A highly sensitive, indirect double sandwich fluorogenic enzyme-linked
immunosorbent assay (FELISA), has been developed for the detection of
staphylococcal enterotoxin B (SEB). The described FELISA allows a SEB
quantification of 0.1 fg/ml for purified toxin and a detection limit
of at least 10 pg/g of contaminated food. Given the sensitivity of FEL
ISA elaborate procedures for the extraction and concentration of enter
otoxin from food samples became unnecessary. The monoclonal anti-SEB a
ntibody (MCA a-SEB) used in the described method reacted with SEB only
. The FELISA is simple to perform and, provided the reaction plates ar
e pre-prepared, the results can be obtained in approximately 3 h.