Inspection of lymph nodes for caseous lymphadenitis and its effect on the density of microbes on sheep carcasses

This study aimed to measure the amount of microbial contamination caused by inspecting the lymph nodes of adult sheep carcasses for caseous lymphadenitis (CLA). Surface swabs from carcasses pre-inspection (N=296) and post-inspection (N=296) were obtained for enumeration of indicator organisms at three commercial abattoirs. At the scapular site, inspection doubled the probability of detecting E. coli (Pr before=0.35, Pr after=0.67) and increased the expected count of E. coli from 2cfu/cm(2) to 13cfu/cm(2). Inspection at the rump site increased the probability of detecting E. coli by 1.1 times (Pr before=0.84, Pr after=0.93) and increased the expected count from 32cfu/cm(2) to 45cfu/cm(2). Effects were also observed for Enterobacteriaceae and total viable count. The findings show that routine inspection of adult sheep carcasses for CLA has a detrimental impact on carcass microbiological traits.     

Recovery of bacteria from poultry carcasses by rinsing,swabbing or excision of skin

Groups of 25 uneviscerated or eviscerated carcasses were obtained at four points in a commercial broiler chicken carcass dressing process. Carcasses from each point in the process were sampled by excision of skin from randomly selected sites, excision of skin from necks, swabbing carcasses with cellulose acetate sponges, or by rinsing whole carcasses. Total aerobic counts, coliforms and Escherichia coli recovered from each sample were enumerated. Values for the log mean number cm⁻² (log A) and the log of the total numbers recovered 25 cm⁻² (N) were calculated for each set of 25 counts. For sets of counts for the same group of bacteria obtained from carcasses at the same stage of processing, the three values for log A or three values for N for sets of counts obtained by excision of skin from randomly selected sites or necks, or by rinsing differed by < 0.5 log unit. However, about half the values for log A or N for sets of counts obtained by swabbing differed by >0.5 log unit from the corresponding values for sets of counts obtained by the other methods. Those data indicate that sampling of poultry carcasses by excision of skin from randomly selected sites or necks, or by rinsing will recover similar numbers of bacteria per unit area of carcass surface.     

Development of an immunosensor based on surface plasmon resonance for enumeration of Escherichia coli in water samples

An immunosensor for the rapid, sensitive and selective detection of generic Escherichia coli in water samples was developed on the basis of surface plasmon resonance (SPR). Antibodies against E. coli were immobilized on a sensor surface and water samples with different concentrations of E. coli were injected to the flow cell. The changes in the response unit (RU) due to the binding of different concentrations of bacteria were computed and a linear correlation (R² = 0.976) was obtained between log E. coli concentration and the change in the RU with a working range of 9 × 10¹ and 1.8 × 10⁵ cfu ml⁻¹. The complete regeneration of the sensor surface was realized by using 1% SDS solution. The selectivity of the developed sensor was examined with Enterobacter aerogenes and Enterobacter dissolvens which did not produce any significant response. The ability of the developed sensor to detect E. coli in real water samples was investigated and the results were closed to that obtained from plate counting method. Based on these results, the developed immunosensor can be employed for rapid, label-free, sensitive and selective detection of E. coli in water samples.     

Polymorphonuclear neutrophils and Escherichia coli proteases involved in proteolysis of casein during experimental E. coli mastitis

An Escherichia coli mastitis model was used to characterize enzymes involved in bovine mammary tissue damage and proteolysis in milk. One-quarter each of four cows were inoculated with a suspension (10⁴ cfu mL⁻¹) of E. coli P4:O32. Blood and milk were collected before inoculation and for 216 h afterwards. Intracellular elastase, collagenase and cathepsin activities were measured by flow cytometry of peripheral blood leukocytes and milk polymorphonuclear neutrophils (PMNs). Leukopenia occurred in peripheral blood 9 h after infection, concomitant with an increase in somatic cell count in milk. Milk PMNs had lower activity of cathepsins and collagenase than peripheral blood PMNs. In parallel, milk samples were studied by zymography, and several proteases were detected in mastitic milk. These activities increased after infection, to reach a peak in 6 h. However, total protease profiles and plasmin activities differed. It was concluded that proteases released by PMNs and E. coli contribute to proteolysis of casein during mastitis, as well as plasmin.     

The growth and survival of Escherichia coli O157:H7 on minced bison and pieces of bison meat stored at 5 and 10 °C

This study investigated the growth and survival of Escherichia coli O157:H7 on minced and whole pieces of bison meat. Growth curves of native microflora, including Pseudomonas spp. and Enterobacteriaceae were also generated. A marked E. coli O157:H7 strain was inoculated onto minced and whole pieces of bison meat at an initial level of 1.5 log₁₀ cfu g⁻¹. The inoculated meat was stored at either 5 °C for 28 days or 10 °C for 21 days. Survival, but no growth, of E. coli O157:H7 was observed on both forms of bison meat stored at 5 °C, while significant growth of the organism was observed at 10 °C. E. coli O157:H7 counts on whole pieces were generally higher than counts observed on minced bison meat, and reached their highest population by 14 days, with a total increase of 3.36 log₁₀ cfu g⁻¹ on whole pieces and 2.12 log₁₀ cfu g⁻¹on minced bison meat stored at 10 °C. Under the same storage temperature, Pseudomonas spp. and total counts displayed similar growth patterns on both pieces and minced bison meat, while the Enterobacteriaceae showed a slower growth rate. This study showed that the growth of E. coli O157:H7 on bison meat is similar to that observed in studies of beef.     

Combinations of nisin with organic acids or salts to control Listeria monocytogenes on sliced pork bologna stored at 4°C in vacuum packages

This study evaluated dipping solutions of nisin with or without organic acids or salts, as inhibitors of Listeria monocytogenes introduced on sliced cooked pork bologna before vacuum packaging and storage at 4°C for 120 days. Inoculated (10²–10³ cfu/cm²) slices were immersed in nisin (5000 IU/ml), or in lactic or acetic acid (1, 3, 5 g/100 ml), sodium acetate or diacetate (3, 5 g/100 ml), and potassium benzoate or sorbate (3 g/100 ml), each combined with nisin. Additional slices were immersed in nisin, inoculated and then immersed in acid or salt solutions without nisin. Nisin reduced L. monocytogenes by 1.0–1.5 log cfu/cm² at treatment (day-0) followed by a listeriostatic effect for 10 days. Thereafter, however, the pathogen multiplied in treatments without acid or salts, with growth being faster on slices immersed in nisin after as compared to before inoculation. Nisin in combination with 3 or 5 g/100 ml acetic acid or sodium diacetate or 3 g/100 ml potassium benzoate, applied individually or as mixtures, did not permit growth before day-90. Other treatments were of variable and lesser effectiveness (20–70 days), whereas in untreated or water-treated (control) bologna L. monocytogenes increased at 6–7 log cfu/cm² at day-20. Based on the antilisterial efficacy and effects of treatments on product pH, nisin with 3 g/100 ml sodium diacetate may be the most promising combination in dipping solutions to control L. monocytogenes on sliced cured pork bologna.     

Microbial safety considerations of flooding in primary production of leafy greens: A case study

This study evaluated the effects of a flood event, floodplain and climatic parameters on microbial contamination of leafy greens grown in the floodplains. Additionally, correlations between pathogenic bacteria and levels of indicator microorganisms have been also determined. To diagnose the microbial contamination after the flood event, sampling was carried out in weeks 1, 3, 5 and 7 after the flooding in four flooded lettuce fields. To assess the impact of flooding on the microbial contamination of leafy greens, indicator microorganisms (coliforms, Escherichia coli and Enterococcus) and pathogenic microorganisms (Salmonella spp., VTEC (E. coli O157:H7 and other verocytotoxin producing E. coli, O26, O103, O111, O145) and Listeria monocytogenes) were evaluated. Irrigation water, soil and lettuce samples showed levels of coliforms and E. coli higher than 5 and 3 log cfu/g or 100 mL, respectively when sampled 1 week after flooding. However, bacterial counts drastically declined three weeks after the flooding. Climatic conditions after flooding, particularly the solar radiation (6–8 MJ/m²), affected the survival of bacteria in the field. L. monocytogenes was not detected in lettuce samples, except for 2 samples collected 3 weeks after the flooding. The presence of Salmonella was detected in irrigation water, soil and lettuce by multiplex PCR one week after the flooding, but only 2 samples of soil and 1 sample of water were confirmed by colony isolation. Verotoxigenic E. coli was detected in soil and lettuce samples by multiplex PCR. Therefore, the implication of flood water as the source of VTEC contamination of soil and lettuce was not clear. E. coli counts in irrigation water were positively correlated with those in lettuce. A significant correlation (P < 0.005) was found between the presence of pathogens and E. coli counts, highlighting a higher probability of detection of pathogens when high levels of E. coli are found. The results obtained in the present study confirm previous knowledge which defined flooding as a main risk factor for the microbial contamination of leafy greens.     

The microbiological conditions of the carcasses of six species after dressing at a small abattoir

At a small abattoir, samples were collected from carcasses of cattle, pigs, deer, bison, ostriches and emus at the ends of the dressing processes. A single sample was collected from each of 50 or 25 carcasses of each species, by swabbing a randomly selected area of 100 cm². Total aerobes, coliforms and Escherichia coli were enumerated in each sample. The microbiological conditions of the carcasses were assessed by reference to the log mean numbers of total aerobes, coliforms and E. coli estimated from sets of counts recovered from 25 samples, or to the log total numbers of coliforms and E. coli recovered from each set of 25 samples. The log mean numbers of total aerobes on beef carcasses were about 2·5 log cfu cm⁻². The log mean numbers of aerobes on deer carcasses were similar, but the log mean numbers on other types of carcass were 0·5–1 log unit more. The coliforms recovered from carcasses were largely E. coli, except for pig carcasses where E. coli were only about 10% of the coliforms recovered. Escherichia coli were recovered from the majority of samples from beef and pig carcasses, at log mean numbers about 1·5 and 2·5 log cfu 100 cm⁻², respectively, and log total numbers recovered >3 log cfu 2500 cm⁻². Escherichia coli were recovered from minorities of samples from deer, buffalo, ostrich and emu carcasses at log total numbers about 2 log cfu 2500 cm⁻². The findings indicate that when carcasses of different species are dressed at an abattoir, similar microbiological contamination of the various types of carcass cannot be assumed.     

Kinetics of destruction ofEscherichia coliandPseudomonas fluorescensinoculated in ewe's milk by high hydrostatic pressure

Ewe's1999199919991999 Academic PressAcademic PressAcademic PressAcademic Pressmilk standardized to 6% fat was inoculated with Escherichia coliand Pseudomonas fluorescensat a concentration of 10⁷and 10⁸ cfu ml⁻¹respectively, and treated by high hydrostatic pressure. Treatments consisted of combinations of pressure (50-300 MPa), temperature (2, 10, 25 and 50°C), and time (5, 10 and 15 min). Violet red bile agar and crystal-violet-tetrazolium count were used to determineE. coliandP. fluorescensrespectively. Pressurization at low and moderately high temperatures produced higher P. fluorescensinactivation than treatments at room temperature, while pressurization at only moderately high temperature produced high E. coliinactivation; low and room temperatures produced similar reductions. On E. coli,reductions of 6.055 log units were produced with 300 MPa for 15 min at 50°C, while on P. fluorescens,reductions of 5.059 log units were produced with 250 MPa for 15 min at 50°C. Both micro-organisms showed a first-order kinetics of destruction in the range 0-30 min, with D-values (at different temperatures and pressures from 150 to 300 MPa) between 2.055 and 18.058 min for E. coli,and 2.058-23.053 min for P. fluorescens.Abaroprotective effect of ewe's milk (6% fat) on both micro-organisms was observed, in comparison with other studies using different means and similar pressurization conditions.     

Inactivation of Escherichia coli O157:H7 by cinnamic aldehyde purified from Cinnamomum cassia shoot

Escherichia coli O157:H7 is a pathogen, which causes the hemorrhagic colitis, hemolytic uremic syndrome and thrombotic thrombocytopenic purpura in humans. Control of the bacterial cells in foods is an important factor to reduce outbreaks of the foodborne diseases. In this study, cinnamic aldehyde possessing antimicrobial activity against the bacterial cells was purified from the extract of cinnamon (Cinnamomum cassia Blume) shoot by sequential fractionation with various solvents and silica gel column chromatography. When E. coli O157:H7 cells were incubated at 37°C for 12 h in the presence of 500 μg ml⁻¹ of the purified from cinnamic aldehyde, the viable counts decreased dramatically (from 4.9×10⁶ to 1.0×10² cfu ml⁻¹). In the presence of 1000 μg ml⁻¹ of the substance, most of the cells were killed after 2 h of incubation suggesting that the antimicrobial activity of cinnamic aldehyde is bacteriocidal in E. coli. Scanning electron microscopic observations revealed that the bacterial cells treated with the cinnamic aldehyde suffered from severe damages in their surface structure. Minimal inhibitory concentration of the cinnamic aldehyde was determined to be 250 μg ml⁻¹ against E. coli strains O157:H7 and O26 or 500 μg ml⁻¹ against strains ATCC11105 and O111.     

UV-C treatment of soymilk in coiled tube UV reactors for inactivation of Escherichia coli W1485 and Bacillus cereus endospores

Coiled tube UV reactors were used to investigate the influence of tube diameter (1.6 mm ID, and 3.2 mm ID) and Reynolds number (Re) to inactivate Escherichia coli W1485 and Bacillus cereus spores in raw soymilk (RSM). Four levels of Re (343, 686, 1029 and 1372) were tested in RSM inoculated separately with each bacterium and treated in the UV reactors at a constant residence time of 11.3 s with UV-C dose of 11.187 mJ/cm² at 253.7 nm. Inactivation efficiency of both microorganisms increased with Re. Maximum reductions of 5.6 log₁₀ CFU/ml of E. coli and 3.29 log₁₀ CFU/ml of B. cereus spores were achieved in the 1.6 mm ID UV reactor. Inactivation efficiency was higher in the 1.6 mm ID UV reactor than the 3.2 mm ID UV reactor for both the organisms. Effect of UV-C light on lipid oxidation of untreated RSM, measured as malondialdehyde and other reactive substances (MORS) content, was much higher (95 nmol/ml) than the UV-treated (58 nmol/ml) and thermally pasteurized (55 nmol/ml) RSM during the storage period of 7 days. The UV-C treatment can be effectively used for reducing E. coli cells and B. cereus spores in soymilk without compromising its quality.     

The influence of lactoperoxidase,heat and low pH on survival of acid-adapted and non-adapted Escherichia coli O157:H7 in goat milk

In hot climates where quality of milk is difficult to control, a lactoperoxidase (LP) system can be applied in combination with conventional preservation treatments at sub-lethal levels to inhibit pathogenic microbes. This study investigated the effect of combined heat treatments (55 °C, 60 °C and 72 °C) and milk acidification (pH 5.0) on survival of acid-adapted and non-adapted Escherichia coli O157:H7 strains UP10 and 1062 in activated LP goat milk. Heat treatment at 72 °C eliminated E. coli O157:H7. Acid-adapted strains UP10 and 1062 cells showed resistance to combined LP and heat at 60 °C in fresh milk. The inhibition of acid-adapted and non-adapted E. coli O157:H7 in milk following combined LP-activation, heat (60 °C) and milk acidification (pH 5.0) suggests that these treatments can be applied to reduce E. coli O157:H7 cells in milk when they occur at low numbers (<5 log₁₀ cfu mL^?1) but does not eliminate E. coli O157:H7 to produce a safe product.     

Reduction effect of the selected chemical and physical treatments to reduce L. monocytogenes biofilms formed on lettuce and cabbage

As people shift their attention away from unhealthy foods, healthy fresh produce has become popular. However, fresh produce has contributed to many outbreaks of Listeria monocytogenes, which can form a mature biofilm within 24 h. Recent control strategies have proved ineffective in ensuring safe food production. This study focuses on L. monocytogenes biofilms formed on lettuces and cabbages using a viable plate count method and field emission electron microscopy. We investigated the reduction efficacy of treatment with 200 parts per million (ppm) chlorine, 2% each of citric, lactic, and malic acids, 32 Hz ultrasonication (US), 390 mJ/cm² ultraviolet-C (UV-C), or 750 mJ/cm² cold oxygen plasma (COP) on L. monocytogenes biofilms. Following treatment, the quality of the vegetables was analyzed with standard procedures. UV-C and COP showed the best CFU reduction, regardless of the nature of the vegetable surface, while US failed to produce any significant reduction (P > 0.05). Furthermore, chemical treatments reduced count by < 1 log colony forming unit (CFU)/cm² on lettuces, whereas a > 2 log reduction was observed on cabbages. The effect of chemical treatment largely depended on the particular vegetable, while UV-C and COP achieved high reduction regardless of the vegetable, and had no effect on quality. We, therefore, speculate that UV-C and COP show promise in overcoming L. monocytogenes biofilms on food produce.     

Influence of supplementing vitamin C to yearling steers fed a high sulfur diet during the finishing period on meat color,tenderness and protein degradation,and fatty acid profile of the longissimus muscle

The objective was to determine the influence of vitamin C (VC) supplemented for approximately 102 d during the finishing period on color, tenderness, and fatty acid profile of longissimus thoracis (LT; n = 136) from steers fed a 0.55% sulfur diet. Treatments included 4 supplemental VC concentrations: 1) 0 (CON), 2) 5 (5VC), 3) 10 (10VC), or 4) 20 (20VC) g VC·h^− 1∙ d^− 1 in a common diet. Increasing supplemental VC decreased (P < 0.01) L*, but increased (P < 0.01) vitamin E and tended to increase (P ≤ 0.07) calcium and iron content of steaks. No VC (P ≥ 0.25) effect was noted for WBSF, calpain-1 autolysis, troponin T degradation, or most fatty acid profiles. A quadratic effect (P ≤ 0.03) was observed for cholesterol and CLA content of LT. Under the conditions of our study, supplementing VC to steers fed a 0.55% sulfur diet late in the finishing period did not influence color or tenderness, but increased the vitamin E content.     

Effect of tomato by-products in the diet of Comisana sheep on composition and conjugated linoleic acid content of milk fat

To evaluate the effect of supplementing the diet of Comisana sheep with by-products from industrial tomato manufacture on the fat composition and conjugated linoleic acid (CLA) content of milk fat, two groups of 50 ewes each were fed either total mixed ration standard (TMRS) or total mixed ration with added tomato by-products (TMRA). Milk fat composition was determined by high-resolution gas chromatography (HRGC). The milk fat content for the animals fed the TMRA diet increased by 6.41% (P < 0.01) after six weeks, compared with the animals fed the TMRS diet. The CLA content in the milk fat for the group of animals fed the TMRA diet was 19.8% (P < 0.05) higher than for those fed the TMRS diet, and reached 1.33 g 100 g^?1 fat, while the polyunsaturated fatty acid (PUFA) content increased by a 6.43% (P < 0.05) and reached 7.12 g 100 g^?1 fat. The fatty acid composition showed an increase in the amount of polyunsaturated fatty acids. The n ? 3:n ? 6 ratio increased by 13% in the milk from sheep fed with the TMRA diet. These observations were confirmed by triglyceride analysis, which showed a decrease in the amount of short-chain (C₂₈–C₃₂) and medium-chain (C₃₄–C₄₂) triglycerides after six weeks, while the opposite was observed for the long-chain triglycerides (C₄₄–C₅₄).     

Survival of Escherichia coli O157:H7 in soil and on carrots and onions grown in fields treated with contaminated manure composts or irrigation water

Many foodborne outbreaks of enterohemorrhagic Escherichia coli O157:H7 infection have been associated with the consumption of contaminated vegetables. On-farm contaminations through contaminated manure or irrigation water application were considered likely sources of the pathogen for several outbreaks. Field studies were done to determine the survival of E. coli O157:H7 on two subterranean crops (carrots and onions), and in soil fertilized with contaminated manure compost or irrigated with contaminated water. Three different types of composts, PM-5 (poultry manure compost), 338 (dairy manure compost) and NVIRO-4 (alkaline stabilized dairy manure compost), and irrigation water were inoculated with an avirulent strain of E. coli O157:H7 at 10⁷ cfu g⁻¹ and 10⁵ cfu ml⁻¹, respectively. A split-plot block design plan was used for each crop, with five treatments (one without compost, three with each of the three composts, and one without compost but with contaminated irrigation water applied) and five replicates for a total of 25 plots, each measuring 1.8×4.6 m², for each crop. Composts were applied to soil as a strip at a rate of 4.5 metric tons ha⁻¹ before carrots and onions were sown. Contaminated irrigation water was sprayed once on the vegetables at the rate of 2 l per plot for this treatment 3 weeks after carrots and onions were sown. E. coli O157:H7 survived in soil samples for 154–196 days, and was detected for 74 and 168 days on onions and carrots, respectively. E. coli O157:H7 survival was greatest in soil amended with poultry compost and least in soil containing alkaline-stabilized dairy manure compost. Survival profiles of E. coli O157:H7 on vegetables and soil samples, contaminated either by application of contaminated compost or irrigation water, were similar. Hence, preharvest contamination of carrots and onions with E. coli O157:H7 for several months can occur through both contaminated manure compost and irrigation water.     

Conjugated linoleic acid production by immobilized cells of Lactobacillus delbrueckii ssp. bulgaricus and Lactobacillus acidophilus

Lactobacillus delbrueckii ssp. bulgaricus (CCRC14009) and L. acidophilus (CCRC14079), immobilized with chitosan and polyacrylamide, were tested for CLA production. A 10-ml aliquot of L. delbrueckii ssp. bulgaricus cell suspension (3.59 × 10⁷ CFU/ml) was adsorbed to 0.5 g chitosan and polyacrylamide, mixed with 0.2 ml linoleic acid (0.9 g/ml), and incubated at 37 °C for 24 h at pH 5, 6, 7, and 8 for CLA production. CLA levels, produced by immobilized cells of L. delbrueckii ssp. bulgaricus and L. acidophilus with increasing cell counts to 1.08 and 1.28 × 10¹⁰ CFU/ml, respectively, at optimal reaction pHs were evaluated. More CLA was formed at pH 8 of chitosan and pH 7 of polyacrylamide-immobilized L. delbrueckii ssp. bulgaricus cell treatments. Increase in cell count resulted in higher CLA production. The adsorption of L. delbrueckii ssp. bulgaricus cells onto polyacrylamide at pH 7 showed significant improvement in total CLA level. Results demonstrated a potential for enhancing CLA production through immobilization.     

Antimicrobial activity of pediocin-producing Lactococcus lactis on Listeria monocytogenes,Staphylococcus aureus and Escherichia coli O157:H7 in cheese

The antimicrobial activity of two pediocin-producing transformants obtained from wild strains of Lactococcus lactis on the survival of Listeria monocytogenes, Staphylococcus aureus and Escherichia coli O157:H7 during cheese ripening was investigated. Cheeses were manufactured from milk inoculated with the three pathogens, each at approximately 6 log cfu mL⁻¹. Pediococcus acidilactici 347 (Ped⁺), Lc. lactis ESI 153, Lc. lactis ESI 515 (Nis⁺) and their respective pediocin-producing transformants Lc. lactis CL1 (Ped⁺) and Lc. lactis CL2 (Nis⁺, Ped⁺) were added at 1% as adjuncts to the starter culture. After 30 d, L. monocytogenes, S. aureus and E. coli O157:H7 counts were 5.30, 5.16 and 4.14 log cfu g⁻¹ in control cheese made without adjunct culture. On day 30, pediocin-producing derivatives Lc. lactis CL1 and Lc. lactis CL2 lowered L. monocytogenes counts by 2.97 and 1.64 log units, S. aureus by 0.98 and 0.40 log units, and E. coli O157:H7 by 0.84 and 1.69 log units with respect to control cheese. All cheeses made with nisin-producing LAB exhibited bacteriocin activity throughout ripening. Pediocin activity was only detected throughout the whole ripening period in cheese with Lc. lactis CL1. Because of the antimicrobial activity of pediocin PA-1, its production in situ by strains of LAB growing efficiently in milk would extend the application of this bacteriocin in cheese manufacture.     

Inactivation of Escherichia coli O157:H7 and Listeria monocytogenes in milk by caprylic acid and monocaprylin

Listeria monocytogenes and Escherichia coli O157:H7 are major foodborne pathogens implicated in various outbreaks involving pasteurized or unpasteurized milk, and various dairy products. The objective of this study was to determine the antibacterial effect of caprylic acid (CA, C_8:0) and its monoglyceride, monocaprylin (MC) on L. monocytogenes and E. coli O157:H7 in whole milk. A five-strain mixture of E. coli O157:H7 or L. monocytogenes was inoculated in autoclaved milk (10⁶ CFU/ml) containing 0, 25, or 50 mM of CA or MC. At 37°C, all the treatments, excepting 25 mm CA, reduced the population of both pathogens by approximately 5.0 log CFU/ml in 6 h. At 24 h of storage at 8°C, MC at both levels and CA at 50 mM decreased L. monocytogenes and E. coli O157:H7, respectively by >5.0 log CFU/ml. At 48 h of 4°C storage, populations of L. monocytogenes and E. coli O157:H7 were decreased to below detection level (enrichment negative) by 50 mm of MC and CA, respectively. Results indicate that MC could potentially be used to inhibit L. monocytogenes and E. coli O157:H7 in milk and dairy products, but sensory studies need to be conducted before recommending their use.     

Enterobacteriaceae in beef products from retail outlets in the Republic of Ireland and comparison of the presence and counts of E. coli O157:H7 in these products

This study investigated the prevalence and numbers of Enterobacteriaceae in minced beef and beef burgers purchased from supermarkets and butcher shops in the Republic of Ireland (RoI). Samples (n=1303) collected between June 2001 and April 2002 from every county in the RoI (∼60 per county) were examined for the presence of Enterobacteriaceae using method BS 5763. Overall, in the 43 beef products in which E. coli O157:H7 was present the Enterobacteriaceae counts ranged from 0.52 to 6.98 log₁₀ cfu g⁻¹. There was no correlation between the number of Enterobacteriaceae and the presence of E. coli O157:H7. There were no significant differences between Enterobacteriaceae numbers in fresh, unpackaged, minced beef samples from butcher shops and supermarkets, or in fresh, unpackaged, beef burgers from butcher shops and supermarkets. However, there were significant differences among the numbers of Enterobacteriaceae detected in different minced beef products. The numbers of Enterobacteriaceae in fresh, unpackaged, minced beef (6.54–6.98 log₁₀ cfu g⁻¹) were considerably higher than in preprepared or prepackaged minced beef (2.95–3.62 log₁₀ cfu g⁻¹).