Literature DB >> 3425033

Specific interaction of bovine IgG1 and IgG2 subclasses with different chlamydial antigens.

N Schmeer1, K Schnorr, J Storz, J Perez-Martinez, H Krauss.   

Abstract

Antigens of the immunotype 1 strain B-577 of Chlamydia psittaci, which were separated by SDS-PAGE and electrophoretically transferred to nitrocellulose membranes were used to probe sequential serum samples of cattle with experimentally induced or naturally occurring chlamydial infections. Applying IgG1- and IgG2-specific markers in an enzyme immunoassay procedure, a predominance of IgG2 reactions with different proteins was determined. The interaction of IgG1 with antigens such as the genus-specific lipopolysaccharide and the major outer membrane protein was usually limited to periods immediately following overt clinical disease. Some other antigens like the 60,000 and 62,000 D proteins, for example, were recognized by both subclasses over the entire period of investigation. This indicates that it may be possible to determine the phase of infection through analysis of the IgG1 and IgG2 responses with the Western blot technique. The different IgG1 and IgG2 responses of cattle infected with different strains of Chlamydia psittaci as well as the diverse reactions of cattle from different herds with naturally occurring chlamydial infections further indicate that it may be feasible to distinguish the strains causing these chlamydial infections using different antigens in the Western blot technique. The results obtained by this method may have implications for the production of a subunit vaccine as well as for serodiagnostic purposes.

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Year:  1987        PMID: 3425033     DOI: 10.1016/s0176-6724(87)80044-5

Source DB:  PubMed          Journal:  Zentralbl Bakteriol Mikrobiol Hyg A        ISSN: 0176-6724


  2 in total

1.  Enzyme-linked immunosorbent fluorescence assay and high-pressure liquid chromatography for analysis of humoral immune responses to Coxiella burnetti proteins.

Authors:  N Schmeer; H P Müller; W Baumgärtner; J Wieda; H Krauss
Journal:  J Clin Microbiol       Date:  1988-12       Impact factor: 5.948

2.  Serological diagnosis of ovine enzootic abortion by comparative inclusion immunofluorescence assay, recombinant lipopolysaccharide enzyme-linked immunosorbent assay, and complement fixation test.

Authors:  P C Griffiths; J M Plater; M W Horigan; M P Rose; C Venables; M Dawson
Journal:  J Clin Microbiol       Date:  1996-06       Impact factor: 5.948

  2 in total

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