This Article
Right arrow Full Text
Right arrow Full Text (PDF)
Right arrow Supplemental material
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 Lybarger, S. R.
Right arrow Articles by Sandkvist, M.
Right arrow Search for Related Content
PubMed
Right arrow PubMed Citation
Right arrow Articles by Lybarger, S. R.
Right arrow Articles by Sandkvist, M.

 Previous Article  |  Next Article 

Journal of Bacteriology, May 2009, p. 3149-3161, Vol. 191, No. 9
0021-9193/09/$08.00+0     doi:10.1128/JB.01701-08
Copyright © 2009, American Society for Microbiology. All Rights Reserved.

Docking and Assembly of the Type II Secretion Complex of Vibrio cholerae{triangledown} ,{dagger}

Suzanne R. Lybarger, Tanya L. Johnson, Miranda D. Gray, Aleksandra E. Sikora, and Maria Sandkvist*

Dept. of Microbiology and Immunology, University of Michigan Medical School, 1150 West Medical Center Drive, Ann Arbor, Michigan 48109

Received 5 December 2008/ Accepted 12 February 2009

Secretion of cholera toxin and other virulence factors from Vibrio cholerae is mediated by the type II secretion (T2S) apparatus, a multiprotein complex composed of both inner and outer membrane proteins. To better understand the mechanism by which the T2S complex coordinates translocation of its substrates, we are examining the protein-protein interactions of its components, encoded by the extracellular protein secretion (eps) genes. In this study, we took a cell biological approach, observing the dynamics of fluorescently tagged EpsC and EpsM proteins in vivo. We report that the level and context of fluorescent protein fusion expression can have a bold effect on subcellular location and that chromosomal, intraoperon expression conditions are optimal for determining the intracellular locations of fusion proteins. Fluorescently tagged, chromosomally expressed EpsC and EpsM form discrete foci along the lengths of the cells, different from the polar localization for green fluorescent protein (GFP)-EpsM previously described, as the fusions are balanced with all their interacting partner proteins within the T2S complex. Additionally, we observed that fluorescent foci in both chromosomal GFP-EpsC- and GFP-EpsM-expressing strains disperse upon deletion of epsD, suggesting that EpsD is critical to the localization of EpsC and EpsM and perhaps their assembly into the T2S complex.


* Corresponding author. Mailing address: Dept. of Microbiology and Immunology, University of Michigan Medical School, 1150 West Medical Center Drive, Ann Arbor, MI 48109. Phone: (734) 764-3552. Fax: (734) 764-3562. E-mail: mariasan{at}umich.edu

{triangledown} Published ahead of print on 27 February 2009.

{dagger} Supplemental material for this article may be found at http://jb.asm.org/.


Journal of Bacteriology, May 2009, p. 3149-3161, Vol. 191, No. 9
0021-9193/09/$08.00+0     doi:10.1128/JB.01701-08
Copyright © 2009, American Society for Microbiology. All Rights Reserved.




This article has been cited by other articles:

  • Janakiraman, A., Fixen, K. R., Gray, A. N., Niki, H., Goldberg, M. B. (2009). A Genome-Scale Proteomic Screen Identifies a Role for DnaK in Chaperoning of Polar Autotransporters in Shigella. J. Bacteriol. 191: 6300-6311 [Abstract] [Full Text]  
  • Slightom, R. N., Buchan, A. (2009). Surface Colonization by Marine Roseobacters: Integrating Genotype and Phenotype. Appl. Environ. Microbiol. 75: 6027-6037 [Abstract] [Full Text]  
  • Sikora, A. E., Beyhan, S., Bagdasarian, M., Yildiz, F. H., Sandkvist, M. (2009). Cell Envelope Perturbation Induces Oxidative Stress and Changes in Iron Homeostasis in Vibrio cholerae. J. Bacteriol. 191: 5398-5408 [Abstract] [Full Text]