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Assessment of transformability of bacteria associated with tomato and potato plants

Published online by Cambridge University Press:  12 September 2007

Leo van Overbeek
Affiliation:
Wageningen University and Research Centre, Plant Research International B.V., Wageningen, Droevendaalsesteeg 1, The Netherlands
Jessica Ray
Affiliation:
Department of Pharmacy, Faculty of Medicine, University of Tromsø, 9037, Tromsø, Norway
Jan Dirk van Elsas
Affiliation:
University of Groningen, Centre for Ecology and Evolutionary studies, Department of Microbial Ecology, Kerklaan 30, 9751 NN Haren, The Netherlands

Abstract

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Transformation of plant-associated bacteria by plant DNA has never been demonstrated in agricultural fields. In total 552 bacterial isolates from stems of Ralstonia solanacearum-infected and healthy tomato plants and from stems and leaves of healthy potato plants were tested for natural genetic competence using plasmid pSKTG DNA and homologous DNA extracts. Control strain Acinetobacterbaylyi ADP1 was transformable with both DNA extracts. No transformable isolates were observed after treatment with plasmid pSKTG DNA. Two isolates, P34, identified as Pseudomonas trivialis and A19, identified as Pseudomonas fragi, were selected on the basis of the consistently higher Rp-resistant CFU numbers after treatment with DNA from Rp-resistant cells than with that from wild-type cells. P34 showed 2.1-fold and A19 1.5-fold higher Rp-resistant CFU numbers after treatment with DNA from homologous Rp-resistant cells versus that from wild-type cells. It is concluded that bacteria capable of in vitro capture and integration of exogenous DNA into their genomes are relatively rare in culturable bacterial communities associated with tomato and potato plants, or that conditions conducive to transformation were not met in transformation assays.


Type
Research Article
Copyright
© ISBR, EDP Sciences, 2007

References

Ausubel FM, Brent R, Kingston RE, Moore DD, Seidman JG, Smith JA, Struhl K (1988) Current protocols in molecular biology. John Wiley and Sons, New York, USA
Ceccherini, MT, Poté, J, Kay, E, Van Tran, V, Maréchal, J, Pietramellara, G, Nannipieri, P, Vogel, TM, Simonet, P (2003) Degradation and transformability of DNA from transgenic leaves. Appl. Environ. Microbiol. 69: 673-678 CrossRef
De Vries, J, Wackernagel, W (2004) Microbial horizontal gene transfer and the DNA release from transgenic crop plants. Plant Soil 266: 91-104 CrossRef
Demanèche, S, Kay, E, Gourbière, F, Simonet, P (2001) Natural transformation of Pseudomonas fluorescens and Agrobacterium tumefaciens in soil. Appl. Environ. Microbiol. 67: 2617-2621 CrossRef
Friedrich, A, Hartsch, T, Averhoff, B (2001) Natural transformation in mesophilic and thermophilic bacteria: identification and characterization of novel, closely related competence genes in Acinetobacter sp. strain BD413 and Thermus thermophilus HB27. Appl. Environ. Microbiol. 67: 3140-3148 CrossRef
Friedrich, A, Prust, C, Hartsch, T, Henne, A, Averhoff, B (2002) Molecular analyses of the natural transformation machinery and identification of pilus structures in the extremely thermophilic bacterium Thermus thermophilus strain HB27. Appl. Environ. Microbiol. 68: 745-755 CrossRef
Heuer, H, Smalla, K (1999) Bacterial phyllosphere communities of Solanum tuberosum L. and T4-lysozym-producing transgenic variants. FEMS Microbiol. Ecol. 28: 357-371 CrossRef
Heuer, H, Krsek, M, Baker, P, Smalla, K, Wellington, EMH (1997) Analysis of actinomycete communities by specific amplification of genes encoding 16S rRNA and gel-electrophoretic separation in denaturing gradients. Appl. Environ. Microbiol. 63: 3233-3241
Jeffrey WH, Paul JH, Stewart GJ (1990) Natural transformation in a marine Vibrio species by plasmid DNA. Microb. Ecol. 19: 259-268
Kay, E, Bertolla, F, Vogel, TM, Simonet, P (2002) Opportunistic colonization of Ralstonia solanacearum-infected plants by Acinetobacter sp. and its natural competence development. Microb. Ecol. 43: 291-297 CrossRef
Kay, E, Chabrillat, G, Vogel, TM, Simonet, P (2003) Intergeneric transfer of chromosomal and conjugative plasmid genes between Ralstonia solanacearum and Acinetobacter sp. BD413. Mol. Plant Microbe Interact. 16: 74-82 CrossRef
Nielsen, KM, Bones, AM, Smalla, K, Van Elsas, JD (1998) Horizontal gene transfer from transgenic plants to terrestrial bacteria – a rare event? FEMS Microbiol. Rev. 22: 79-103 CrossRef
Nielsen, KM, Smalla, K, Van Elsas, JD (2000a) Natural transformation of Acinetobacter sp. strain BD413 with cell lysates of Acinetobacter sp., Pseudomonas fluorescens, and Burkholderia cepacia in soil microcosms. Appl. Environ. Microbiol. 66: 206-212 CrossRef
Nielsen, KM, Van Elsas, JD, Smalla, K (2000b) Transformation of Acinetobacter sp. strain BD413 (pFG4 $\rm \Delta $ nptII) with transgenic plant DNA in soil microcosms and effects of kanamycin on selection of transformants. Appl. Environ. Microbiol. 66: 1237-1242 CrossRef
Sambrook J, Fritsch EF, Maniatis T (1989) Molecular cloning: a laboratory manual. Cold Spring Harbor Laboratory, Cold Spring Harbor, New York
Smit E, Van Elsas JD (1992) Methods for studying conjugative gene transfer in soil. In Wellington EMH, van Elsas JD, eds, Genetic interactions between microorganisms in the natural environment. Pergamon Press, London, pp 113-125
Thomas, CM, Nielsen, KM (2005) Mechanisms of, and barriers to, horizontal gene transfer between bacteria. Nat. Rev. Micro. 3: 711-721 CrossRef
Van Vuurde JWL, Van der Wolf JM (1995) Immunofluorescence colony-staining (IFC). In Molecular Microbial Ecology Manual, Akkermans ADL, van Elsas JD, de Bruijn FJ, eds, Kluwer Academic Publishers, Dordrecht, section 4.1.3
Vaneechoutte M, Young DM, Ornston N, De Baere T, Nemec A, Van der Reijden T, Carr E, Tjernberg I, Dijkshoorn L (2006) Naturally transformable Acinetobacter sp. strain ADP1 belongs to the newly described species Acinetobacter baylyi. Appl. Environ. Microbiol. 72: 932-936