Antibody response of patients infected with verocytotoxin-producing Escherichia coli to protein antigens encoded on the LEE locus

Citation
C. Jenkins et al., Antibody response of patients infected with verocytotoxin-producing Escherichia coli to protein antigens encoded on the LEE locus, J MED MICRO, 49(1), 2000, pp. 97-101
Citations number
16
Categorie Soggetti
Microbiology
Journal title
JOURNAL OF MEDICAL MICROBIOLOGY
ISSN journal
00222615 → ACNP
Volume
49
Issue
1
Year of publication
2000
Pages
97 - 101
Database
ISI
SICI code
0022-2615(200001)49:1<97:AROPIW>2.0.ZU;2-A
Abstract
Sera from patients infected with verocytotoxin-producing Escherichia coli ( VTEC) O157, from patients with antibodies to E. coli O157 lipopolysaccharid e (LPS) and from healthy controls were examined for antibodies to proteins involved in expressing the attaching and effacing phenotype, After SDS-PAGE , purified recombinant intimin, EspA-filament structural protein, transloca ted protein EspB and three separate domains of the translocated intimin rec eptor (Tir) were tested for reaction with patients' sera by immunoblotting, An ELISA was also used to detect antibodies to intimin in sera from E, col i O157 LPS antibody-positive individuals. Seven of nine culture-positive pa tients and one control patient had antibodies to EspA, Five of these patien ts and two controls had serum antibodies to the intimin-binding region of T it, whereas none of the sera contained antibodies binding to either of the intracellular domains of Tir, By immunoblotting, 10 of 14 culture-positive patients had antibodies to the conserved region of intimin, eight of whom w ere infected with E, coli O157 phage type 2, Thirty-six of 60 sera from cul ture-negative but E coli O157 LPS antibody-positive patients had antibodies to intimin as determined by ELISA, The secreted proteins are expressed in vivo during infection and are considered as pathogenic markers. Antibodies to these proteins may form the basis of a serodiagnostic test for the detec tion of patients infected with VTEC which carry the locus for the enterocyt e effacement pathogenicity island and provide an adjunct test to the establ ished serological tests based on VTEC LPS.