The MOPC 467 Bio-Enzabeadm enzyme immunoassay (EIA) identified 335 (92.8%) of 361 Salmonella strains tested and gave false positive reactions with 5 (6.5%) of 77 strains of nonsalmonellae. Lack of specificity was particularly prominent with 5. fyphi but not mstricted to any one of the 25 somatic groupings represented in this study. Four of the five false-positive reactions were attributed to Citrobucrerfreundii. The EIA assay identified 27 (96%) of 28 naturally contaminated foods and produced 16 (25%) false positive reactions which were mainly associated with Citrobucrer spp. Attempts at method brevity underlined the importance of M broth post-enrichment and centrifugation for maximum method sensitivity and the inadequacy of EIA for detection of Salmonella in preemichment and enrichment cultures.
INTRODUCTIONRECENT ATTEMPTS to develop rapid, cost-efficient methods for the detection of Salmonella in foods have met with limited success. A minimum of 4-5 days are presently required to obtain presumptive evidence of salmonellae in foods by standard methods of analysis (Health Protection Branch, 1978; U.S. Food and Drug Administration, 1978). Such a delay in obtaining results generally precipitates costly storage of finished products. Novel diagnostic approaches involving immunofluorescent (Thomason, 1981), serological (Sperber and Deibel, 1969), DNA-DNA hybridization (Fitts et al., 1983) and ELISA (Minnich et al., 1982) techniques yield presumptive results l-2 days earlier than with standard cultural techniques. Lack of research interest in preenrichment cultures as test material apparently has stemmed from an apprehension that large populations of competing microorganisms in these cultures would present an insurmountable challenge to the specificity and/or sensitivity of new analytical techniques.The present study evaluates the sensitivity and specificity of the Bio-Enzabeada enzyme immunoassay (EIA) technique (Mattingly, 1984). The assay is based on the ability of a murine myeloma protein (MOPC 467) to detect nonserotypic flagellar antigens in heated extracts of cultured material. Specifically, the study investigates the ability of the technique to detect salmonellae in pure cultures and in the preenrichment, selective enrichment and direct enrichment cultures of foods; it also considers the effects of post-enrichment in M broth and the number of salmonellae in test samples as affected by centrifugation on the sensitivity of the EIA method.