The occurrence of indicator bacteria on hands and aprons of food handlers in the delicatessen sections of a retail group

Despite an increase in the number of food handlers receiving food hygiene training, a high number of food poisoning outbreaks still occur as a result of improper food handling practices in the retail industry. In this study, samples were collected from the hands and aprons of food handlers in the delicatessen sections of a prominent South African retail group and analysed for the presence of total viable counts (TVC), total coliforms, Escherichia coli, members of the family Enterobacteriaceae and Staphylococcus aureus in order to assess the levels of contamination and to establish possible relationships. Noteworthy TVC were present on 98% of hands and 84% of aprons sampled and conformed to the national standard of 1 × 10² cfu cm⁻² without exception. Coliforms were present on 40% of food handler’s hands and on 26% of aprons and when compared to the literature which suggests a target value of <2.5 cfu cm⁻², 32% of food handlers exceeded the target with regard to hands and 8% with regard to aprons. E. coli was found to only exceed the limit in the case of one food handler. Enterobacteriaceae were present on the hands of food handlers (44%) and on aprons (16%), ranging between 5 and 1.8 × 10¹ cfu cm⁻² on hands and between 5 and 2.9 × 10¹ cfu cm⁻² on aprons. S. aureus counts were present on 88% of hands and 48% of aprons and ranged between negligible and 9.8 × 10¹ cfu cm⁻² for hands and up to 6.2 × 10¹ cfu cm⁻² for aprons. No significant statistical correlation occurred between the organisms on hands and aprons, indicating that the latter were not likely to be cross-contaminated by hands.     

Synthesis,characterization and comparative study of nano-Ag–TiO2 against Gram-positive and Gram-negative bacteria under fluorescent light

Currently, some of the major problems affecting the world are air pollution as well as microbial contamination. Every time we breathe, we are risking our lives by inhaling dangerous chemicals and biological contaminants that have found their way into the air. Therefore this work focuses on the antibacterial activity of Ag–TiO₂ to overcome the microbial contaminant and infectious disease. Ag–TiO₂ nanosolution were synthesized by sol–gel method and found to be an effective visible light driven photocatalyst. The nanosolutions were characterized by X-ray diffraction (XRD), transmittance electron microscopy (TEM), photoluminescence (PL) spectra, and X-ray photoelectron spectroscopy (XPS). At the concentration of 0.2–0.1 M, Ag–TiO₂ caused 100% inhibition of bacterial growth. The antibacterial efficacy of Ag–TiO₂ was evaluated with two kinds of bacteria; Gram-positive and Gram-negative. The colony count of Ag–TiO₂ against Gram-negative were evaluated with stain such as Escherichia coli, Pseudomonas aeruginosa and Shigella while for Gram-positive were investigated with Staphylococcus aureus, Bacillus subtilis, Bacillus cereus. Colony count results indicated that Ag–TiO₂ able to kill bacteria at the lowest concentration of 0.05 M that contains 0.06 mol % Ag. From the SEM and TEM observation, the survival of the Gram-positive was low and the decomposition was rapid as compared to Gram-negative bacteria.     

Microbiological quality of legume-based traditional fermented foods marketed in West Bengal,India

A total of 105 samples of six different types of legume-based popular fermented foods, namely amriti, dhokla, dosa, idli, papad and wadi, purchased from retail outlets in West Bengal, was analysed to determine their microbiological safety status. While dhokla and idli were of high-moisture foods (62 g (100 g)⁻¹), others had a lower moisture level (14–27 g (100 g)⁻¹). Papad was alkaline (pH 8.7), whereas all the other foods were acidic (pH 4.4–5.8). Every sample was found contaminated with total aerobic mesophilic bacteria (detection limit, 10 cfu g⁻¹); 38% (40/105) of the samples contained more than 10⁶ cfu g⁻¹. Aerobic mesophilic bacterial spores were found in 88% (92/105) of the samples (detection limit, 100 cfu g⁻¹), whereas their anaerobic counterparts were present in 39% (41/105) of the samples (detection limit, 10 cfu g⁻¹). Although all the samples, excepting one, were free from Staphylococcus aureus (detection limit, 100 cfu g⁻¹), 20% (21/105) of the samples were found contaminated with Bacillus cereus (detection limit, 100 cfu g⁻¹). Enterobacteriaceae were found in 46% (48/105) of the samples (detection limit, 10 cfu g⁻¹). Of the Enterobacteriaceae isolates, 92% were coliforms and 57% were faecal coliforms. Escherichia coli (detection limit, 10 cfu g⁻¹) was found in only one sample each of wadi and idli, at a load of 10³–10⁴ g⁻¹. Salmonella (detection limit, 1 cell (25 g)⁻¹) occurred in 12 samples of wadi, idli and papad, however was absent in the other three products. Clostridium perfringens (detection limit, 10 cfu g⁻¹) and Shigella (detection limit, 1 cell (25 g)⁻¹) could not be detected. The results obtained in the present study indicated that these foods were manufactured using poor-quality starting materials, processed under unhygienic conditions, or/and temperature-abused during transportation and storage. Based on these results, a guideline is recommended for obtaining safe products.     

Validation studies on an online monitoring system for reducing faecal and microbial contamination on beef carcasses

The objective of this research was to establish the reduction in the incidence of carcass faecal contamination and microbial counts that could be achieved in a beef slaughter plant using a novel information technology based online monitoring system. On 18 separate visits over the course of 6 months, every carcass (approximately 500 per day) was examined at the final inspection stand for visible faecal contamination. Each incidence was attributed to dehiding or evisceration operations. On each visit, 10 carcasses were swabbed at the trimming stand, at the hock, rump, anus, brisket and flank to determine total viable counts (TVC), Escherichia coli counts (ECC), total enteric counts (TEC) and total coliform counts (TCC). Over the course of this study, faecal contamination rates for dehiding and evisceration were reduced from 54.2% to 28.2% and from 32.5% to 13.7%, respectively. TVC remained constant at approximately 3.0 log₁₀ cfu cm⁻² while ECC, TEC and TCC decreased by 0.56 log₁₀ cfu cm⁻², 0.83 log₁₀ cfu cm⁻² and 0.9 log₁₀ cfu cm⁻², respectively. Online monitoring is therefore an effective means of reducing the incidence of bovine carcass faecal and enteric counts.     

Microbiological changes in farm reared freshwater prawn (Macrobrachium rosenbergii de Man) in ice

The microbiological changes in farm reared freshwater prawn (Macrobrachium rosenbergii de Man) during ice storage were studied. A total of 156 bacterial cultures from fresh and ice-stored farmed freshwater prawn were isolated and characterized. Total aerobic, mesophilic and psychrotrophic counts and hydrogen sulphide producing bacterial counts were determined. The total aerobic counts at 20 and 37 °C on fresh prawn was in the range of 4–5 log₁₀ cfu g⁻¹. Aerobic counts on M. rosenbergii at 20 °C and 7 °C exceeded 10⁷ cfu g⁻¹ by the end of storage, of which 40–52% were H₂S producers. Gram-negative bacteria constituted 73% of the total flora of fresh prawn and Enterobacteriaceae and Aeromonadaceae dominated. After 19 days of iced storage, more than 80% of the bacterial flora of prawn were Gram-negative. Pseudomonas, Aeromonas hydrophila, A. veronii boivar sobria and Shewanella putrefaciens were identified as the dominant spoilage organisms of farm reared M. rosenbergii stored in ice. This study confirms that freshwater prawn carry significant numbers of motile aeromonads capable of growth at low temperature. The results of the study indicated that the shelf-life of freshwater prawn as determined by microbiological data is 12–16 days. Immediate icing of harvested M. rosenbergii is essential to improve the microbiological stability.     

Development of a real-time PCR procedure for quantification of viable Escherichia coli in populations of E. coli exposed to lactic acid,and the acid tolerance of verotoxigenic E. coli (VTEC) from cattle hides

The aims of this study were to develop a real-time PCR procedure for determining the effects on Escherichia coli of treatment for decontaminating beef carcasses with lactic acid solution, and determining if there were differences in the acid tolerance of E. coli generally and verotoxigenic E. coli (VTEC). Suspensions of E. coli were incubated with 4% lactic acid at pH 3.6. The numbers of surviving E. coli at different incubation times were determined from plate counts and from quantification by real-time PCR of the uidA gene in DNA preparations. The numbers of viable E. coli progressively declined, by about 4 log units during incubation for 6 h. The mean cycle threshold (Ct) values for uidA in DNA from samples collected at different times and treated or not treated with propidium monoazide (PMA) before DNA extraction were similar. Treatment with 1% sodium deoxycholate (SD) before PMA treatment resulted in an increase of >6 Ct when the reduction in viable cell number was around 1 log. When E. coli incubated with 4% lactic acid solutions of pH 2.4, 2.8, 3.2 or 3.6 were resuscitated in half strength brain heart infusion (BHI) for 2 h before treatments with SD and PMA, the slope of the plot relating Ct values to the numbers of viable E. coli was 1.85 Ct log cfu⁻¹ with the correlation coefficient (R²) being 0.80. The findings indicate that while the membranes of E. coli inactivated by 4% lactic acid were largely impermeable to PMA, the membranes of both dead and injured cells were rendered permeable to PMA by treatment with 1% SD. Resuscitation in BHI restored the membrane barrier properties of the injured cells. Treatment with lactic acid resulted in increases in Ct values of 4.1, 3.7, 2.5 and 1.5 for the uidA, stx₁, stx₂ and eae genes, respectively; and the increases in Ct values for the latter two genes were significantly different (p < 0.05) from that for the uidA gene. This indicates that VTEC carrying stx₂ and/or eae were more acid resistant than other E. coli. Thus, caution should be exercised when using generic E. coli as an indicator for VTEC for assessment of the antimicrobial efficacy of organic acid decontaminating treatments at abattoirs.     

Radio frequency heating of comminuted meats - considerations in relation to microbial challenge studies

Bacillus cereus and Clostridium perfringens vegetative cell and spore cocktails in maximum recovery diluent (MRD) were inoculated into pork luncheon meat to challenge a previously developed radio frequency (RF) cooking protocol. After RF cooking and cooling microbial enumeration results showed a reduction in B. cereus vegetative cell and spores of 5.4 and 1.8 log₁₀ cfu g⁻¹, respectively while the corresponding reduction for C. perfringens vegetative cells and spores were 6.8 and 4.1 log₁₀ cfu g⁻¹, respectively. However, post cooking temperatures within the product were lower than anticipated. Subsequent analysis of product thermal and dielectric properties indicated that MRD addition and compositional variations within meat ingredients altered thermal and dielectric properties which in turn contributed to reduced and less uniform temperatures. The study shows that for RF microbial challenge studies, adjustment of product formulation prior to MRD addition is critical to ensure a similar composition to the normal product and a true picture of microbial inactivation.     

A visual detection method for Salmonella Typhimurium based on aptamer recognition and nanogold labeling

A rapid, specific and visible detection method for Salmonella Typhimurium was developed based on the recognition of aptamers coupled with nanogold labeling and silver signal amplification. Briefly, biotinylated aptamer 1, which was specific to Salmonella Typhimurium, was immobilized onto the surface of microtiter plate-wells modified with streptavidin through the binding of biotin and streptavidin. Then, the target bacteria, Salmonella Typhimurium, and the aptamer 2-gold nanoparticle (aptamer 2-AuNPs) conjugates were incubated in the wells to form sandwich-type aptamer/bacteria/aptamer-AuNPs complexes. Under optimal conditions, the correlation between the concentration of Salmonella Typhimurium and the intensity of the signals was observed to be linear within the range of 10–10⁶ cfu mL⁻¹ (R² = 0.9913), and the detection limit of the proposed method was observed to be 7 cfu mL⁻¹ This developed method offers the potential for rapid, sensitive and visible detection of Salmonella Typhimurium in samples.     

Antimicrobial effect of cranberry juice and extracts

The antimicrobial effect of cranberry juice and of three cranberry extracts (water-soluble (E1) and apolar phenolic compounds (E2), and anthocyanins (E3)) was investigated against seven bacterial strains (Enterococcus faecium resistant to vancomycin (ERV), Escherichia coli O157:H7 EDL 933, Escherichia coli ATCC 25922, Listeria monocytogenes HPB 2812, Pseudomonas aeruginosa ATCC 15442, Salmonella Typhimurium SL1344, and Staphylococcus aureus ATCC 29213). Each cranberry sample was analyzed to determine the minimum inhibitory concentration (MIC) and the maximal tolerated concentration (MTC) at neutral pH. The results, reported in μg phenol/mL, indicated that all the bacterial strains, both Gram-positive and Gram-negative, were selectively inhibited by the cranberry phenolic compounds. The extract rich in water-soluble phenolic compounds caused the most important growth inhibitions. The bacteria ERV, and to a lesser degree, P. aeruginosa, S. aureus and E. coli ATCC 25922, were the most sensitive to the antimicrobial activity of extract E1. The growth of P. aeruginosa and E. coli ATCC was also affected by the presence of the anthocyanin-rich cranberry extract E3, although the observed antibacterial effect was not as important as with extract E1. In general, L. monocytogenes, E. coli O157:H7 and S. Typhimurium were the most resistant to the antibacterial activity of the cranberry extracts. Within 30 min of exposure with pure neutralized cranberry juice, L. monocytogenes and ERV were completely inactivated.     

The effect of non-thermal processing technologies on microbial inactivation: An investigation into sub-lethal injury of Escherichia coli and Pseudomonas fluorescens

In recent years, there has been an increased interest in food processing technologies that could lessen the thermal impact on food products. In the present study, thermosonication (TS) and pulsed electric fields (PEF), applied individually or in combination (TS/PEF), were investigated to determine their effects on inactivation and sub-lethal injury of Pseudomonas fluorescens and Escherichia coli. TS was applied at a low (L) and high (H) wave amplitude (18.6 μm and 27.9 μm, respectively), while PEF was applied at a low and high electrical field strength (29 kV cm⁻¹ and 32 kV cm⁻¹, respectively). In addition, the inhibitory effects of TS/PEF combined were assessed. For P. fluorescens, when applied individually, TS and PEF resulted in ≤9% and ≤47% inactivation, respectively, with 8% sub-lethal injury following PEF treatment. However, TS/PEF treatment caused ≤48% inactivation and ≤34% sub-lethal injury, respectively. For E. coli, TS caused ≤6% inactivation, and ≤2% sub-lethal injury, while PEF treatment alone caused inactivation and sub-lethal injury of 86% and 29%, respectively. TS/PEF caused a maximum of 66% inactivation, while sub-lethally injuring approximately 26% of the of E. coli population. The present study confirms the ability of TS and PEF to inactivate microorganisms, but shows that some bacteria were not killed, but sub-lethally injured.     

Potential bio-activity of whey fermented extract as sanitizer of organic grown lettuce

Consumption of vegetables is increasing due to demand for healthy products in peoples' diets. To reduce microbial contamination and maintain freshness, industrial processes in Portugal rely on minimally processing of vegetables with hypochlorite as sanitizer. Formation of toxic chlorine derivatives has raised concern restrictions to its use and alternatives with whey permeate as a disinfection agent has been attempted. The aim of this work was to evaluate the bio potential of fermented cheese whey, for use on disinfection of minimally processed lettuce organically grown.Assays were made with whey obtained from inoculated milk during cheese processing, fermented for 120 h at 37 °C, after which, among other carbohydrates, lactic acid was measured by HPLC, giving average yields of 18 g L⁻¹.The sanitizing effect of whey, undiluted, 75 and 50% solutions, was compared with 110 ppm sodium hypochlorite, after rinsing. Aerobic Microorganisms (AM), Psychrotrophic Microorganisms (PM) and Enterobacteriaceae (ENT), were used as indicators for hygiene quality. For a level of significance of P < 0.05, the hygiene quality standards of lettuce samples, were better using 75% whey solution (AM 6.62, PM 7.48 cfu g⁻¹), than using sodium hypochlorite (AM 7.48, PM 8.15 cfu g⁻¹), for the 7 days of shelf life studied. Evaluation of Enterobacteriaceae showed significant differences after 3 days, between water (ENT 4.98 cfu g⁻¹) sodium hypochlorite (ENT 4.81 cfu g⁻¹) and 75% solution of whey (ENT 4.63 cfu g⁻¹).Considering the actual limitations imposed to chlorine sanitation, these results point a good alternative to the food industry, especially for organic fresh vegetables, which are chemical free brands.     

Behaviour of Escherichia coli O157 (VTEC), Salmonella Typhimurium and Listeria monocytogenes during the manufacture,ripening and shelf life of low fat salami

The aim of this study was to evaluate the behaviour of Escherichia coli, Salmonella Typhimurium and Listeria monocytogenes in an innovative semi-dry reduced fat Italian salami. The product is made from pork meat and it is characterized by less than 20% fat, lactose-, gluten- and milk protein-free. It is developed in Italy according to EC Regulation No. 1924/2006 “on nutrition and health claims made on foods”. Multi-strain cocktails of each pathogen were used to inoculate (5 log cfu g⁻¹) separately the salami batter. During the manufacture and ripening, E. coli, S. Typhimurium, and L. monocytogenes decreased by 2.5, 1.65 and 0.5 log cfu g⁻¹ respectively from the initial inoculated levels. Experimental data indicated that, during the shelf life in a condition of moderate thermal abuse (8–12 °C), the portioned and vacuum packed low fat salami are not able to support the growth of L. monocytogenes.     

Effect of pressure,depressurization rate and pressure cycling on the inactivation of Escherichia coli by supercritical carbon dioxide

This work is focused on the use of supercritical carbon dioxide to inactivate the pathogenic Escherichia coli. For this purpose, the experimental design methodology was employed to evaluate the effects of pressure (8–28 MPa), depressurization rate (1–11 MPa min^?1) and pressure cycling (1–5 cycles) on the microorganism inactivation using the static-synthetic method in a variable-volume reactor. The number of pressure cycles and system pressure showed a significant influence on E. coli inactivation with supercritical CO₂, indicating that the increase in the number of pressure cycles and system pressure improve inactivation efficiency. Microbial inactivation followed first order reaction kinetics, where the rates increased with increasing pressure from 8 to 16 MPa. The decimal reduction times (D) ranged from 1.03 to 5.35 min. The pressure dependence of the E. coli specific inactivation rates can be described by the z value, which was found to be 11.4. The results reported here may be useful to provide an effective non-thermal sterilization of foods in pilot/industrial scale.     

Combined sustainable sanitising treatments to reduce Escherichia coli and Salmonella Enteritidis growth on fresh-cut kailan-hybrid broccoli

The effects of peroxyacetic acid (PA), neutral electrolysed water (NEW), ultraviolet C light (UV-C) and superatmospheric O₂ packaging (HO), single or combined, on the growth rate of Escherichia coli and S. Enteritidis inoculated onto fresh-cut kailan-hybrid broccoli were studied throughout 14 days of shelf life at 5 and 10 °C. As controls, unwashed, water-washed and NaClO-washed were used. PA and NEW showed a better sanitising effect than NaClO against both E. coli/S. Enteritidis with reductions of 2.2/2.7 and 2.6/2.6 log CFU g⁻¹, respectively. UV-C attained E. coli/S. Enteritidis decreases of 1.3–1.4/2.1–2.2 log CFU g⁻¹ compared to unwashed samples. The bacteriostatic effects of PA or NEW were improved when they were combined with UV-C, decreasing E. coli and S. Enteritidis counts by about 3 log CFU g⁻¹. After 14 days, PA and NEW-treated samples attained E. coli/S. Enteritidis reductions at 5 °C of 2.3/1.4 and about 1 log CFU g⁻¹, respectively. Storage of those samples at 10 °C masked that sanitising effect. At both storage temperatures, UV-C-treated samples registered lower E. coli and S. Enteritidis reductions (or higher increases for S. Enteritidis at 10 °C) regarding conventional NaClO-sanitized samples or other single treatments. However, PA, NEW or UV-C-treated samples under HO at both storage temperatures showed better bacterial control than individual treatments with the greatest effectiveness for UV-C + HO. Triple combination did not imply an enhanced benefit over double combinations. Conclusively, PA, NEW and UV-C seems to be effective emergent alternatives to NaClO to reduce initial E. coli and S. Enteritidis populations in fresh-cut kailan-hybrid broccoli. Storage at 5 or 10 °C under HO greatly controlled microbial growth.     

Influence of argon modified atmosphere packaging on the growth potential of strains of Listeria monocytogenes and Escherichia coli

Modified atmosphere packaging (MAP) based on carbon dioxide (CO₂) – nitrogen (N₂) gas mixtures has been applied to maintain the safety and quality of ready-to-eat (RTE) meat products. The use of argon (Ar) gas as a supplement to CO₂–N₂ mixtures or as substitute for N₂ is a current approach to enhance the effectiveness of MAP. As there is limited information on the effect of Ar MAP on the growth behaviour or the survival of pathogenic bacteria in RTE foods, the aim of the present study was to assess the influence of Ar in MAP on the growth of Listeria monocytogenes and Escherichia coli strains under different conditions. For this purpose, a CO₂–N₂ (20:80) atmosphere was compared with a CO₂–N₂–Ar (30:30:40) and CO₂–Ar (30:70) atmosphere based on the assessment of bacterial growth (δ) on a gelatin-agar medium and ham. Additionally, a shelf life monitoring study was performed to evaluate the effect of these treatments on the background microflora of ham. The findings suggest that under the CO₂–N₂ MAP the product matrices supported the growth (δ > 0.5 log CFU g⁻¹) of L. monocytogenes throughout an observation period of 21 days at 4 ± 2 °C. On the contrary, both MAP containing Ar were equally able to reduce the δ below 0.5 log CFU g⁻¹. In this regard it was irrelevant whether L. monocytogenes was inoculated in depth (per slice) or at the surface (top slice) of the ham. Regarding the influence of the different gas atmospheres on E. coli all gas mixtures applied had the capacity to reduce the δ of E. coli below −0.5 log CFU g⁻¹. Further, shelf-life extension could not be managed with the gas atmospheres considered.     

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 (>4 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.     

Antimicrobial action and effects on beef quality attributes of a gaseous ozone treatment at refrigeration temperatures

The effects of gaseous ozone treatment at refrigeration temperatures, on microbial counts (total aerobic mesophilic heterotrophic microorganisms and inoculated Escherichia coli) in culture media and in beef samples were analyzed. The influence of ozone on beef quality properties such as surface color and rancidity was measured.The effect of gaseous ozone (154 × 10^?6 kg m^?3) in culture media inoculated with E. coli after 3- or 24-h treatment at 0° and 4 °C caused a total inactivation of this microorganism.For beef samples treated with the same gaseous ozone concentration, the highest microbial inhibition was observed at 0 °C and after 24-h exposure, producing a decrease of 0.7 and 2.0 log₁₀ cycles in E. coli and total aerobic mesophilic heterotrophic microorganism counts respectively; however, both the surface color and lipid oxidation of these beef samples were unacceptable. Shorter exposure times (3 h) to the tested ozone concentration at both temperatures (0–4 °C), reduced 0.5 log₁₀ cycles the counts of total aerobic mesophilic heterotrophic microorganisms and 0.6–1.0 log₁₀ cycles the counts of E. coli, without changing the color or producing rancidity in beef.     

Effect of combination of ultraviolet light and hydrogen peroxide on inactivation of Escherichia coli O157:H7, native microbial loads,and quality of button mushrooms

Mushrooms are prone to microbial spoilage and browning during growing and processing. Ultraviolet light (254 nm, UV-C) has been used as an alternative technology to chemical sanitizersfor food products. Hydrogen peroxide (H₂O₂) is classified as generally recognized as safe for use in foods as a bleaching and antimicrobial agent, and could control the bacterial blotch and browning of mushrooms. This study investigated the effects of water wash (control), 3% H₂O₂ wash, 0.45 kJ m⁻² UV-C, and combination of H₂O₂ and UV-C (H₂O₂ + UV) on microbial loads and product quality of mushrooms during storage for 14 days at 4 °C. Additionally, the inactivation of Escherichia coli O157:H7 inoculated on mushrooms was determined. Results showed that water wash, H₂O₂, UV-C and H₂O₂ + UV resulted in 0.44, 0.77, 0.85, and 0.87 logs CFU g⁻¹ reduction of E. coli O157:H7, respectively. Hydrogen peroxide, UV-C and the combination reduced total aerobic plate counts on the surface of mushrooms by 0.2–1.4 logs CFU g⁻¹ compared to the control, while there was no significant difference among the three treatments during storage. After storage, UV-C treated mushrooms had similar L* and a* values as the control while H₂O₂ and H₂O₂ + UV-C treated mushrooms had higher L* (lighter) and lower a* (less brown) values than the control. Compared to water wash, all the treatments inhibited lesion development on the mushroom surface on day 14. The combination of H₂O₂ and UV achieved the best overall dual control of lesion and browning. There was no significant difference in ascorbic acid and total phenolic content among the treatments. Overall our results suggested that H₂O₂ + UV reduced microbial loads, and extended storage life by reducing lesion development without causing deterioration in nutritional quality of button mushrooms. Therefore, when properly utilized, H₂O₂ + UV could potentially be used for maintaining postharvest quality while marginally reducing populations of E. coli O157:H7 and background microflora.     

In vitro antibacterial activity of Australian native herb extracts against food-related bacteria

The antibacterial activities of water, ethanol and hexane extracts of five Australian herbs (Backhousia citriodora, Anetholea anisata, Eucalyptus staigerana, Eu. olida and Prostanthera incisa) against seven food-related bacteria (Enterococcus faecalis, Escherichia coli, Listeria monocytogenes, Pseudomonas aeruginosa, Salmonella Enteritidis, Sal. Typhimurium and Staphylococcus aureus) were determined by the microtitre broth microdilution assay. The water extracts of all the herbs displayed no or low antimicrobial activity against all of the bacteria tested with the exception of S. aureus. Relatively high levels of activity (minimum inhibitory concentrations of 125–15.6 μg ml⁻¹) against this pathogen were present in water extracts from all herbs except P. incisa. The ethanol and hexane extracts of all herbs displayed some activity against a number of the bacteria tested, with no one particular herb displaying an obviously higher level or range of activity. Staphylococcus aureus proved to be the most sensitive of the bacteria tested against the solvent extracts with all extracts displaying activity ranging from 125 to 7.8 μg ml⁻¹, while E. coli and L. monocytogenes, on the other hand, proved the least sensitive with only five of 15 herb/extract combinations displaying any activity against these pathogens. The extracts of the Australian native herbs examined in this study have potential for application in foods to increase shelf-life or promote safety.     

Antimicrobial effect of acidified sodium chlorite,sodium chlorite,sodium hypochlorite,and citric acid on Escherichia coli O157:H7 and natural microflora of fresh-cut cilantro

Fresh-cut cilantro is particularly susceptible to microbial growth and, therefore, use of an effective sanitizer on this product is of great importance. The objective of this study was to evaluate the efficacy of different sanitizing treatments on reducing Escherichia coli O157:H7 populations, aerobic mesophilic bacterial, yeast and mould counts on fresh-cut cilantro. Cut cilantro was treated with sodium hypochlorite (SH) at 0.2 g L^?1 free chlorine and acidified sodium chlorite (ASC) at 0.1, 0.25, 0.5 and 1 g L^?1, along with the components of ASC, i.e., citric acid (CA) at 6 g L^?1 and sodium chlorite (SC) at 1 g L^?1. In the present study, it was found that SH inactivated, at maximum, 1–1.3 log cfu g^?1 of background or pathogenic microflora present on cut cilantro. However, reductions of more than 3 log cfu g^?1 were observed after washing with 1 g L^?1 of ASC. Moreover, when lower concentrations of ASC were used (0.25 and 0.5 g L^?1), microbial populations were reduced by about 2 log cfu g^?1. SC was as effective as ASC at 1 g L^?1 in reducing aerobic mesophilic bacteria and E. coli O157:H7 populations, although it was not as effective as ASC in reducing yeast and mould populations.