Utility of UV-C radiation as anti-Salmonella decontamination treatment for desiccated coconut flakes

This study established the ultraviolet-C (UV-C)-mediated reduction of a cocktail of Salmonella enterica serovars, artificially inoculated onto desiccated coconut flakes. Inoculated cells exhibited biphasic inactivation behavior, characterized by an initial, log-linear population reduction, followed by a slower log-linear population decline where sublethal injury accumulated. Decimal reduction times in the faster inactivation phase (D_fast) ranged from 0.65 to 0.82 min, equivalent to UV-C energy dose of 86.58–109.22 mJ/cm². The D_slow values ranged from 21.19 to 24.21 min, equivalent to energy dose of 2822.51–3224.78 mJ/cm². A total of 3-log cycles reduction in inoculated Salmonella were observed after 40 min exposure of desiccated coconut to UV-C. Further, this 40-min process resulted in changes in the Hunter L*, a* and b* color parameter values, but were not detected by a test consumer panel as evident in the non-significant difference in the color acceptability of UV-C treated and untreated coconut flakes. The UV-C process also did not affect the general acceptability of baked coconut macaroons made from UV-C treated coconut flakes. The results obtained in this work may serve as baseline information in the development of an in- or post-process integration of a UV-C radiation step against Salmonella spp. in the desiccated coconut production process flow.     

Inactivation of Staphylococcus saprophyticus in chicken meat and purge using thermal processing,high pressure processing,gamma radiation,and ultraviolet light (254 nm)

Staphylococcus saprophyticus is a common contaminant in meat and poultry, and causes urinary tract infections after colonization of the gastrointestinal tract, followed by accidental transfer of contaminated feces to the urethra. There is limited information regarding the inactivation kinetics of S. saprophyticus in meat and poultry. When S. saprophyticus was suspended in ground chicken meat (GCM) the thermal processing D₁₀ was 6.26, 0.60 and 0.09 min at 55, 60 and 65 °C, respectively. When S. saprophyticus was inoculated into GCM and subjected to high pressure processing (5 °C, 0–25 min) at 200, 300 or 400 MPa the HPP D₁₀ was 15.5, 9.43, and 3.54 min, respectively. When the S. saprophyticus cocktail was inoculated into GCM and irradiated (5 and −20 °C) the gamma radiation D₁₀ were 0.64 and 0.77 kGy, respectively. When S. saprophyticus was inoculated into chicken purge which was then placed on food contact surfaces including stainless steel, and high density polyethylene and polypropylene and treated with UV-C (0–60 mJ/cm²) the UV-C D₁₀ ranged from 14.9 to 18.5 mJ/cm². These results indicate the inactivation kinetics for S. saprophyticus are consistent with those for other foodborne pathogens and could be controlled in poultry meat and purge without difficulty.     

Thermal death times of acid-habituated Escherichia coli and Salmonella enterica in selected fruit beverages

The study established the decimal reduction times at 60 and 73 °C (D₆₀ and D₇₃) of each of acid-adapted cocktails of Escherichia coli (NRRL 3704, ATCC 8739, ATCC 92522) and Salmonella enterica serovars Typhimurium (NRRL B-4420), Typhi (NRRL B-573), and Enteritidis (Biotech 1963) in some fruit beverages. Tested beverages included apple and orange juices, which are most commonly reported vectors of diseases; and tropical fruit beverages such as mango, guava, and soursop nectars, which are not frequently used as suspending media in thermal inactivation studies. The fruit beverages had pH of 3.30–4.73, titratable acidities of 0.15–0.64% organic acid, and soluble solids of 11.13–14.33 °Brix. At 60 °C, E. coli and Salmonella were 1.26–3.13 and 1.21–2.33 folds, respectively, more resistant to heating than at 73 °C. At 60 °C, E. coli and S. enterica had D₆₀ value ranges of 5.90 s (orange juice) to 12.42 s (guava nectar) and 7.50 s (orange juice) to 11.46 s (soursop nectar), respectively. At 73 °C, E. coli had D₇₃ values ranging from 3.56 s (apple juice) to 5.82 s (soursop nectar), while those of S. enterica ranged from 3.59 s (guava nectar) to 9.74 s (soursop nectar). The variations in the observed heat resistance in both heating temperatures were attributed to the differences in the physicochemical properties of the suspending fruit beverages. The results obtained in this work contribute to further understanding the behaviors of these pertinent pathogens in heat-treated fruit beverages. These data also provide baseline information for the establishment of heat pasteurization process schedules for better control of fruit juice product safety.     

Inactivation behaviors of foodborne microorganisms in multi-frequency power ultrasound-treated orange juice

This study established the inactivation kinetic parameters of some pathogenic bacteria including Escherichia coli O157:H7, Salmonella enterica serotypes, and Listeria monocytogenes; and spoilage yeasts namely, Debaryomyces hansenii, Clavispora lusitaniae, Torulaspora delbrueckii, Pichia fermentans, and Saccharomyces cerevisiae in orange juice subjected to multi-frequency Dynashock power ultrasound treatment. All test organisms exhibited a biphasic inactivation behavior with a sigmoidal inactivation curve consisted of an initial inactivation lag, followed by logarithmic linear inactivation. Injury accumulation in the inactivation lag phase was established in acid-adapted bacteria. The time necessary to reduce initial inoculated populations by 5 log cycles (99.999%), T_5D values, significantly increased with acid adaptation. The T_5D of E. coli, S. enterica, and L. monocytogenes increased from 37.64, 36.87, and 34.59 respectively; to 54.72, 40.38, and 37.83 min respectively after acid exposure. Temperature increase due to sensible heat propagation during ultrasound treatment decreased the resistance of the test bacteria. The cocktail of E. coli O157:H7 had significantly greater resistance towards ultrasound treatment (T_5D = 54.72 min) than any of the individual strain (T_5D = 41.48–47.48 min) in the mix. Similar results were found in the composited (T_5D = 60.02 min) and individual species (T_5D = 20.31–59.04 min). The results established in this work provide baseline information on microbial behavior in multi-frequency ultrasound-treated orange juice for establishment of pasteurization process schedules.     

Effectiveness of UV light as a means to reduce Salmonella contamination on tomatoes and food contact surfaces

The effectiveness of ultraviolet light at a wavelength of 254 nm to reduce Salmonella contamination on tomatoes and food contact surfaces was evaluated. Inoculated tomatoes were exposed to UV-C light at doses ranging from 0 to 223.1 mJ/cm². All UV treatments significantly reduced Salmonella populations (p < 0.05). The effectiveness of UV-C light in reducing Salmonella contamination on different locations on tomato surfaces under various UV doses (0–117.2 mJ/cm²) was also explored. Results indicated that regardless of the locations, UV treatment was shown to be effective in decreasing Salmonella populations. Subsequent studies evaluated possible photoreactivation or dark repair of injured Salmonella post-UV treatment. Following UV light exposure at doses of 0, 22.3, 44.6, and 89.2 mJ/cm², tomatoes were either exposed to visible light for 0, 3, and 5 h or stored in the dark for the same amount of time. Photoreactivation was not detected, nor was dark repair. UV light was also evaluated for its effectiveness to reduce Salmonella contamination on food contact surfaces (stainless steel, HDPE, waxed cardboard and PVC). Contaminated coupons were exposed to UV-C light at 0, 3.3, and 19.7 mJ/cm². Significant differences were observed between coupons treated with UV light and the controls (p < 0.05). Coupons exposed for longer time had greater Salmonella population reductions, except for waxed cardboard coupons. Application of UV-C light to reduce Salmonella contamination in tomato handling facilities is feasible.     

High pressure processing pretreatment enhanced the thermosonication inactivation of Alicyclobacillus acidoterrestris spores in orange juice

The spoilage of high acid fruit juices and nectars by Alicyclobacillus acidoterrestris is a major concern to juice manufacturers around the world since it is difficult to detect. In this study, thermosonication (ultrasound and heat, TS) and thermal inactivation of A. acidoterrestris spores in pretreated orange juice were carried out and resistance parameters were estimated. First, the effect of TS acoustic energy density (AED, 0.3–20.2 W/mL) on the inactivation at 75 °C was investigated. Then, the influence of TS temperature (70–78 °C) on the spore inactivation (AED = 20.2 W/mL) was studied. Next, we explored the effect of high pressure processing (HPP) pretreatment of juice on the 20.2 W/mL TS inactivation at the best temperature (78 °C). Lastly, the thermal inactivation of spores in juice heat shocked + 1 min sonicated vs. untreated juice was also investigated.Results of TS showed higher spore inactivation for higher AED (D_75°C-value of 49 min for 20.2 W/mL vs. 217 min for 0.33 W/mL). Lower D-values were obtained at higher temperatures (D_78°C-value of 28 min vs. D_70°C-value of 139 min at 20.2 W/mL). The TS D_78°C-value (at 20.2 W/mL) decreased further from 28 min to 14 min when the orange juice was previously submitted to 600 MPa for 15 min. Thermal treatment alone at 78 °C resulted in almost no spore inactivation, whereas the heat shock + ultrasound pretreatment of juice enhanced the thermal inactivation of spores (D_85°C-value decreased from 69 to 29 min). To conclude, HPP-assisted TS provided the best method for spore inactivation, indicating the benefit of high pressure and power ultrasound technology in addition to heat. TS required at least 8 °C lower temperatures than thermal treatments to achieve the same spore inactivation, which could enhance juice quality and energy savings.     

Decimal reduction times of acid-adapted and non-adapted Escherichia coli O157:H7, Salmonella spp., and Listeria monocytogenes in young Cocos nucifera Linn. liquid endosperm

The study established the decimal reduction times at 55 °C (D_55 °C values) of acid-adapted and non-adapted Escherichia coli O157:H7, Salmonella enterica, and Listeria monocytogenes in young coconut liquid endosperm. Acid adaptation of the test pathogens was conducted by cultivating cells in a gradually acidifying nutrient broth supplemented with 1% glucose. Results showed that acid adaptation had varying influence on the subsequent thermal resistances of the pathogens. The non-adapted E. coli O157:H7 exhibited the greatest resistance among the tested pathogens with a D_55 °C of 23.20 min. Prior adaptation to acidity decreased the D_55 °C to 16.16 min. On the other hand, acid adaptation increased the D_55 °C values of S. enterica and L. monocytogenes from 8.76 to 10.55 min, and from 7.47 to 18.09 min, respectively. The D_55 °C of the non-adapted E. coli O157:H7 was used to establish a pasteurization process schedule with an order of lethality equal to 5-logarithmic (99.999%) reduction. Sensory evaluation revealed that the overall acceptability, color, aroma, coconut flavor, and freshness characteristics of non-pasteurized and pasteurized liquid endosperms were not significantly different (p > 0.05). Moreover, the sensory quality attributes of coconut beverages (80:20 vol/vol endosperm-to-water ratio, soluble solids adjusted to 10 °Brix with sucrose) prepared from both non-pasteurized and pasteurized liquid endosperm samples did not significantly vary. The results obtained from the study may be used in the establishment and validation of thermal process schedules for young coconut liquid endosperm beverages.     

Effects of UV-C on physicochemical quality attributes and Salmonella enteritidis inactivation in liquid egg products

The perspectives of UV-C radiation as a non-thermal treatment for liquid egg products were evaluated from the point of view of the effects on egg quality attributes and the decontamination efficiency against the main egg contaminant Salmonella enterica subsp. enterica Ser. Enteritidis. UV-C treated egg fractions (egg yolk, egg white and whole egg) were analyzed for changes in pH, color, temperature-dependent viscosity and TBARS index, and were inoculated with S. enteritidis (ATCC 13076). Contrary to heat treatments, UV-C was not affecting viscosity and pH. Browning due to Maillard was perceptible in egg yolk and whole egg at low UV-C doses, but the corresponding browning indexes were always lower than in heat pasteurized egg fractions. Major changes were only due to lipid oxidation. TBARS values at the highest UV-C doses were larger than in pasteurized egg yolk and whole egg; under dynamic conditions and 0.61 J cm^?2, results were not significantly different to natural untreated samples. And UV-C was effective to inactivate S. enteritidis. In egg white, a load reduction up to 5.3 log₁₀ was achieved under dynamic conditions (9.22 J cm^?2, 39 min), while 3.3 log₁₀ and 3.8 log₁₀ reductions were recorded in egg yolk and whole egg. Static treatments were less efficient, but still, load reductions between 1.7 and 2.8 log₁₀ were obtained. At 3.94 mW cm^?2, time necessary to achieve a 4D reduction of Salmonella cells was estimated to be around 7.4 min in egg white.     

Biofilm forming Salmonella strains exhibit enhanced thermal resistance in wheat flour

The biofilm lifestyle of bacteria confers a remarkably increased tolerance to antimicrobial interventions and environmental stresses, however little is known about influence of biofilms on thermal resistance of Salmonella in low-moisture foods. This study was aimed to assess the correlation between the ability of biofilm formation of Salmonella Enteritidis (S. Enteritidis) strains and their capacity to survive desiccation and thermal treatment in wheat flour as a model for low-moisture food. The production of the biofilm in S. Enteritidis strains was analyzed qualitatively and quantitatively using calcoflour fluorescence, congo-red binding, pellicle formation and microtiter-plate test. Subsequently, three biofilm-forming and four non-forming S. Enteritidis strains were selected. Survival after desiccation was evaluated by population counts before and after equilibration for 4–5 days at 45% RH. Thermal resistance (D_{80 °C, 0.45 aw}) of S. Enteritidis in wheat flour was evaluated by fitting the thermal inactivation kinetic data with the first order kinetics model. The biofilm forming ability was not associated with resistance to desiccation. However, thermal resistance (D_{80 °C, 0.45 aw}) and pre-formed biofilm amount (OD_492 nm) showed a linear correlation (Spearmen correlation ρ = 0.8, p < 0.05), indicating more biofilm production confers more thermal resistance. Average thermal resistance (D_{80 °C, 0.45 aw}) was significantly (p < 0.05) higher among biofilm formers (14.1 ± 0.6 min) when compared with non-formers (6.0 ± 0.2 min). This study shows that the amount of biofilm produced by Salmonella on congo red-calcofluor media is linearly correlated with the thermal resistance of Salmonella in wheat flour. The findings reinforce the necessity of appropriate management in sanitation and biofilm removal in plants that process low-moisture foods.     

Synergistic effect of a combination of ultraviolet–C irradiation and sodium hypochlorite to reduce Listeria monocytogenes biofilms on stainless steel and eggshell surfaces

The present study demonstrates the synergistic effect of treatment with a combination of ultraviolet (UV)C (300, 600, 1200, and 1800 mWs/cm²) irradiation and sodium hypochlorite (NaOCl) (50, 100, 150, and 200 ppm) on Listeria monocytogenes ATCC 19113 biofilms formed on stainless steel and eggshell surfaces. The synergistic effect was not dependent on the dose of UV–C irradiation or the concentration of NaOCl. Synergistic reductions of biofilms after UV–C/NaOCl treatment on stainless steel and eggshells were 0.95–3.68 log CFU/cm² and –0.22 to 1.02 log CFU/cm², respectively. The largest synergistic reductions of biofilms were 3.68 log CFU/cm² using 1800 mWs/cm² UV–C and 200 ppm NaOCl on stainless steel, and 1.02 CFU/cm² using 600 mWs/cm² UV–C and 50 ppm NaOCl on eggshells. The Hunter colors of L*, a*, and b* were not significantly (P > 0.05) changed on eggshell surfaces treated with all single and combined treatments. The results in this study indicate that the combination treatment of 1800 mWs/cm² UV–C/200 ppm NaOCl could be feasible for use on stainless steel surfaces in industrial kitchens, facilities, and restaurants. In addition, the combination of 600 mWs/cm² UV–C/500 ppm NaOCl could possibly be used in egg production, processing, and distribution processes to enhance food safety without causing changes to the eggshell surface color.     

Alicyclobacillus acidoterrestris spore inactivation by high pressure combined with mild heat: Modeling the effects of temperature and soluble solids

High pressure processing (HPP) comprises the application of pressures between 100 and 1000 MPa to foods for microbial inactivation and food preservation. HPP has been commercially applied to pasteurize fruit juices with the advantage of retaining its bioactive constituents and original organoleptic properties. Alicyclobacillus acidoterrestris has been suggested as a reference in the design of pasteurization for high-acid fruit products, due to spore resistance and spoilage incidents in fruit juices. In this study, A. acidoterrestris spore inactivation by 600 MPa combined with mild heat (35–65 °C) in malt extract broth adjusted to 10, 20 and 30 °Brix was carried out and the inactivation was modeled.The soluble solids increased the resistance of the spores to 600 MPa-thermal process, while the temperature decreased its resistance. Although the nonlinear Weibull model gave better fittings, the first-order kinetic parameters were also determined. For example for 600 MPa at 55 °C D_10°Brix = 4.2 min, D_20°Brix = 7.6 min, D_30°Brix = 13.7 min, and z_T-values were 20–21 °C. The z-values for the effect of soluble solids on D_T-values were 39–40 °Brix for 45 and 55 °C 600 MPa HPP. The results obtained with broth were validated with fruit juices and concentrates. The combination of HPP with heat was an effective alternative to conventional thermal processing for the inactivation of A. acidoterrestris spores in juices up to 30 °Brix, allowing the use of less 30–40 °C of temperature for the same microbial inactivation, which potentially results in more nutritious, fresher and tastier juices/concentrates.     

Antimicrobial efficacy of vacuum impregnation washing with malic acid applied to whole paprika,carrots, king oyster mushrooms and muskmelons

Antimicrobial effect of vacuum impregnation (VI) applied to organic acid washing against Salmonella Typhimurium, Escherichia coli O157:H7 and Listeria monocytogenes on paprika fruit, carrots, king oyster mushrooms and muskmelons was investigated. Samples were treated with intermittent VI with 21.3 kPa and compared with dipping washing in 2% malic acid. The initial sample pathogen levels were approximately 10⁵–10⁷ CFU/cm². Enumerations of the three pathogens on paprika and carrots treated with VI washing were reduced to below the detection limit (= 1 log₁₀ CFU/cm²) after 3–5 min and 15–20 min, respectively. For each time point where populations of the three pathogens were reduced to below the detection limit by VI treatment, populations of 1.2–1.9 log CFU/cm² and 2.5 to 2.8 log CFU/cm² survived on paprika and carrots, respectively, when subjected to dipping treatment. After 20 min of dipping treatment, surviving populations of the three pathogens ranged from 3.5 to 4.1 and 3.3 to 4.4 log CFU/cm² on king oyster mushrooms and muskmelons, respectively. After 20 min of VI treatment, surviving populations of the three pathogens ranged from 3.0 to 3.6 log and 3.1 to 4.1 log CFU/cm², respectively, on king oyster mushrooms and muskmelons. Additionally, there were no significant (P ≥ 0.05) differences in pathogen reductions between dipping and VI treatment for both king oyster mushrooms and muskmelons. King oyster mushrooms (R_a = 6.02 ± 1.65 μm) and muskmelons (R_a = 11.43 ± 1.68 μm) had relatively large roughness values compared to those of paprika (R_a = 0.60 ± 0.10 μm) and carrots (R_a = 2.51 ± 0.50 μm). Scanning electron photomicrographs showed many deep protected sites in king oyster mushrooms and muskmelons with many microbes located deep in these sites following VI treatment. Instrumental color, texture and titratable acidity values of paprika and carrots subjected to VI washing treatment with 2% malic acid for 5 and 20 min were not significantly (P ≥ 0.05) different from those of untreated control samples during 7 day storage.     

Inactivation of Salmonella Typhimurium and quality preservation of cherry tomatoes by in-package aerosolization of antimicrobials

The purpose of the present study was to investigate the efficacy of in-package aerosolized aqueous sanitizers in reducing populations of Salmonella enterica serovar Typhimurium on tomato fruit and in maintaining fruit quality. Cherry tomatoes were inoculated with a cocktail of attenuated S. Typhimurium ATCC 53647 and 53648 strains on the smooth skin surface and stem scar area. Next, 200 ppm free chlorine, and peroxyacetic acid (PAA) and aqueous ClO₂ at different concentrations, 2% lactic acid + 2% acetic acid + 2% levulinic acid, and 3% acetic acid + 3% lactic acid were aerosolized into a clamshell container containing cherry tomatoes. Results showed that S. Typhimurium populations on smooth tomato surfaces were reduced by more than 5 log CFU/fruit with 400 ppm PAA, 2% lactic acid + 2% acetic acid + 2% levulinic acid, 3% acetic acid + 3% lactic acid, and aqueous ClO₂ (100 and 400 ppm). On the stem scar area, 400 ppm aqueous ClO₂ was more effective in reducing S. Typhimurium populations than other treatments, achieving 4.89 log CFU/fruit reduction, followed by 400 ppm PAA (2.62 log CFU/fruit). The efficacy of ClO₂ and acid combination treatments increased during 3-week storage at 10 °C, achieving >3 log CFU/fruit inactivation with the acid combination and ca. 6 log with for 400 ppm with ClO₂. None of the treatments significantly (p > 0.05) affected color, appearance, firmness, vitamin C, lycopene or antioxidant values of tomatoes during 3 weeks of storage; although, an acidic odor was detected for samples treated with the organic acids in the earlier period of the storage. These results suggest that in-package aerosolized sanitizers can be used as a novel method for the inactivation of Salmonella on tomato fruit.     

Comparison of spore inactivation with novel agitating retort,static retort and combined high pressure-temperature treatments

Optimization of food preservation technologies is necessary for improved product quality and nutrition as well as energy and environmental sustainability. In the current study, inactivation of Bacillus subtilis spores in a model soup (pH 6.1) with agitating retort, static retort and combined high pressure-temperature treatments was investigated. With isothermal experiments, D_95° C and z values for B. subtilis spores in the soup were obtained as 4.67 min and 8.65 °C. Log-linear model performed well for describing isothermal spore inactivation kinetics with satisfactory R²_adj values (0.94–0.97). Agitating retort treatments caused a dramatic reduction in processing times, as 17 min processing in agitating mode was required for 7-log inactivation of B. subtilis spores, compared to 53 min in static mode at 110 °C. For agitating process, observed and predicted lethality values were similar. This implied a homogenous heat load distribution within the soup with the help of high frequency agitation. Combined HPP and mild temperature treatments were highly synergistic for elimination of B. subtilis spores in the same model soup used in heat treatments. HPP treatments combining 650 MPa and 55–65 °C for 10 min resulted in up to 4.5 log kill effect on spores. The findings from the current study can be utilized in selection of test conditions for similar products in future safety studies. Results clearly showed that using novel mechanisms in food processing provide an opportunity for milder processing which can lead to better food quality and sustainability.     

Influences of vanillin and licorice root extract supplementations on the decimal reduction times of Escherichia coli O157:H7 in mildly heated young coconut liquid endosperm

This study determined the influences of supplementing different combinations of vanillin (0–500 ppm) and licorice root extract (LRE, 0–420 ppm) on the mild heat (55 °C) decimal reduction times (D₅₅-values) of a cocktail of Escherichia coli O157:H7 in young coconut liquid endosperm. The maximum level of supplementation per additive tested was previously established not to result in the lowering of general consumer acceptability of the liquid endosperm. The D₅₅-values ranged from 15.08 to 31.40 min. The influences of both additives on the D₅₅-value fitted significantly into a 2-factor, interaction model with only the joint effect of the additives having significant effect on D₅₅. The combined efficacies of the additives were most significant at concentrations above 250 ppm vanillin and 210 ppm LRE. The results obtained may be used in the establishment of mild heat pasteurization processes for supplemented young coconut liquid endosperm, for better control of quality and safety.     

Growth and inhibition by spices of growth from spores of enterotoxigenic Bacillus cereus in cooked rice

Bacillus cereus is a pathogenic spore-forming bacterium implicated in cases of diarrheal and emetic type of foodborne illness. We previously found that enterotoxigenic B. cereus is widely present in retail spices. Here we analyzed the spore heat resistance of nine diarrheal strains isolated from spices. Seven had D_95°C values ranging from 0.64 to 3.53 min while two emetic strains had D_95°C values of 7.04 min and 6.64 min. The ability of selected strains to grow in cooked rice at temperatures 20 °C, 17 °C and 12 °C was determined as well as their toxin expression capability. After 48 h, B. cereus levels of 1.26 × 10⁷ and 3.8 × 10⁷ CFU/g were obtained in cooked rice maintained at 17 °C and 20 °C respectively. At 12 °C, counts did not reach 10⁴ CFU/g even after 48 h of incubation. The increase in the aerobic, mesophilic bacterial population (APC) and B. cereus population naturally present in 0.1% crushed pepper added to cooked rice was determined over a period of 48 h at 20 °C and 17 °C. Levels of B. cereus in pepper/rice samples reached a maximum of 1600 MPN/g at 20 °C while the APC was 2.4 × 10⁸/g at this temperature. When thyme, containing the same initial natural level of B. cereus, was added to rice in place of pepper, more than a five-fold greater level of B. cereus was detected at 20 °C. Since thyme contained initial APC of 2.5 log₁₀ less than pepper we conclude that the high APC functions in a competitive-exclusion manner, minimizing the growth of B. cereus and potentially other agents of foodborne illness. This is particularly relevant in instances of temperature abuse of foods and may explain the low incidence of foodborne illness due to B. cereus despite its widespread presence shown in previous surveys of market spices.     

The effect of stopping alcoholic fermentation on the variability of H,C and O stable isotope ratios of ethanol

Stopping fermentation using chemical or physical agents is an oenological procedure carried out in order to leave a pleasant amount of residual sugar in the wine. This process is typically used in the production of some Italian sweet wines (such as the famous Moscato d’Asti), where alcoholic fermentation is stopped once the alcoholic content reaches 4.5–10%. In this study, we investigated the effect of stopping fermentation on the isotopic values of (D/H)_I, (D/H)_II, δ¹³C and δ¹⁸O of ethanol obtained from wine. We examined 126 samples obtained by partially fermenting five different must samples (N = 4 fresh musts, N = 1 desulphited must) and 18 commercial Italian sweet wines. Fermentation stage was positively correlated with the δ¹³C and, in particular, the (D/H)_II values of ethanol, but not with the (D/H)_I and δ¹⁸O values. Partially fermented musts and traditional sweet wines were characterized by lower δ¹³C and (D/H)_II isotopic values. The (D/H)_II values were outside the normal range of variability for natural wines, which means that particular care must be taken in assessing the (D/H)_II of sweet wines in order to avoid misinterpreting the results.     

Use of chemical treatments applied alone and in combination to reduce Campylobacter on raw poultry

Research focussing on the use of chemicals to decontaminate poultry carcasses to reduce pathogenic and spoilage organisms has increased in recent years. The objective of this study was to evaluate the efficacy of 12% (w/v) trisodium phosphate (TSP), 2% (w/v) citric acid (CA) and 5% (w/v) capric acid sodium salt (CP) in reducing Campylobacter, total viable counts and total Enterobacteriaceae counts on poultry. These chemicals were also used in various combinations (TSP + CA, TSP + CP and CA + CP) to determine if sequential treatments would enhance microbial reductions. TSP (1.9–2.3 log₁₀ cfu cm²) and CP (2.2–2.4 log₁₀ cfu cm²) gave the largest Campylobacter jejuni reductions while TSP was the most effective at reducing TVC (0.9 log₁₀ cfu cm²) and TEC (0.9 log₁₀ cfu cm²). TSP + CP was the most effective combination treatment (2.9 log₁₀ cfu cm²) for reducing C. jejuni counts and was significantly (P < 0.05) greater than any of the single chemical treatments, with the exception of CP treatment against strain 1146 (2.4 log₁₀ cfu cm²). The TVC and TEC populations proved more resistant to combination treatments as only TSP + CP showed a significantly (p < 0.05) enhanced reductive efficacy in comparison to single CP treatment. This study provides further data on the efficacy of a number of potential chemicals used alone and in combination for the decontamination of raw poultry.     

Determination of melamine in dairy products by HILIC-UV with NH2 column

A HPLC method using a NH₂ column for determination of melamine was reported, with acetonitrile-H₃PO₄ (15 mmol L⁻¹, pH = 6.5) (V/V = 88:12) as mobile phase and UV detection at 215 nm. The tested parameters included mobile phase composition, percentage of organic solvent, and buffer concentration, and pH value and UV detection wavelength. Good linearity was observed within the concentration range of 0.005-32 mg L⁻¹ (n = 7, r = 0.9997), the detection limit was 0.003 mg L⁻¹ (S/N = 3). The chromatography mode was considered to be hydrophilic interaction chromatography (HILIC). The method was successfully applied to determine melamine in several dairy products, with acetonitrile as extract solvent of melamine and also as protein precipitant. The spike recovery of melamine was within 73-96%.     

Thermal inactivation of Salmonella Typhimurium on dressed chicken skin previously exposed to acidified sodium chlorite or carvacrol

Salmonella is a leading cause of foodborne illness and live poultry is a main reservoir of this pathogen, worldwide. Cross-contamination and transportation of contaminated poultry meat act as an important vehicle of Salmonella infections in humans. In this study, we assessed the effect of two antimicrobials; acidified sodium chlorite (ASC) and carvacrol followed by thermal treatment to inactivate Salmonella Typhimurium on dressed chicken skin. D-values (time in min for the pathogen to decrease by 90%) of Salmonella Typhimurium at 56, 60 and 64 °C on dressed chicken skin in the control samples, determined by linear regression, were 6.17, 3.16, 1.32 min, respectively. Two D-values calculated using a logistic model, ranged from 6.28 (D_1, major population, plus T_L) and 11.66 (D_2, heat-resistant subpopulation, plus T_L) min at 56 °C to 1.08 (D₁ plus T_L), and 2.07 (D₂ plus T_L) min at 64 °C. Pre-dipping in 100–300 ppm ASC or 0.02–0.06% carvacrol rendered the pathogen more sensitive to the lethal effect of heat. Thus, combination of antimicrobials with thermal inactivation was more effective in reducing heat resistance of the pathogen on dressed chicken surface. The model developed will assist poultry processors in estimating the time required for specific log reductions of Salmonella Typhimurium on chicken skin and thus, will contribute in designing acceptance limits at critical control points for chicken skins at lower times and temperatures for cooking.