Detection and quantification of cytokines is important to better understand
disease processes in populations. This study assessed the feasibility of q
uantifying wildlife orthologues for tumor necrosis factor (TNF) and interle
ukin-6 (IL-6) using two bioassays combined with an in vitro model for immun
e stimulation. For all species, heparinized blood (1 ml) was exposed to lip
opolysaccharide (LPS; 10 pg to 50 mug) for 6 hr (37 degreesC) after which p
lasma was collected. Neutralizing antibodies were used to demonstrate that
grizzly bear (Ursus arctos) TNF can be quantified with a WEHI-164 bioassay,
and expression of TNF in the LPS stimulated model is dose-dependent. A B9
bioassay demonstrated LPS-dose-dependent production of IL-6 for grizzly bea
rs, although neutralizing antibodies were not available to confirm that IL-
6 was responsible for these results. The B9 assay may have detected IL-6 or
thologues for bighorn sheep (Ovis canadensis canadensis), elk (Cervus elaph
us) and bison (Bison bison). These assays combined with the LPS stimulated
blood model could provide a rapid means for assessing immunological effects
of pathogens and toxicants.