Search

The Canadian Food Inspection Agency is developing an Establishment-based Risk Assessment (ERA) model for commercial and on-farm mills involved in the manufacture, storage, packaging, labeling, or distribution of livestock feed (ERA-Feed Mill model). This model will help inform the allocation of inspection resources on the basis of feed safety risk, including animal health and food safety risk. In a previous study, 34 risk factors, grouped into inherent, mitigation, and compliance clusters, along with assessment criteria were selected. The objective of this current study was to estimate the relative risk (RR) of the 203 assessment criteria on the basis of the impact on feed safety to design an ERA-Feed Mill model algorithm. Furthermore, the intent of this study was to assess the maximum increase or decrease of risk obtained when multiple criteria belonging to a same cluster were identified in a specific feed mill. To do so, a two-round face-to-face expert elicitation was conducted with 28 Canadian feed experts. Results showed no significant association between respondent profiles (years of experience and work sector) and estimated RR. Uniformity of answers between experts improved between rounds. Criteria having the highest increase in risk (median RR ≥ 4) included the presence of materials prohibited to be fed to ruminants in a facility that produces ruminant feed, the presence of multiple livestock species on-site, and historical noncompliances related to the inspection of the feed mill's process control and end-product control programs. Risk mitigation criteria having the highest impact on decreasing the risk were the implementation of feed safety certifications, the use of dedicated manufacturing lines (prohibited materials or medications), and having a hazard sampling plan in place for finished feed. The median RR assigned to each criterion and cluster will be used to build an algorithm of the Canadian Food Inspection Agency's ERA-Feed Mill model. HIGHLIGHTS

The Canadian Food Inspection Agency (CFIA) is developing a risk assessment model aimed at quantifying the food safety risk associated with food establishments under its jurisdiction. To support the development of this model, the current study was undertaken to quantify the relative importance of selected criteria considered for inclusion in the model. This process also aimed at estimating the risk associated with specific clusters of criteria. Overall, 173 criteria were presented to experts during a two-round face-to-face expert elicitation to estimate their relative risk to human health. Twenty-nine Canadian experts participated in the expert elicitation including members from academia (31%), industry (31%), and government (38%). A good consensus on the relative risks given to most criteria and clusters of criteria was achieved, and experts assessed them as significantly affecting the risk related to a food establishment. None of the experts expressed opposition to the inclusion of any criterion or to the way they were clustered. Experts assigned a relative risk of ≤4, of 4–8, and of ≥8–67% (116), 29.5% (51), and 3.5% (6) of the 173 criteria identified, respectively. Those having the highest impact on establishment food safety risk were: historical food safety recalls and lack of compliance for the sanitation program, the control of critical control points, followed by the equipment maintenance and calibration program, and the general food hygiene program. Having a sampling plan with trend analysis and follow-up actions was considered as an important mitigation factor. As a result, the median values calculated for each criterion and cluster will be used in the new Canadian Food Inspection Agency Establishment-based risk assessment model to support the allocation of inspection resources based on risk.

Biofilms are known to play important roles in bacterial survival and persistence in food-processing environments. This study aimed to determine the ability of the top 7 STEC serotypes to form biofilms on polystyrene (POL) and stainless steel (SS) plates and to quantify their survival and transfer from dry-surface biofilms to lettuce pieces. The ability of 14 STEC strains to form biofilms on these two materials at different exposure times and temperatures was assessed using crystal violet, Congo red and SEM. At 10 °C all serotypes were weak biofilm producers on both surfaces. In contrast, serotypes O45-040, O45-445, O103-102, O103-670 and O157-R508 were strong biofilm producers at 25 °C. Strains O103-102, O103-670, O111-CFS, O111–053 and O157:H7-R508 were expressers of curli. Under scanning electron microscopy, strains O103-670, O111-CFS, O157-R508, and O121-083 formed more discernible multilayer, mature biofilms on SS coupons. Regardless of the surface (POL/SS), all STEC strains were able to transfer viable cells onto fresh lettuce within a short contact time (2 min) to varying degrees (up to 6.35 log cfu/g). On POL, viable cell of almost all serotypes exhibited decreased detachment (p = 0.001) over 6 days; while after 30 days on SS, serotypes O45-040, O103-102, O103-670, O111-053, O111-CFS, O121-083, O145-231 O157:H7-R508 and O157:H7-122 were transferred to lettuce. After enrichment, all 14 STEC strains were recovered from dry-surface biofilms on POL and SS plates after 30 days. Results demonstrated that the top 7 STEC remained viable within dry-surface biofilms for at least 30 days, transferring to lettuce within 2 min of exposure and acting as a source of adulteration.

The safety of livestock feed is recognized worldwide as a prerequisite for the protection of animal and human health. In this context, the Canadian Food Inspection Agency is developing an Establishment-based Risk Assessment model for livestock feed mills (ERA-Feed Mill) to assist in the allocation of inspection resources based on feed safety risk. The objectives of the present study were to identify and select animal health and food safety-related risk factors along with their assessment criteria, pertaining to Canadian feed mill practices, to be included in the ERA-Feed Mill model. To do so, a review of the scientific literature and consultations with feed experts were conducted. A final list of 34 risk factors was generated, 21 identified from the scientific literature and 13 from feed expert advice. Risk factors were grouped into three clusters: inherent risk factors, mitigation factors and compliance factors for which 4, 10 and 20 factors were identified, respectively. Criteria for quantitatively assessing each risk factor were defined based on common practices found in the Canadian feed industry. These findings contributed to the initial steps of the CFIA's ERA-Feed Mill model development. By assessing the feed safety risk factors related to feed mills in Canada, this tool will help inform the CFIA on the level of oversight required to manage these risks, and will contribute to the production and maintenance of healthy livestock and the production of safe food.

Decreasing the health burden caused by foodborne pathogens is challenging and it depends on the identification of the most significant hazards and food sources causing illnesses, so adequate mitigation strategies can be implemented. In this regard, the Canadian Food Inspection Agency (CFIA) has developed the Establishment-based Risk Assessment (ERA) model, so that a more effective and efficient allocation of resources can be assigned to the highest food safety risk areas. To assess risk, the model considers the type of food sub-products being manufactured by establishments and its scope is limited to the 17 most important foodborne pathogens representing the highest level of food safety risk. However, the information on source attribution at the sub-product level based on a structured approach is limited. To overcome this challenge, an expert elicitation was conducted in 2016 to estimate the relative contribution and associated certainty of each sub-product for 31 pathogen-commodity combinations to the total Canadian health burden associated with foodborne illnesses (expressed in DALYs). These DALYs represent 78% of the total Canadian health burden associated with federally-regulated food commodities considered within the model. A total of 49 Canadian experts recruited using a “snow ball” sampling strategy participated in the study by completing an electronic survey. Results of the elicitation displayed variable levels of health burden allocation between the pathogens and the different commodity sub-products. Assessment of the certainty levels showed some combinations being evaluated with more confidence (e.g., Campylobacter and eggs/poultry sub-products) than others, where a bimodal distribution of certainty was observed (e.g., Toxoplasma in pork sub-products). Furthermore, no participant raised concerns on the food classification scheme, suggesting their agreement with the proposed sub-products categorization of the elicitation. Relative contribution estimates will be included in the CFIA ERA model and used to enhance its applicability for risk prioritization and effective resource allocation during food establishment inspections. While substantial uncertainty around the central tendency estimates was found, these estimates provide a good basis for regulatory oversight and public health policy.

The glucosinolate sinigrin (SNG) is converted by endogenous plant myrosinase or by bacterial myrosinase-like activity to form the potent antimicrobial allyl isothiocyanate. In order to use SNG as a natural antimicrobial precursor in food, it became important to better understand the ability of bacteria to synthesize the enzyme(s) and understand factors influencing this synthesis at a constant SNG concentration. Eight spoilage, pathogenic, or starter culture bacteria were grown separately in medium containing individual or combined salts with SNG. SNG degradation by the bacteria and the formation of its major degradation product, allyl isothiocyanate, were followed for 12 days at 30 or 35°C. The bacterial strains varied in their ability to metabolize SNG, and this was enhanced by NaCl and/or NaNO(3). SNG hydrolysis took place after 4 days, and the greatest amount occurred by day 12. At 12 days, Escherichia coli O157:H7 showed the greatest capacity to hydrolyze SNG (45.3% degradation), followed by Staphylococcus carnosus (44.57%), while Pseudomonas fluorescens was not active against SNG. The ability of tested strains to metabolize SNG, in decreasing order, was as follows: Escherichia coli O157:H7Staphylococcus carnosusStaphylococcus aureusPediococcus pentosaceusSalmonella TyphimuriumListeria monocytogenesEnterococcus faecalisPseudomonas fluorescens.

Previous studies have reported that the mechanism of bactericidal action of the plant oil aromatics, eugenol, carvacrol and cinnamaldehyde involves inhibition of adenosine triphosphate generation and membrane disruption. In this study the capacity of the aromatics to inhibit the membrane bound ATPase activity of Escherichia coli and Listeria monocytogenes was investigated by experiments on isolated membranes. Inhibition of the ATPase activity of E. coli membranes was observed with 5 mM or 10 mM eugenol or carvacrol. Progressively greater inhibition by cinnamaldehyde was observed as concentration increased from 0.1 to 10 mM. L. monocytogenes ATPase activity was significantly inhibited by eugenol (5 or 10 mM), carvacrol (10 mM) and cinnamaldehyde (10 mM). Lactobacillus sakei is highly resistant to cinnamaldehyde compared to E. coli and L. monocytogenes. To determine whether this resistance was related to the relative hydrophobicity of the cell surface and hence the ability of the cell to take up the aromatics, the percentage of the three organisms partitioning in dodecane was compared. No significant difference was found between the partitioning percentage of L. monocytogenes (17.2%) and L. sakei (13.8%), indicating that surface hydrophobicity does not explain the differing sensitivity to cinnamaldehyde of these two organism. The percent partitioning of E. coli was significantly greater than both other organisms (23.3%) and may explain the greater sensitivity of E. coli to all three aromatics.

The role of membrane disruption in the bactericidal activity of the plant oil aromatic compounds eugenol, carvacrol and cinnamaldehyde was investigated using confocal laser scanning microscopy, changes in ATP levels and cell viability. In 25 mM HEPES buffer pH 7 at 20 degrees C, 10 mM eugenol or carvacrol increased uptake of propidium iodide by Escherichia coli, Listeria monocytogenes and Lactobacillus sakei over a 10-min period. The same treatments resulted in lowered viability, rapid depletion of cellular ATP and release of ATP, with the exception of Lb. sakei treated with carvacrol. Eugenol or carvacrol at 5 mM to 10 mM inhibited E. coli and L. monocytogenes motility. Lb. sakei was resistant to cinnamaldehyde. Thus, its effects were only studied on E. coli and L. monocytogenes. At 10 mM, cinnamaldehyde caused a slight but statistically significant increase in propidium iodide staining of E. coli, but had no effect on L. monocytogenes. Cinnamaldehyde treatment of E. coli at 10 mM and L. monocytogenes at 40 mM resulted in decreased cellular ATP, but there was no concomitant release of ATP. Cinnamaldehyde at 5 and 10 mM inhibited E. coli and L. monocytogenes motility. Results for eugenol and carvacrol are consistent with non-specific permeabilization of the cytoplasmic membrane. Evidence for increased membrane permeability by cinnamaldehyde is less conclusive. The release of ATP from eugenol and carvacrol-treated cells and absence of release from cinnamaldehyde-treated cells could indicate that eugenol and carvacrol possess ATPase inhibiting activity. Secondary effects would also be consistent with membrane disruption.

Commercial allyl isothiocyanate (AIT) was examined for its ability to reduce numbers of Escherichia coli O157:H7 inoculated in fresh ground beef packaged under nitrogen and stored refrigerated or frozen. A five-strain cocktail of E. coli O157:H7 containing 3 or 6 log10 cfu/g was inoculated into 100 g ground beef and formed into 10x1-cm patties. A 10-cm diameter filter paper disk treated with AIT suspended in sterile corn oil was placed on top of a single patty. One patty and paper disk were placed in a bag of Nylon/EVOH/PE with O2 permeability of 2.3 cm3 m(-2) 24 h atm at 23 degrees C. The bags were back-flushed with 100% nitrogen, heat-sealed and stored at 10, 4 and -18 degrees C for 8, 21 or 35 days, respectively. During storage, the AIT levels in the package headspaces were determined by gas liquid chromatography, and mesophilic bacteria and E. coli O157:H7 were counted. The mesophilic aerobic bacteria in ground beef patties were largely unaffected by the addition of AIT. At an initial population of 3 log10 cfu/g, E. coli O157:H7 was reduced by AIT to undetectable levels after 18 days at 4 degrees C or 10 days at -18 degrees C. In samples inoculated with 6 log10 cfu/g, a3 log10 reduction of E. coli O157:H7 was observed after 21 days at 4 degrees C, while a 1 log10 reduction was observed after 8 and 35 days at 10 and -18 degrees C, respectively. The final AIT concentrations in the headspaces after storage at 10, 4, and -18 degrees C were 444, 456, and 112 microg/ml at 8, 21, and 35 days, respectively. Results showed that AIT can substantially reduce numbers of E. coli O157:H7 in fresh ground beef during refrigerated or frozen storage.

This study was undertaken to determine whether the glucosinolates naturally present in non-deheated mustard flour could serve as a source of allyl and other isothiocyanates in sufficient quantity to kill Escherichia coli O157:H7 inoculated in ground beef at three different levels, during refrigerated storage of the meat under nitrogen. Mustard flour was mixed at 5%, 10% or 20% (w/w) with freshly ground beef, then the beef was inoculated with a cocktail of five strains of E. coli O157:H7 at either 3, 6 oror =1.6 log10 cfu/g. The ground beef was formed into 100 g patties and each was placed in a bag of Nylon/EVOH/PE, which was back-flushed with 100% N2, heat-sealed and stored at 4 degrees C foror =21 days. During storage, the allyl isothiocyanate (AIT) levels in package headspaces were determined by gas liquid chromatography. By 21 days, the levels present in treatments were not significantly different. After 21 days storage, there were 0.5, 3 and 5.4 log10 decreases in numbers of E. coli O157:H7 from the initial levels of 6 log10 cfu/g in meat containing 5%, 10% and 20% mustard flour, respectively. When inoculated at 3 log10 cfu/g, E. coli O157:H7 was reduced to undetectable levels after 18, 12 and 3 days with 5%, 10% and 20% mustard flour, respectively. When immunomagnetic separation (IMS) was used for E. coli recovery following its inoculation ator =1.6 log10 cfu/g, 5% mustard did not completely eliminate the pathogen from ground beef stored for 6 days. The natural microflora of the ground beef which developed in vacuum packages was unaffected by the addition of 5% mustard flour but some inhibition was found at higher concentrations. Sensory evaluation of the cooked ground beef showed that there were no significant differences in the acceptability of meat treated with 5 or 10% mustard flour. However, panelists could distinguish untreated controls from mustard treatments, but considered the mustard-treated meat to be acceptable. These results showed that it is possible to use mustard flour at levels of5-10% to eliminate E. coli O157:H7 from fresh ground beef.

The temperatures and ages of 5389 packs of beef in 10 multiple shelf display cabinets were determined. The median temperature of the packs in each cabinet was 7 °C. All packs in three cabinets were ⩽2 days old. The percentages of packs older than 2 days were

A feed supplement, SCB, containing Saccharomyces cerevisiae subsp. boulardii, produced substances which were successful in inhibiting strains of E. coli O157:H7 in a spot agar assay. Growth and/or survival of E. coli O157:H7 in ruminal fluid in the presence of SCB was investigated in a batch culture incubation and in continuous culture using a Rumen Simulation Technique (Rusitec). In the batch culture incubation, E. coli O157:H7 (EC) was inoculated (104 CFU/ml final concentration) into 100 ml of clarified ruminal fluid amended with SCB at 0 (control), 5 (SCB5), 10 (SCB10), 15 (SCB15) or 20 (SCB20) mg/ml (n=3). Treatments were incubated at 39 °C, and EC was enumerated after 0, 12, 24 and 48 h by plating onto selective medium. Treatments SCB15 and SCB20 completely eradicated 104 CFU EC/ml within 48 h (P 0.05). In the Rusitec incubation, fermentations were established in 12 Rusitec vessels using ruminal inoculum confirmed negative for E. coli O157. Each vessel was inoculated with EC (104 CFU/ml), then 8 h later, with stock solutions of SCB yielding initial concentrations of 0 (control), 5 (SCB5) or 20 (SCB20) mg/ml (n=4). Enumerations of EC were conducted 0, 4, 8, 12 and 24 h after EC inoculation, and daily thereafter for 6 days. Counts of EC did not differ (P>0.05) from the control with either level of SCB, at any of the time points assessed. The inhibitory effect of SCB on E. coli O157:H7 observed in batch culture at 48 h was not observed in continuous culture (Rusitec). Lack of an effect of SCB on E. coli O157:H7 in the Rusitec suggests that the production of inhibitory substances by S. cerevisiae may not occur in the mixed microflora of the rumen. Also, diffusion of inhibitory substances in the rumen or degradation of inhibitory substance by rumen microorganisms may have reduced their effectiveness against E. coli O157:H7.

Cilantro oil is an essential oil preparation extracted from the plant Coriandrum sativium. A series of experiments were conducted to evaluate the ability of cilantro oil to control the growth of Listeria monocytogenes on vacuum-packed ham. The in vitro minimal inhibitory concentration for five strains of L. monocytogenes was found to vary from 0.074% to 0.018% depending on strain. Cilantro oil treatments were then tested on ham disks inoculated with a cocktail of the five L. monocytogenes strains. The treatments studied were 0.1%, 0.5%, and 6% cilantro oil diluted in sterile canola oil or incorporated into a gelatin gel in which lecithin was used to enhance incorporation of the cilantro oil. Gelatin gel treatments were also conducted with 1.4% monolaurin with or without 6% cilantro oil to determine if an interaction between the antimicrobials could increase inhibition of L. monocytogenes. Treated ham was then vacuum-packed and stored at 10 °C for up to 4 weeks. The only cilantro oil treatment which inhibited growth of L. monocytogenes on the ham samples was 6% cilantro oil gel. Samples receiving this treatment had populations of L. monocytogenes 1.3 log CFU/ml lower than controls at week 1 of storage, though there was no difference between treatments from week 2 onward. It appears that immobilization of the antimicrobial in a gel enhanced the effect of treatments. Cilantro oil does not appear to be a suitable agent for the control of L. monocytogenes on ham. The possible reasons for reduced effectiveness of cilantro oil against L. monocytogenes on ham are discussed.

There is a growing interest in modelling microbial growth as an alternative to time-consuming, traditional, microbiological enumeration techniques. Several statistical models have been reported to describe the growth of different microorganisms, but there are accuracy problems. An alternate technique 'artificial neural networks' (ANN) for modelling microbial growth is explained and evaluated. Published data were used to build separate general regression neural network (GRNN) structures for modelling growth of Aeromonas hydrophila, Shigella flexneri, and Brochothrix thermosphacta. Both GRNN and published statistical model predictions were compared against the experimental data using six statistical indices. For training data sets, the GRNN predictions were far superior than the statistical model predictions, whereas the GRNN predictions were similar or slightly worse than statistical model predictions for test data sets for all the three data sets. GRNN predictions can be considered good, considering its performance for unseen data. Graphical plots, mean relative percentage residual, mean absolute relative residual, and root mean squared residual were identified as suitable indices for comparing competing models. ANN can now become a vehicle whereby predictive microbiology can be applied in food product development and food safety risk assessment.

Biogenic amines are formed in foods as a result of amino acid decarboxylation catalyzed by bacterial enzymes. When consumed in sufficient quantities, these compounds will cause headache, hypertension, fever, and heart failure. Technologies such as vacuum packaging and carbon dioxide-modified atmosphere packaging (CO2-MAP), when combined with low-temperature storage (-1.5 degrees C), allow fresh pork to have a storage life long enough for export to overseas markets. During low-temperature storage of pork in these packaging systems, the lactic acid bacteria (LAB), which possess the enzymes for biogenic amine formation, dominate the microflora. The objectives of this study were to determine the quantities of biogenic amines in packaged fresh pork, to monitor LAB growth, and to determine the storage life by sensory evaluation. Vacuum-packaged and CO2-MAP pork were stored at -1.5+/-0.5 degrees C for 9 and 13 weeks, respectively. Phenylethylamine, putrescine, cadaverine, histamine, tyramine, spermidine, and spermine concentrations were determined weekly by high-performance liquid chromatography and capillary gel electrophoresis. LAB and carnobacteria were enumerated weekly. Samples were evaluated for odor and appearance. The CO2-MAP was successful in delaying bacterial growth and the development of unacceptable off-odors compared with the vacuum packaging. The storage lives of the vacuum-packaged and CO2-MAP pork were 5 and 13 weeks, respectively. High-performance liquid chromatography was the superior method for biogenic amine quantification. Tyramine and phenylethylamine in pork of both packaging treatments approached levels considered to be potentially toxic. Given Canada's increasing role in the export of fresh meat to foreign markets, it is recommended that the formation of biogenic amines in vacuum-packaged and CO2-MAP pork be further investigated.

A previously-designed insulated container was modified to improve the hold period (variable) nitrogen (N 2 ) use of the cryogenic system used to cool the container. Although fresh meat storage life is longest at −1.5±0.5°C, the target temperature range for the system was changed to −1.0±0.5°C to eliminate any economic loss caused by the freezing of meat. A centrifugal fan, with its motor mounted outside the container, provided a uniform temperature within the container and lowered the hold period N 2 use of the system. Chilling of the product from an initial temperature of 7.0°C to −1.0°C required on average 33.7, 31.7, 34.7, and 30.6 kg of N 2 at outside temperatures of 30, 15, 0, and −15°C, respectively. Average hold period N 2 use for maintaining the required temperature was 4.8, 2.8, 1.2, and 0.1 kg/h at outside temperatures of 30, 15, 0, and −15°C, respectively, and these were an improvement over the previous design. The overall maximum temperature of the container during the trials was −0.3°C, while the overall minimum was −1.4°C. A vacuum insulated transfer line decreased hold period N 2 use by 51% in comparison with a steel braided transfer line. A simulated N 2 failure of the system resulted in an average temperature increase of 0.5 o C/h within the container.

Centralized packaging of retail meat cuts is growing more popular because of its economies and potential to maintain quality, enhance safety, and extend the shelf life of fresh meat. Requirements for optimizing shelf life of centrally prepared retail cuts for periods up to 15 weeks are slightly different from those needed to extend the shelf life of fresh, chilled meat. Chilled meat primarily deteriorate at the cut or uncut muscle surface. In long-term storage, primal cuts are placed in an atmosphere saturated with carbon dioxide and containing very low residual oxygen. These cuts are held at -1.5+/-0.5 degrees C. When the meat is removed, it is fabricated into retail or food service cuts. New fresh surfaces are created in the process, revitalizing the meat's appearance. After being prepared for retail display, the meat normally has four more days of shelf life. Depending on the meat species, shelf life is usually limited by development of undesirable organoleptic changes, usually defects in color, which are independent of microbial presence. The microbes consist of a lactic acid bacterial population that maximizes under storage conditions at about 10(8) CFU/cm2 well before shelf life ends. Circumstances are different with centralized distribution of retail-ready fresh meat. The wholesale storage period following initial packaging of the retail cuts is about 20 to 30 days. Prepared products must withstand retail display for up to 2 days without further manipulation of package contents. Retail packages are simply moved from their storage container (usually a unit or overwrap containing a modified atmosphere) to retail display, where desirable meat color develops upon exposure to air. Three gas atmospheres have some potential to satisfy storage needs for centralized distribution of retail-ready packages: 100% CO2, 100% N2, or 70% N2 + 30% CO2. Shelf life is limited by undesirable changes in surfaces exposed at initial packaging, caused by growth of psychrotrophic bacteria. If 100% CO2 is used, these are all lactic acid bacteria (LAB). Therefore, initial bacterial numbers on the meat and storage temperature become critical to success. The most attractive storage option is 100% CO2 used at - 1.5 +/-0.5 degrees C. This review presents the reason for that recommendation, along with basic concepts of meat chemistry, a discussion of modified atmosphere packaging, meat microbiology, and current results with simulated centralized packaging of retail-ready meats.

Heat resistance, germination and sensitivity to selected antimicrobials was investigated using Penicillium roqueforti , Penicillium aurantiogriseum and Penicillium viridicatum spores, produced on potato dextrose agar (PDA) adjusted to 0.88 a W using either glycerol or NaCl. Results indicated that spores produced on media without a W adjustment (0.99 a W ; control) appeared more heat resistant (55°C, 10 min) compared to those produced at 0.88 a W (treatment). For treatment spores only, heat resistance was observed to decrease further when initially incubated (25°C, 48 h) in sterile, distilled water. All treatment spores were more sensitive to benzoate and sorbate but more resistant to cycloheximide. The time taken for germination, especially for P. roqueforti spores appeared to vary depending on the a W and solute used during spore production. ©

A model for studying spoilage in sliced cooked delicatessen meats using conventional plating procedures was characterized by following the transfer of adventitious lactic acid bacteria (LAB), thermotolerant LAB and pediococci from a dry fermented sausage to cooked ham and bologna during a simultaneous slicing procedure. The major group of organisms present in these products was LAB. Each of the three groups of organisms was transferred to the cooked meats, but during storage under vacuum at 7°C, only the adventitious lactobacilli from the sausage appeared to contribute to cooked meat spoilage. Pediococci declined within 28 days of co-slicing, thermotolerant LAB grew slowly and never reached levels of >5 log 10 cfu cm −2 , but transferred adventitious LAB from the sausage grew and reached peak populations 4 weeks earlier in the co-sliced cooked meats than in controls. During storage at 7°C co-sliced cooked meats spoiled, as assessed by purge (liquid) and ropy slime formation, 2–4 weeks faster than the separately-sliced and vacuum-packaged products. The distribution of organisms on package slices differed. In control cooked products numbers of bacteria present on center package slices were lower than on outside slices. Bacterial numbers were greatest at the meat surface–packaging film interface. In co-sliced cooked products organisms were evenly distributed throughout slices in the packages. Based on findings from use of the co-slice model, in vacuum packages of sliced cured meats where >10 5 cfu bacteria cm −2 are equally distributed throughout package slices, poor slicing hygiene is the cause. Commercially-sliced bologna was repackaged with allyl isothiocyanate (AIT) to test its ability to delay bacterial growth at the meat surface. The preservative effects of AIT were tested under vacuum or when backflushed with CO 2 . CO 2 alone was more effective than AIT in delaying LAB growth but neither treatment was particularly effective.