Background: Apoptosis is an active cell death process mediated by
caspases activation, in which different extrinsic or intrinsic
signalling pathways result in direct activation of effector caspases.
Caspase-3 is considered to be the most important of the executioner
caspases, which cause the morphological and biochemical changes
detected in apoptotic cells. Different bacterial and virus pathogens
have developed different strategies to survive inside the host and
overcome natural protections, one of them is inducing apoptotic death
in infected cells. We have demonstrated previously that Piscirickettsia
salmonis activates this process in monocytes/macrophages from
salmonid RTS11 cell line both by morphological and caspase detection
assays; nevertheless, recognition of caspase activation by western blot
was impossible since most of the commercially available antibodies for
mammalian caspases are not cross-reacting. Results: We have generated a
monospecific polyclonal antibody directed to an epitope region of
salmonid caspase-3; the selected epitope present high homology with
caspase-3 from others teleost species and includes the active site of
the enzyme. The peptide was designed using bioinformatics tools and was
chemically synthesized using the Fmoc strategy, analysed by RP-HPLC,
its molecular weight confirmed by mass spectrometry and its structure
analyzed by circular dichroism. The synthetic peptide was immunized and
antibodies from ascitic fluid were enriched for immunoglobulins using
caprylic acid and then purified by activated affinity columns. The
anti-peptide activity of purified antibodies was verified by ELISA, and
the ability of the anti-peptide to recognize salmonid caspase-3
activation was demonstrated with the molecule in P. salmonis RTS11
infected cells by western blotting, ELISA and immunocytochemistry.
Conclusions: This is the first antibody available for a fish caspase,
specifically for trout caspase-3, whose applications were validated by
different immunological assays