Evaluation of an enzyme-linked immunosorbent assay (ELISA) for the detection of Campylobacter jejuni antibodies, and comparison with a complement fixation test (CFT). 1985

J Oosterom, and C H den Uyl, and J R Bänffer, and S Lauwers, and J Huisman, and A E Busschbach, and F G Poelma, and R Bellemans

An enzyme-linked immunosorbent assay (ELISA) was developed for the detection of total anti-Campylobacter immunoglobulins in human sera. In this assay disintegrated Campylobacter bacteria were used as the antigen. Absorption tests including other possibly enteropathogenic bacterial species showed that the ELISA system displayed a high immunological specificity for Campylobacter. Using this ELISA it was found that in about 80% of Campylobacter patients these Campylobacter antibodies are produced to almost maximal levels within 8 days after onset of disease, and that they may persist for at least 4 months. Indeed, Campylobacter antibodies were demonstrated at low levels in a large number of control sera. However, accepting an antibody titre of 1:640 as indicative of Campylobacter infection, the statistical sensitivity of the ELISA system was 77% and the specificity 95%. In an epidemiological survey a high association was demonstrated between the severity of Campylobacter-related symptoms and antibody titre values. Assessment of Campylobacter antibody titres by means of this ELISA and by a complement fixation test in 92 sera from index patients and contacts with and without symptoms showed a high association of results.

UI MeSH Term Description Entries
D007136 Immunoglobulins Multi-subunit proteins which function in IMMUNITY. They are produced by B LYMPHOCYTES from the IMMUNOGLOBULIN GENES. They are comprised of two heavy (IMMUNOGLOBULIN HEAVY CHAINS) and two light chains (IMMUNOGLOBULIN LIGHT CHAINS) with additional ancillary polypeptide chains depending on their isoforms. The variety of isoforms include monomeric or polymeric forms, and transmembrane forms (B-CELL ANTIGEN RECEPTORS) or secreted forms (ANTIBODIES). They are divided by the amino acid sequence of their heavy chains into five classes (IMMUNOGLOBULIN A; IMMUNOGLOBULIN D; IMMUNOGLOBULIN E; IMMUNOGLOBULIN G; IMMUNOGLOBULIN M) and various subclasses. Globulins, Immune,Immune Globulin,Immune Globulins,Immunoglobulin,Globulin, Immune
D002167 Campylobacter A genus of bacteria found in the reproductive organs, intestinal tract, and oral cavity of animals and man. Some species are pathogenic.
D002169 Campylobacter Infections Infections with bacteria of the genus CAMPYLOBACTER. Campylobacter Infection,Campylobacteriosis,Infections, Campylobacter,Campylobacterioses,Infection, Campylobacter
D003168 Complement Fixation Tests Serologic tests based on inactivation of complement by the antigen-antibody complex (stage 1). Binding of free complement can be visualized by addition of a second antigen-antibody system such as red cells and appropriate red cell antibody (hemolysin) requiring complement for its completion (stage 2). Failure of the red cells to lyse indicates that a specific antigen-antibody reaction has taken place in stage 1. If red cells lyse, free complement is present indicating no antigen-antibody reaction occurred in stage 1. Complement Absorption Test, Conglutinating,Conglutination Reaction,Conglutinating Complement Absorption Test,Complement Fixation Test,Conglutination Reactions,Fixation Test, Complement,Fixation Tests, Complement,Reaction, Conglutination,Reactions, Conglutination,Test, Complement Fixation,Tests, Complement Fixation
D004797 Enzyme-Linked Immunosorbent Assay An immunoassay utilizing an antibody labeled with an enzyme marker such as horseradish peroxidase. While either the enzyme or the antibody is bound to an immunosorbent substrate, they both retain their biologic activity; the change in enzyme activity as a result of the enzyme-antibody-antigen reaction is proportional to the concentration of the antigen and can be measured spectrophotometrically or with the naked eye. Many variations of the method have been developed. ELISA,Assay, Enzyme-Linked Immunosorbent,Assays, Enzyme-Linked Immunosorbent,Enzyme Linked Immunosorbent Assay,Enzyme-Linked Immunosorbent Assays,Immunosorbent Assay, Enzyme-Linked,Immunosorbent Assays, Enzyme-Linked
D006801 Humans Members of the species Homo sapiens. Homo sapiens,Man (Taxonomy),Human,Man, Modern,Modern Man
D000907 Antibodies, Bacterial Immunoglobulins produced in a response to BACTERIAL ANTIGENS. Bacterial Antibodies
D000942 Antigens, Bacterial Substances elaborated by bacteria that have antigenic activity. Bacterial Antigen,Bacterial Antigens,Antigen, Bacterial
D013997 Time Factors Elements of limited time intervals, contributing to particular results or situations. Time Series,Factor, Time,Time Factor

Related Publications

J Oosterom, and C H den Uyl, and J R Bänffer, and S Lauwers, and J Huisman, and A E Busschbach, and F G Poelma, and R Bellemans
February 1983, Journal of clinical pathology,
J Oosterom, and C H den Uyl, and J R Bänffer, and S Lauwers, and J Huisman, and A E Busschbach, and F G Poelma, and R Bellemans
July 1982, Kansenshogaku zasshi. The Journal of the Japanese Association for Infectious Diseases,
J Oosterom, and C H den Uyl, and J R Bänffer, and S Lauwers, and J Huisman, and A E Busschbach, and F G Poelma, and R Bellemans
July 1985, New Zealand veterinary journal,
J Oosterom, and C H den Uyl, and J R Bänffer, and S Lauwers, and J Huisman, and A E Busschbach, and F G Poelma, and R Bellemans
December 1982, Acta pathologica, microbiologica, et immunologica Scandinavica. Section B, Microbiology,
J Oosterom, and C H den Uyl, and J R Bänffer, and S Lauwers, and J Huisman, and A E Busschbach, and F G Poelma, and R Bellemans
February 1979, Journal of clinical pathology,
J Oosterom, and C H den Uyl, and J R Bänffer, and S Lauwers, and J Huisman, and A E Busschbach, and F G Poelma, and R Bellemans
March 1986, Veterinary parasitology,
J Oosterom, and C H den Uyl, and J R Bänffer, and S Lauwers, and J Huisman, and A E Busschbach, and F G Poelma, and R Bellemans
June 1984, American journal of veterinary research,
J Oosterom, and C H den Uyl, and J R Bänffer, and S Lauwers, and J Huisman, and A E Busschbach, and F G Poelma, and R Bellemans
November 1983, The Veterinary record,
J Oosterom, and C H den Uyl, and J R Bänffer, and S Lauwers, and J Huisman, and A E Busschbach, and F G Poelma, and R Bellemans
October 1984, Journal of immunological methods,
J Oosterom, and C H den Uyl, and J R Bänffer, and S Lauwers, and J Huisman, and A E Busschbach, and F G Poelma, and R Bellemans
January 1994, Veterinary research communications,
Copied contents to your clipboard!