Journal of Bacteriology, April 2005, p. 2286-2296, Vol. 187, No. 7
0021-9193/05/$08.00+0 doi:10.1128/JB.187.7.2286-2296.2005
Copyright © 2005, American Society for Microbiology. All Rights Reserved.
Strong Decrease in Invasive Ability and Outer Membrane Vesicle Release in Crohn's Disease-Associated Adherent-Invasive Escherichia coli Strain LF82 with the yfgL Gene Deleted
Nathalie Rolhion,
Nicolas Barnich,
Laurent Claret, and
Arlette Darfeuille-Michaud*
Pathogénie Bactérienne Intestinale, Laboratoire de Bactériologie, Université d'Auvergne, Clermont-Ferrand, France
Received 22 December 2004/
Accepted 28 December 2004
Adherent-invasive Escherichia coli strain LF82 recovered from a chronic lesion of a patient with Crohn's disease is able to invade cultured intestinal epithelial cells. Three mutants with impaired ability to invade epithelial cells had the Tn5phoA transposon inserted in the yfgL gene encoding the YfgL lipoprotein. A yfgL- negative isogenic mutant showed a marked decrease both in its ability to invade Intestine-407 cells and in the amount of the outer membrane proteins OmpA and OmpC in the culture supernatant, as shown by analysis of the culture supernatant protein contents by sodium dodecyl sulfate-polyacrylamide gel electrophoresis and matrix-assisted laser desorption ionization-time of flight mass spectrometry. Transcomplementation of the LF82-
yfgL isogenic mutant with the cloned yfgL gene restored invasion ability and outer membrane protein release in the culture supernatant. The outer membrane proteins in the culture supernatant of strain LF82 resulted from the formation of vesicles. This was shown by Western blot analysis of periplasmic and outer membrane fraction markers typically found in outer membrane vesicles and by transmission electron microscopic analysis of ultracentrifuged cell-free LF82 supernatant pellets, indicating the presence of vesicles with a bilayered structure surrounding a central electron-dense core. Thus, deletion of the yfgL gene in strain LF82 resulted in a decreased ability to invade intestinal epithelial cells and a decreased release of outer membrane vesicles.
* Corresponding author. Mailing address: Pathogénie Bactérienne Intestinale, Laboratoire de Bactériologie, Université d'Auvergne, CBRV, 28 Place Henri Dunant, 63001 Clermont-Ferrand, France. Phone: 33 4 73 17 79 97. Fax: 33 4 73 17 83 71. E-mail: arlette.darfeuille-michaud{at}u-clermont1.fr.
Journal of Bacteriology, April 2005, p. 2286-2296, Vol. 187, No. 7
0021-9193/05/$08.00+0 doi:10.1128/JB.187.7.2286-2296.2005
Copyright © 2005, American Society for Microbiology. All Rights Reserved.
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Copyright © 2005 by the American Society for Microbiology. All rights reserved.