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Clinical and Diagnostic Laboratory Immunology, March 1998, p. 242-246, Vol. 5, No. 2
U.S. Meat Animal Research Center, USDA
Agricultural Research Service, Clay Center,
Nebraska,1 and
National Animal
Disease Center, USDA Agricultural Research Service, Ames,
Iowa2
Received 11 September 1997/Returned for modification 12 November
1997/Accepted 24 November 1997
The O157 antigen of Escherichia coli shares structural
elements with lipopolysaccharide (LPS) antigens of other bacterial species, notably Brucella abortus and Yersinia
enterocolitica O9, a fact that confounds the
interpretation of assays for anti-O157 antibodies. To address this
problem, a blocking enzyme-linked immunosorbent assay (bELISA) was
designed with E. coli O157:H7 LPS as the antigen and a
monoclonal antibody specific for E. coli O157, designated
13B3, as the competing antibody. The bELISA had equivalent sensitivity
to, and significantly higher specificity than, the indirect ELISA
(iELISA), detecting anti-O157 antibodies in sera from cattle
experimentally inoculated with O157:H7. Only 13% of sera from naive
heifers vaccinated for or experimentally infected with B. abortus had increased anti-O157 bELISA titers, while 61% of
anti-O157 iELISA titers were increased. The bELISA is a sensitive and
specific method for the detection of serum antibodies resulting from
exposure to E. coli O157.
1071-412X/98/$04.00+0
Copyright © 1998, American Society for Microbiology. All rights reserved.
Development of a Blocking Enzyme-Linked Immunosorbent Assay for
Detection of Serum Antibodies to O157 Antigen of
Escherichia coli
*
Corresponding author. Mailing address: USDA, ARS, U.S.
Meat Animal Research Center, P.O. Box 166, State Spur 18D, Clay Center, NE 68933. Phone: (402) 762-4177. Fax: (402) 762-4375. E-mail: laegreid{at}aux.marc.usda.gov.
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