Jm. Murtiningsih,"cox, EVALUATION OF THE SEROBACT(TM) AND MICROBACT(TM) SYSTEMS FOR THE DETECTION AND IDENTIFICATION OF LISTERIA SPP, Food control, 8(4), 1997, pp. 205-210
The Serobact(TM) Listeria latex agglutination reagent and Microbact(TM
) 12L system were evaluated, respectively, for the detection and ident
ification of Listeria in foods. The Serobact(TM) reagent proved effect
ive, compared with conventional cultural methods, in the detection of
low levels (1-10 cells/25 g) of both L. monocytogenes and L. innocua a
rtificially inoculated into a range of foods, following enrichment. Ex
tended incubation of either the primary or secondary enrichment increa
sed the number of samples positive for Listeria by both Serobact(TM) a
nd conventional culture, but also increased the number of false positi
ve reactions. The Serobact(TM) reagent also proved effective in screen
ing enrichment cultures of potentially contaminated retail food sample
s. Using the USDA enrichment procedure, the Serobact(TM) reagent yield
ed 100% sensitivity and 93.9% specificity, when compared to convention
al culture. Identification of 81 Listeria isolates using the Microbact
(TM) 12L System was compared with conventional biochemical and physiol
ogical tests. While identification after 4 h was poor; due to negative
or incomplete fermentation of carbohydrates and lack of haemolysis, i
dentification of all but two of 81 isolates was achieved after 24h. (C
) 1997 Elsevier Science Ltd.