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Microbiology 152 (2006), 567-577; DOI  10.1099/mic.0.28405-0
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Microbiology 152 (2006), 567-577; DOI  10.1099/mic.0.28405-0
© 2006 Society for General Microbiology

Transcriptional and translational expression patterns associated with immobilized growth of Campylobacter jejuni

Balamurugan Sampathkumar3,{dagger}, Scott Napper1,{dagger}, Catherine D. Carrillo2, Philip Willson1, Eduardo Taboada2, John H. E. Nash2, Andrew A. Potter1, Lorne A. Babiuk1 and Brenda J. Allan1

1 Vaccine and Infectious Disease Organization, University of Saskatchewan, 120 Veterinary Road, Saskatoon, Saskatchewan, Canada S7N 5E3
2 Institute for Biological Sciences, National Research Council of Canada, 100 Sussex Road, Ottawa, Ontario, Canada K1A 0R6
3 Agriculture and Agri-Food Canada, Lacombe Research Centre, 6000 C&E Trail, Lacombe, Alberta, Canada T4L 1W1

Correspondence
Brenda J. Allan
brenda.allan{at}usask.ca

Although Campylobacter jejuni is a leading cause of food-borne illness, little is known about the mechanisms by which this pathogen mediates prolonged environmental survival or host cell virulence. Although these behaviours represent distinct phenotypes, they share a common requirement of an immobilized state. In order to understand the cellular mechanisms that facilitate a surface-associated lifestyle, transcriptional and translational expression profiles were determined for sessile and planktonic C. jejuni. These investigations indicate that the immobilized bacteria undergo a shift in cellular priorities away from metabolic, motility and protein synthesis capabilities towards emphasis on iron uptake, oxidative stress defence and membrane transport. This pattern of expression partially overlaps those reported for Campylobacter during host colonization, as well as for other species of bacteria involved in biofilms, highlighting common adaptive responses to the conserved challenges within each of these phenotypes. The adaptation of Campylobacter to immobilized growth may represent a quasi-differentiated state that functions as a foundation for further specialization towards phenotypes such as biofilm formation or host cell virulence.


The Gene Expression Omnibus Repository accession number for the microarray experiments reported in this paper is GSE3028.

{dagger}These authors contributed equally to this work.




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