Serodiagnosis of infection with Verocytotoxin-producing Escherichia coli

Citation
C. Jenkins et H. Chart, Serodiagnosis of infection with Verocytotoxin-producing Escherichia coli, J APPL MICR, 86(4), 1999, pp. 569-575
Citations number
32
Categorie Soggetti
Biology,Microbiology
Journal title
JOURNAL OF APPLIED MICROBIOLOGY
ISSN journal
13645072 → ACNP
Volume
86
Issue
4
Year of publication
1999
Pages
569 - 575
Database
ISI
SICI code
1364-5072(199904)86:4<569:SOIWVE>2.0.ZU;2-E
Abstract
Human sera (167) were screened for antibodies to lipopolysaccharide (LPS) p repared from strains of Verocytotoxin-producing Escherichia coli (VTEC) bel onging to a range of serogroups, secreted proteins expressed by attaching a nd effacing VTEC, enterohaemolysin and H = 7 flagellar proteins. Twelve ser a (about 7%) contained antibodies to the LPS of E, coli 05 (one), 026 (two) , 0145(one), 0145 (one), 0163 (one) and 0165 (five). Sera containing antibo dies to the LPS off. roll O26 and O145 also contained antibodies to secrete d proteins of 100 and 40 kDa. An additional 34 sera, known to contain antib odies to the lipopolysaccharide of E. roll O157, were examined for antibodi es to enterohaemolysin, H = 7 flagellar antigens and bacterial cell surface -associated proteins of 5, 6 and 22 kDa. Three sera contained antibodies to enterohaemolysin and one serum contained antibodies to flagellar proteins. Antibodies to membrane-associated proteins were not detected. It was concl uded that enterohaemolysin, H = 7 flagellar proteins and the cell surface-a ssociated proteins were unsuitable for use in immunoassays for providing ev idence of infection with VTEC.