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Journal of Clinical Microbiology, December 1999, p. 3822-3827, Vol. 37, No. 12
Department of Biochemistry Imperial College
of Science,
Received 7 May 1999/Returned for modification 24 June 1999/Accepted 23 August 1999
Enteropathogenic Escherichia coli (EPEC) and
enterohemorrhagic E. coli (EHEC) constitute a significant
risk to human health worldwide. A hallmark of both pathogens is their
ability to produce characteristic attaching-and-effacing (A/E) lesions
in intestinal epithelial cells. Genes encoding A/E lesion formation map
to a chromosomal pathogenicity island termed the locus of enterocyte effacement (LEE). Intimin, an LEE-encoded bacterial adhesion molecule, mediates the intimate bacterium-host cell interaction characteristic of
A/E lesions. On the basis of characterization of the C-terminal 280-amino-acid cell binding domain of intimin
(Int280661-939), four distinct Int280 types (types
0095-1137/99/$04.00+0
Copyright © 1999, American Society for Microbiology. All rights reserved.
Development of a Universal Intimin Antiserum and PCR
Primers

,
,
, and
) have been identified. Importantly, Int280
and
Int280
antisera specifically recognized their respective intimin
types. Using a conserved region of the intimin molecule
(Int388-667) and primers synthesized to generate the
recombinant Int388-667, we have now generated universal
intimin antiserum and PCR primers that are reactive with the different
intimin types expressed by both human and animal A/E lesion-forming
strains. Use of immunogold electron microscopy to visualize intimin on
the surfaces of EPEC and EHEC strains revealed, in general, a uniform
distribution on the bacterial cell surface. However, a filamentous
staining pattern was observed with a few strains expressing intimin
. Cloning of the intimin eae gene from one such strain
(strain ICC57) into strain CVD206, an EPEC strain which harbors a null
deletion in eae, produced a uniform intimin staining
pattern indicating that, if the filamentous staining pattern defines a
filamentous form of intimin
, it is dependent upon the genetic
background of the strain and is not a feature of the intimin molecule.
*
Corresponding author. Mailing address: Department of
Biochemistry, Imperial College, Exhibition Rd., London SW7 2AZ, United Kingdom. Phone: 44-71-594-5253. Fax: 44-71-594-5255. E-mail:
g.frankel{at}ic.ac.uk.
Present address: Institute of Microbiology and Genetics, University
of Vienna, Dr. Bohrgasse 9, A-1030 Vienna, Austria.
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