This Article
Right arrow Full Text
Right arrow Full Text (PDF)
Right arrow Alert me when this article is cited
Right arrow Alert me if a correction is posted
Services
Right arrow Similar articles in this journal
Right arrow Similar articles in PubMed
Right arrow Alert me to new issues of the journal
Right arrow Download to citation manager
Right arrowReprints and Permissions
Right arrow Copyright Information
Right arrow Books from ASM Press
Right arrow MicrobeWorld
Citing Articles
Right arrow Citing Articles via HighWire
Right arrow Citing Articles via Google Scholar
Google Scholar
Right arrow Articles by Purdy, D.
Right arrow Articles by Park, S. F.
Right arrow Search for Related Content
PubMed
Right arrow PubMed Citation
Right arrow Articles by Purdy, D.
Right arrow Articles by Park, S. F.
Agricola
Right arrow Articles by Purdy, D.
Right arrow Articles by Park, S. F.

 Previous Article  |  Next Article 

Applied and Environmental Microbiology, June 1999, p. 2540-2546, Vol. 65, No. 6
0099-2240/99/$04.00+0
Copyright © 1999, American Society for Microbiology. All rights reserved.

Generation of a Superoxide Dismutase (SOD)-Deficient Mutant of Campylobacter coli: Evidence for the Significance of SOD in Campylobacter Survival and Colonization

Desmond Purdy,1 Sean Cawthraw,2 Joanne H. Dickinson,3 Diane G. Newell,2 and Simon F. Park4,*

School of Biological Sciences, University of Surrey, Guildford GU2 5XH,4 Veterinary Laboratories Agency, New Haw, Addlestone KT15 3NB,2 Centre for Applied Microbiology Research, Porton Down, Salisbury SP4 0JG,1 and University of Nottingham, Sutton Bonington Campus, Loughborough LE12 5RD,3 United Kingdom

Received 8 December 1998/Accepted 10 March 1999

The microaerophilic nature of Campylobacter species implies an inherent sensitivity towards oxygen and its reduction products, particularly the superoxide anion. The deleterious effects of exposure to superoxide radicals are counteracted by the activity of superoxide dismutase (SOD). We have shown previously that Campylobacter coli possesses an iron cofactored SOD. The sodB gene of C. coli UA585 was insertionally inactivated by the site-specific insertion of a tetO cassette. Organisms harboring the inactivated gene failed to produce a biologically functional form of the enzyme. While the ability of this mutant to grow in aerobic conditions was unchanged relative to the parental strain, its survival was severely compromised when nongrowing cells were exposed to air. Accordingly, the SOD-deficient mutant was unable to survive for prolonged periods in model foods. Furthermore, inactivation of the sodB gene decreased the colonization potential in an experimental infection of 1-day-old chicks. In contrast, strain CK100, which is deficient in catalase activity, showed the same survival and colonization characteristics as the parental strain. These results indicate that SOD, but not catalase, is an important determinant in the ability of C. coli to survive aerobically and for optimal colonization within the chicken gut.


* Corresponding author. Mailing address: School of Biological Sciences, University of Surrey, Guildford GU2 5XH, United Kingdom. Phone: 44 (0) 1483-259024. Fax: 44 (0) 1483-300374. E-mail: s.park{at}surrey.ac.uk.


Applied and Environmental Microbiology, June 1999, p. 2540-2546, Vol. 65, No. 6
0099-2240/99/$04.00+0
Copyright © 1999, American Society for Microbiology. All rights reserved.



This article has been cited by other articles:

  • Lin, A. E., Krastel, K., Hobb, R. I., Thompson, S. A., Cvitkovitch, D. G., Gaynor, E. C. (2009). Atypical Roles for Campylobacter jejuni Amino Acid ATP Binding Cassette Transporter Components PaqP and PaqQ in Bacterial Stress Tolerance and Pathogen-Host Cell Dynamics. Infect. Immun. 77: 4912-4924 [Abstract] [Full Text]  
  • Azizoglu, R. O., Osborne, J., Wilson, S., Kathariou, S. (2009). Role of Growth Temperature in Freeze-Thaw Tolerance of Listeria spp.. Appl. Environ. Microbiol. 75: 5315-5320 [Abstract] [Full Text]  
  • Wright, J. A., Grant, A. J., Hurd, D., Harrison, M., Guccione, E. J., Kelly, D. J., Maskell, D. J. (2009). Metabolite and transcriptome analysis of Campylobacter jejuni in vitro growth reveals a stationary-phase physiological switch. Microbiology 155: 80-94 [Abstract] [Full Text]  
  • Atack, J. M., Kelly, D. J. (2008). Contribution of the stereospecific methionine sulphoxide reductases MsrA and MsrB to oxidative and nitrosative stress resistance in the food-borne pathogen Campylobacter jejuni. Microbiology 154: 2219-2230 [Abstract] [Full Text]  
  • Bingham-Ramos, L. K., Hendrixson, D. R. (2008). Characterization of Two Putative Cytochrome c Peroxidases of Campylobacter jejuni Involved in Promoting Commensal Colonization of Poultry. Infect. Immun. 76: 1105-1114 [Abstract] [Full Text]  
  • Grant, A. J., Coward, C., Jones, M. A., Woodall, C. A., Barrow, P. A., Maskell, D. J. (2005). Signature-Tagged Transposon Mutagenesis Studies Demonstrate the Dynamic Nature of Cecal Colonization of 2-Week-Old Chickens by Campylobacter jejuni. Appl. Environ. Microbiol. 71: 8031-8041 [Abstract] [Full Text]  
  • Stintzi, A., Marlow, D., Palyada, K., Naikare, H., Panciera, R., Whitworth, L., Clarke, C. (2005). Use of Genome-Wide Expression Profiling and Mutagenesis To Study the Intestinal Lifestyle of Campylobacter jejuni. Infect. Immun. 73: 1797-1810 [Abstract] [Full Text]  
  • Palyada, K., Threadgill, D., Stintzi, A. (2004). Iron Acquisition and Regulation in Campylobacter jejuni. J. Bacteriol. 186: 4714-4729 [Abstract] [Full Text]  
  • Gaynor, E. C., Cawthraw, S., Manning, G., MacKichan, J. K., Falkow, S., Newell, D. G. (2004). The Genome-Sequenced Variant of Campylobacter jejuni NCTC 11168 and the Original Clonal Clinical Isolate Differ Markedly in Colonization, Gene Expression, and Virulence-Associated Phenotypes. J. Bacteriol. 186: 503-517 [Abstract] [Full Text]  
  • Ishikawa, T., Mizunoe, Y., Kawabata, S.-i., Takade, A., Harada, M., Wai, S. N., Yoshida, S.-i. (2003). The Iron-Binding Protein Dps Confers Hydrogen Peroxide Stress Resistance to Campylobacter jejuni. J. Bacteriol. 185: 1010-1017 [Abstract] [Full Text]  
  • Valderas, M. W., Gatson, J. W., Wreyford, N., Hart, M. E. (2002). The Superoxide Dismutase Gene sodM Is Unique to Staphylococcus aureus: Absence of sodM in Coagulase-Negative Staphylococci. J. Bacteriol. 184: 2465-2472 [Abstract] [Full Text]  
  • Luke, N. R., Karalus, R. J., Campagnari, A. A. (2002). Inactivation of the Moraxella catarrhalis Superoxide Dismutase SodA Induces Constitutive Expression of Iron-Repressible Outer Membrane Proteins. Infect. Immun. 70: 1889-1895 [Abstract] [Full Text]  
  • Ahmed, I. H., Manning, G., Wassenaar, T. M., Cawthraw, S., Newell, D. G. (2002). Identification of genetic differences between two Campylobacter jejuni strains with different colonization potentials. Microbiology 148: 1203-1212 [Abstract] [Full Text]  
  • Seyler, R. W. Jr., Olson, J. W., Maier, R. J. (2001). Superoxide Dismutase-Deficient Mutants of Helicobacter pylori Are Hypersensitive to Oxidative Stress and Defective in Host Colonization. Infect. Immun. 69: 4034-4040 [Abstract] [Full Text]  
  • Kelly, A. F., Park, S. F., Bovill, R., Mackey, B. M. (2001). Survival of Campylobacter jejuni during Stationary Phase: Evidence for the Absence of a Phenotypic Stationary-Phase Response. Appl. Environ. Microbiol. 67: 2248-2254 [Abstract] [Full Text]  
  • Stead, D., Park, S. F. (2000). Roles of Fe Superoxide Dismutase and Catalase in Resistance of Campylobacter coli to Freeze-Thaw Stress. Appl. Environ. Microbiol. 66: 3110-3112 [Abstract] [Full Text]  
  • Fry, B. N., Feng, S., Chen, Y.-Y., Newell, D. G., Coloe, P. J., Korolik, V. (2000). The galE Gene of Campylobacter jejuni Is Involved in Lipopolysaccharide Synthesis and Virulence. Infect. Immun. 68: 2594-2601 [Abstract] [Full Text]