Incidence,internalization and behavior of Salmonella in mangoes,var. Tommy Atkins

Mangoes imported from South America were responsible for two Salmonella multistate outbreaks in the USA. The hot water immersion treatment utilized for fly larvae control was pointed out as the probably responsible for bacterial internalization in these fruits. The objective of this study was to evaluate: the presence of Salmonella in mangoes, the occurrence of internalization of these bacteria during a laboratory-simulated hydrothermal treatment and the bacterial behavior in mangoes in the rind surfaces and in different portions: stem end, middle side and blossom-end after storage at 8 and 22 °C, for 24 and 144 h. One hundred samples were analyzed; Salmonella was not found in any of the 33 samples destined for the export market, but in two of the remaining samples, destined for the internal market, the presence of that bacterium was detected. The results from the laboratory-simulated experiments proved that bacterial internalization occurred in the intact fruit. In the stem portion the log of MPN/g of bacteria was statistically higher than in the remaining parts of the fruit (p < 0.05), demonstrating that the stem is the route for bacterial entrance. At 22 °C bacterial multiplication was observed in all portions (the rind surface, stem end, middle side and blossom-end) analyzed. However, at 8 °C the growth was lower, and in the rind surface there was a decrease in the number of bacteria. Thus, microorganisms present in the water used for hydrothermal treatments can migrate to the interior of mangoes, survive and grow in all fruit portions.     

Effect of catechin and ferulic acid on melanosis and quality of Pacific white shrimp subjected to prior freeze–thawing during refrigerated storage

Melanosis of Pacific white shrimp (Litopenaeus vannamei) subjected to freeze–thawing with different thawing methods and various cycles were monitored during subsequent refrigerated storage (4 °C) up to 4 days. Melanosis score was lower in Pacific white shrimp thawed at 4 °C, compared with that found in samples thawed at room temperature or using tap water. Polyphenol oxidase (PPO) activity increased as freeze–thaw cycles increased (P < 0.05). Enhanced PPO activity was most likely associated with increased melanosis. Pacific white shrimp treated with catechin (0.05%, 0.1% and 0.2% (w/v)) or ferulic acid (1%, 2% and 3% (w/v)) and subjected to freeze–thawing with various cycles showed the retarded melanosis during the subsequent refrigerated storage of 4 days, compared with the control (P < 0.05). Treatment of shrimp with both phenolic compounds could impede the growth of psychrophilic bacteria and the spoilage as evidenced by the lowered psychrophilic bacteria count and total volatile base content (TVB). Sample treated with 0.2% catechin or 3% ferulic acid also exhibited the retarded lipid oxidation during the subsequent refrigerated storage, compared with the control (P < 0.05). Thus, either catechin or ferulic acid could be used as the potential additive to lower melanosis of shrimp with prior freeze–thawing.     

Effects of lactic acid and lauricidin on the survival of Listeria monocytogenes,Salmonella enteritidis and Escherichia coli O157:H7 in chicken breast stored at 4 °C

Lauricidin and lactic acid were evaluated for their effects on growth and survival of Listeria monocytogenes (L55), Salmonella enteritidis (S552) and Escherichia coli O157:H7 (E19) inoculated onto raw chicken breast. Fresh, raw chicken breasts were purchased immediately after slaughter and transported on ice to the laboratory within 20 min. Each chicken breast was decontaminated by briefly dipping in 70% ethanol and passed through a flame of a Bunsen burner and then allowed to cool. The decontaminated Chicken breast was dipped in TSB broth, at room temperature (25 °C) for 15 min, containing approximately log 9 CFU/ml of L. monocytogenes, S. enteritidis or E. coli O157:H7. Initial counts of L. monocytogenes, S. enteritidis or E. coli O157:H7 counts in chicken breast immediately after dipping in TSB broth were in the range of log 7–log 8 CFU/g. After inoculation, the chicken breasts were kept at room temperature for 20 min to allow attachment. Each inoculated chicken breast (25 °C) was dipped in 0 (control – sterile water), 0.5%, 1%, 1.5% or 2% of lauricidin (w/v) or lactic acid (v/v) for 10, 20 or 30 min and then individually placed in oxygen-permeable polyethylene bags. Breasts were subjected to microbiological analyses after treatment (day 0) and after storage for 2, 5, 7, 10 and 14 d at 4 °C. Initial counts of L. monocytogenes, S. enteritidis and E. coli O157:H7, in chicken breast treated with lauricidin decreased by 2.90, 1.31 and 2.27 log CFU/g, respectively. Lauricidin was more effective in reducing L. monocytogenes population than S. enteritidis and E. coli O157:H7 population. Dipping chicken breast in lauricidin for 30 min caused a significant reduction of L. monocytogenes, S. enteritidis and E. coli O157:H7 population compared to 10 and 20 min dipping. Initial L. monocytogenes, S. enteritidis and E. coli O157:H7 counts on chicken breast treated with lactic acid decreased by 1.97, 1.71 and 2.59 log CFU/g, respectively. Lactic acid caused a higher reduction in initial S. enteritidis and E. coli O157:H7 counts compared to lauricidin.     

Aqueous extracts of Hibiscus sabdariffa calyces as an antimicrobial rinse on hot dogs against Listeria monocytogenes and methicillin-resistant Staphylococcus aureus

Contamination of ready-to-eat meat products by foodborne pathogens is a major concern in the food industry. Novel methods to control foodborne pathogens are made necessary by continuing outbreaks as well as the development of antibiotic-resistant pathogens. Hibiscus sabdariffa extracts could be useful as a natural source of antimicrobial rinse on ready-to-eat products to control pathogens. In this study, lyophilized Hibiscus flower extracts were examined for their antimicrobial activity as a rinse on all-beef hot dogs against Listeria monocytogenes and methicillin-resistant Staphylococcus aureus (MRSA). Beef hot dogs were dip inoculated in overnight cultures of 1:1 mixtures of L. monocytogenes strains Scott A and 101 or MRSA strains ATCC 33591 and ATCC 33593 and were placed at 4 °C overnight to allow for bacterial attachment. Hot dogs were rinsed with extracts (120, 240 mg/mL) or water (control) for 5, 15, 30, or 60 min and then plated immediately (0 h; no storage) or stored at 4 °C overnight and plated at 24 h. Serial dilutions were plated in duplicate on both TSA and selection media, Modified Oxford (Listeria) or Baird Parker (MRSA), and the entire experiment was replicated 3 times. Higher extract concentrations, longer rinse times, and longer storage times were the most effective at inhibiting and/or killing L. monocytogenes and MRSA on hot dogs. L. monocytogenes was reduced to ca. 1.5 log CFU/g while MRSA was reduced to undetectable levels following rinsing of hot dogs with extracts at 240 mg/mL for 60 min and stored for 24 h. Both L. monocytogenes and MRSA were reduced ca. 2 log CFU/g following rinsing of hot dogs with extracts at 120 mg/mL for 60 min and stored for 24 h. This research demonstrates the effectiveness of Hibiscus extracts against L. monocytogenes and MRSA as an antimicrobial rinse on ready-to-eat meat products.     

Inactivation of Salmonella,E. coli and Listeria monocytogenes in phosphate-buffered saline and apple juice by ultraviolet and heat treatments

Two strains of Escherichia coli (K-12 and O157:H7), Salmonella (enteritidis and typhimurium) and Listeria monocytogenes (AS-1 and M24-1) were individually suspended in phosphate-buffered saline (PBS) and apple juice prior to exposure to UV radiation (220–300 nm) and heating at 55 °C. The calculated decimal reduction times (D value, min) varied with suspending medium and mode of inactivation. The AS-1 and M24-1 strains of L. monocytogenes were found to be most resistant to UV in PBS (0.28–0.29 min) while the AS-1 strain was most resistant in juice (1.26 min). The AS-1 strain of L. monocytogenes and E. coli O157:H7 were most heat resistant when suspended in PBS (4.41 min) and juice (4.43 min), respectively. Results obtained from this study may be used by apple juice processors in selecting appropriate organisms for UV irradiation or heat treatment lethality validations.     

Effect of organic acids,hydrogen peroxide and mild heat on inactivation of Escherichia coli O157:H7 on baby spinach

Minimally processed baby spinach contaminated with Escherichia coli O157:H7 has been associated with multiple outbreaks of foodborne illnesses recently. Chlorinated water is widely used to wash vegetables commercially, but this washing procedure has limited efficacy and can lead to the formation of carcinogenic substances. This study was conducted to determine the effects of organic acids and hydrogen peroxide alone and in binary combinations with or without mild heat (40 and 50 °C) on the inactivation of Escherichia coli O157:H7 on baby spinach. Baby spinach leaves were dip-inoculated with E. coli O157:H7 to a level of 6 log CFU/g and stored at 4 °C for 24 h before treatment. Individual washing solutions (1% and 2% lactic acid [LA], citric acid [CA], malic acid [MA], tartaric acid [TA], acetic acid [AA], hydrogen peroxide [H₂O₂] as well as binary combinations of LA, CA, MA and H₂O₂ at final concentrations of 1% were used to decontaminate spinach leaves at 22, 40 or 50 °C for 2–5 min to test their efficacy in reducing E. coli O157:H7. Chlorinated water (200 ppm free chlorine) decreased the population of E. coli O157:H7 on baby spinach by only 1.2–1.6 log CFU/g, which was not significantly different from DI water washing. Washing with 1% LA at 40 °C for 5 min was the most effective treatment achieving a 2.7 log reduction of E. coli O157:H7 which is significantly higher than chlorine washing. Washing with LA + CA or LA + HP at 40 °C for 5 min was equally effective against E. coli O157:H7, resulting in a 2.7 log reduction of E. coli O157:H7. The application of mild heat significantly enhanced the efficacy of washing solutions on the inactivation of E. coli O157:H7. There was, however, no significant difference between treatments at 40 °C for 5 min and 50 °C for 2 min. The results suggested that the use of organic acids in combination with mild heat can be a potential intervention to control E. coli O157:H7 on spinach.     

Efficiency of high pressure treatment on inactivation of pathogenic microorganisms and enzymes in apple,orange, apricot and sour cherry juices

The purpose of this study was to investigate the effect of high hydrostatic pressure with a mild heat treatment on Staphylococcus aureus 485, Escherichia coli O157:H7 933 and Salmonella Enteritidis FDA in apple, orange, apricot and sour cherry juices. The effectiveness of the treatment on polyphenol oxidase activity in apple juice and pectinesterase activity in orange juice were also determined. An inoculum of microorganisms was completely inactivated at 350 MPa and 40 °C in 5 min. The residual polyphenol oxidase activity in apple juice after treatment at 450 MPa and 50 °C for 60 min was obtained as 9 ± 2.2%. The residual pectinesterase activity in orange juice after treatment at 450 MPa and 50 °C for 30 min was determined as approximately 7 ± 1.6%. It compares with 12 ± 0.2% at a treatment of 40 °C and 450 MPa for 60 min. Pressure resistant isoenzymes were thought to be responsible for the final residual activity. The inactivation is irreversible and the enzyme is not reactivated upon storage. High pressure processing constitutes an effective technology to inactivate the enzymes in fruit juices. Pressures higher than 400 MPa can be combined with mild heat (<50 °C) to accelerate enzyme inactivation.     

Antimicrobial activity of clove (Syzgium aromaticum) oil in inhibiting Listeria monocytogenes on chicken frankfurters

The ability of Listeria monocytogenes to survive and grow at refrigeration temperature in some ready to eat (RTE) poultry products is a public health concern. The inhibitory effect of clove oil (1% and 2%, v/w) applied to the surface of RTE chicken frankfurters was determined on seven strains of L. monocytogenes inoculated at low (10²–10³ cfu/g) or high cell numbers (10⁴–10⁶ cfu/g), and stored at 5 °C for 2 weeks or at 15 °C for 1 week. All strains of L. monocytogenes survived and grew on control frankfurters at 5 °C and 15 °C but growth was inhibited under both storage conditions in the presence of either 1% or 2% clove oil. Depending on the sensory considerations, the addition of clove oil to frankfurters may be an effective strategy to control L. monocytogenes in chicken frankfurters.     

Application of an optimized 18-h method involving one step culturing and single primer-based PCR assay for detection of Salmonella spp. in foods

A polymerase chain reaction (PCR) using 20-mer oligonucleotide single primer (named primer 3) randomly designed on the basis of Salmonella Typhimurium gatD gene encoding galactitol-1-phosphate dehydrogenase could produce the specific DNA product of approximate 770-bp in all 38 Salmonella strains used. No 770-bp DNA band was amplified from any DNA samples of 20 non-Salmonella bacteria. The DNA band was detected by 1% agarose gel electrophoresis and ethidium bromide staining. The sensitivity of the RAPD–PCR assay for detection of pure genomic DNA from S. Typhimurium ATCC 13311 and Salmonella Enteritidis DMST 15676 was as few as 0.01 ng. When simple boiling in TE buffer for 5 min was used for extraction both Salmonella spp. DNA, the detection limits were at least 230 and 320 cells, respectively. By using the RAPD–PCR assay following at least 14 h pre-enrichment in nutrient broth (NB), as few as 1 CFU of S. Typhimurium ATCC 13311 or S. Enteritidis DMST 15676 per 25 g of autoclaved chicken meat was detected. When the optimized 18-h method involving pre-enrichment in NB and DNA extraction by boiling protocol followed by RAPD–PCR using primer 3 was evaluated in comparison with the conventional method on 195 possibly naturally-contaminated food samples, 36 samples were found positive by both methods. In addition, the results of the developed RAPD–PCR-based assay proved to be identical to those by the conventional method. The optimized 18-h method was simple, rapid and sensitive, achieved the same detection limit as the conventional method and produced a zero level of false-negative results.     

Non-thermal inactivation of Escherichia coli K12 in buffered peptone water using a pilot-plant scale supercritical carbon dioxide system with a gas–liquid porous metal contactor

This study evaluated the effectiveness of a supercritical carbon dioxide (SCCO₂) system, with a gas–liquid porous metal contactor, for reducing Escherichia coli K12 in diluted buffered peptone water. 0.1% (w/v) buffered peptone water inoculated with E. coli K12 was processed using the SCCO₂ system at CO₂ concentrations of 3.1–9.5 wt%, outlet temperatures of 34, 38, and 42 °C, a system pressure of 7.6 MPa, and a flow rate of 1 L/min. Increased CO₂ concentrations and temperatures significantly (P < 0.05) enhanced microbial reduction. A maximum reduction of 5.8-log was obtained at 8.2% CO₂ and 42 °C. To achieve a 5-log reduction of E. coli K12 in 0.1% buffered peptone water, minimum CO₂ concentrations of 9.5%, 5.5%, and 5.3% were needed at 34, 38, and 42 °C, respectively. Further reductions of cells were observed after storage for 7 days at 4 °C. But storage at 25 °C increased the number of viable cells to 8-log cfu/mL after 7 days. This study showed the potential of the pilot scale SCCO₂ system with a gas–liquid porous metal contactor for microbial inactivation in liquid food.     

Decontamination of fresh produce by the use of slightly acidic hypochlorous water following pretreatment with sucrose fatty acid ester under microbubble generation

Treatment by slightly acidic hypochlorous water (SAHW) in combination of pretreatment with sucrose fatty acid ester under microbubble generation was effective for decontamination of lettuce. Sufficient contact time of SAHW containing 30 mg/L of available chlorine on reduction of viable counts of lettuce was determined to be 5 min. For 5 min at 18–20 °C, treatment with 30 mg/L of available chlorine in SAHW appeared more effective in the reduction of bacteria on lettuce compared with 15 mg/L. The treatment of lettuce at 50 °C with SAHW at 30 mg/L of available chlorine showed a 2 log reduction of bacterial counts without injury in the tissue. The treatment at 50 °C, SAHW also delayed browning on cut lettuce for the first 5–6 days of subsequent storage at 6 °C. Among two sucrose fatty acid esters tested, sucrose monopalmitate at 100 mg/L had a higher efficacy for pretreatment under microbubble generation. After pretreatment for 5 min with 100 mg/L sucrose monopalmitate under microbubble generation and subsequent treatment with SAHW at 50 °C for 5 min, viable counts of lettuce were decreased by about 3–4 logs. After the same treatment, Pseudomonas sp. predominant on lettuce decreased drastically. These results indicate the effectiveness of the combined treatments of sucrose fatty acid ester under microbubble generation and SAHW at 50 °C for decontamination of fresh produce.     

Efficacy of sanitizers in reducing Escherichia coli O157:H7, Salmonella spp. and Listeria monocytogenes populations on fresh-cut carrots

Shredded carrots were inoculated with Escherichia coli O157:H7, Salmonella or Listeria monocytogenes and washed for 1 or 2 min with chlorine (Cl; 200 ppm), peroxyacetic acid (PA; 40 ppm) or acidified sodium chlorite (ASC; 100, 200, 500 ppm) under simulated commercial processing conditions. After washed, the carrots were spin dried, packaged and stored at 5 °C for up to 10 days. Bacterial enumeration was significantly (P ⩽ 0.05) reduced by 1, 1.5 and 2.5 log CFU/g after washing with ASC 100, 250 and 500 ppm, respectively. All sanitizers reduced pathogen load below that of tap water wash and unwashed controls. During storage at 5 °C the bacterial load of all treatments increased gradually, but to different extent in different treatments. ASC inhibited bacterial growth more effectively than the other sanitizers and also maintained the lowest pathogen counts (<1 log CFU/g) during storage. Organic matter in the process water significantly (P ⩽ 0.05) reduced the antibacterial efficacy of Cl, but not that of PA or ASC. Therefore, ASC shows the potential to be used as a commercial sanitizer for washing shredded carrots.     

Effects of lactic acid and hot water treatments on Salmonella Typhimurium and Listeria monocytogenes on beef

The present study is designed to determine alone and combined effects of lactic acid (LA) and hot water (HW) treatments. Hot water and different concentrations of lactic acid were evaluated for their reduction effects on Salmonella Typhimurium and Listeria monocytogenes on contaminated beef during refrigerated storage at 4 °C. The reductions were 0.05–1.19 and 0.09–1.14 log for S. Typhimurium and L. monocytogenes on day 0 respectively, while it was 0.43–1.78 and 1.69–3.84 log respectively on day 5 of storage. Results of this study suggest that LA and HW treatments can be used to reduce S. Typhimurium and L. monocytogenes which provide an additional measure of safety in production line.     

Superheated steam reduction of deoxynivalenol in naturally contaminated wheat kernels

Contamination of wheat with the Fusarium mycotoxin deoxynivalenol (DON) is a concern to the ethanol industry as it is stable during most processing operations and will be concentrated in the spent grains, which are potentially a valuable feedstock. Superheated steam at four processing temperatures (110, 135, 160, and 185 °C), three steam velocities (0.65, 1.3, and 1.5 m/s), and processing times of 2–15 min were used to treat wheat kernels naturally contaminated with DON to find the best processing parameters for the reduction of DON. A commercial enzyme-linked immunosorbent assay (ELISA) kit was used to determine DON levels in the wheat samples. Samples became increasingly toasted, displaying a brown color with increasing processing temperatures and times, and became friable after processing at temperatures of 160 and 185 °C. Only samples processed at 185 °C and 1.3 m/s exhibited any starch gelatinization. Significant (P < 0.05) reductions in DON levels were seen at 160 and 185 °C but were not generally seen at 110 and 135 °C and the effect of velocity was not significant (P > 0.05). Reductions of up to 52% were achieved at 185 °C and 6 min processing time and were due only to thermal degradation and not to solubilization and extraction.     

The effect of high pressure on microbial population,meat quality and sensory characteristics of chicken breast fillet

High hydrostatic pressure (300, 450 and 600 MPa) was used to investigate its effect on microbial population, meat quality and sensory characteristics of chicken breast fillets. Pressures of 450 and 600 MPa almost completely eliminated all the 3 major pathogens Salmonella typhimurium (KCTC 1925), Escherichia coli (KCTC 1682), and Listeria monocytogenes (KCTC 3569) and therefore improved safety of chicken breast fillets. The 600 MPa treatment reduced bacteria count by 6–8 log (CFU/g) for 7–14 days, and the 450 MPa treatment reduced bacteria count by 4–8 log (CFU/g) for 3–14 days, depending on the microorganism. The increased pressure had an impact on flavour, aroma strength and juiciness. The 300 MPa pressure significantly reduced flavour, aroma strength and juiciness, and 450 MPa produced breast fillets with the weakest aroma. Increasing pressure increased cooking loss and colour by increasing L*, a* and b* values. Moreover, elevated pressure increased hardness, cohesiveness, gumminess and chewiness, as well as improved freshness of meat by reducing VBN. Pressure of 450 MPa and higher induced lipid oxidation. The results demonstrate that high pressure treatment is an effective technology in reducing bacterial spoilage and extending shelf-life of chicken breast fillet, however it may have a negative impact on some quality and sensory characteristics.     

Incidence of pathogenic psychrotrophs in ice creams sold in some retail outlets in Mumbai,India

With a view to determine the microbial quality of ice creams, 30 samples of commercial brands of three flavours sold in the `open' and `packaged, (cone, cup)' forms were analyzed for their total bacterial counts (TBC), yeast and mold counts (YMC), coliforms and pathogenic psychrotrophs; Bacillus cereus, Staphylococcus aureus, Listeria monocytogenes, Yersinia enterocolitica and Salmonella spp. In general in both the types of ice creams bacterial load (2.3 × 10⁴–8.5 × 10⁶ cfu/ml) was higher; particularly coliform levels were 10–100 fold higher (3.0 × 10²–5.8 × 10⁴ cfu/ml) than the safety limits prescribed by Indian Standards Institute (ISI). Staph. aureus was detected in both the types of ice creams but occurrence of B. cereus was more frequent in open samples (40%) than in packed ones (26.6%). Salmonella was not detected in any of the 30 samples tested. While 53% of the packed and 100% of the open ice creams exhibited Listeria contamination, Yersinia were detected in 33% of packed and 40% of open ones. L. monocytogenes and/or Y. enterocolitica was detected only in one of the open ice cream samples. Growth profile of Y. enterocolitica 5692 and L. monocytogenes 036 at simulated temperature abuse conditions during commercial frozen storage showed that after 10 days L. monocytogenes could grow to >1 log and 1 log cycle at 8–10°C and 2–4°C, respectively and Y. enterocolitica grew 2 log cycles at both the temperatures. Results are discussed in the context of present microbiological specifications and the need for its implementation by regulatory agencies to ward off possible health hazards arising from pathogens.     

Use of gamma irradiation for inactivation of pathogens inoculated into Kimbab,steamed rice rolled by dried laver

The effect of gamma irradiation for inactivating the pathogens inoculated into the ready-to-eat Kimbab, steamed rice rolled by dried laver, was investigated. The pathogens used were Salmonella Typhimurium, Escherichia coli, Staphylococcus aureus and Listeria ivanovii which are important for public health. The growth of four test organisms inoculated (about 10⁶–10⁷ CFU/g) into the Kimbab were sustained by an irradiation treatment during 24 h of storage regardless of the temperature at 10, 20 and 30 °C. Four pathogen inoculated into Kimbab decreased 2–3 log CFU/g by 1 kGy treatment and was not detected after 3 kGy. The D₁₀ value of pathogens inoculated into the Kimbab were 0.31–0.44 kGy among the four organisms. This study indicated that a low dose irradiation can maintain microbial safety for ready-to-eat Kimbab, steamed rice rolled by dried laver.     

Behavior of Salmonella Rubislaw on ground black pepper (Piper nigrum L.)

Among spices, black pepper is highly appreciated and Brazil is one of the largest producers of it in the world. However, spices may reach consumers presenting poor quality, due to the loss of volatile compounds, microbial contamination or even due to insect infestation. Salmonella spp. frequently contaminate ground black pepper and may be recovered from products with low levels of free water, even after they have been submitted to high temperatures. The objective of this trial was to evaluate the behavior of a Salmonella Rubislaw strain on ground black pepper (Piper Nigrum L.), as well as to study the effects of water activity (A_w) and storage temperature (5, 25 and 35 °C) for 2 and 15 days. The most probable number technique was used for the quantification of the S. Rubislaw. Data obtained in the present trial indicate that differences in the reduction in counts were observed in relation to A_w (P = 0.006) and storage temperature (P = 0.000). Nevertheless, there was no significance as to the interaction of the two factors (P’s > 0.05). Bonferroni multiple comparisons tests have shown significant differences only when related to the A_w: 0.663, 0.815 and 0.887 (P’s < 0.05). When the product is stored at 5 °C, the number of surviving cells is even greater (P = 0.000). Considering the data obtained, we may conclude that, after contamination, S. Rubislaw remains viable in pepper for up to 15 days.     

Comparison of aluminum thermal-death-time disks with a pilot-scale pasteurizer on the thermal inactivation of Escherichia coli K12 in apple cider

This study was conducted to compare thermal inactivation kinetics obtained using a pilot-scale pasteurizer and a bench-scale processing system. Pilot-scale pasteurizers are useful for product development, but comparisons on thermal inactivation kinetics with smaller scale systems are lacking. Using an Armfield pilot-scale pasteurizer and aluminum thermal-death-time (TDT) disks, the D-values and z-values of Escherichia coli K12 in apple cider were determined in the temperature range of 54–62 °C. Come-up times to 58 °C were also measured and were 35 and 61 s for the TDT disks and pasteurizer, respectively. The D-values from the TDT disks were 9.66, 4.01, 1.44 and 0.44 min at temperatures of 54, 56, 58, and 60 °C, respectively. The D-values from the pasteurizer were 3.48, 1.22, 0.10 and 0.05 min at temperatures of 56, 58, 60, and 62 °C, respectively. The z-values from the TDT disks and the pasteurizer were 4.68 and 3.60 °C, respectively. There was no significant (P > 0.05) difference in the D-values of the TDT disks and pasteurizer at 56 and 58 °C, while there was a significant (P < 0.05) difference in the D-value at 60 °C and in the z-value. This study revealed that the thermal inactivation kinetics obtained using bench scale TDT disks and an Armfield pilot-scale pasteurizer under certain conditions are similar. However, based on ease of use and other factors, TDT disks are preferable for acquiring thermal inactivation kinetics.     

Prevalence of foodborne pathogens in open markets and supermarkets in Thailand

This study was conducted in Thailand (Bangkok and Pathum Thani provinces), from June 2006 to July 2007, in order to assess the prevalence of Listeria monocytogenes, Escherichia coli O157, Salmonella, Shigella and Vibrio parahaemolyticus in foods. Retail raw meats and seafood, including chicken (n = 109), pork (n = 80), beef (n = 108), shrimp (n = 43) and oysters (n = 48), from open markets and supermarkets were analyzed. Salmonella was found in 22 of 61 (36%) open market samples (48% of chicken, none of pork and beef, and 53% of shrimp) and in 12 of 75 (16%) samples from supermarkets (57%, 12%, 24%, 0% respectively). However, a small number of L. monocytogenes were isolated, where 6 of 217 (3%) were samples from open markets (6% of chicken and 3% of pork) and 17 of 171 (10%) were from supermarkets (3% of beef, 4% of chicken, and 32% of pork). In both markets, L. monocytogenes was not detected from shrimps, neither from oysters. E. coli O157, Shigella and tdh-positive V. parahaemolyticus were not isolated in this collection. Several Salmonella and L. monocytogenes isolates were multidrug-resistant. Both markets would need better assessment, since multidrug-resistant strains have been isolated and they may lead to therapeutic failure.