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 Beltrametti, F.
Right arrow Articles by Guzmán, C. A.
Right arrow Search for Related Content
PubMed
Right arrow PubMed Citation
Right arrow Articles by Beltrametti, F.
Right arrow Articles by Guzmán, C. A.

 Previous Article  |  Next Article 

Journal of Bacteriology, June 1999, p. 3409-3418, Vol. 181, No. 11
0021-9193/99/$04.00+0
Copyright © 1999, American Society for Microbiology. All rights reserved.

Transcriptional Regulation of the esp Genes of Enterohemorrhagic Escherichia coli

Fabrizio Beltrametti, Andreas U. Kresse, and Carlos A. Guzmán*

Department of Microbial Pathogenicity and Vaccine Research, Division of Microbiology, GBF-National Research Centre for Biotechnology, D-38124 Braunschweig, Germany

Received 21 December 1998/Accepted 31 March 1999

We have determined that the genes encoding the secreted proteins EspA, EspD, and EspB of enterohemorrhagic Escherichia coli (EHEC) are organized in a single operon. The esp operon is controlled by a promoter located 94 bp upstream from the ATG start codon of the espA gene. The promoter is activated in the early logarithmic growth phase, upon bacterial contact with eukaryotic cells and in response to Ca2+, Mn2+, and HEPES. Transcription of the esp operon seems to be switched off in tightly attached bacteria. The activation process is regulated by osmolarity (induction at high osmolarities), modulated by temperature, and influenced by the degree of DNA supercoiling. Transcription is sigma S dependent, and the H-NS protein contributes to its fine tuning. Identification of the factors involved in activation of the esp operon and the signals responsible for modulation may facilitate understanding of the underlying molecular events leading to sequential expression of virulence factors during natural infections caused by EHEC.


* Corresponding author. Mailing address: Department of Microbial Pathogenicity and Vaccine Research, Division of Microbiology, GBF-National Research Centre for Biotechnology, Mascheroder Weg 1, D-38124 Braunschweig, Germany. Phone: 49-531-6181558. Fax: 49-531-6181411. E-mail: cag{at}gbf.de.


Journal of Bacteriology, June 1999, p. 3409-3418, Vol. 181, No. 11
0021-9193/99/$04.00+0
Copyright © 1999, American Society for Microbiology. All rights reserved.



This article has been cited by other articles:

  • Bergholz, T. M., Vanaja, S. K., Whittam, T. S. (2009). Gene Expression Induced in Escherichia coli O157:H7 upon Exposure to Model Apple Juice. Appl. Environ. Microbiol. 75: 3542-3553 [Abstract] [Full Text]  
  • White-Ziegler, C. A., Davis, T. R. (2009). Genome-Wide Identification of H-NS-Controlled, Temperature-Regulated Genes in Escherichia coli K-12. J. Bacteriol. 191: 1106-1110 [Abstract] [Full Text]  
  • Mellies, J. L., Larabee, F. J., Zarr, M. A., Horback, K. L., Lorenzen, E., Mavor, D. (2008). Ler interdomain linker is essential for anti-silencing activity in enteropathogenic Escherichia coli. Microbiology 154: 3624-3638 [Abstract] [Full Text]  
  • Torres, A. G., Slater, T. M., Patel, S. D., Popov, V. L., Arenas-Hernandez, M. M. P. (2008). Contribution of the Ler- and H-NS-Regulated Long Polar Fimbriae of Escherichia coli O157:H7 during Binding to Tissue-Cultured Cells. Infect. Immun. 76: 5062-5071 [Abstract] [Full Text]  
  • Vareille, M., Rannou, F., Thelier, N., Glasser, A.-L., de Sablet, T., Martin, C., Gobert, A. P. (2008). Heme Oxygenase-1 Is a Critical Regulator of Nitric Oxide Production in Enterohemorrhagic Escherichia coli-Infected Human Enterocytes. J. Immunol. 180: 5720-5726 [Abstract] [Full Text]  
  • Mellies, J. L., Barron, A. M. S., Carmona, A. M. (2007). Enteropathogenic and Enterohemorrhagic Escherichia coli Virulence Gene Regulation. Infect. Immun. 75: 4199-4210 [Full Text]  
  • Torres, A. G., Lopez-Sanchez, G. N., Milflores-Flores, L., Patel, S. D., Rojas-Lopez, M., Martinez de la Pena, C. F., Arenas-Hernandez, M. M. P., Martinez-Laguna, Y. (2007). Ler and H-NS, Regulators Controlling Expression of the Long Polar Fimbriae of Escherichia coli O157:H7. J. Bacteriol. 189: 5916-5928 [Abstract] [Full Text]  
  • Ando, H., Abe, H., Sugimoto, N., Tobe, T. (2007). Maturation of functional type III secretion machinery by activation of anaerobic respiration in enterohaemorrhagic Escherichia coli. Microbiology 153: 464-473 [Abstract] [Full Text]  
  • Walters, M., Sperandio, V. (2006). Autoinducer 3 and Epinephrine Signaling in the Kinetics of Locus of Enterocyte Effacement Gene Expression in Enterohemorrhagic Escherichia coli.. Infect. Immun. 74: 5445-5455 [Abstract] [Full Text]  
  • Navarre, W. W., Porwollik, S., Wang, Y., McClelland, M., Rosen, H., Libby, S. J., Fang, F. C. (2006). Selective Silencing of Foreign DNA with Low GC Content by the H-NS Protein in Salmonella. Science 313: 236-238 [Abstract] [Full Text]  
  • Zhang, L., Chaudhuri, R. R., Constantinidou, C., Hobman, J. L., Patel, M. D., Jones, A. C., Sarti, D., Roe, A. J., Vlisidou, I., Shaw, R. K., Falciani, F., Stevens, M. P., Gally, D. L., Knutton, S., Frankel, G., Penn, C. W., Pallen, M. J. (2004). Regulators Encoded in the Escherichia coli Type III Secretion System 2 Gene Cluster Influence Expression of Genes within the Locus for Enterocyte Effacement in Enterohemorrhagic E. coli O157:H7. Infect. Immun. 72: 7282-7293 [Abstract] [Full Text]  
  • Sharma, V. K., Zuerner, R. L. (2004). Role of hha and ler in Transcriptional Regulation of the esp Operon of Enterohemorrhagic Escherichia coli O157:H7. J. Bacteriol. 186: 7290-7301 [Abstract] [Full Text]  
  • Li, M., Rosenshine, I., Tung, S. L., Wang, X. H., Friedberg, D., Hew, C. L., Leung, K. Y. (2004). Comparative Proteomic Analysis of Extracellular Proteins of Enterohemorrhagic and Enteropathogenic Escherichia coli Strains and Their ihf and ler Mutants. Appl. Environ. Microbiol. 70: 5274-5282 [Abstract] [Full Text]  
  • Bertin, Y., Boukhors, K., Livrelli, V., Martin, C. (2004). Localization of the Insertion Site and Pathotype Determination of the Locus of Enterocyte Effacement of Shiga Toxin-Producing Escherichia coli Strains. Appl. Environ. Microbiol. 70: 61-68 [Abstract] [Full Text]  
  • Hulsmann, A., Rosche, T. M., Kong, I.-S., Hassan, H. M., Beam, D. M., Oliver, J. D. (2003). RpoS-Dependent Stress Response and Exoenzyme Production in Vibrio vulnificus. Appl. Environ. Microbiol. 69: 6114-6120 [Abstract] [Full Text]  
  • Roe, A. J., Yull, H., Naylor, S. W., Woodward, M. J., Smith, D. G. E., Gally, D. L. (2003). Heterogeneous Surface Expression of EspA Translocon Filaments by Escherichia coli O157:H7 Is Controlled at the Posttranscriptional Level. Infect. Immun. 71: 5900-5909 [Abstract] [Full Text]  
  • Tatsuno, I., Nagano, K., Taguchi, K., Rong, L., Mori, H., Sasakawa, C. (2003). Increased Adherence to Caco-2 Cells Caused by Disruption of the yhiE and yhiF Genes in Enterohemorrhagic Escherichia coli O157:H7. Infect. Immun. 71: 2598-2606 [Abstract] [Full Text]  
  • Dahan, S., Dalmasso, G., Imbert, V., Peyron, J.-F., Rampal, P., Czerucka, D. (2003). Saccharomyces boulardii Interferes with Enterohemorrhagic Escherichia coli-Induced Signaling Pathways in T84 Cells. Infect. Immun. 71: 766-773 [Abstract] [Full Text]  
  • Abe, H., Tatsuno, I., Tobe, T., Okutani, A., Sasakawa, C. (2002). Bicarbonate Ion Stimulates the Expression of Locus of Enterocyte Effacement-Encoded Genes in Enterohemorrhagic Escherichia coli O157:H7. Infect. Immun. 70: 3500-3509 [Abstract] [Full Text]  
  • McIngvale, S. C., Elhanafi, D., Drake, M. A. (2002). Optimization of Reverse Transcriptase PCR To Detect Viable Shiga-Toxin-Producing Escherichia coli. Appl. Environ. Microbiol. 68: 799-806 [Abstract] [Full Text]  
  • Sandner, L., Eguiarte, L. E., Navarro, A., Cravioto, A., Souza, V. (2001). The elements of the locus of enterocyte effacement in human and wild mammal isolates of Escherichia coli: evolution by assemblage or disruption?. Microbiology 147: 3149-3158 [Abstract] [Full Text]  
  • McNally, A., Roe, A. J., Simpson, S., Thomson-Carter, F. M., Hoey, D. E. E., Currie, C., Chakraborty, T., Smith, D. G. E., Gally, D. L. (2001). Differences in Levels of Secreted Locus of Enterocyte Effacement Proteins between Human Disease-Associated and Bovine Escherichia coli O157. Infect. Immun. 69: 5107-5114 [Abstract] [Full Text]  
  • White-Ziegler, C. A., Villapakkam, A., Ronaszeki, K., Young, S. (2000). H-NS Controls pap and daa Fimbrial Transcription in Escherichia coli in Response to Multiple Environmental Cues. J. Bacteriol. 182: 6391-6400 [Abstract] [Full Text]  
  • Kresse, A. U., Beltrametti, F., Müller, A., Ebel, F., Guzmán, C. A. (2000). Characterization of SepL of Enterohemorrhagic Escherichia coli. J. Bacteriol. 182: 6490-6498 [Abstract] [Full Text]  
  • Indergand, S., Graf, J. (2000). Ingested Blood Contributes to the Specificity of the Symbiosis of Aeromonas veronii Biovar Sobria and Hirudo medicinalis, the Medicinal Leech. Appl. Environ. Microbiol. 66: 4735-4741 [Abstract] [Full Text]  
  • Ogierman, M. A., Paton, A. W., Paton, J. C. (2000). Up-Regulation of Both Intimin and eae-Independent Adherence of Shiga Toxigenic Escherichia coli O157 by ler and Phenotypic Impact of a Naturally Occurring ler Mutation. Infect. Immun. 68: 5344-5353 [Abstract] [Full Text]  
  • Weyand, N. J., Low, D. A. (2000). Regulation of Pap Phase Variation. Lrp IS SUFFICIENT FOR THE ESTABLISHMENT OF THE PHASE OFF pap DNA METHYLATION PATTERN AND REPRESSION OF pap TRANSCRIPTION IN VITRO. J. Biol. Chem. 275: 3192-3200 [Abstract] [Full Text]  
  • Kresse, A. U., Rohde, M., Guzman, C. A. (1999). The EspD Protein of Enterohemorrhagic Escherichia coli Is Required for the Formation of Bacterial Surface Appendages and Is Incorporated in the Cytoplasmic Membranes of Target Cells. Infect. Immun. 67: 4834-4842 [Abstract] [Full Text]