Comparison of Heat Resistance of Listeria monocytogenes in Milk as Determined by Two Methods

1987 ◽  
Vol 50 (1) ◽  
pp. 14-17 ◽  
Author(s):  
CATHERINE W. DONNELLY ◽  
ELIZABETH H. BRIGGS ◽  
L. SCOTT DONNELLY
Keyword(s):  
Listeria Monocytogenes ◽  
Thermal Resistance ◽  
Heat Resistance ◽  
Thermal Inactivation ◽  
Test Tube ◽  
Initial Population ◽  
Tube Versus

The thermal resistance of 3 strains of Listeria monocytogenes was compared using test tube versus sealed tube methods of thermal inactivation. All L. monocytogenes strains were rapidly inactivated in milk when survival was measured using sealed tube thermal inactivation methods. Calculated D62°C values ranged between 0.1–0.4 min for the three strains tested. In contrast, total inactivation of L. monocytogenes populations using test tube methods of thermal inactivation could not be accomplished within 30 min at 62°C. Extensive tailing of survivor curves was consistently observed. When an initial population of 5 × 106 L. monocytogenes/ml was heated at 72, 82, or 92°C, consistent survival of a population of 102–103 L. monocytogenes/ml after 30 min was observed. The results prove that the test tube method for measuring thermal resistance of L. monocytogenes is inaccurate. Reports of extraordinary heat resistance based upon this method are correspondingly inaccurate. L. monocytogenes cells, dispersed freely in milk, will not survive pasteurization.

Modeling the Effects of Temperature, Sodium Chloride, and Green Tea and Their Interactions on the Thermal Inactivation of Listeria monocytogenes in Turkey†

2014 ◽  
Vol 77 (10) ◽  
pp. 1696-1702 ◽  
Author(s):  
VIJAY K. JUNEJA ◽  
JIMENA GARCIA-DÁVILA ◽  
JULIO CESAR LOPEZ-ROMERO ◽  
ETNA AIDA PENA-RAMOS ◽  
JUAN PEDRO CAMOU ◽  
...  
Keyword(s):  
Listeria Monocytogenes ◽  
Sodium Chloride ◽  
Protective Effect ◽  
Heat Resistance ◽  
Green Tea ◽  
Thermal Inactivation ◽  
Heating Temperature ◽  
Lethal Effect ◽  
Interactive Effects ◽  
D Values

The interactive effects of heating temperature (55 to 65°C), sodium chloride (NaCl; 0 to 2%), and green tea 60% polyphenol extract (GTPE; 0 to 3%) on the heat resistance of a five-strain mixture of Listeria monocytogenes in ground turkey were determined. Thermal death times were quantified in bags that were submerged in a circulating water bath set at 55, 57, 60, 63, and 65°C. The recovery medium was tryptic soy agar supplemented with 0.6% yeast extract and 1% sodium pyruvate. D-values were analyzed by second-order response surface regression for temperature, NaCl, and GTPE. The data indicated that all three factors interacted to affect the inactivation of the pathogen. The D-values for turkey with no NaCl or GTPE at 55, 57, 60, 63, and 65°C were 36.3, 20.8, 13.2, 4.1, and 2.9 min, respectively. Although NaCl exhibited a concentration-dependent protective effect against heat lethality on L. monocytogenes in turkey, addition of GTPE rendered the pathogen more sensitive to the lethal effect of heat. GTPE levels up to 1.5% interacted with NaCl and reduced the protective effect of NaCl on heat resistance of the pathogen. Food processors can use the predictive model to design an appropriate heat treatment that would inactivate L. monocytogenes in cooked turkey products without adversely affecting the quality of the product.

Thermal Inactivation of Listeria monocytogenes in Chicken Gravy

1992 ◽  
Vol 55 (7) ◽  
pp. 492-496 ◽  
Author(s):  
I-PING D. HUANG ◽  
AHMED E. YOUSEF ◽  
ELMER H. MARTH ◽  
M. EILEEN MATTHEWS
Keyword(s):  
Heat Treatment ◽  
Listeria Monocytogenes ◽  
Heat Resistance ◽  
Thermal Inactivation ◽  
Refrigerated Storage ◽  
Department Of Agriculture ◽  
Large Numbers ◽  
Z Value ◽  
D Values ◽  
The U.S

Heat resistance of Listeria monocytogenes strains V7 and Scott A in chicken gravy and changes in heat resistance during refrigerated storage were studied. After chicken gravy was made, it was cooled to 40°C, inoculated with 105 CFU L. monocytogenes per ml of gravy, and then stored at 7°C for 10 d. Gravy was heated at 50, 55, 60, and 65°C immediately after inoculation and after 1, 3, 5, and 10 d of refrigerated storage. The D values for strains Scott A and V7 in gravy heated at 50°C at day 0 were 119 and 195 min and at day 10 they were 115 and 119 min, respectively, whereas at 65°C comparable values at day 0 were 0.48 and 0.19 min and at day 10 they were 0.014 and 0.007 min. Heat resistance (expressed as D values) was greater at day 0 than at the end of refrigerated storage. The z values ranged from 3.41 to 6.10°C and were highest at the early stages of chill storage and then decreased at the later stages. Strain V7 was more heat resistant than Scott A at 50°C. Strain Scott A always had a higher z value than did strain V7 at the same storage interval. A heat treatment greater than the 4-D process recommended by the U.S. Department of Agriculture was required to inactivate the large numbers of L. monocytogenes that developed in chicken gravy during refrigerated storage.

Evaluation of Microbiological Safety of Shrimp Cooked in a Microwave Oven

1995 ◽  
Vol 58 (7) ◽  
pp. 742-747 ◽  
Author(s):  
SRIKANTH GUNDAVARAPU ◽  
YEN-CON HUNG ◽  
ROBERT E. BRACKETT ◽  
P. MALLIKARJUNAN
Keyword(s):  
Mathematical Model ◽  
Listeria Monocytogenes ◽  
Heat Resistance ◽  
Constant Temperature ◽  
Microwave Power ◽  
Thermal Inactivation ◽  
Microwave Oven ◽  
D Values ◽  
Cooking Times ◽  
Temperature Water

The effect of different microwave power levels (240, 400, 560, and 800 W) on the survival of Listeria monocytogenes in inoculated shrimp was investigated. Thermal inactivation rates (D-values) of L. monocytogenes were determined using constant temperature water baths to establish the heat resistance of L. monocytogenes in shrimp. Shrimp were inoculated with approximately 5 × 105 CFU/g of a five-strain mixture of L. monocytogenes. One hundred grams of shrimp were cooked in the microwave oven at different power levels using cooking times predicted by a mathematical model as well as 20% longer times than those obtained from the model. No viable L. monocytogenes were detected in uninoculated shrimp after microwave cooking, but at least one replication of inoculated shrimp tested positive for the presence of Listeria. No viable L. monocytogenes were detected in shrimp cooked at 120% of predicted times.

Thermal Destruction of Listeria monocytogenes in Ice Cream Mix

1992 ◽  
Vol 55 (4) ◽  
pp. 234-237 ◽  
Author(s):  
V. H. HOLSINGER ◽  
P. W. SMITH ◽  
J. L. SMITH ◽  
S. A. PALUMBO
Keyword(s):  
Listeria Monocytogenes ◽  
Thermal Resistance ◽  
Heat Resistance ◽  
Thermal Destruction ◽  
Variable Viscosity ◽  
Ice Cream ◽  
High Fructose Corn Syrup ◽  
Corn Syrup ◽  
High Fructose ◽  
Solids Content

Thermal destruction of Listeria monocytogenes strain Scott A was studied in refrigerated ice cream mixes to evaluate the relationship of mix composition to heat resistance with differing heat treatments. A central composite response surface design with two independent variables (high fructose corn syrup solids content and milkfat content) and one dependent variable (viscosity of the mix) was developed. High fructose corn syrup solids (HFCSS) content ranged from 1 to 7%, milkfat (MF) content from 4 to 18%, and total solids content from 28 to 44%. Sucrose content (11%) and milk-solids-not-fat content (10%) were kept constant. D140°F values were established in the mixes with a simulated batch pasteurization procedure using closed vials. Survivor data indicated sigmoidal responses with initial shoulders and tailing, but shoulder values were not significantly affected by either HFCSS or MF. D and F (F = 7D + shoulder) values were significantly (p = 0.01, R2 = .88; p = 0.01, R2 = .89, respectively) correlated to HCFSS content with increasing heat resistance conferred at higher concentrations. MF content had little or no effect on thermal death time but had a greater effect on viscosity of the mix than did content of HFCSS. Increased thermal resistance of LM was associated with the common ice cream stabilizer used; stabilizer contained guar gum and carrageenan. Pasteurization guidelines for ice cream mix are adequate to ensure inactivation of LM. Since results suggest that major ingredients in ice cream, ice milk, and shake mixes increase thermal resistance of LM, it is important that every precaution be taken to inactivate the organism.

Thermal Inactivation of Conidia From Aspergillus flavus and Aspergillus parasiticus

1975 ◽  
Vol 38 (11) ◽  
pp. 678-682 ◽  
Author(s):  
M. P. DOYLE ◽  
E. H. MARTH
Keyword(s):  
Thermal Resistance ◽  
Heat Resistance ◽  
Aspergillus Flavus ◽  
Positive Relationship ◽  
Thermal Inactivation ◽  
Aspergillus Parasiticus ◽  
Moist Heat ◽  
Heat Resistant ◽  
D Values ◽  
Strain Dependent

Thermal resistance at 45, 50, 55, and 60 C of conidia from various strains of Aspergillus flavus and Aspergillus parasiticus was determined using a heating menstruum buffered at pH 7.0 with KH2PO4-NaOH. Heat resistance of conidia from both molds was strain-dependent. With moist heat at 45 C, D-values for conidia from various strains ranged from 14 to >161 h, whereas at 60 C the range was from 8 to 59 sec. At 50 and 55 C, D values ranged from 16 to 987 and 3 to 29 min, respectively. There appeared to be a positive relationship between the degree of heat resistance of conidia and the amount of aflatoxin produced by the different aspergilli. Conidia that were 15 and 20 days old were less resistant to heat than when they were 7 or 10 days old. Conidia that were produced on a substrate low in protein and high in glucose were more heat resistant than were those produced on a more proteinaceous substrate that contained little glucose.

Heat Resistance of Fungi Isolated from Frozen Blueberries

2008 ◽  
Vol 71 (10) ◽  
pp. 2030-2035 ◽  
Author(s):  
YUTAKA KIKOKU ◽  
NOBUHIRO TAGASHIRA ◽  
HIROYUKI NAKANO
Keyword(s):  
Thermal Resistance ◽  
Heat Resistance ◽  
Thermal Inactivation ◽  
Heat Resistant ◽  
Death Time ◽  
Naturally Occurring ◽  
Thermal Death ◽  
D Values ◽  
Thermal Death Time

This study dealt with the isolation, characterization, and identification of the fungal microflora of frozen blueberries imported from Canada. The thermal inactivation rates of the rarely studied isolated heat-resistant molds, Devriesia spp. and Hamigera striata, in naturally and artificially contaminated blueberry slurries were also determined. The D-values of naturally contaminating Devriesia spp. at 70, 80, 85, and 90°C were 714, 114, 44.4, and 14.1 min, respectively. The D-values of H. striata at 70, 80, 85, and 90°C were 909, 286, 42.6, and 10.3 min, respectively. The z-values calculated from the thermal death time curves were 11.0 and 6.9°C for Devriesia spp. and H. striata, respectively. Results also showed that in both test mold species, the naturally occurring molds had significantly higher thermal resistance than did the artificially contaminated counterparts. The results established by this study may be used by blueberry processors to prevent losses due to spoilage caused by the heat-resistant microorganisms.

scholarly journals Effect of Physical Structures of Food Matrices on Heat Resistance of Enterococcus faecium NRRL-2356 in Wheat Kernels, Flour and Dough

Foods ◽  
2020 ◽  
Vol 9 (12) ◽  
pp. 1890
Author(s):  
Biying Lin ◽  
Yufei Zhu ◽  
Lihui Zhang ◽  
Ruzhen Xu ◽  
Xiangyu Guan ◽  
...  
Keyword(s):  
Thermal Resistance ◽  
Heat Resistance ◽  
Enterococcus Faecium ◽  
Thermal Inactivation ◽  
Distribution Model ◽  
Heat Resistant ◽  
Wheat Kernel ◽  
First Order Kinetics ◽  
Food Matrices ◽  
Wheat Kernels

Nonpathogenic surrogate microorganisms, with a similar or slightly higher thermal resistance of the target pathogens, are usually recommended for validating practical pasteurization processes. The aim of this study was to explore a surrogate microorganism in wheat products by comparing the thermal resistance of three common bacteria in wheat kernels and flour. The most heat-resistant Enterococcus faecium NRRL-2356 rather than Salmonella cocktail and Escherichia coli ATCC 25922 was determined when heating at different temperature–time combinations at a fixed heating rate of 5 °C/min in a heating block system. The most heat-resistant pathogen was selected to investigate the influences of physical structures of food matrices. The results indicated that the heat resistance of E. faecium was influenced by physical structures of food matrices and reduced at wheat kernel structural conditions. The inactivation of E. faecium was better fitted in the Weibull distribution model for wheat dough structural conditions while in first-order kinetics for wheat kernel and flour structural conditions due to the changes of physical structures during heating. A better pasteurization effect could be achieved in wheat kernel structure in this study, which may provide technical support for thermal inactivation of pathogens in wheat-based food processing.

Development of a Dry Inoculation Method for Thermal Challenge Studies in Low-Moisture Foods by Using Talc as a Carrier for Salmonella and a Surrogate (Enterococcus faecium)

2015 ◽  
Vol 78 (6) ◽  
pp. 1106-1112 ◽  
Author(s):  
ELENA ENACHE ◽  
AI KATAOKA ◽  
D. GLENN BLACK ◽  
CARLA D. NAPIER ◽  
RICHARD PODOLAK ◽  
...  
Keyword(s):  
Thermal Resistance ◽  
Heat Resistance ◽  
Water Activity ◽  
Enterococcus Faecium ◽  
Thermal Inactivation ◽  
Death Time ◽  
Significant Difference ◽  
Growth Method ◽  
Low Moisture Foods ◽  
Inoculum Preparation

The objective of this study was to obtain dry inocula of Salmonella Tennessee and Enterococcus faecium, a surrogate for thermal inactivation of Salmonella in low-moisture foods, and to compare their thermal resistance and stability over time in terms of survival. Two methods of cell growth were compared: cells harvested from a lawn on tryptic soy agar (TSA-cells) and from tryptic soy broth (TSB-cells). Concentrated cultures of each organism were inoculated onto talc powder, incubated at 35°C for 24 h, and dried for additional 24 h at room temperature (23 ± 2°C) to achieve a final water activity of ≤0.55 before sieving. Cell reductions of Salmonella and E. faecium during the drying process were between 0.14 and 0.96 log CFU/g, depending on growth method used. There was no difference between microbial counts at days 1 and 30. Heat resistance of the dry inoculum on talc inoculated into a model peanut paste (50% fat and 0.6 water activity) was determined after 1 and 30 days of preparation, using thermal death time tests conducted at 85°C. For Salmonella, there was no significant difference between the thermal resistance (D85°C) for the TSB-cells and TSA-cells (e.g. day 1 cells D85°C = 1.05 and 1.07 min, respectively), and there was no significant difference in D85°C between dry inocula on talc used either 1 or 30 days after preparation (P > 0.05). However, the use the dry inocula of E. faecium yielded different results: the TSB-grown cells had a significantly (P < 0.05) greater heat resistance than TSA-grown cells (e.g. D85°C for TSB-cells = 3.42 min versus 2.60 min for TSA-cells). E. faecium had significantly (P < 0.05) greater heat resistance than Salmonella Tennessee regardless what cell type was used for dry inoculum preparation; therefore, it proved to be a conservative but appropriate surrogate for thermal inactivation of Salmonella in low-moisture food matrices under the tested conditions.

Effect of Prior Growth Conditions on the Thermal Inactivation of 13 Strains of Listeria monocytogenes in Two Heating Menstrua

2005 ◽  
Vol 68 (1) ◽  
pp. 168-172 ◽  
Author(s):  
SHARON G. EDELSON-MAMMEL ◽  
RICHARD C. WHITING ◽  
SAM W. JOSEPH ◽  
ROBERT L. BUCHANAN
Keyword(s):  
Listeria Monocytogenes ◽  
Thermal Resistance ◽  
Stationary Phase ◽  
Thermal Tolerance ◽  
Thermal Inactivation ◽  
Brain Heart Infusion ◽  
Acid Resistance ◽  
Growth Conditions ◽  
Ph Values ◽  
Ph Dependent

The thermal tolerance of 13 Listeria monocytogenes strains was tested using a submerged heating coil apparatus. The strains were grown individually for 18 h at 37°C in acidogenic tryptic soy broth (without dextrose) supplemented with 1% glucose and 1% glutamine (TSB+G) or nonacidogenic tryptic soy broth supplemented with 1% glutamine but containing no glucose (dextrose) (TSB−G). The former medium results in cells induced for pH-dependent, stationary-phase acid resistance, whereas the latter medium allows L. monocytogenes to grow to high numbers in the absence of glucose, yielding cells that are not induced for pH-dependent, stationary-phase acid resistance. The average final pH values of the 18-h TSB+G and the TSB−G cultures were 4.7 and 6.7, respectively. The cells grown in the acid resistance–inducing and non–acid resistance–inducing media were then tested in two heating menstrua that consisted of brain heart infusion broth adjusted to pH 3.0 and water activity (aw) of 0.987 or pH 7.0 and aw 0.970. In 14 of the 26 menstruum-strain combinations tested, the acid resistance–induced strains were more heat resistant then the equivalent noninduced cultures. No difference in the pattern of thermal resistance in response to induction of acid resistance was apparent among the different serovars tested. The results suggest that the ability of prior induction of acid resistance to enhance thermal resistance can vary substantially among L. monocytogenes strains.

Heat Resistance and Growth of Listeria monocytogenes in Liquid Whole Egg1,2

1990 ◽  
Vol 53 (1) ◽  
pp. 9-14 ◽  
Author(s):  
PEGGY M. FOEGEDING ◽  
SUSAN B. LEASOR
Keyword(s):  
Listeria Monocytogenes ◽  
Thermal Resistance ◽  
Heat Resistance ◽  
Growth Temperature ◽  
Generation Times ◽  
Liquid Whole Egg ◽  
D Values ◽  
Whole Egg

Listeria monocytogenes F5069, ATCC 19111, Scott A, and two L. monocytogenes strains isolated from egg were evaluated for growth and thermal resistance in liquid whole egg. Each strain grew in liquid whole egg at temperatures between 4 and 30°C, except Scott A which did not grow at 4 or 10°C. Generation times ranged from 24 h for F5069 to 51 h for ATCC 19111 at 4°C and from 7.8 h for one of the egg isolates to 31 h for ATCC 19111 at 10°C. Maximum populations for each strain increased with increasing growth temperature and were between 105 and 3 × 108 CFU/g. Decimal reduction times (D-values) of each L. monocytogenes strain in raw liquid whole egg were similar to D-values reported in milk. The heat resistance of all strains was similar. For L. monocytogenes F5069, D-values ranged from 22.6 min at 51°C to 0.20 min at 66°C. The zD-value for F5069 was 7.2°C. Minimal pasteurization parameters (60°C, 3.5 min) for liquid whole egg would result in 99 to 99.9% inactivation (populations reduced 2 to 3 log cycles) of the L. monocytogenes strains tested.

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