For accreditation of CSIRO specific pathogen-free flocks, chicken sera
are routinely tested for antibody to chicken anaemia virus (CAV) usin
g a commercially available ELISA kit. On some occasions recently, up t
o 18.2% positive reactions have been found in individual isolators, wi
th an overall reaction rate of 2.7%. On subsequent bleeding the majori
ty of the suspected birds have given negative reactions, indicating th
at the earlier reactions were false-positives. The protein composition
of the sera that appeared CAV-negative or -positive in the ELISA were
compared using various chromatographic techniques. Separation of seru
m proteins by high resolution size exclusion chromatography revealed t
hat in the false-positive sera the antigen-binding activity is associa
ted with a protein fraction which was different from mat found in the
true-positive sera.