Abstract:Aims: To determine the prevalence and number of Salmonella and Campylobacter in sausages and to evaluate their destruction during cooking. Methods and Results: One hundred and sixty-two packs of uncooked economy or catering sausages, comprising 53 packs of frozen and 109 of chilled sausages, were purchased in Devon between March and July 2000. All were tested for the presence of Salmonella and 51 packs of chilled sausages were also examined for the presence of Campylobacter spp. To investigate the heat toleran… Show more
“…According to Mattick et al (2002), one of the main problems in the isolation of Salmonella in foods is the small number of these bacteria considering the rate of bacterial contamination. According to Bennett et al (1998), the BAX® system always produced a positive result when the cell count of Salmonella spp.…”
“…According to Mattick et al (2002), one of the main problems in the isolation of Salmonella in foods is the small number of these bacteria considering the rate of bacterial contamination. According to Bennett et al (1998), the BAX® system always produced a positive result when the cell count of Salmonella spp.…”
“…Our results were similar to those obtained by Seydi and Sylla (1996) in Dakar, but were clearly inferior to those of Elhag et al (2014) in Khartoum who revealed that 97.5% of the studied sausage samples were contaminated by these bacteria. Many studies showed than the Salmonella can be isolated from various types of sausages (Abrahim et al, 1998;Mattick et al, 2002;Özbey et al, 2007). The high incidence of these bacteria could be due to the faeces contamination of the chopped meat used for the production of pork-butchery, contaminated water, the environment and bad hygiene of workers (Reid et al, 2002).…”
In order to assess the microbiological quality of Merguez and influence of temperature on the rate of contamination, from April 2 to May 12, 2016, a study was undertaken in two types of meat retailing in the region of M'Sila, Algeria. A total of 60 samples of Merguez were collected in ten sites from five markets and five independent butcher's shops, for purposes of microbiological analysis. The majority of the samples were contaminated by coagulase positive staphylococci and thermotolerant coliforms. The average counting in both types combined trade were 2.0±0.2 log 10 cfu/g for thermotolerant coliforms and 2.2±0.2 log 10 cfu/g for coagulase positive staphylococci. However, all samples were free of Salmonella spp. and sulphite-reducing Clostridium. Compared to the days of sampling, both bacterial indicators counted in covered markets were significantly different from one day to another (p<0.05). However, no significant difference (p>0.05) were reported between daily concentration for these two groups of bacteria counted in samples from independent butchers. These results show disrespect the rules of good hygienic practices during preparation, storage and sale of Merguez. The potential consequences of the consumption of these foods on the health of consumers should motivate disease control measures.
“…The four-strain composite culture was used to inoculate various substrates in order to prepare the inocula under representative environmental conditions (inoculum origin). The control inoculum (TSB) was obtained by inoculating (5 log CFU/ml) TSB-G with the composite E. coli O157:H7 culture (1 ml), and, after overnight incubation at 35°C, the resulting cell suspension was diluted (1,000-fold) in sterilized maximum-recovery diluent (MRD; 1.0 g peptone [Difco] and 8.5 g sodium chloride [Fisher Scientific, Fair Lawn, NJ] in 1 liter distilled water) (18).…”
This study evaluated the impact of inoculum preparation and storage conditions on the response of Escherichia coli O157:H7 exposed to consumer-induced stresses simulating undercooking and digestion. Lean beef tissue samples were inoculated with E. coli O157:H7 cultures prepared in tryptic soy broth or meat decontamination runoff fluids (WASH) or detached from moist biofilms or dried biofilms formed on stainless steel coupons immersed in inoculated WASH. After inoculation, the samples were left untreated or dipped for 30 s each in hot (75°C) water followed by lactic acid (2%, 55°C), vacuum packaged, stored at 4 (28 days) or 12°C (16 days), and periodically transferred to aerobic storage (7°C for 5 days). During storage, samples were exposed to sequential heat (55°C; 20 min) and simulated gastric fluid (adjusted to pH 1.0 with HCl; 90 min) stresses simulating consumption of undercooked beef. Under the conditions of this study, cells originating from inocula of planktonic cells were, in general, more resistant to heat and acid than cells from cultures grown as biofilms and detached prior to meat inoculation. Heat and acid tolerance of cells on meat stored at 4°C was lower than that of cells on nondecontaminated meat stored at 12°C, where growth occurred during storage. Decontamination of fresh beef resulted in injury that inhibited subsequent growth of surviving cells at 12°C, as well as in decreases in resistance to subsequent heat and acid stresses. The shift of pathogen cells on beef stored under vacuum at 4°C to aerobic storage did not affect cell populations or subsequent survival after sequential exposure to heat and simulated gastric fluid. However, the transfer of meat stored under vacuum at 12°C to aerobic storage resulted in reduction in pathogen counts during aerobic storage and sensitization of survivors to the effects of sequential heat and acid exposure.
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