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 Guichon, A.
Right arrow Articles by Zychlinsky, A.
Right arrow Search for Related Content
PubMed
Right arrow PubMed Citation
Right arrow Articles by Guichon, A.
Right arrow Articles by Zychlinsky, A.

 Previous Article  |  Next Article 

Journal of Bacteriology, February 2001, p. 1269-1276, Vol. 183, No. 4
0021-9193/01/$04.00+0   DOI: 10.1128/JB.183.4.1269-1276.2001
Copyright © 2001, American Society for Microbiology. All rights reserved.

Structure-Function Analysis of the Shigella Virulence Factor IpaB

Andrea Guichon,1 David Hersh,1 Mark R. Smith,2 and Arturo Zychlinsky1,*

The Skirball Institute and Department of Microbiology, New York University Medical Center, New York, New York 10016,1 and Intramural Research Support Program, SAIC Frederick, National Cancer Institute, Frederick Cancer Research and Development Center, Frederick, Maryland 217022

Received 18 October 2000/Accepted 16 November 2000

Infection by the gram-negative bacterium Shigella flexneri results in dysentery, an acute inflammatory disease of the colon. Essential events in the pathogenesis of Shigella infections include bacterial invasion of epithelial cells, escape from the phagosome, and induction of apoptosis in macrophages. The Shigella virulence factor invasion plasmid antigen B (IpaB) is required for all of these processes. Induction of apoptosis is dependent on IpaB binding to the cysteine protease caspase-1 (Casp-1). The activation of this enzyme triggers both apoptosis and release of the proinflammatory cytokine interleukin-1beta . Several IpaB mutants were generated to correlate function with protein subdomains. We determined that the N-terminal portion of IpaB is necessary for stable expression of IpaB. A putative amphipathic alpha -helical domain preserves the structure of IpaB. We found 10 consecutive residues within the amino terminus of the hydrophobic region that play a critical role in invasion, phagosomal escape, and cytotoxicity. An IpaB mutant carrying a mutation in this region binds to Casp-1 yet is not cytotoxic, even following direct delivery to the macrophage cytoplasm. These results indicate that the association between IpaB and Casp-1 is only a step in the activation of macrophage apoptosis.


* Corresponding author. Mailing address: Skirball Institute, New York University Medical Center, 540 First Avenue, New York, NY 10016. Phone: (212) 263-7058. Fax: (212) 263-5711. E-mail: zychlins{at}saturn.med.nyu.edu.


Journal of Bacteriology, February 2001, p. 1269-1276, Vol. 183, No. 4
0021-9193/01/$04.00+0   DOI: 10.1128/JB.183.4.1269-1276.2001
Copyright © 2001, American Society for Microbiology. All rights reserved.



This article has been cited by other articles:

  • Schroeder, G. N., Hilbi, H. (2008). Molecular Pathogenesis of Shigella spp.: Controlling Host Cell Signaling, Invasion, and Death by Type III Secretion. Clin. Microbiol. Rev. 21: 134-156 [Abstract] [Full Text]  
  • Schroeder, G. N., Jann, N. J., Hilbi, H. (2007). Intracellular type III secretion by cytoplasmic Shigella flexneri promotes caspase-1-dependent macrophage cell death. Microbiology 153: 2862-2876 [Abstract] [Full Text]  
  • Matarrese, P., Falzano, L., Fabbri, A., Gambardella, L., Frank, C., Geny, B., Popoff, M. R., Malorni, W., Fiorentini, C. (2007). Clostridium difficile Toxin B Causes Apoptosis in Epithelial Cells by Thrilling Mitochondria: INVOLVEMENT OF ATP-SENSITIVE MITOCHONDRIAL POTASSIUM CHANNELS. J. Biol. Chem. 282: 9029-9041 [Abstract] [Full Text]  
  • Farshad, S., Sheikhi, R., Japoni, A., Basiri, E., Alborzi, A. (2006). Characterization of Shigella Strains in Iran by Plasmid Profile Analysis and PCR Amplification of ipa Genes.. J. Clin. Microbiol. 44: 2879-2883 [Abstract] [Full Text]  
  • Petnicki-Ocwieja, T., van Dijk, K., Alfano, J. R. (2005). The hrpK Operon of Pseudomonas syringae pv. tomato DC3000 Encodes Two Proteins Secreted by the Type III (Hrp) Protein Secretion System: HopB1 and HrpK, a Putative Type III Translocator. J. Bacteriol. 187: 649-663 [Abstract] [Full Text]  
  • Koterski, J. F., Nahvi, M., Venkatesan, M. M., Haimovich, B. (2005). Virulent Shigella flexneri Causes Damage to Mitochondria and Triggers Necrosis in Infected Human Monocyte-Derived Macrophages. Infect. Immun. 73: 504-513 [Abstract] [Full Text]  
  • van der Velden, A. W. M., Velasquez, M., Starnbach, M. N. (2003). Salmonella Rapidly Kill Dendritic Cells via a Caspase-1- Dependent Mechanism. J. Immunol. 171: 6742-6749 [Abstract] [Full Text]  
  • Hathaway, L. J., Griffin, G. E., Sansonetti, P. J., Edgeworth, J. D. (2002). Human Monocytes Kill Shigella flexneri but Then Die by Apoptosis Associated with Suppression of Proinflammatory Cytokine Production. Infect. Immun. 70: 3833-3842 [Abstract] [Full Text]