1887

Abstract

Summary: A mutant (PF24) of the race 1 strain, 299A, of pv. has been characterized in terms of its interactions with pea () cultivars. The mutant showed a changed reaction (avirulence to virulence) with a group of pea cultivars, including cvs. Belinda and Puget, previously thought to contain resistance genes R1 and R3. Avirulence towards cv. Puget was restored by transfer of any one of five cosmid clones from a race 3 (strain 870A) gene library to a rifampicin-resistant derivative of PF24. These observations were in agreement with a revised race-specific resistance genotype for Belinda and similar cultivars comprising a single resistance gene, R3. An incompatible interaction was observed between strain PF24 and cvs. Vinco (postulated to harbour race-specific resistance genes R1, R2, R3 and R5) and Hurst’s Greenshaft (R4 and possibly R1), indicating that the mutant retains at least one avirulence gene (A1 or A1 and A4). Mutant PF24 showed loss of a cryptic plasmid (pA V212) compared with its progenitor, strain 299A. A subclone (pAV233) of one of the race 3 restoration clones showed strong hybridization with similar-sized digestion fragments in race 3 plasmid DNA, confirming the A3 gene to be plasmid-borne. Strong cross-hybridization was also observed with a single 3·27 kb RI fragment of plasmid DNA present in strain 299A but absent from strain PF24. This is consistent with the corresponding A3 determinant being located on pAV212 in the race 1 strain 299A. The novel avirulence gene corresponding to A3 in strain 870A is provisionally designated . A spontaneous race-change variant (strain 1759, which expressed no avirulence phenotype toward the pea differential cultivars) was derived from the race 3 strain 870A. This race 6 strain and a wild isolate of a race 6 strain both lacked plasmid DNA sequences corresponding to the insert in pA V233.

Loading

Article metrics loading...

/content/journal/micro/10.1099/00221287-137-9-2231
1991-09-01
2024-04-24
Loading full text...

Full text loading...

/deliver/fulltext/micro/137/9/mic-137-9-2231.html?itemId=/content/journal/micro/10.1099/00221287-137-9-2231&mimeType=html&fmt=ahah

References

  1. Atherton G. T. 1987; The genetics of pathogenicity and host specificity of Pseudomonas syringae pathovar pisi. PhD thesis, CNAA, Bristol Polytechnic
    [Google Scholar]
  2. Clewell D. B., Helinski D. R. 1969; Supercoiled circular protein-DNA complex in Escherichia coli: purification and induced conversion to an open circular DNA form. Proceedings of the National Academy of Sciences of the United States of America 621159–1166
    [Google Scholar]
  3. Clowes R. C., Hayes W. 1968 Experiments in Microbial Genetics Oxford & Edinburgh: Blackwell Scientific Publications;
    [Google Scholar]
  4. Datta N., Hedges R. W., Shaw E. J., Sykes R. B., Richmond M. H. 1971; Properties of an R factor from Pseudomonas aeruginosa. Journal of Bacteriology 108:1244–1249
    [Google Scholar]
  5. Eckhardt T. 1978; A rapid method for the identification of plasmid DNA in bacteria. Plasmid 1:584–588
    [Google Scholar]
  6. Figurski D. H., Helinski D. R. 1979; Replication of an origin-containing derivative of plasmid RK2 dependent on a plasmid function provided in trans. Proceedings of the National Academy of Sciences of the United States of America 761648–1652
    [Google Scholar]
  7. Flor H. H. 1956; The complementary genetic systems in flax and flax rust. Advances in Genetics 8:29–54
    [Google Scholar]
  8. Keen N. T., Tamaki S., Kobayashi D., Stayton M., Gerhold D., Shen H., Gold S., Lorang J., Thordal-Christensen H. 1989; Characterization and function of avirulence genes from Pseudomonas syringae pv. tomato. Signal Molecules in Plants and Plant-Microbe interactions (NATO ASI series H36183–188 Lugtenberg B. J. J. Berlin & Heidelberg: Springer-Verlag;
    [Google Scholar]
  9. King E. O., Ward M. K., Raney D. E. 1954; Two simple media for the demonstration of pyocyanin and fluorescin. Journal of Laboratory and Clinical Medicine 44:301–337
    [Google Scholar]
  10. Klement Z. 1963; Rapid detection of pathogenicity of phytopatho-genic Pseudomonads. Nature, London 199:299–300
    [Google Scholar]
  11. Kobayashi D. Y., Tamaki S. J., Keen N. T. 1990; Molecular characterization of avirulence gene D from Pseudomonas syringae pv. tomato. Molecular Plant-Microbe Interactions 3:94–102
    [Google Scholar]
  12. Malik A. N. 1985; Genetic studies with Pseudomonas syringae pathovar pisi. PhD thesis, CNAA, Thames Polytechnic
    [Google Scholar]
  13. Malik A. N., Vivian A., Taylor J. D. 1987; Isolation and partial characterization of three classes of mutant in Pseudomonas syringae pathovar pisi with altered behaviour towards their host, Pisum sativum. Journal of General Microbiology 133:2393–2399
    [Google Scholar]
  14. Maniatis T., Fritsch E. F., Sambrook J. 1982 Molecular Cloning: a Laboratory Manual Cold Spring Harbor, NY: Cold Spring Harbor Laboratory;
    [Google Scholar]
  15. Murray N. E., Brammar W. J., Murray K. 1977; Lambdoid phages that simplify the recovery of in vitro recombinants. Molecular and General Genetics 150:53–61
    [Google Scholar]
  16. Simon R., Priefer U., Puhler A. 1983; A broad host range mobilization system for in vitro genetic engineering: transposon mutagenesis in Gram negative bacteria. Bio/Technology 1:784–789
    [Google Scholar]
  17. Stall R. E., Loschke D. C., Jones J. B. 1986; Linkage of copper resistance and avirulence loci on a self-transmissible plasmid in Xanthomonas campestris pv. vesicatoria. Phytopathology 76:240–243
    [Google Scholar]
  18. Staskawicz B., Dahlbeck D., Keen N., Napoli C. 1987; Molecular characterization of cloned avirulence genes from race 0 and race 1 of Pseudomonas syringae pv. glycinea. Journal of Bacteriology 169:5789–5794
    [Google Scholar]
  19. Swanson J., Kearney B., Dahlbeck D., Staskawicz B. 1988; Cloned avirulence gene of Xanthomonas campestris pv. vesicatoria complements spontaneous race-change mutants. Molecular Plant-Microbe Interactions 1:5–9
    [Google Scholar]
  20. Tamaki S., Dahlbeck D., Staskawicz B., Keen N. T. 1988; Characterization and expression of two avirulence genes cloned from Pseudomonas syringae pv. glycinea. Journal of Bacteriology 170:4846–4854
    [Google Scholar]
  21. Taylor J. D. 1972a; Specificity of bacteriophages and antiserum for Pseudomonas pisi. New Zealand Journal of Agricultural Research 15:421–431
    [Google Scholar]
  22. Taylor J. D. 1972b; Races of Pseudomonas pisi and sources of resistance in field and garden peas. New Zealand Journal of Agricultural Research 15:441–447
    [Google Scholar]
  23. Taylor J. D., Dye D. W. 1972; A survey of the organisms associated with bacterial blight of peas. New Zealand Journal of Agricultural Research 15:432–440
    [Google Scholar]
  24. Taylor J. D., Bevan J. R., Crute I. R., Reader S. L. 1989; Genetic relationship between races of Pseudomonas syringae pathovar pisi and cultivars of Pisum sativum. Plant Pathology 38:364–375
    [Google Scholar]
  25. Vivian A., Atherton G. T., Bevan J. R., Crute I. R., Mur L. A. J., Taylor J. D. 1989; Isolation and characterization of cloned DNA conferring specific avirulence in Pseudomonas syringae pv. pisi to pea (Pisum sativum) cultivars, which possess the resistance allele, R2. Physiological and Molecular Plant Pathology 34:335–344
    [Google Scholar]
http://instance.metastore.ingenta.com/content/journal/micro/10.1099/00221287-137-9-2231
Loading
/content/journal/micro/10.1099/00221287-137-9-2231
Loading

Data & Media loading...

This is a required field
Please enter a valid email address
Approval was a Success
Invalid data
An Error Occurred
Approval was partially successful, following selected items could not be processed due to error