Gm. Wyatt et al., FURTHER-STUDIES ON THE FEASIBILITY OF ONE-DAY SALMONELLA DETECTION BYENZYME-LINKED-IMMUNOSORBENT-ASSAY, Applied and environmental microbiology, 59(5), 1993, pp. 1383-1390
A model system previously developed for the rapid detection of Salmone
lla typhimurium in foods was improved and extended to many other Salmo
nella serotypes. The original protocol, which consisted of an overnigh
t nonselective culture followed by a specific enzyme-linked immunosorb
ent assay (ELISA), was modified and improved. A sandwich ELISA which u
sed polyclonal antibodies for the capture stage and a cocktail of mono
clonal antibodies for the detector stage was developed. The assay reco
gnized a wide range of Salmonella serotypes; S. enteritidis, the most
important serotype in the United Kingdom had a detection limit in the
ELISA of about 4 x 10(2) cells ml-1. The cultural stage prior to the E
LISA was either a single nonselective broth (incubated for 28 h) or a
preenrichment broth (incubated for 7 h) plus a selective broth (incuba
ted for 21 h). Antibodies which bind to cells grown in the unfavorable
conditions of a selective medium were selected. It was concluded that
, in the future, the shortened protocols for the detection of Salmonel
la spp. in foods described here will be of considerable value.