Skip to main content
Log in

Genetic engineering for resistance to bacteria in transgenic plants by introduction of foreign genes

  • Mini-Review
  • Published:
Molecular Breeding Aims and scope Submit manuscript

This is a preview of subscription content, log in via an institution to check access.

Access this article

Price excludes VAT (USA)
Tax calculation will be finalised during checkout.

Instant access to the full article PDF.

Institutional subscriptions

References

  1. Allefs JJHM, de Jong ER, Florack DEA, Hoogendoorn J, Stiekema WJ: Erwinia soft rot resistance of potato cultivars expressing antimicrobial peptide tachyplesin. I. Mol Breed 2: 97–105 (1996).

    Google Scholar 

  2. Allefs SJHM, Florack DEA, Hoogendoorn C, Stiekema WJ: Erwinia soft rot resistance of potato cultivars transformed with a gene construct coding for antimicrobial peptide cecropin B is not altered. Am Potato J 72: 437–445 (1995).

    Google Scholar 

  3. Anzai H, Yoneyama K, Yamaguchi I: Transgenic tobacco resistant to a bacterial disease by the detoxification of a pathogenic toxin. Mol Gen Genet 219: 429–494 (1989).

    Google Scholar 

  4. Bain RA, Pérombelon MCM: Methods of testing potato cultivars for resistance to soft rot tubers caused by Erwinia carotovora subsp. atroseptica. Plant Path 37: 431–437 (1991).

    Google Scholar 

  5. Baker CJ, Orlandi EW: Active oxygen in plant pathogenesis. Ann Rev Phytopath 33: 299–321 (1995).

    Google Scholar 

  6. Bednarek SY, Raikhel NV: Intracellular trafficking of secretory proteins. Plant Mol Biol 20: 133–150 (1992).

    Google Scholar 

  7. Belknap WR: Field performance of transgenic Russet Burbank and Lemhi Russet potatoes. In: Third International Symposium on the Molecular Biology of the Potato, Santa Cruz (Abstracts) p. 49 (1993).

  8. Boman HG: Antibacterial peptides: key components needed in immunity: Cell 65: 205–207 (1991).

    Google Scholar 

  9. Bonas U, Conrads-Strauch J, Balbo I: Resistance in tomato to Xanthomonas campestris pv. vesicatoria is determined by alleles of the pepper-specific avirulence gene avrBs3. Mol Gen Genet 238: 261–2696 (1993).

    Google Scholar 

  10. Carmona MJ, Molina A, Fernández JA, López-Fando JJ, Garcia-Olmedo F: Expression of the α-thionin gene from barley in tobacco confers enhanced resistance to bacterial pathogens. Plant J 3: 457–462 (1993).

    Google Scholar 

  11. Chrispeels MJ: Sorting of proteins in the secretory system. Annu Rev Plant Physiol Plant Mol Biol 42: 21–53 (1991).

    Google Scholar 

  12. Chrispeels MJ, Tague BW: Protein sorting in the secretory system of plant cells. Int Rev Cytol 125: 1–45 (1991).

    Google Scholar 

  13. Collmer A: Pectic enzymes and bacterial invasion of plants. In: Kosuge T, Nester EW (eds) Plant-Microbe Interactions, vol. 2, pp. 253–284. Macmillan Publishing Corporation, New York, (1987).

    Google Scholar 

  14. Collmer A, Keen NT: The role of pectic enzymes in plant pathogenesis: Annu Rev Phytopath 24: 383–409 (1986).

    Google Scholar 

  15. Cutt JR, Klessig D: Pathogenesis-related proteins. In: Boller T, Meins F (eds) Plant Gene Research, Genes involved in Plant Defense, pp. 209–243. Springer-Verlag, Wien (1992).

    Google Scholar 

  16. de la Fuente-Martinez JM, Mosquada-Cano G, Alavarez-Morales A, Herrera-Estrella L. Expression of a bacterial phaseolotoxin-resistant ornithyl transcarbamylase in transgenic tobacco confers resistance to Pseudomonas syringae pv. phaseolicola. Bio/technology 10: 905–909 (1992).

    Google Scholar 

  17. Destéfano-Beltran L, Nagpala P, Jaeho K, Dodds JH, Jaynes JM: Genetic transformation of potato to enhance nutritional value and confer disease resistance. In: Dennis ES, Llewellyn DJ (eds) Plant Gene Research: Molecular Approaches to Crop Improvement, pp. 17–32. Springer-Verlag, Wien/New York (1991).

    Google Scholar 

  18. Düring K: Can lysozymes mediate antibacterial resistance in plants? Plant Mol Biol 23: 209–214 (1993).

    Google Scholar 

  19. Düring K, Porsch P, Fladung M, Lörz H: Transgenic potato plants resistant to the phytopathogenic bacterium Erwinia carotovora. Plant J 3: 587–598 (1993).

    Google Scholar 

  20. Düring K: A plant transformation vector with a minimal T-DNA. Transgen Res 3: 138–140 (1994).

    Google Scholar 

  21. Düring K: Differential patterns of bacteriolytic activities in potato in comparison to bacteriophage T4 and hen egg white lysozymes. J Phytopath 141: 159–164 (1994).

    Google Scholar 

  22. Firek S, Draper J, Owen MRL, Gandecha A, Cockburn B, Whitelam GC: Secretion of functional single-chain Fv protein in transgenic tobacco plants and cell suspension cultures. Plant Mol Biol 23: 861–870 (1993).

    Google Scholar 

  23. Florack DEA, Dirkse WG, Visser B, Heidekamp F, Stiekema WJ: Expression of biologically active hordothionins in tobacco. Effects of pre- and pro-sequences at the amino and carboxyl termini of the hordothionin precursor on mature protein expression and sorting. Plant Mol Biol 24: 83–96 (1994).

    Google Scholar 

  24. Florack D, Allefs S, Bollen R, Bosch D, Visser B, Stiekema W: Expression of giant silkmoth cecropin B genes in tobacco. Transgen Res 4: 132–141 (1995).

    Google Scholar 

  25. Griffiths AD, Williams SC, Hartley O, Tomlinson IM, Waterhouse P, Crosby WL, Kontermann RE, Jones PT, Low NM, Allison TJ, Prospero TD, Hoogenboom HR, Nissim A, Cox JPL, Harrison JL, Zaccolo M, Gherardi E, Winter G: Isolation of high affinity human antibodies directly from large synthetic repertoires. EMBO J 13: 3245–3260 (1994).

    Google Scholar 

  26. Gudmundsson GH, Lidhol DA, Asling B, Gan R, Boman HG: The cecropin locus: cloning and expression of a gene encoding three antibacterial peptides in Hyalophora cecropia. J Biol Chem 266: 11510–11517 (1991).

    Google Scholar 

  27. Herbers K, Conrads-Strauch J, Bonas U: Race-specificity of plant to resistance to bacterial spot disease determined by repetitive motifs in a bacterial avirulence protein. Nature 356: 172–174 (1992).

    Google Scholar 

  28. Hightower R, Baden C, Penzes E, Dunsmuir P: The expression of cecropin peptide in transgenic tobacco does not confer resistance to Pseudomonas syringae pv. tabact. Plant Cell Rep 13: 295–299 (1994).

    Google Scholar 

  29. Hippe S, Düring K, Kreuzaler F: In situ localization of a foreign protein in transgenic plants by immunoelectron microscopy following high pressure freezing, freeze substitution and low temperature embedding. Eur J Cell Biol 50: 230–234 (1989).

    Google Scholar 

  30. Holm L, Sander C: Structural similarity of plant chitinase and lysozymes from animals and phage. An evolutionary connection. FEBS Lett 340: 129–132 (1994).

    Google Scholar 

  31. Hu P, Leong S, Sequeira L: Molecular cloning of genes that specify virulence in Pseudomonas solanacearum. J Bact 170: 617–622 (1988).

    Google Scholar 

  32. Jaynes JM, Nagpala P, Destefano-Beltran L, Hong-Hung J, Kim J, Denny T, Cetiner S: Expression of a cecropin B lytic peptide analogue in transgenic tobacco confers enhanced resistance to bacterial wilt caused by Pseudomonas solanacearum. Plant Sci 8: 43–53 (1993).

    Google Scholar 

  33. Jones S, Yu B, Bainton NJ, Birdsall M, Bycroft BW, Chhabra SR, Cox AJR, Golby P, Reeves PF, Stephens S, Winson MK, Salmond GPC, Stewart GSAB, Williams P: The lux autoinducer regulates the production of exoenzyme virulence factor determinants in Erwinia carotovora and Pseudomonas aeruginosa. EMBO J 12: 2477–2482 (1993).

    Google Scholar 

  34. Keen NT: The molecular biology of disease resistance. Plant Mol Biol 19: 109–122 (1992).

    Google Scholar 

  35. Ma JKC, Hiatt A, Hein M, Vine ND, Wang F, Stabila P, van Dolleweerd C, Mostov K, Lehner T: Generation and assembly of secretory antibodies in plants. Science 268: 716–719 (1995).

    Google Scholar 

  36. Majeau N, Trudel J, Asselin A: Diversity of cucumber chitinase isoforms and characterization of one seed basic chitinase with lysozyme activity. Plant Sci 68: 9–16 (1990).

    Google Scholar 

  37. Matthews BW, Remington SJ, Gruetter MG, Anderson WF: Relation between hen egg white lysozyme and bacteriophage T4 lysozyme: evolutionary implications. J Mol Biol 147: 545–558 (1981).

    Google Scholar 

  38. Nissim A, Hoogenboom HR, Tomlinson IM, Flynn G, Midgeley C, Lane D, Winter G: Antibody fragments from a ‘singlepot’ phage display library as immunochemical reagents. EMBO J 12: 692–698 (1994).

    Google Scholar 

  39. Nordeen RD, Sinden SL, Jaynes JM, Owens LD: Activity of cecropin SB37 against protoplasts from several plant species and their bacterial pathogens. Plant Sci 82: 101–107 (1992).

    Google Scholar 

  40. Norelli JL, Aldwinckle HS, Destefano-Beltran L, Jaynes JM: Transgenic ‘Malling 26’ apple expressing the attacin E gene has increased resistance to Erwinia amylovora. Euphytica 77: 123–128 (1994).

    Google Scholar 

  41. Pérombelon MCM: The impaired host and soft rot bacteria. In: Mount MS, Lacey GH (eds) Phytopathogenic Prokaryotes, pp. 55–69. Academic Press, New York (1982).

    Google Scholar 

  42. Pirhonen M, Flego D, Heikinheimo R, Palva ET: A small diffusible signal molecule is responsible for the global control of virulence and exoenzyme production in the plant pathogen Erwinia carotovora. EMBO J 12: 2467–2476 (1993).

    Google Scholar 

  43. Salmond GPC: Secretion of extracellular virulence factors by plant pathogenic bacteria. Annu Rev Phytopath 32: 181–200 (1994).

    Google Scholar 

  44. Salmond GPC, Bycroft BW, Stewart GSAB, Williams P: The bacterial ‘enigma’: cracking the code of cell-cell communication. Mol Microbiol 16: 615–624 (1995).

    Google Scholar 

  45. Tavladoraki P, Benvenuto E, Trinca S, De Martinis D, Cattaneo A, Galeffi P: Transgenic plants expressing a functional single-chain Fv antibody are specifically protected from virus attack. Nature 366: 469–472 (1993).

    Google Scholar 

  46. Taylor NG, Walker EA, Firek S, Draper J: Novel plant disease resistance strategies by secretion of single chain antibodies. In: Seventh International Symposium on Molecular Plant-Microbe Interactions, Edinburgh (Abstracts) p. 139 (1994).

  47. Trudel J, Audy P, Asselin A: Electrophoretic forms of chitinase activity in Xanthi-nc tobacco healthy and infected with tobacco mosaic virus. Mol Plant-Microbe Int 2: 315–324 (1989).

    Google Scholar 

  48. van Engelen FA, Schouten A, Molthoff JW, Roosien J, Salinas J, Dirkse WG, Schots A, Bakker J, Gommers FJ, Jongsma MA, Bosch D, Stiekema W: Coordinate expression of antibody subunit genes yields high levels of functional antibodies in roots of transgenic tobacco Plant Mol Biol 26: 1701–1710 (1994).

    Google Scholar 

  49. Vaughan TJ, Williams AJ, Pritchard K, Osbourn JK, Pope AR, Earnshaw JC, McCafferty J, Hodits RA, Wilton J, Johnson KS: Human antibodies with sub-nanomolar affinities isolated from a large non-immunized phage display library. Nature Biotechnol 14: 309–314 (1996).

    Google Scholar 

  50. Voss A, Niersbach M, Hain R, Hirsch HJ, Liao YC, Kreuzaler F, Fischer R: Reduced virus infectivity in N. tabacum secreting a TMV-specific full-size antibody. Mol Breed 1: 39–50 (1995).

    Google Scholar 

  51. Weber J, Olsen O, von Wettstein D: Digalacturonates induce defense against soft rot in potato tubers. In: Seventh International Symposium on Molecular Plant-Microbe Interactions, Edinburgh (Abstracts), p. 112 (1994).

  52. Wharam S, Mulholland V, Salmond GPC: Conserved virulence factor regulation and secretion apparatus in bacterial pathogens of plants and animals. Eur J Plant Path 101: 1–13 (1995).

    Google Scholar 

  53. Wu G, Shortt BJ, Lawrence EB, Levine EB, Fitzsimmons KC, Shah DM: Disease resistance conferred by expression of a gene encoding H2O2-generating glucose oxidase in transgenic potato plants. Plant Cell 7: 1357–1368 (1995).

    Google Scholar 

Download references

Author information

Authors and Affiliations

Authors

Rights and permissions

Reprints and permissions

About this article

Cite this article

Düring, K. Genetic engineering for resistance to bacteria in transgenic plants by introduction of foreign genes. Mol Breeding 2, 297–305 (1996). https://doi.org/10.1007/BF00437908

Download citation

  • Received:

  • Accepted:

  • Issue Date:

  • DOI: https://doi.org/10.1007/BF00437908

Key words

Navigation