Effect of Different Pre-Growth Temperatures on the Survival Kinetics of Salmonella enterica and Listeria monocytogenes in Fresh-Cut Salad during Refrigerated Storage

The effect of the pre-growth temperature of bacterial cultures on their subsequent survival kinetics in fresh-cut produce during refrigerated storage was investigated in this study. Three-strain cocktails of Listeria monocytogenes and Salmonella enterica, cultured at different growth temperatures (4, 21, and 37 °C) were inoculated on fresh-cut mixed salad and on individual produce in the mixed salad. The inoculated samples were stored at 4 °C and 80 ± 2% relative humidity (RH) for up to 72 h and the growth, survival, or death kinetics were determined at regular intervals. The results indicate that depending upon the type of pathogen tested, the pre-growth temperature(s) and the type of produce showed a significant (p ≤ 0.05) effect on the survival kinetics. Among the tested produce, mixed salad showed the highest reduction in L. monocytogenes pre-grown at 37 °C (1.33 log CFU/g) followed by red cabbage (0.56 log CFU/g), iceberg lettuce (0.52 log CFU/g), and carrot (−0.62 log CFU/g), after 72 h, respectively. In the case of Salmonella, carrot showed the highest reduction (1.07 log CFU/g for 37 °C pre-grown culture) followed by mixed salad (0.78 log CFU/g for 37 °C pre-grown culture), cabbage (0.76 log CFU/g for 21 °C pre-grown culture), and lettuce (0.65 log CFU/g for 4 °C pre-grown culture), respectively. Among the tested ComBase predictive models, the Baranyi–Roberts model better fitted the experimental data. These findings indicate that the appropriate selection of pre-growth environmental conditions is critical to better understand the kinetics of foodborne pathogens

Pre-Growth Environmental Stresses Affect Foodborne Pathogens Response to Subsequent Chemical Treatments

Foodborne pathogens such as Salmonella, E. coli O157:H7, and Listeria monocytogenes are known to survive under different environmental stresses with an effect on their physiological properties. The purpose of this study was to determine the effect of different environmental stresses on the foodborne pathogens response to subsequent chemical treatments. Three types of pathogens Salmonella, E. coli O157:H7, and Listeria monocytogenes were subjected to different environmental stresses: (i) Desiccation (ii) high salt (iii) low pH, and (iv) temperatures (14, 23, and 37 °C) during their growth. The cells harvested at their early stationary growth phase were subsequently subjected to chlorine (100 or 200 ppm), peracetic acid (40 or 80 ppm), and 0.5% lactic acid treatments. The results showed that pre-growth stress conditions have significant effect on the reduction of tested pathogens depending upon the type of chemical treatment. Salmonella showed the highest sensitivity against all these treatments when compared to E. coli O157:H7 and Listeria monocytogenes. In addition, Listeria monocytogenes showed the highest percentage of sub-lethally injured cells. These findings highlighted the need to consider pre-growth conditions as an important factor for the validation of physical and chemical intervention treatments

Effect of ultraviolet light treatment on microbiological safety and quality of fresh produce: An overview

Fresh and fresh-cut fruits and vegetables have been associated in several foodborne illness outbreaks. Although investigations from those outbreaks reported that the contamination with pathogenic microorganisms may occur at any point in the farm to fork continuum, effective control strategies are still being widely investigated. In that direction, the concept of hurdle technology involving a sequence of different interventions have been widely explored. Among those interventions, ultraviolet (UV) light alone or in combination with other treatments such as use of organic acids or sanitizer solutions, has found to be a promising approach to maintain the microbiological safety and quality of fresh and fresh-cut produce. Recent advances in using UV as a part of hurdle technology on the safety of fresh produce at different stages are presented here. Furthermore, this review discusses the mechanism of UV induced antimicrobial activity, factors that influence antimicrobial efficacy and its effect on produce. In addition, the challenges, and prospects of using UV irradiation as an intervention treatment were also discussed

Photocatalytic TiO2 coating of plastic cutting board to prevent microbial cross-contamination

Kitchen cutting boards are one common source of microbial cross-contamination in foods. In this study, a method was developed to create an antimicrobial coating on HDPE cutting board using UV-activated TiO2 nanoparticles (NPs). The antimicrobial efficacy of the developed coatings was tested against E. coli O157: H7 for 3 h at 0.5 ± 0.05 mW/cm2 UVA light intensity. In addition, the effect of NP loading (0.0125, 0.0625, and 0.125 mg/cm2), and surface treatment of coatings by oxygen plasma for 1–15 min on the bactericidal efficacy was investigated. Further, the bactericidal efficacy of the TiO2 coated cutting board on repeated use (i.e. 1, 2, 3 and 5 times) was also evaluated. The results showed that by increasing the NP loading from 0 to 0.125 mg/cm2 has increased the log reduction from 0.37 to 1.18 CFU/cm2. However, no significant difference (P \u3e 0.05) in the reduction was observed between NP loadings at 0.0625 and 0.125 mg/cm2. Oxygen plasma treatment of the coated surfaces for 5–15 min significantly increased (P ≤ 0.05) the log reduction compared to control sample without plasma treatment. Under the tested conditions, TiO2 coating with 0.0625 mg/cm2 NP loading followed by oxygen plasma treatment for 5 min was found to achieve the greatest reduction up to 2.67 log CFU/cm2. Also, the coated-surfaces were found to retain the original bactericidal property even after up to 5 times washing treatment. The developed TiO2 coating on cutting board showed promise to mitigate the risk of microbial cross-contamination by providing a stable antimicrobial activity for extended use. Plasma treatment further enhanced the bactericidal property of the developed coatings without affecting physical stability

Effect of binder on the physical stability and bactericidal property of titanium dioxide (TiO2) nanocoatings on food contact surfaces

TiO2 is a promising photocatalyst for use in food processing environment as an antimicrobial coating. The purpose of this study was to determine the effect of different binding agents on the physical stability and bactericidal property of TiO2 nanocoatings created on stainless steel surfaces. A total of six different coating suspensions were prepared by mixing TiO2 (Aeroxide® P-25) nanoparticles (NPs) with three different types of binders (Shellac (A), polyuretahne (B), and polycrylic (C)) at a 1:4 to 1:16 NP to binder weight ratio. Bactericidal activity of these TiO2 coatings against Escherichia coli O157:H7 (5-strain) was determined at three different UV-A light intensities (0.25, 0.50 and 0.75 mW/cm2) for 3 h. The type of binder used in the coating had a significant effect on the log reduction of E. coli O157:H7. TiO2 coatings with binder C showed highest reduction (\u3e4 log CFU/cm2) followed by TiO2 coating with binder B and A. Increasing the binder concentration in the formulation from a 1:4 to 1:16 weight ratio decreased the log reduction of E. coli O157:H7. Increasing the UV-A light intensity from 0.25 to 0.75 mW/cm2 increased the log reduction of bacteria for all the TiO2 coatings. The physical stability of the TiO2 coatings was determined using ASTM procedures. TiO2 coatings with binder B showed highest adhesion strength and scratch hardness when compared to coatings with other binders. However, on repeated use experiments (1, 3, 5, and 10 times), TiO2 coatings with binder C were found to be physically more stable and able to retain their original bactericidal property. The results of this study showed promise in developing durable TiO2 coatings with strong photocatalytic bactericidal property on food contact surfaces using appropriate binding agents to help ensure safe food processing environment

Effect of pecan variety and the method of extraction on the antimicrobial activity of pecan shell extracts against different foodborne pathogens and their efficacy on food matrices

The shells of pecans are a rich source of bioactive compounds with potential inhibitory activity against various pathogenic microorganisms. This study investigated the antimicrobial activity of pecan shell extracts as effected by the type of cultivar and the method of extraction against various foodborne bacterial pathogens. Defatted shell powders of 19 different pecan cultivars were subjected to aqueous and ethanolic extraction (1:20 w/v) procedures, respectively. The minimum inhibitory concentration (MIC) and minimum bactericidal concentration (MBC) of lyophilized pecan shell extracts dissolved in deionized water containing 5% DMSO (v/v) were determined against multiple strains of Listeria monocytogenes, Salmonella enterica, and Escherichia coli O157:H7. The antimicrobial activity of pecan shell extracts was found to be pathogen specific and strain dependent. Overall, L. monocytogenes was found to be least resistant to treatment with pecan shell extracts with an MIC and/or MBC values ranging from 1.25 to 5 mg/mL followed by Salmonella enterica (2.5 to ≥5 mg/mL) and E. coli O157:H7 (≥5 mg/mL). Type of cultivar and the method of extraction found to have a variable effect on the antimicrobial activity. Furthermore, the challenge studies on fresh-cut cantaloupes and thawed catfish fillets treated with 5 mg/mL pecan shell extracts and stored at 4 °C for up to 5 days showed aL. monocytogenes when compared to the controls with no treatment. No significant change in the color quality of treated food samples was observed with pecan shell extract treatment. The results of this study showed promise to use pecan shell extracts as a natural antimicrobial agent to inhibit the growth of tested foodborne bacterial pathogens

Analysis of Sanitizer Rotation on the Susceptibility, Biofilm Forming Ability and Caco-2 Cell Adhesion and Invasion of Listeria

The purpose of this study was to determine the effect of sanitizer use conditions on the susceptibility, biofilm forming ability and pathogenicity of Listeria monocytogenes. Two different strains of L. monocytogenes and a non-pathogenic L. innocua were exposed to sodium hypochlorite, benzalkonium chloride and peroxyacetic acid at different concentrations (4 to 512 ppm) and treatment times (30 s to 5 min), respectively. Under the tested conditions, no significant difference (p \u3e 0.05) in reduction was observed among the three tested sanitizers. A reduction of 1 to 8 log CFU/mL was observed depending upon the sanitizer concentration and treatment times. The survived cells at the highest sublethal concentration and treatment time of a particular sanitizer upon re-exposure to the same or different sanitizer showed either no change or increased susceptibility when compared to parent strains. Upon repeated exposure to sanitizers at progressively increasing concentrations from 1 to 128 ppm, L. innocua was able to survive concentrations of up to 32 ppm benzalkonium chloride and 64 ppm peroxyacetic acid treatments, respectively. At the tested sub-lethal concentrations, no significant difference (p \u3e 0.05) in biofilm formation was observed among the tested strains. Caco-2 interaction with L. innocua showed a reduction in invasion ability with sublethal concentrations of sanitizers

Antioxidant Properties of Pecan Shell Bioactive Components of Different Cultivars and Extraction Methods

Pecan shells are a rich source of various bioactive compounds with potential antioxidant and antimicrobial properties. This study investigated the effect of pecan variety and method extraction on the antioxidant property of shell extracts. Twenty different varieties of pecan shells were subjected to either aqueous or ethanolic extraction and were examined for total phenolics and antiradical activity. The phenolic content and antiradical activity of shell extracts were significantly (p \u3c 0.05) varied with different pecan cultivars. The total phenolic content of ethanol extracts ranged from 304.2 (Caddo) to 153.54 (Cherokee) mg GAE/g of dry extract and was significantly greater (p \u3c 0.05) than those obtained by aqueous extraction. The antiradical activity of ethanol extracts ranged from 840.6 (Maramec) to 526.74 (Caper Fear) mg TEg−1, while aqueous extracts ranged from 934.9 (Curtis) to 468.3 (Elliot) mg TEg−1. Chemical profiling of the crude and acid hydrolyzed extracts was performed by reverse phase high performance liquid chromatography and flow injection electrospray ionization mass spectrometry. Lignin degradation products such as lignols, dilignols, trilignols, and oligolignols were found to be the major components of tested extracts. Phenolic content and antiradical activity of pecan shell extracts are significantly varied with cultivars and methods of extraction

Hot water treatment as a kill-step to inactivate Escherichia coli O157:H7, Salmonella enterica, Listeria monocytogenes and Enterococcus faecium on in-shell pecans

In-shell pecans are susceptible to microbial contamination. This study was performed to investigate feasibility of using hot water treatment as a kill-step for food-borne pathogens during pecan shelling. In-shell pecans were subjected to hot water at 70, 80 or 90 °C for 1, 2, 3, 4 or 5 min. The time-temperature treatments to achieve a 5-log reduction of Salmonella enterica, Escherichia coli O157:H7, Listeria monocytogenes, and non-pathogenic Enterococcus faecium were determined. Thermal death values were determined for each tested condition. L. monocytogenes was most susceptible to heat treatment and were reduced by 4.6 ± 0.35 log CFU/g at 70 °C for 5 min, while 3–5 min at 80 and 90 °C treatments was required to achieve a similar reduction level for S. enterica, E. coli O157:H7, and E. faecium. S. enterica were most resistant and required 4 min treatment time to achieve a 5-log reduction at 80 and 90 °C. The D-values ranged from 1.15 to 1.72, 0.83 to 1.19, and 0.41–0.92 min at 70, 80 and 90 °C, respectively. E. faecium had the highest D-value (1.72 min at 70 °C), indicating a potential surrogate for process validation for pecan industries. Utilizing proper hot water treatment during pecan shelling could reduce food safety risk

Effect of hot water treatment of in-shell pecans on physicochemical properties and consumer acceptability of roasted pecan kernels

The effect of hot water pre-treatment of in-shell pecans on physicochemical properties, consumer acceptance and purchase intent of dehulled and roasted kernels was evaluated. In-shell pecans were first subjected to hot water at 70, 80 and 90 °C for 8.6, 6.6 and 4.6 min respectively and kernels were later dry roasted at 160 °C for 10 min. The physicochemical properties of hot water treated and untreated nuts, before and after roasting were determined. Furthermore, consumer acceptance and purchase intent of the roasted kernels were determined. Hot water treatment, alone and subsequent roasting had minimal effect on pecans’ physicochemical properties. Consumers liked (P \u3c 0.05) the colour and aroma of treated pecans. No effect (P \u3e 0.05) of pre-treatment was observed on the acceptability of other sensory attributes. Safety claim increased treated pecans’ overall liking; however, it decreased purchase intent. Hot water treatment showed promise as a post-harvest microbial intervention strategy without affecting the physicochemical properties and consumer acceptability