Furthermore, the BAX system failed to detect one sample inoculated with 5 CFU/25 g of S. Agona. The same sample was detected using the real-time PCR method although the Ct value was rather high (Ct value of 33). Finally, two samples (5 CFU/25 g of S. Infantis and 2 CFU/25 g of S. Agona) were not detected by the real-time PCR method although being positive with the BAX system. For one of these samples, however, the IAC was negative as well, prompting a re-examination of the sample. However, at low inoculation levels the cell number added can vary due of statistical reasons thereby affecting the probability

of detection [23]. From these data, it can be concluded that the real-time PCR is equivalent to the BAX system in detecting Salmonella AZD4547 in learn more artificially contaminated meat samples Conclusion In conclusion, the real-time

PCR method was validated in comparative and collaborative trials according to guidelines given by NordVal. The PCR method was found to perform well. Results from this study together with published data on selectivity of the real-time PCR assay [6] formed the basis for obtaining NordVal approval as an alternative method for detection of Salmonella in meat and environmental (carcass swabs) samples [24]. After a successful comparison with a commercially available SYBR-Green PCR-based method currently used by a number of meat producers, the real-time PCR method is now being implemented as a routine analysis method by leading poultry and pork producers in Denmark for qualitative detection of Salmonella in raw meat and carcass swabs. Methods DNA extraction Five-ml aliquots from the pre-enrichments were drawn for DNA-extraction. For the automated DNA extraction method, the aliquots were centrifuged at 3000 × g for 5 min, and DNA-extraction performed on a KingFisher (Thermo Labsystems, Helsinki, Finland), as previously described [13], using a DNA isolation kit for blood, stool, cells and tissue (Magnesil KF, Genomic system, Promega, Madison, WI) as specified by the

manufacturer with a total of 75 μl of magnetic particles. Real-time PCR A TaqMan real-time PCR method [6], targeting a region within the ttrRSBCA locus, for the specific detection Galeterone of Salmonella, was employed as previously described [13] using 9 μl of the purified DNA as template in a total reaction volume of 25 μl. Reference culture based method The detection of Salmonella spp. was conducted in accordance with the recommendations from the Nordic Committee on Food Analyses (NMKL) [3] as previously described [13]. However, 25 g of sample (meat) or one swab was transferred to pre-heated buffered peptone water (1:10, BPW; Oxoid, Basingstoke, United Kingdom) and incubated at 37°C for 18 ± 2 h.