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Infection and Immunity, September 2008, p. 4129-4136, Vol. 76, No. 9
0019-9567/08/$08.00+0 doi:10.1128/IAI.00334-08
Copyright © 2008, American Society for Microbiology. All Rights Reserved.

INRA, UR 1282 Infectiologie Animale et Santé Publique, Laboratoire de Pathogénie Bactérienne, F-37380 Nouzilly, France
Received 13 March 2008/ Returned for modification 25 April 2008/ Accepted 21 June 2008
IbeA in extraintestinal pathogenic Escherichia coli (ExPEC) strains was previously described for its role in invasion. Here we investigated the role of IbeA and IbeT, encoded by a gene located downstream of ibeA, in the adhesion of the avian ExPEC strain BEN2908 to human brain microvascular endothelial cells (HBMEC). The
ibeA mutant was less adhesive to HBMEC than the wild-type strain BEN2908 was. Because strain BEN2908 also expresses type 1 fimbriae, we measured the adhesion specifically due to IbeA by comparing the adhesive properties of a
fim derivative of strain BEN2908 to those of a double
fim
ibeA mutant. No differences were observed, indicating that the reduction of adhesion in BEN2908
ibeA could be due to a decrease in type 1 fimbria expression. We indeed showed that the decreased adhesion of BEN2908
ibeA was correlated with a decrease in type 1 fimbria expression. Accordingly, more bacteria had a fim promoter orientated in the off position in a culture of BEN2908
ibeA than in a culture of BEN2908. Expression of fimB and fimE, two genes encoding recombinases participating in controlling the orientation of the fim promoter, was decreased in BEN2908
ibeA. A reduction of type 1 fimbria expression due to a preferential orientation of the fim promoter in the off position was also seen in an ibeT mutant of strain BEN2908. We finally suggest a role for IbeA and IbeT in modulating the expression of type 1 fimbriae through an as yet unknown mechanism.
Published ahead of print on 30 June 2008.
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