Affiliation:
1. Department of Biochemistry, Imperial College of Science, Technology and Medicine, London SW7 2AZ,1 and
2. Institute of Child Health, The University of Birmingham B16 8ET,2 United Kingdom, and
3. Departmento de Microbiologia, Instituto de Ciências Biomédicas, Universidade de São Paulo, São Paulo, Brazil3
Abstract
ABSTRACT
Intimins are outer membrane proteins expressed by enteric bacterial pathogens capable of inducing intestinal attachment-and-effacement lesions. A eukaryotic cell-binding domain is located within a 280-amino-acid (Int280) carboxy terminus of intimin polypeptides. Polyclonal antiserum was raised against Int280 from enteropathogenic
Escherichia coli
(EPEC) serotypes O127:H6 and O114:H2 (anti-Int280-H6 and anti-Int280-H2, respectively), and Western blot analysis was used to explore the immunological relationship between the intimin polypeptides expressed by different clinical EPEC and enterohemorrhagic
E. coli
(EHEC) isolates, a rabbit diarrheagenic
E. coli
strain (RDEC-1), and
Citrobacter rodentium
. Anti-Int280-H6 serum reacted strongly with some EPEC serotypes, whereas anti-Int280-H2 serum reacted strongly with strains belonging to different EPEC and EHEC serotypes, RDEC-1, and
C. rodentium
. These observations were confirmed by using purified Int280 in an enzyme-linked immunosorbent assay and by immunogold and immunofluorescence labelling of whole bacterial cells. Some bacterial strains were recognized poorly by either antiserum (e.g., EPEC O86:H34 and EHEC O157:H7). By using PCR primers designed on the basis of the intimin-encoding
eae
gene sequences of serotype O127:H6, O114:H2, and O86:H34 EPEC and serotype O157:H7 EHEC, we could distinguish between different
eae
gene derivatives. Accordingly, the different intimin types were designated α, β, δ, and γ, respectively.
Publisher
American Society for Microbiology
Cited by
252 articles.
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