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Appl. Environ. Microbiol., 04 1995, 1341-1347, Vol 61, No. 4
M Uyttendaele, R Schukkink, B van Gemen and J Debevere
An assay to detect Campylobacter jejuni in foods that uses a short
selective enrichment culture, a simple and rapid isolation procedure, NASBA
amplification of RNA, and a nonradioactive in solution hybridization was
studied. The presence of high numbers of indigenous flora affected the
sensitivity of the assay. However, detection of C. jejuni was possible up
to a ratio of indigenous flora to C. jejuni of 10,000:1. Interference by
food components was eliminated by centrifugation following the enrichment
step. Fourteen food samples artificially inoculated with C. jejuni (1 to
1,000 CFU/10 g) were analyzed with the NASBA assay and the conventional
culture method with Campylobacter charcoal differential agar (CCDA). A few
false-negative results were obtained by both NASBA (1.42%) and CCDA (2.86%)
isolation. Yet the use of enrichment culture and NASBA shortened the
analysis time from 6 days to 26 h. The relative simplicity and rapidity of
the NASBA assay make it an attractive alternative for detection of C.
jejuni in food samples.
Copyright © 1995, American Society for Microbiology
Detection of Campylobacter jejuni added to foods by using a combined selective enrichment and nucleic acid sequence-based amplification (NASBA)
Department of Food Technology and Nutrition, Faculty of Agricultural and Applied Biological Sciences, University of Ghent, Belgium.
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