Skip to main content
Journal of Bacteriology logoLink to Journal of Bacteriology
. 2012 Jul;194(14):3733–3734. doi: 10.1128/JB.00567-12

Draft Genome Sequence of Pseudomonas syringae Pathovar Syringae Strain FF5, Causal Agent of Stem Tip Dieback Disease on Ornamental Pear

Kee Hoon Sohn a, Jonathan D G Jones a, David J Studholme a,b,
PMCID: PMC3393499  PMID: 22740663

Abstract

Pseudomonas syringae FF5 causes stem tip dieback disease on ornamental pear (Pyrus calleryana). Its genome encodes a complete type III secretion system (T3SS) and HopAC1, HopM1, AvrE1, HopI1, HopAA1, HopJ1, HopAH2, HopAH1, HopAG1, and HopAZ1. Lacking detectable homologues of other T3SS effectors, it may encode novel, undiscovered effectors.

GENOME ANNOUNCEMENT

Pseudomonas syringae is a Gram-negative bacterial pathogen that causes disease on a broad range of important crops and uncultivated plants, but individual strains show a high degree of host specificity. The species P. syringae is subdivided into about 50 pathovars, with each defined primarily by its host range (3, 6). A major determinant of ability to evade the host's defenses is the bacterium's type III secretion system (T3SS) and its substrates, the T3SS effector proteins (2, 8, 9).

Pseudomonas syringae pv. syringae strain FF5 was originally isolated (15) in Oklahoma, where it was causing stem tip dieback disease on ornamental pear (Pyrus calleryana). It is a common laboratory strain used in molecular studies (1, 4, 7, 1012, 1419).

The draft genome sequence assembly of P. syringae pv. syringae FF5 contains 79 supercontigs consisting of 4,578 contigs assembled from 100× deep genome-wide sequencing with Illumina GAII paired reads. The de novo assembly was performed using Velvet 0.7.48 (20).

Strain FF5 belongs to clade 2b in the phylogeny of Sarkar and Guttman (13) based on multilocus sequence analysis. A complete closed genome sequence is available for P. syringae pv. syringae B728a (5), which is also a member of clade 2c. Approximately 83% of the B728a genome is conserved in FF5; the two genomes share 95.3% nucleotide sequence identity in this conserved portion of their genomes. The remaining 17% of their genomes share no detectable nucleotide sequence similarity. P. syringae pv. syringae FF5 encodes a complete T3SS and homologues of the effectors HopAC1, HopM1, AvrE1, HopI1, HopAA1, HopJ1, HopAH2, HopAH1, HopAG1, and HopAZ1. However, it lacks detectable homologues of any other T3SS effectors found in P. syringae pv. syringae B278a and other sequenced strains of this species. This suggests that either P. syringae pv. syringae FF5 has an unusually small repertoire of T3SS effectors or, more likely, it encodes several as-yet-unidentified novel effectors.

Nucleotide sequence accession numbers.

Sequence data from this whole-genome shotgun project have been deposited at GenBank under the accession number ACXZ00000000. The version described in this paper is the first version, ACXZ00000000.1. The genome project was also deposited in the Genomes OnLine Database as project number Gi04242, and the NCBI taxonomy identification number is 591153.

ACKNOWLEDGMENTS

This work was supported in part by The Gatsby Charitable Foundation. K. H. Sohn was supported in part by a grant (project no. PJ007850201006) from the Rural Development Administration (Republic of Korea).

REFERENCES

  • 1. Couch R, O'Connor SE, Seidle H, Walsh CT, Parry R. 2004. Characterization of CmaA, an adenylation-thiolation didomain enzyme involved in the biosynthesis of coronatine. J. Bacteriol. 186:35–42 [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 2. Cunnac S, Lindeberg M, Collmer A. 2009. Pseudomonas syringae type III secretion system effectors: repertoires in search of functions. Curr. Opin. Microbiol. 12:53–60 [DOI] [PubMed] [Google Scholar]
  • 3. Dye DW, et al. 1980. International standards for naming pathovars of phytopathogenic bacteria and a list of pathovar names and pathotype strains. Rev. Plant Pathol. 59:153–168 [Google Scholar]
  • 4. Fakhr MK, Peñaloza-Vázquez A, Chakrabarty AM, Bender CL. 1999. Regulation of alginate biosynthesis in Pseudomonas syringae pv. syringae. J. Bacteriol. 181:3478–3485 [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 5. Feil H, et al. 2005. Comparison of the complete genome sequences of Pseudomonas syringae pv. syringae B728a and pv. tomato DC3000. Proc. Natl. Acad. Sci. U. S. A. 102:11064–11069 [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 6. Hirano SS, Upper CD. 2000. Bacteria in the leaf ecosystem with emphasis on Pseudomonas syringae—a pathogen, ice nucleus, and epiphyte. Microbiol. Mol. Biol. Rev. 64:624–653 [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 7. Kim JJ, Sundin GW. 2001. Construction and analysis of photolyase mutants of Pseudomonas aeruginosa and Pseudomonas syringae: contribution of photoreactivation, nucleotide excision repair, and mutagenic DNA repair to cell survival and mutability following exposure to UV-B radiation. Appl. Environ. Microbiol. 67:1405–1411 [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 8. Lindeberg M, et al. 2006. Closing the circle on the discovery of genes encoding Hrp regulon members and type III secretion system effectors in the genomes of three model Pseudomonas syringae strains. Mol. Plant Microbe Interact. 19:1151–1158 [DOI] [PubMed] [Google Scholar]
  • 9. Mansfield JW. 2009. From bacterial avirulence genes to effector functions via the hrp delivery system: an overview of 25 years of progress in our understanding of plant innate immunity. Mol. Plant Pathol. 10:721–734 [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 10. Peñaloza-Vázquez A, Fakhr MK, Bailey AM, Bender CL. 2004. AlgR functions in algC expression and virulence in Pseudomonas syringae pv. syringae. Microbiology 150:2727–2737 [DOI] [PubMed] [Google Scholar]
  • 11. Peñaloza-Vázquez A, Kidambi SP, Chakrabarty AM, Bender CL. 1997. Characterization of the alginate biosynthetic gene cluster in Pseudomonas syringae pv. syringae. J. Bacteriol. 179:4464–4472 [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 12. Penaloza-Vazquez A, Sreedharan A, Bender CL. 2010. Transcriptional studies of the hrpM/opgH gene in Pseudomonas syringae during biofilm formation and in response to different environmental challenges. Environ. Microbiol. 12:1452–1467 [DOI] [PubMed] [Google Scholar]
  • 13. Sarkar SF, Guttman DS. 2004. Evolution of the core genome of Pseudomonas syringae, a highly clonal, endemic plant pathogen. Appl. Environ. Microbiol. 70:1999–2012 [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 14. Seidle HF, Couch RD, Parry RJ. 2006. Characterization of a nonspecific phosphopantetheinyl transferase from Pseudomonas syringae pv. syringae FF5. Arch. Biochem. Biophys. 446:167–174 [DOI] [PubMed] [Google Scholar]
  • 15. Sundin GW, Bender CL. 1993. Ecological and genetic analysis of copper and streptomycin resistance in Pseudomonas syringae pv. syringae. Appl. Environ. Microbiol. 59:1018–1024 [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 16. Sundin GW, Bender CL. 1996. Molecular analysis of closely related copper- and streptomycin-resistance plasmids in Pseudomonas syringae pv. syringae. Plasmid 35:98–107 [DOI] [PubMed] [Google Scholar]
  • 17. Sundin GW, Kidambi SP, Ullrich M, Bender CL. 1996. Resistance to ultraviolet light in Pseudomonas syringae: sequence and functional analysis of the plasmid-encoded rulAB genes. Gene 177:77–81 [DOI] [PubMed] [Google Scholar]
  • 18. Sundin GW, Murillo J. 1999. Functional analysis of the Pseudomonas syringae rulAB determinant in tolerance to ultraviolet B (290-320 nm) radiation and distribution of rulAB among P. syringae pathovars. Environ. Microbiol. 1:75–87 [DOI] [PubMed] [Google Scholar]
  • 19. Yu J, Peñaloza-Vázquez A, Chakrabarty AM, Bender CL. 1999. Involvement of the exopolysaccharide alginate in the virulence and epiphytic fitness of Pseudomonas syringae pv. syringae. Mol. Microbiol. 33:712–720 [DOI] [PubMed] [Google Scholar]
  • 20. Zerbino DR, Birney E. 2008. Velvet: algorithms for de novo short read assembly using de Bruijn graphs. Genome Res. 18:821–829 [DOI] [PMC free article] [PubMed] [Google Scholar]

Articles from Journal of Bacteriology are provided here courtesy of American Society for Microbiology (ASM)

RESOURCES