Evaluation of Canine and Human Antisera as Diagnostic Reagents for Use in the Identification of Immunoglobulins of Steller Sea Lions (Eumetopiasjubatus) and Harbor Seals (Phoca vitulina)
Abstract
The status of the humoral immune system can be assessed through the use of
immunoassays that measure immunoglobulin concentrations in serum. Using species specific
reagents in primary binding assays maximizes sensitivity and specificity; however, the
availability of commercial antisera for non-domestic or exotic animals is often limited.
Currently, this laboratory is developing species specific antisera for Steller sea lion
immunoglobulin isotypes. In an effort to obtain preliminary results, canine (a common ancestral
relation to pinnipeds) and human reagents (including purified immunoglobulins and antisera
specific for the immunoglobulins) were checked for cross reactivity against Steller sea lion and
harbor seal serum. The canine reagents were obtained from Bethyl laboratories and Sigma; the
human reagents were from Sigma. Analysis of the pinniped serum proteins was performed through
several immunoassays including Ouchterlony (double immunodiffusion) and Western
blot/Immunostaining analysis.
The Ouchterlony assays revealed that anti-dog gamma, anti-dog mu, and
anti-dog IgG (whole molecule) reagents have cross-reactivity with both harbor seal and Steller
sea lion serum. Similar results were obtained with Western blot/Immunostaining analysis. The
anti-human gamma had a weak interaction with Steller sea lion serum and no reaction with the
harbor seal serum in the Ouchterlony procedure. Anti-human mu was cross-reactive with Steller
sea lion serum in both immunoassays performed, but was cross-reactive with harbor seal serum
only in the Ouchterlony procedure. While the results with Western blot/Immunostaining analysis
were ambiguous, the Ouchterlony assay showed definitively that Steller sea lion serum was
cross-reactive with anti-dog alpha, but not with anti-human alpha. Harbor seal serum did not
react with either the anti-dog alpha or anti-human alpha antisera by either immunoassay
methods.
The results indicate that anti-dog gamma, mu, and alpha, and anti-human mu
will be used as reagents in a capture ELISA to measure concentrations of specific immunoglobulin
isotypes in Steller secretion and harbor seal serum.