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.     

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

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

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.     

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.     

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.     

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

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

Estimation of growth parameters of Listeria monocytogenes after sublethal heat and slightly acidic electrolyzed water (SAEW) treatment

Time to detection experiments (TTD) based on turbidometry using an automatic Bioscreen C is a useful and straightforward method for estimating microbial growth parameters (lag time (λ), growth rate (μ) and “work to be done” (h₀)) at constant temperature. This study investigated the effects of slightly acidic electrolyzed water (SAEW) and heat treatment on Listeria monocytogenes growth at different recovery temperatures (10 °C, 15 °C, 25 °C, and 30 °C). Similar surviving and sublethally injured L. monocytogenes populations were obtained by heat treatment (55 °C for 10 min) and SAEW treatment (available chlorine concentration of 30 mg/l and ratio of bacteria against SAEW of 8:2 for 30 s). In these experimental conditions, stresses had greater impact on the λ and h₀ parameter in comparison with recovery temperature while there was no great change in growth rate under isothermal conditions. Larger λ values and h₀ parameters were observed in sublethal-heat injured L. monocytogenes (the maximum λ and h₀ parameters are 30.199 h and 1.6492) as compared to SAEW groups (the maximum λ and h₀ parameters are 22.634 h and 1.4396). The sensitivity analysis of SAEW and heat treatments on h₀ parameter indicated that SAEW treatment showed a higher influence. The collinearity diagnostics of independent variables [recovery temperature (T), μ, λ] for dependent variable (h₀ parameter) demonstrated that T, μ and λ had strong collinearity. In addition, the established secondary models in this study have good performances on predicting the effect of recovery temperature on bacterial growth parameters.     

Transmission of Listeria monocytogenes from raw chicken meat to cooked chicken meat through cutting boards

Listeria monocytogenes (L. monocytogenes) is a food-borne pathogen contaminating poultry products. Ready-to-eat (RTE) cooked chicken meat can easily be contaminated with L. monocytogenes in post-processing activities. This study aimed to determine transmission of L. monocytogenes from raw chicken meat to hot and cooled chicken meat through polyethylene and wooden cutting boards. Raw chicken breast samples were purchased from retail markets and were artificially contaminated with L. monocytogenes at concentration of 7.35 ± 0.22 log CFU/ml. Contaminated raw samples were placed on polyethylene and wooden cutting boards to simulate bacterial transfer to cutting boards. Cooked chicken samples (hot and cooled) were then placed on the same cutting boards to simulate transfer of bacteria from cutting boards to cooked meat. L. monocytogenes successfully attached to polyethylene and wooden cutting boards and recovered after holding time up to 1 h. Transmissions of L. monocytogenes to cooled cooked samples from both types of cutting boards were relatively higher than hot cooked samples. Moreover, transfer rates of L. monocytogenes from wooden cutting boards at holding time of 1 h to both cooled and hot cooked samples were lower than those from polyethylene cutting board. It is recommended to use different cutting boards for raw and cooked materials and apply detergents and hot water for cleaning procedure to eliminate L. monocytogenes attached to the cutting boards and prevent cross-contamination of final products.     

Growth of Listeria monocytogenes in salmon roe – A kinetic analysis

The objective of this study was to investigate the growth kinetics of Listeria monocytogenes in unsalted and salted (3%) salmon roe. Growth curves, developed using inoculated samples incubated at constant temperatures between 5 and 30 °C, were analyzed by curve-fitting to the Huang and Baranyi models using the USDA IPMP 2013. The experimental results showed that L. monocytogenes in salted samples exhibited approximately 40% longer lag times than the cells in unsalted samples under the same temperature condition, while the rates of bacterial growth were not affected by the addition of salt. The Ratkowsky square-root (RSR) model, Huang square-root (HSR) model, and an Arrhenius-type model were all shown suitable for evaluating the effect of temperature on specific growth rates. The estimated nominal minimum growth temperature in the RSR model was −0.5 °C, whereas the minimum growth temperature in HSR model was 2.57 °C. The HSR models may be more suitable for describing the temperature effect in salted salmon roe. The lag times of L. monocytogenes were found to change log-linearly with the specific growth rates. The mean h₀ in the Baranyi model was 0.742 in unsalted samples and 1.193 in salted samples, and did not appear to change with temperature in a systematic manner. In summary, kinetic models were developed for examining the effect of temperature on growth of L. monocytogenes in unsalted and salted salmon roe samples. The results may be used by the food industry and regulatory agencies to estimate the growth of L. monocytogenes in salmon roe, and to conduct risk assessments of this microorganism.     

The influence of acid stress on the growth of Listeria monocytogenes and Escherichia coli O157:H7 on cooked ham

Acid solutions are increasingly being used for decontaminating meat surfaces. On the surfaces of acid-treated meat, the population of microorganism is reduced due to the low pH of acids, and the subsequent growth of the microorganism is reduced due to the residual acids on meat surfaces. Microbial cells on meat surfaces subjected to acid treatments may cross-contaminate untreated meat surfaces, e.g., microorganisms on the surfaces of acid-treated cooked ham cross contaminate the untreated surfaces during slicing. The objective of this study was to examine this scenario in determining the subsequent growth of acid-treated Listeria monocytogenes and Escherichia coli O157:H7 on the surfaces of untreated meat. Cells of multiple-strain L. monocytogenes or E. coli O157:H7 were exposed to HCl solutions of pH 3, 4, or 5 and deionized water at room temperature for 24 h. The acid or deionized water-treated cells were inoculated separately onto cooked ham. Samples inoculated with L. monocytogenes were stored at 4 and 8 °C and samples inoculated with E. coli O157:H7 were stored at 10 and 12 °C. Populations of the pathogens on ham were enumerated during storage, and the lag phase durations (LPD, h) and growth rates (GR, log CFU/h) of the pathogens were determined. The populations of L. monocytogenes and E. coli O157:H7 in pH 5, 4, and 3 solutions were 1.2–3.1 and 0.6–2.4 log CFU/ml, respectively, lower than those in deionized water, indicating an increased acid stress on both microorganisms at lower pHs. L. monocytogenes subjected to pH 3 and pH 4 stresses and E. coli O157:H7 subjected to pH 3 stress exhibited significantly (p < 0.05) extended LPDs and reduced GRs on cooked ham. The growth of L. monocytogenes on ham was more readily reduced by acid stress than that of E. coli O157:H7. This study showed that acid treatments reduced the viability of L. monocytogenes and E. coli O157:H7and the acid stress reduced their subsequent growth ability on untreated ham. Therefore, cross-contamination of L. monocytogenes or E. coli O157:H7 cells from acid-treated meat surfaces onto untreated meat surfaces may not impose increased risk to the product.     

Ripening conditions: A tool for the control of Listeria monocytogenes in uncooked pressed type cheese

The effect of ripening conditions (two temperatures, 9 °C and 13 °C, and two relative humidities 93% and 97%) on the growth of Listeria monocytogenes and other microbial populations was evaluated in the cores and rinds of uncooked pressed type cheeses prepared with pasteurised milk and inoculated either with Streptococcus thermophilus only or with an anti-listerial consortium. Regardless of temperature and relative humidity (RH), inhibition by the anti-listerial consortium was stronger in the cheese cores than in the rinds. Temperature had no significant effect on L. monocytogenes counts in cores or rinds. However, at the beginning of ripening in the consortium cheese, L. monocytogenes growth was more strongly inhibited at 13 °C than at 9 °C. Regardless of inoculation type and ripening temperature, counts of L. monocytogenes were significantly lower in the cores and rinds of cheeses ripened at 93% than at 97% RH. Lactobacilli counts were higher at 13 °C than at 9 °C and at 93% than at 97% RH. Lactobacilli can help to inhibit L. monocytogenes by catabolising galactose and producing lactate. Further investigations will be needed to evaluate the effect of ripening at 13 °C and 93% RH on the sensorial properties of cheese.     

Thermal inactivation of Listeria monocytogenes from alheiras,traditional Portuguese sausage during cooking

D values were calculated at 55, 60 and 65 °C for five Listeria monocytogenes isolates using alheira (traditional Portuguese sausage) food matrix as heating menstrum. z values were also calculated and combined with internal alheiras temperature profiles during cooking in multiple ways, allowed estimations of percentages of L. monocytogenes survival.Survival percentages estimations showed that except for roasting, the remaining evaluated cooking methods might not be sufficient to inactivate this foodborne pathogen in alheiras at the minimum temperature profiles. However, it is important to note that all evaluated cooking methods were able to inactivate L. monocytogenes in alheiras at their maximum internal temperature profiles.     

Dynamic analysis of growth of Salmonella Enteritidis in liquid egg whites

Salmonella Enteritidis (SE) is a common foodborne pathogen associated with eggs and egg products. This research was conducted to study the kinetics of growth and survival of SE in liquid egg whites (LEW). A dynamic temperature profile that exposed SE to suboptimal temperatures and below the minimum growth temperature (T_min) was used with two isothermal conditions to develop kinetic models. One-step dynamic analysis was used to directly construct a tertiary model for describing the growth and survival of SE and determine the kinetic parameters.The results of kinetic analysis showed that the T_min was 7.7 °C and SE may die off at a rate of 2.78 × 10⁻³ log CFU/ml per h per °C below the T_min. The root mean square error (RMSE) of the model was 0.5 log CFU/ml, with 76.6% of the residual errors within ±0.5 log CFU/ml of the experimental observations. The model was validated under both dynamic temperature and isothermal conditions. Both growth and survival of SE was accurately predicted, with the RMSE of validation at < 0.5 log CFU/ml. For all the validation tests, nearly 75% of the residual errors were within ±0.5 log CFU/ml of the experimental observations.This study clearly demonstrated that the one-step dynamic analysis method is an accurate and efficient method for direct construction of predictive models and estimation of the associated kinetic parameters that govern the growth and survival of microorganisms in food. Since the mathematical model has been validated, it can be used to predict the growth and survival of SE in LEW during storage and distribution and for conducting risk assessment of this microorganism.     

Efficacy of electrolyzed oxidizing water as a pretreatment method for reducing Listeria monocytogenes contamination in cold-smoked Atlantic salmon (Salmo salar)

Listeria monocytogenes contamination in ready-to-eat (RTE) fish products, in particular in cold-smoked salmon is an important food safety concern. This study evaluated the antimicrobial activity of electrolyzed oxidizing (EO) water as a pretreatment method during the process of cold-smoked salmon to inactivate L. monocytogenes. In addition, the effect of EO water treatment on the sensory and textural quality of the final product was also evaluated. Raw Atlantic salmon (Salmo salar) fillets were inoculated with L. monocytogenes (with an approximately cell number of 6 × 10⁵ CFU/g L. monocytogenes ATCC 19114) and treated with EO water at three different temperatures (20, 30, and 40 °C) and at three different exposure time of 2, 6, and 10 min before the cold-smoking process. A combination of EO water and a mild temperature (40 °C) had reduced L. monocytogenes populations by 2.85 log₁₀ CFU/g. The sensory as evaluated by a consumer panel (N = 71) and texture, which was measured by texture analysis showed no significant changes between EO and mild temperature treated samples and the control.     

Behavior of Listeria monocytogenes type1 355/98 (85) in meat emulsions as affected by temperature,pH, water activity,fat and microbial preservatives

The aim of this work was to analyze the effect of temperature (10–30 °C), fat content (20–50%), sodium chloride (2.5–5.0%) and preservative concentrations: sodium nitrite (0–150 ppm), lactic acid (50–500 mM) and nisin (0–100 IU/g (international units per gram)) on the growth of Listeria monocytogenes in a meat emulsion system.Individual and simultaneous effects of the parameters were tested and the results were mathematical modeled; inhibition indexes were calculated in each case. The addition of 7.5% NaCI inhibited the growth of L. monocytogenes at 20 and 30 °C, however, at 10 °C, microbial counts reached approximately 10⁶ CFU/g. The addition of 50 mM of lactic acid to obtain a pH ≤ 5 inhibited the growth of L. monocytogenes. The combinations of lactic acid with sodium nitrite or with nisin showed an enhancement of the inhibitory effect. However, considering the low toxicity of nisin, the combination of lactic acid (50 mM) and nisin (20 IU/g) would be more acceptable in the prevention of the growth of Listeria monocytogenes.     

Estimating the efficacy of mild heating processes taking into account microbial non-linearities: A case study on the thermisation of a food simulant

Traditional and novel approaches for the calculation of the heat treatment efficiency are compared in this work. The Mild Heat value (MH-value), an alternative approach to the commonly used sterilisation, pasteurisation and cook value (F, P, C-value), is calculated to estimate the efficiency of a mild heat process. MH-value is the time needed to achieve a predefined microbial reduction at a reference temperature and a known thermal resistant constant, z, for log-linear or specific types of non-log-linear microbial inactivation kinetics. An illustrative example is given in which microbial inactivation data of Listeria innocua CLIP 20-595 are used for estimating the inactivation parameters under isothermal conditions of 58, 60, 63 and 66 °C by the use of the log-linear and the Geeraerd et al. (2000) model. Thereafter, dynamic temperature profiles (targeting at 54 and 57 °C) representing milk thermisation are exploited for illustrating the application of MH-value. Finally, the equivalent holding times of different temperatures are calculated taking into account the observed non-linearity.     

Influence of temperature on alkali stress adaptation in Listeria monocytogenes

Listeria monocytogenes cells may induce alkali stress adaptation when exposed to sublethal concentrations of alkaline cleaners and sanitizers that may be frequently used in the food processing environment. In the present study, the effect of temperature on the induction and the stability of such alkali stress adaptation in L. monocytogenes were investigated. Our results demonstrate that temperature plays a critical role in the induction of alkali stress adaptation in L. monocytogenes under sublethal alkaline conditions. Pre-exposure to pH 9.0 tryptic soy broth supplemented with 0.6% yeast extract (TSB-YE) at 37 °C induced pronounced alkali stress adaptation whereas sublethal alkaline pre-exposure at 4 °C failed to induce any alkali stress adaptation. Furthermore, this pattern of alkali stress adaptation in L. monocytogenes was not dependent on the length of pre-exposure time, the concentration of sublethal alkali, the types of alkaline agents and the growth phases of cells. In addition, alkali stress adaptation induced at 37 °C was completely reversed in pH 7.2 TSB-YE within 2 h at 37 °C or within 4 h at 22 °C. However, once it was induced at a higher temperature, alkali stress adaptation in L. monocytogenes remained stable at 4 °C for at least 4 h. Our findings suggest that even though cold temperatures do not induce alkali stress adapted phenotypes, but it can maintain the previously acquired alkali stress adaptation much longer in L. monocytogenes.     

Efficacy of Fir and Qysoom essential oils,alone and in combination,in controlling Listeria monocytogenes in vitro and in RTE meat products model

Listeria monocytogenes, frequently associated with ready-to-eat meat products (RTE-MP), is the causal agent of listeriosis, the virulent foodborne disease. Accordingly, this work aimed to study the effectiveness of essential oils (EOs) of different plants to control growth of L. monocytogenes in RTE-MP model. EOs antilisteric activities were screened by disk diffusion method. Then, efficacy of EOs (1% v/w) with strong inhibition activities were further examined in meat luncheon model, against 2 levels of L. monocytogenes strains cocktail (3 and 6 log CFU/g) coupled with storage at 4 °C for 14 days. The EOs of Fir and Qysoom showed to have the highest significant (p < 0.05) antilisteric activity. In the food model, L. monocytogenes populations in control samples increased by 4 log cycles after 14 days of storage at 4 °C. At the end of storage, for samples with low contamination; Fir, Qysoom, and EOs mixture had approximately 6.37, 6.04, and 5.53 log CFU/g of L. monocytogenes respectively, compared to 6.90 log of control. Whereas in the samples with high contamination level, populations reached to 8.43, 8.88 and 6.75 log CFU/g for Fir, Qysoom, and EOs mixture respectively, compared to 9.90 log of the control. The application of 1% EOs (v/w) to RTE-MP surfaces significantly showed to reduce (p < 0.05) the L. monocytogenes populations growth rate as compared to control in the 2 levels treatments after 14 days of storage at 4 °C. Accordingly, our results suggest that these EOs could be used as natural bio-preservatives in many food products produced in Jordan and worldwide, particularly in RTE-MP.     

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.     

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.