Modeling Surface Transfer of Listeria monocytogenes on Salami during Slicing

ABSTRACT: Listeria monocytogenes has been implicated in several listeriosis outbreaks linked to the consumption of presliced ready‐to‐eat (RTE) deli meats, which has drawn considerable attention in regard to possible cross‐contamination during slicing operation at retail and food service environments. Salami with 15% fat (a moderate fat content deli item) was used to investigate the transfer of L. monocytogenes between a meat slicer and salami slices and to understand its impact on food safety. A 6‐strain cocktail of L. monocytogenes was inoculated onto a slicer blade to an initial level of approximately 3, 5, 6, 7, or 9 log CFU/blade (or approximately 2, 4, 5, 6, or 8 log CFU/cm² of the blade edge area), and then the salami was sliced to a thickness of 1 to 2 mm (case I). For another cross‐contamination scenario, a clean blade was first used to slice salami loaf that was previously surface‐inoculated with L. monocytogenes (approximately 3, 5, 6, 7, 8, or 9 log CFU/100 cm² area), followed by slicing the uninoculated salami loaf (case II). The salami slicing rate was maintained at an average of 3 to 4 slices per minute in all the tests. The results showed that the empirical models developed in this study were reasonably accurate in describing the transfer trend/pattern of L. monocytogenes between the blade and salami slices if the inoculum level was > 5 log CFU on the salami or blade. With an initial inoculum at 3 or 4 log CFU, the experimental data seemed to suggest a rather random pattern of bacterial transfer between blade and salami. The currently developed models are microbial load (n), sequential slice index (X), and contamination route dependent, which might limit their applications to certain conditions. However, the models may be further applied to predict the 3 or 4 log CFU level (and below) cross‐contamination of salami slicing process. Considering only few data are available in the literature regarding food pathogen surface transfer, the empirical models may provide a useful tool in building risk assessment procedures.     

Inactivation of Escherichia Coli O157:H7 and Salmonella Enterica on Blueberries in Water Using Ultraviolet Light

Ultraviolet light (UV) has antimicrobial effects, but the shadowing effect has limited its application. In this study, a novel setup using UV processing in agitated water was developed to inactivate Escherichia coli O157:H7 and Salmonella on blueberries. Blueberries were dip‐ or spot‐inoculated with E. coli or Salmonella. Blueberries inoculated with E. coli were treated for 2 to 10 min with UV directly (dry UV) or immersed in agitated water during UV treatment (wet UV). E. coli was most easily killed on spot‐inoculated blueberries with a 5.2‐log reduction after 10‐min wet UV treatment. Dip‐inoculated blueberries were the most difficult to be decontaminated with only 1.6‐log reduction after 10‐min wet UV treatment. Wet UV treatment generally showed higher efficacies than dry UV treatment, achieving an average of 1.4 log more reduction for spot‐inoculated blueberries. For dip‐inoculated blueberries, chlorine washing and UV treatments were less effective, achieving <2 log reductions of E. coli. Thus, the efficacy of combinations of wet UV with sodium dodecyl sulfate (SDS), levulinic acid, or chlorine was evaluated. Inoculated blueberries were UV‐treated while being immersed in agitated water containing 100 ppm SDS, 0.5% levulinic acid or 10 ppm chlorine. The 3 chemicals did not significantly enhance the wet UV treatment. Findings of this study suggest that UV treatment could be used as an alternative to chlorine washing for blueberries and potentially for other fresh produce.     

Effectiveness of ozone,heat and chlorine for destroying common food spoilage bacteria in synthetic media and biofilms†

Ozone, chlorine and heat applications were compared for killing effectiveness against food spoilage bacteria in synthetic broth. Fresh 24‐h bacterial cultures of Pseudomonas fluorescens (ATCC 948), Pseudomonas fragi (ATCC 4973), Pseudomonas putida (ATCC 795), Enterobacter aerogenes (ATCC 35028), Enterobacter cloacae (ATCC 35030) and Bacillus licheniformis (ATCC 14580) were exposed to ozone (0.6 ppm for 1 min and 10 min), chlorine (100 ppm for 2 min) or heat (77 ± 1°C for 5 min). One‐minute ozonation had little effect against the bacteria. There were significant differences (P < 0.05) among 10‐min ozonation, chlorine or heat inactivation of all bacteria exceptB. licheniformis. Ten‐minute ozonation caused the highest bacterial population reduction, with a mean reduction over all species of 7.3 log units followed by heat (5.4 log reduction) and chlorine (3.07 log reduction). Clean, passivated, sterile stainless steel (SS) metal coupons [2.54 × 2.54 cm², American Society for Testing Materials (ASTM) number 304] were incubated in ultra‐high temperature (UHT) sterile milk inoculated with P. fluorescens (ATCC 948), P. fragi (ATCC 4973) and P. putida (ATCC 795) for 24–72 h. After biofilm formation, the SS metal coupons were rinsed with phosphate‐buffered saline (1 min) and exposed to ozone (0.6 ppm for 10 min) and chlorine (100 ppm for 2 min). Results indicated that both ozone and chlorine significantly reduced the biofilm bacteria adhered to the SS metal coupons as compared to the control (P < 0.05). However, there was no significant difference (P > 0.05) between ozone and chlorine inactivation of the bacteria with the exception of P. putida. Ozone killed P. putida more effectively than chlorine.     

Inhibition of Listeria monocytogenes by Nisin Combined with Grape Seed Extract or Green Tea Extract in Soy Protein Film Coated on Turkey Frankfurters

The objective of this study was to evaluate the inhibitory effect of grape seed extract (GSE), green tea extract (GTE), nisin and their combinations (nisin with either GSE or GTE) against Listeria monocytogenes. The inhibitory effect of these natural compounds was evaluated in phosphate buffer solution (PBS) medium containing approximately 10⁹ colony‐forming units (CFU/mL) of L. monocytogenes. The effectiveness of these compounds in a meat model system was evaluated by surface inoculation (approximately 10⁶ CFU/g) of L. monocytogenes onto turkey frankfurters. The inoculated frankfurters were dipped into soy protein film‐forming solutions with and without the addition of antimicrobial agents (GSE 1% or GTE 1% or nisin 10000 IU or combinations). Samples were stored at either 4 °C or 10 °C. The inhibitory effects of edible coatings were evaluated on a weekly basis for 28 d. The greatest inhibitory effect was observed in the PBS medium containing GSE (1%) and nisin (10000 IU/mL), which caused a 9‐log cycle reduction of L. monocytogenes population after 3 h incubation at 37 °C. In the meat system, the L. monocytogenes population (7.1 CFU/g) was decreased by more than 2 log cycle after 28 d at 4 °C and 10 °C, in the samples containing nisin (10000 IU) combined with either GSE (1%) or GTE (1%). This research has demonstrated that the use of an edible film coating containing both nisin and natural extracts is a promising means of controlling the growth and recontamination of L. monocytogenes on ready‐to‐eat meat products.     

Effect of Hops Beta Acids on the Survival of Unstressed‐ or Acid‐Stress‐Adapted‐Listeria Monocytogenes and on the Quality and Sensory Attributes of Commercially Cured Ham Slices

This study evaluated the antilisterial activity of hops beta acids (HBA) and their impact on the quality and sensory attributes of ham. Commercially cured ham slices were inoculated with unstressed‐ and acid‐stress‐adapted (ASA)‐L. monocytogenes (2.2 to 2.5 log CFU/cm²), followed by no dipping (control), dipping in deionized (DI) water, or dipping in a 0.11% HBA solution. This was followed by vacuum or aerobic packaging and storage (7.2 °C, 35 or 20 d). Samples were taken periodically during storage to check for pH changes and analyze the microbial populations. Color measurements were obtained by dipping noninoculated ham slices in a 0.11% HBA solution, followed by vacuum packaging and storage (4.0 °C, 42 d). Sensory evaluations were performed on ham slices treated with 0.05% to 0.23% HBA solutions, followed by vacuum packaging and storage (4.0 °C, 30 d). HBA caused immediate reductions of 1.2 to 1.5 log CFU/cm² (P < 0.05) in unstressed‐ and ASA‐L. monocytogenes populations on ham slices. During storage, the unstressed‐L. monocytogenes populations on HBA‐treated samples were 0.5 to 2.0 log CFU/cm² lower (P < 0.05) than control samples and those dipped in DI water. The lag‐phase of the unstressed‐L. monocytogenes population was extended from 3.396 to 7.125 d (control) to 7.194 to 10.920 d in the HBA‐treated samples. However, the ASA‐L. monocytogenes population showed resistance to HBA because they had a higher growth rate than control samples and had similar growth variables to DI water‐treated samples during storage. Dipping in HBA solution did not adversely affect the color or sensory attributes of the ham slices stored in vacuum packages. These results are useful for helping ready‐to‐eat meat processors develop operational procedures for applying HBA on ham slices.     

Effects of Zataria multiflora boiss essential oil,ultraviolet radiation and their combination on Listeria monocytogenes biofilm in a simulated industrial model

The objective of this study was to investigate the inhibitory effect of Zataria multiflora boiss essential oils (ZEOs), ultraviolet (UV) radiation and their combination against Listeria monocytogenes biofilm in a simulated industrial model (SIM). The effect of minimal inhibitory concentration (MIC) and sub‐MIC concentration of ZEOs, different contact time of UV and their combination was evaluated in a SIM on 6‐ and 12‐day‐old L. monocytogenes biofilm. In a SIM, 0.3% ZEOs were adequate to completely eliminate 6‐ and 12‐day‐old biofilm grown on stainless steel coupons. The population of viable L. monocytogenes biofilm cells under a 15‐ to 45‐min contact time of UV treatment declined significantly at 6‐ and 12‐day‐old biofilm. The combined effect of ZEO and UV showed antagonist effects. These findings indicated that in the single use, ZEO and UV revealed a suitable antilisteria biofilm activity, while combining them is not a promising method to remove listeria biofilms from stainless steel surfaces.     

Bactericidal Activity of Aqueous Chlorine and Chlorine Dioxide Solutions in a Fish Model System

A commercial ClO₂-producing solution killed mostly Escherichia coli, Listeria monocytogenes Scott A and its streptomycin-resistant (Str^R) strain at 15, 10, and 7.5 ppm, respectively, while aqueous ClO₂ and chlorine achieved similar results against the tested strains at 20 and 25 ppm, respectively. Aqueous ClO₂ and the commercial solution were more effective than aqueous chlorine in killing Str^R-L. monocytogenes inoculated on fish cubes (mangrove snapper) at 3.4 × 10³ or 2.4 × 10⁶ CFU/g, as well as in solutions washed off the cubes. Fish cubes treated with aqueous chlorine or ClO₂ contained negligible chlorine residues, while the commercial treatment samples contained chlorite and some free and combined available chlorine.     

Predictive Modeling of the Effect of ε‐Polylysine Hydrochloride on Growth and Thermal Inactivation of Listeria monocytogenes in Fish Balls

This study aimed to evaluate the effect of ε‐polylysine hydrochloride (ε‐PLH) on the growth and thermal inactivation kinetics of Listeria monocytogenes in fish balls. Samples, supplemented with ε‐PLH (0, 150, or 300 ppm, w/w), were inoculated with a three‐strain cocktail of L. monocytogenes and incubated at constant temperatures of 3.4, 8, 12, or 16 °C for growth studies, or heated at 60, 62.5, 65, or 67.5 °C for thermal inactivation tests. The growth curves were fitted to the Huang primary model, and the Huang and Ratkowsky square‐root models (SRM) were used as the secondary models to evaluate the effect of temperature on bacterial growth. The survival during heating was analyzed with a log‐linear model. The results showed that, while the lag time of L. monocytogenes was affected by both ε‐PLH concentration and temperature, the specific growth rate was unaffected by ε‐PLH. Under the same temperature, a 10‐time in increase of the lag time would be expected for every 565 ppm in the increase of ε‐PLH concentration. Using the Ratkowsky SRM, the estimated nominal minimum growth temperature was –2.04 °C, while the minimum growth temperature was 0.29 °C when estimated with the Huang SRM. Validation at 10 °C showed that the Huang primary model, in combination with either the Huang or Ratkowsky SRM, could accurately predict the growth of L. monocytogenes. On the other hand, the thermal resistance of the pathogen was significantly reduced by increase in temperature or ε‐PLH. The thermal z value of L. monocytogenes was 5.78 °C, and the ε‐PLH z value was 1642 ppm. The results of this study showed that the combined application of ε‐PLH and temperature can be used to control L. monocytogenes in fish balls and to improve food safety and reduce risks to public health.     

The effects of various disinfectants againstListeria monocytogeneson fresh-cut vegetables

Demand for fresh, healthier convenience-type foods has stimulated sales of fresh-cut vegetables in North America. As part of an overall program to better define the microbiological safety of these products, studies were done to examine the effects of various disinfectants againstListeria monocytogeneson fresh-cut vegetables. Some of the more established disinfectants such as chlorine and chlorine dioxide, as well as some of the newer ones including Salmide^Rand trisodium phosphate were tested againstL. monocytogeneson lettuce and cabbage. Different exposure times, as well as concentrations of the disinfectants were evaluated. In addition, organic acids such as lactic and acetic were examined for their ability to inactivateL. monocytogenespresent on the surface of vegetables. Chlorine was also tested in combination with the organic acids and various surfactants. For chlorine (200ppm, 10min), the maximum observed log₁₀reduction ofL. monocytogenesat 4 and 22°C, respectively, was 1.3 and 1.7 for lettuce and 0.9 and 1.2 for cabbage. Chlorine dioxide treatment (5ppm, 10min) of lettuce and cabbage at 4 and 22°C, respectively, resulted in a maximum observed log₁₀reduction ofL. monocytogenesof 1.1 and 0.8 for lettuce and 0.4 and 0.8 for cabbage. In comparison, the highest levels of Salmide^Rused on cabbage and lettuce (200ppm) at 22°C led to maximum reductions of 1.8 and 0.6 logs, respectively. None of the surfactants tested improved the disinfectant efficiency of chlorine, and actually proved to be antagonistic. Trisodium phosphate had almost no effect on reducing numbers ofL. monocytogenes, at levels that did not affect the organoleptic quality of lettuce. Lactic acid proved to be more effective than acetic acid in reducing numbers ofL. monocytogenes, although maximum reductions of only 0.5 and 0.2 logs were observed after a 10min exposure to 1% solutions of each organic acid. In general, therefore, one can expect approximately a 1log reduction in numbers ofL. monocytogenes, regardless of the disinfectant used.     

Inactivation of Escherichia coli O157:H7, Salmonella typhimurium,and Listeria monocytogenes on Stored Iceberg Lettuce by Aqueous Chlorine Dioxide Treatment

ABSTRACT: Inactivation of Escherichia coli O157:H7, Salmonella typhimurium, and Listeria monocytogenes in iceberg lettuce by aqueous chlorine dioxide (ClO₂) treatment was evaluated. Iceberg lettuce samples were inoculated with approximately 7 log CFU/g of E. coli O157:H7, S. typhimurium, and L. monocytogenes. Iceberg lettuce samples were then treated with 0, 5, 10, or 50 ppm ClO₂ solution and stored at 4 °C. Aqueous ClO₂ treatment significantly decreased the populations of pathogenic bacteria on shredded lettuce (P < 0.05). In particular, 50 ppm ClO₂ treatment reduced E. coli O157:H7, S. typhimurium, and L. monocytogenes by 1.44, 1.95, and 1.20 log CFU/g, respectively. The D₁₀‐values of E. coli O157:H7, S. typhimurium, and L. monocytogenes in shredded lettuce were 11, 26, and 42 ppm, respectively. The effect of aqueous ClO₂ treatment on the growth of pathogenic bacteria during storage was evaluated, and a decrease in the population size of these pathogenic bacteria was observed. Additionally, aqueous ClO₂ treatment did not affect the color of lettuce during storage. These results suggest that aqueous ClO₂ treatment can be used to improve the microbial safety of shredded lettuce during storage.     

Predictive Modeling for Growth of Non‐ and Cold‐adapted Listeria monocytogenes on Fresh‐cut Cantaloupe at Different Storage Temperatures

The aim of this study was to determine the growth kinetics of Listeria monocytogenes, with and without cold‐adaption, on fresh‐cut cantaloupe under different storage temperatures. Fresh‐cut samples, spot inoculated with a 4‐strain cocktail of L. monocytogenes (～3.2 log CFU/g), were exposed to constant storage temperatures held at 10, 15, 20, 25, or 30 °C. All growth curves of L. monocytogenes were fitted to the Baranyi, modified Gompertz, and Huang models. Regardless of conditions under which cells grew, the time needed to reach 5 log CFU/g decreased with the elevated storage temperature. Experimental results showed that there were no significant differences (P > 0.05) in the maximum growth rate k (log CFU/g h^?1) and lag phase duration λ (h) between the cultures of L. monocytogenes with or without previous cold‐adaption treatments. No distinct difference was observed in the growth pattern among 3 primary models at various storage temperatures. The growth curves of secondary modeling were fitted on an Arrhenius‐type model for describing the relationship between k and temperature of the L. monocytogenes on fresh‐cut cantaloupe from 10 to 30 °C. The root mean square error values of secondary models for non‐ and cold‐adapted cells were 0.018, 0.021, and 0.024, and 0.039, 0.026, and 0.017 at the modified Gompertz, Baranyi, and Huang model, respectively, indicating that these 3 models presented the good statistical fit. This study may provide valuable information to predict the growth of L. monocytogenes on fresh‐cut cantaloupes at different storage conditions.     

Susceptibility of Listeria monocytogenes strains to disinfectants and chlorinated alkaline cleaners at cold temperatures

Minimal inhibitory concentration (MIC), suspension and biofilm tests were used in evaluating the disinfecting efficacy of eight commercially available disinfectants and four chlorinated alkaline cleaners against 10 strains of Listeria monocytogenes at refrigerated temperatures. The adaptive response and cross-adaptation of L. monocytogenes to the disinfectants and chlorinated alkaline cleaners were investigated. The bactericidal components in the agents used were chlorine, quaternary ammonium compound (QAC), peracetic acid, ethanol and isopropanol. With some exceptions the disinfectants were efficient against the L. monocytogenes strains. One alkaline hypochlorite containing disinfectant was not efficient in the suspension and MIC tests at the lowest concentration recommended by the manufacturer. The chlorinated alkaline cleaners were effective against L. monocytogenes. A QAC-based disinfectant was found to be the least-effective agent on both glass bead-blasted polyethylene and stainless-steel surfaces. Adaptive and cross-adaptive responses of L. monocytogenes strains were observed towards the QAC-based agent, but over 2-fold increases to other agents were not observed. These results suggest that the adaptive responses of L. monocytogenes to disinfectants or chlorinated alkaline cleaners are of a minor concern.     

Reduction of Listeria monocytogenes in cold‐smoked salmon by bacteriophage P100, nisin and lauric arginate,singly or in combinations

Three GRAS antimicrobials including, lauric arginate (LAE), bacteriophage P100 (phage P100) and bacteriocin nisin, were evaluated either singly or in combinations for the reduction of initial load of Listeria monocytogenes in cold‐smoked salmon (CSS). The stability of phage P100 in the presence of LAE (200 ppm) and nisin (500 ppm) or at 10× and 100× of these concentrations was determined at 4 °C or 30 °C for 24 h in a broth model. Phage P100 was found to be highly stable in the presence of these antimicrobial agents as plaque‐forming units (PFU) did not vary between control and antimicrobial‐treated phage. The survival of L. monocytogenes in the presence of phage P100, nisin and LAE showed remarkable reduction within 24 h both at 4 °C or 30 °C in broth. Treatment of CSS containing 3.5 log CFU cm^?2 L. monocytogenes with phage P100 (10⁸ PFU mL^?1), nisin (500 ppm) and LAE (200 ppm) showed strong listericidal action and reduced the L. monocytogenes by 2–3 log CFU cm^?2 after 24 h. Among the combined treatments, phage P100 + LAE or nisin + LAE exhibited the most listericidal action in which L. monocytogenes cells were reduced to undetectable level within 24 h in CSS.     

Efficacy of Combined Sous Vide‐Microwave Cooking for Foodborne Pathogen Inactivation in Ready‐to‐Eat Chicory Stems

There is a variety of different food processing methods, which can be used to prepare ready‐to‐eat foods. However, the need to preserve the freshness and nutritional qualities leads to the application of mild technologies which may be insufficient to inactivate microbial pathogens. In this work, fresh chicory stems were packed under a vacuum in films, which were transparent to microwaves. These were then exposed to microwaves for different periods of time. The application of sous vide microwave cooking (SV‐MW, 900 W, 2450 MHz), controlled naturally occurring mesophilic aerobic bacteria, yeasts and molds for up to 30 d when vacuum‐packed vegetables were stored at 4 °C. In addition, the process lethality of the SV‐MW 90 s cooking was experimentally validated. This treatment led to 6.07 ± 0.7 and 4.92 ± 0.65 log cfu/g reduction of Escherichia coli and Listeria monocytogenes inoculated over the chicory stems (100 g), respectively. With an initial load of 9 log cfu/g for both pathogens, less than 10 cfu/g of surviving cells were found after 90 s cooking. This shows that short‐time microwave cooking can be used to effectively pasteurize vacuum‐packed chicory stems, achieving >5 log cfu/g reduction of E. coli and L. monocytogenes.     

Effects of Antimicrobial Coatings and Cryogenic Freezing on Survival and Growth of Listeria innocua on Frozen Ready‐to‐Eat Shrimp during Thawing

Foodborne pathogens such as Listeria monocytogenes could pose a health risk on frozen ready‐to‐eat (RTE) shrimp as the pathogen could grow following thawing. In this study, antimicrobial‐coating treatments alone, or in combination with cryogenic freezing, were evaluated for their ability to inhibit the growth of Listeria innocua, a surrogate for L. monocytogenes, on RTE shrimp. Cooked RTE shrimp were inoculated with L. innocua at 3 population levels and treated with coating solutions consisting of chitosan, allyl isothiocyanate (AIT), or lauric arginate ester (LAE). The treated shrimp were then stored at –18 °C for 6 d before being thawed at 4, 10, or 22 °C for either 24 or 48 h. Results revealed that antimicrobial coatings achieved approximately 5.5 to 1 log CFU/g reduction of L. innocua on RTE shrimp after the treatments, depending on the inoculated population levels. The coating‐treated shrimp samples had significantly (P < 0.05) less L. innocua than controls at each thawing temperature and time. Cryogenic freezing in combination with coating treatments did not achieve synergistic effects against L. innocua. Antimicrobial coatings can help to improve product safety by reducing Listeria on RTE shrimp.     

COMPUTER‐CONTROLLED MICROWAVE HEATING TO IN‐PACKAGE PASTEURIZE BEEF FRANKFURTERS FOR ELIMINATION OF LISTERIA MONOCYTOGENES†

The objective of this study was to develop an in‐package pasteurization technology to kill Listeria monocytogenes in ready‐to‐eat meats using microwave heating. This technology utilized an infrared sensor to monitor the surface temperature of beef frankfurters during microwave heating. The aim was to increase the surface temperature of frankfurters to a set point lethal to L. monocytogenes. A feedback control mechanism was used to control the power to the microwave oven. Results indicated that the simple on‐off control mechanism was able to maintain the surface temperature of beef frankfurters near the respective set points of 75, 80 or 85C used in this study. This pasteurization process was able to achieve a 7‐log reduction of L. monocytogenes in inoculated beef frankfurters using a 600‐W nominally rated microwave oven within 12–15 min. If optimized, this system may provide the food industry with a terminal, postlethality pasteurization technology to kill L. monocytogenes in ready‐to‐eat meats within the final packages.     

D and z Values of Salmonella, Listeria innocua, and Listeria monocytogenes in Fully Cooked Poultry Products

: The D and z values of Salmonella, Listeria innocua, and Listeria monocytogenes were obtained for different ready‐to‐eat poultry products, including chicken, turkey, and duck. The D values of Salmonella, L. innocua, and L. monocytogenes were 151.5 to 0.1 min at 55 to 70°C, and the z values of Salmonella, L. innocua, and L. monocytogenes were 4.9 to 7.0 °C. Significant differences were found for the heat resistance of Salmonella, L. innocua, and L. monocytogenes among turkey, duck, and chicken products, indicating that the kinetic values of a certain pathogen in a specific product should be used for determining process lethality in fully cooked and vacuum‐packaged poultry products during post‐cook heat treatments.     

Combined Effect of Thermosonication and Slightly Acidic Electrolyzed Water to Reduce Foodborne Pathogens and Spoilage Microorganisms on Fresh‐cut Kale

This study evaluated the efficacy of individual treatments (thermosonication [TS+DW] and slightly acidic electrolyzed water [SAcEW]) and their combination on reducing Escherichia coli O157:H7, Listeria monocytogenes, and spoilage microorganisms (total bacterial counts [TBC], Enterobacteriaceae, Pseudomonas spp., and yeast and mold counts [YMC]) on fresh‐cut kale. For comparison, the antimicrobial efficacies of sodium chlorite (SC; 100 mg/L) and sodium hypochlorite (SH; 100 mg/L) were also evaluated. Each 10 g sample of kale leaves was inoculated to contain approximately 6 log CFU/g of E. coli O157:H7 or L. monocytogenes. Each inoculated or uninoculated samples was then dip treated with deionized water (DW; control), TS+DW, and SAcEW at various treatment conditions (temperature, physicochemical properties, and time) to assess the efficacy of each individual treatment. The efficacy of TS+DW or SAcEW was enhanced at 40 °C for 3 min, with an acoustic energy density of 400 W/L for TS+DW and available chlorine concentration of 5 mg/L for SAcEW. At 40 °C for 3 min, combined treatment of thermosonication 400 W/L and SAcEW 5 mg/L (TS+SAcEW) was more effective in reducing microorganisms compared to the individual treatments (SAcEW, SC, SH, and TS+DW) and combined treatments (TS+SC and TS+SH), which significantly (P < 0.05) reduced E. coli O157:H7, L. monocytogenes, TBC, Enterobacteriaceae, Pseudomonas spp., and YMC by 3.32, 3.11, 3.97, 3.66, 3.62, and >3.24 log CFU/g, respectively. The results suggest that the combined treatment of TS+SAcEW has the potential as a decontamination process in fresh‐cut industry.     

USE OF A CONTROLLED CHLORINE DIOXIDE (CLO2) RELEASE SYSTEM IN COMBINATION WITH MODIFIED ATMOSPHERE PACKAGING (MAP) TO CONTROL THE GROWTH OF PATHOGENS

ABSTRACT

Salmonella Typhimurium and Listeria monocytogenes are major bacterial pathogens associated with poultry products. A controlled released ClO₂ sachet applied with modified atmosphere packaging (MAP) was evaluated for its ability to control the growth of S. Typhimurium and L. monocytogenes on raw chicken breast during refrigerated storage. The fresh chicken samples were inoculated with one or the other of the pathogens at 10⁴ cfu/g, and the packages (with and without ClO₂ sachet) were flushed with ambient air or 30% CO₂/70% N₂ before sealing, and then stored at 4C for up to 21 days. The maximum reduction in MAP plus ClO₂ (compared with MAP alone) was 0.68 log cfu/g for S. Typhimurium and 1.87 log cfu/g for L. monocytogenes. Color and pH changes of the chicken breast were observed at 8 µg/h of ClO₂ during the storage period.

PRACTICAL APPLICATIONS

We think that the results of the study with the combined treatment of chlorine dioxide (ClO₂) and modified atmosphere packaging may enhance the effectiveness of antimicrobials, reduce the amount of agent needed, and decrease the risk of off‐flavors. The applications of the results will be useful for poultry industry to give the significant improvement in shelf life for packaged fresh products.     

Bactericidal activity of lauric arginate in milk and Queso Fresco cheese against Listeria monocytogenes cold growth

Lauric arginate (LAE) at concentrations of 200 ppm and 800 ppm was evaluated for its effectiveness in reducing cold growth of Listeria monocytogenes in whole milk, skim milk, and Queso Fresco cheese (QFC) at 4°C for 15 to 28 d. Use of 200 ppm of LAE reduced 4 log cfu/mL of L. monocytogenes to a nondetectable level within 30 min at 4°C in tryptic soy broth. In contrast, when 4 log cfu/mL of L. monocytogenes was inoculated in whole milk or skim milk, the reduction of L. monocytogenes was approximately 1 log cfu/mL after 24 h with 200 ppm of LAE. When 800 ppm of LAE was added to whole or skim milk, the initial 4 log cfu/mL of L. monocytogenes was nondetectable following 24 h, and no growth of L. monocytogenes was observed for 15 d at 4°C. With surface treatment of 200 or 800 ppm of LAE on vacuum-packaged QFC, the reductions of L. monocytogenes within 24 h at 4°C were 1.2 and 3.0 log cfu/g, respectively. In addition, the overall growth of L. monocytogenes in QFC was decreased by 0.3 to 2.6 and by 2.3 to 5.0 log cfu/g with 200 and 800 ppm of LAE, respectively, compared with untreated controls over 28 d at 4°C. Sensory tests revealed that consumers could not determine a difference between QFC samples that were treated with 0 and 200 ppm of LAE, the FDA-approved level of LAE use in foods. In addition, no differences existed between treatments with respect to flavor, texture, and overall acceptability of the QFC. Lauric arginate shows promise for potential use in QFC because it exerts initial bactericidal activity against L. monocytogenes at 4°C without affecting sensory quality.