp 233–248

    Google Scholar 

  14. Jacques MA, Morris CE (1995) A review of issues related to the quantification of bacteria from the phyllosphere. FEMS Ecol Microbiol 18:1–14

    Article  CAS  Google Scholar 

  15. Lindow SE (1996) Role of immigration and other processes in determining epiphytic bacterial populations: Implications for disease management. In: Morris CE, Nicot PC, Nguyen-The C (eds) Aerial Plant Surface Microbiology. Plenum Press, New York, pp 155–168

    Google Scholar 

  16. Lindow SE, Andersen GL (1996) Influence of immigration on epiphytic bacterial populations on navel orange leaves. Appl Environ Microbiol 62:2978–2987

    PubMed  CAS  Google Scholar 

  17. Mahafee WF, Kloepper JW (1997) Bacterial communities of the rhizosphere and endorhiza associated with field-grown cucumber plants inoculated with a plant growth-promoting rhizobacterium or its genetically modified derivative. Can J Microbiol 43:344–353

    Article  Google Scholar 

  18. Morris CE, Monier JM, Jacques MA (1998) A technique to quantify the population size and composition of the biofilm component in communities of bacteria in the phyllosphere. Appl Environ Microbiol 64:4789–4795

    PubMed  CAS  Google Scholar 

  19. Morris CE, Nguyen-The C (1996) The role of plant surface bacteria in the hygienic and market quality of minimally processed vegetables. In: Morris CE, Nicot PC, Nguyen-The C (eds) Aerial Plant Surface Microbiology. Plenum Press, New York, pp 191–208

    Google Scholar 

  20. Müller T, Seyfarth W (1997) Starvation and nonculturable state in plant-associated lactic acid bacteria. Microbiol Res 152:39–43

    Google Scholar 

  21. O'Brien RD, Lindow SE (1989) Effects of plant species and environmental conditions on epiphytic population sizes ofPseudomonas syringae and other bacteria. Phytopathology 79:619–627

    Google Scholar 

  22. Poole RW (1974) An Introduction to Quantitative Ecology. McGraw-Hill, Kogakusha, Tokyo

    Google Scholar 

  23. Romantschuk M (1992) Attachment of plant pathogenic bacteria to plant surfaces. Annu Rev Phytopathol 30:225–243

    Article  CAS  PubMed  Google Scholar 

  24. Salerno CM, Montero MC, Sagardoy MA (1997) Dynamics of bacteria from the phyllosphere and leaves of soy (Glycine max L. Merrill) in field conditions. Rev Arg Microbiol 29:122–130

    CAS  Google Scholar 

  25. Thompson IP, Bailey MJ, Ellis JE, Lilley AK, McCormack PJ, Purdy KJ, Rainey PB (1995) Short-term community dynamics in the phyllosphere microbiology of field-grown sugar beet. FEMS Microbiol Ecol 16:205–212

    Article  CAS  Google Scholar 

  26. Thompson IP, Bailey MJ, Fenlon JS, Fermor TR, Lilley AK, Lynch JM, McCormack PJ, McQuillen MP, Purdy KJ, Rainey PB, Whipps JM (1993) Quantitative and qualitative seasonal changes in the microbial community from the phyllosphere of sugar beet (Beta vulgaris). Plant Soil 150:177–191

    Article  Google Scholar 

  27. Thompson IP, Ellis JE, Bailey MJ (1995) Autoecology of a genetically modified fluorescent pseudomonad on sugar beet. FEMS Microbiol Ecol 16:205–212

    Article  CAS  Google Scholar 

  28. Willems A, De Vos P, De Ley J (1992) The genusComamonas. In: Balows A, Trüper HG, Dworkin M, Harder W, Shleifer KH (eds) The Prokaryotes. Springer-Verlag, New York, pp 2583–2590

    Google Scholar 

  29. Wilson M, Lindow SE (1992) Relationship of total viable and culturable cells in epiphytic populations ofPseudomonas syringae. Appl Environ Microbiol 58:3908–3913

    PubMed  CAS  Google Scholar 

  30. Wilson M, Lindow SE (1994) Coexistence among epiphytic bacterial populations mediated through nutritional resource partitioning. Appl Environ Microbiol 60:4468–4477

    PubMed  CAS  Google Scholar 

  31. Wilson M, Lindow SE (1994) Inoculum density-dependent mortality and colonization of the phyllosphere byPseudomonas syringae. Appl Environ Microbiol 60:2232–2237

    PubMed  Google Scholar 

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Correspondence to Edouard J. Jurkevitch.

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Jurkevitch, E.J., Shapira, G. Structure and colonization dynamics of epiphytic bacterial communities and of selected component strains on tomato (Lycopersicon esculentum) leaves. Microb Ecol 40, 300–308 (2000). https://doi.org/10.1007/s002480000023

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