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Journal of Bacteriology, August 2004, p. 5486-5495, Vol. 186, No. 16
0021-9193/04/$08.00+0     DOI: 10.1128/JB.186.16.5486-5495.2004
Copyright © 2004, American Society for Microbiology. All Rights Reserved.

Identification of the Secretion and Translocation Domain of the Enteropathogenic and Enterohemorrhagic Escherichia coli Effector Cif, Using TEM-1 ß-Lactamase as a New Fluorescence-Based Reporter

Xavier Charpentier and Eric Oswald*

UMR 1225, Institut National de la Recherche Agronomique, Ecole Nationale Vétérinaire de Toulouse, 31076 Toulouse Cedex, France

Received 1 April 2004/ Accepted 14 May 2004

Enteropathogenic and enterohemorrhagic Escherichia coli (EPEC and EHEC) strains are human and animal pathogens that inject effector proteins into host cells via a type III secretion system (TTSS). Cif is an effector protein which induces host cell cycle arrest and reorganization of the actin cytoskeleton. Cif is encoded by a lambdoid prophage present in most of the EPEC and EHEC strains. In this study, we analyzed the domain that targets Cif to the TTSS by using a new reporter system based on a translational fusion of the effector proteins with mature TEM-1 ß-lactamase. Translocation was detected directly in living host cells by using the fluorescent ß-lactamase substrate CCF2/AM. We show that the first 16 amino acids (aa) of Cif were necessary and sufficient to mediate translocation into the host cells. Similarly, the first 20 aa of the effector proteins Map, EspF, and Tir, which are encoded in the same region as the TTSS, mediated secretion and translocation in a type III-dependent but chaperone-independent manner. A truncated form of Cif lacking its first 20 aa was no longer secreted and translocated, but fusion with the first 20 aa of Tir, Map, or EspF restored both secretion and translocation. In addition, the chimeric proteins were fully able to trigger host cell cycle arrest and stress fiber formation. In conclusion, our results demonstrate that Cif is composed of a C-terminal effector domain and an exchangeable N-terminal translocation signal and that the TEM-1 reporter system is a convenient tool for the study of the translocation of toxins or effector proteins into host cells.

* Corresponding author. Mailing address: UMR 1225, INRA-ENVT, 23 chemin des Capelles, 31076 Toulouse Cedex, France. Phone: 33 561 19 39 91. Fax: 33 561 19 39 75. E-mail: e.oswald{at}envt.fr.

Journal of Bacteriology, August 2004, p. 5486-5495, Vol. 186, No. 16
0021-9193/04/$08.00+0     DOI: 10.1128/JB.186.16.5486-5495.2004
Copyright © 2004, American Society for Microbiology. All Rights Reserved.



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