Inhibition of Listeria monocytogenes in pH-Adjusted Pasteurized Liquid Whole Egg†

2003 ◽  
Vol 66 (6) ◽  
pp. 999-1006 ◽  
Author(s):  
JAMES D. SCHUMAN ◽  
BRIAN W. SHELDON

Although the transmission of L. monocytogenes to humans via pasteurized egg products has not been documented, L. monocytogenes and other Listeria species have been isolated from commercially broken raw liquid whole egg (LWE) in both the United States and Ireland. Recent Listeria thermal inactivation studies indicate that conventional minimal egg pasteurization processes would effect only a 2.1- to 2.7-order-of-magnitude inactivation of L. monocytogenes in LWE; thus, the margin of safety provided by conventional pasteurization processes is substantially smaller for L. monocytogenes than for Salmonella species (a 9-order-of-magnitude process). The objective of this study was to evaluate the inhibitory effects of nisin on the survival and growth of L. monocytogenes in refrigerated and pH-adjusted (pH 6.6 versus pH 7.5) ultrapasteurized LWE and in a liquid model system. The addition of nisin (1,000 IU/ml) to pH-adjusted ultrapasteurized LWE reduced L. monocytogenes populations by 1.6 to >3.3 log CFU/ml and delayed (pH 7.5) or prevented (pH 6.6) the growth of the pathogen for 8 to 12 weeks at 4 and 10°C. Bioactive nisin was detected in LWE at both pH values for 12 weeks at 4°C. In subsequent experiments, Listeria reductions of >3.0 log CFU/ml were achieved within 24 h in both LWE and broth plus nisin (500 IU/ml) at pH 6.6 but not at pH 7.5, and antilisterial activity was enhanced when nisin was added as a solution rather than in dry form.

2001 ◽  
Vol 64 (7) ◽  
pp. 934-938 ◽  
Author(s):  
R. E. BRACKETT ◽  
J. D. SCHUMAN ◽  
H. R. BALL ◽  
A. J. SCOUTEN

The heat resistance of six strains of Salmonella (including Enteritidis, Heidelberg, and Typhimurium) in liquid whole egg and shell eggs was determined. Decimal reduction times (D-values) of each of the six strains were determined in liquid whole egg heated at 56.7°C within glass capillary tubes immersed in a water bath. D-values ranged from 3.05 to 4.09 min, and significant differences were observed between the strains tested (α = 0.05). In addition, approximately 7 log10 CFU/g of a six-strain cocktail was inoculated into the geometric center of raw shell eggs and the eggs heated at 57.2°C using convection currents of humidity-controlled air. D-values of the pooled salmonellae ranged from 5.49 to 6.12 min within the center of intact shell eggs. A heating period of 70 min or more resulted in no surviving salmonellae being detected (i.e., an 8.7-log reduction per egg).


1989 ◽  
Vol 52 (11) ◽  
pp. 777-780 ◽  
Author(s):  
SUSAN B. LEASOR ◽  
PEGGY M. FOEGEDING

Commercially broken raw liquid whole egg (LWE) was obtained from 11 processing establishments across the United States on 3 or 4 occasions over an eight-month period. The samples were evaluated for the presence of Listeria species by the FDA, USDA, and cold enrichment procedures. Forty-five Listeria isolates were obtained from 15 of 42 (36%) egg samples. Both the USDA and FDA methods were useful for isolation of Listeria species, resulting in 12 and 8 positive samples, respectively. Six samples were positive by both procedures. Listeria was isolated from one sample by cold enrichment. The most frequently isolated species was L. innocua, which was found in all (15) of the listeriae-positive samples. L. monocytogenes was the only other species isolated and was obtained from 5% (2) of the egg samples. The USDA and FDA procedures each yielded one L. monocytogenes-positive sample. The two L. monocytogenes-positive samples contained estimated populations of 1 and 8 CFU L. monocytogenes/ml and were obtained from the same plant during the spring and early summer sampling times. Twelve (80%) of the 15 Listeria-positive samples were solids-adjusted LWE. Thus, Listeria species, including the psychrotrophic pathogen L. monocytogenes, are present in commercially broken raw LWE.


2007 ◽  
Vol 70 (6) ◽  
pp. 1402-1409 ◽  
Author(s):  
IGNACIO ALVAREZ ◽  
BRENDAN A. NIEMIRA ◽  
XUETONG FAN ◽  
CHRISTOPHER H. SOMMERS

The effect of combining irradiation and heat (i.e., irradiation followed by heat [IR-H]) on Salmonella Enteritidis and Salmonella Senftenberg inoculated into liquid whole egg (LWE) with added nisin, EDTA, sorbic acid, carvacrol, or combinations of these GRAS (generally recognized as safe) additives was investigated. Synergistic reductions of Salmonella populations were observed when LWE samples containing GRAS additives were treated by gamma radiation (0.3 and 1.0 kGy), heat (57 and 60°C), or IR-H. The presence of additives reduced the initial radiation Dγ-values (radiation doses required to eliminate 90% of the viable cells) by 1.2- to 1.5-fold, the thermal decimal reduction times (Dt-values) by up to 3.5- and 1.8-fold at 57 and 60°C, respectively, and the thermal Dt-values after irradiation treatments by up to 3.4- and 1.5-fold at 57 and 60°C, respectively, for both Salmonella serovars. Of all the additives investigated, nisin at a concentration of 100 IU/ml was the most effective at reducing the heat treatment times needed to obtain a 5-log reduction of Salmonella. Thus, while treatments of 21.6 min at 57°C or of 5 min at 60°C should be applied to achieve a 5-log reduction for Salmonella in LWE, only 5.5 min at 57°C or 2.3 min at 60°C after a 0.3-kGy radiation pretreatment was required when nisin at a concentration of 100 IU/ml was used. The synergistic reduction of Salmonella viability by IR-H treatments in the presence of GRAS additives could enable LWE producers to reduce the temperature or processing time of thermal treatments (current standards are 60°C for 3.5 min in the United States) or to increase the level of Salmonella inactivation.


1996 ◽  
Vol 59 (2) ◽  
pp. 121-126 ◽  
Author(s):  
PETER M. MURIANA ◽  
HUIYING HOU ◽  
RAKESH K. SINGH

A flow-injection system was devised to mimic continuous flow-through pasteurization systems for laboratory thermal inactivation studies. Air bubbles were introduced into the sample stream to create separate moving segments (plugs) of liquid stream during pasteurization while residence time was adjusted by a combination of pump speed and column length. The method was used to obtain thermal inactivation data for Listeria monocytogenes Scott A and Salmonella enteritidis ATCC 13076 in liquid whole eggs at different temperatures and heating times. Thermal inactivation of L. monocytogenes using the capillary tube method (Zcap = 7.3°C) gave results comparable to those obtained with the flow-injection system (Zflow = 7.2°C). The flow-injection system also was used to examine thermal inactivation of S. enteritidis (SE) grown in either tryptic soy broth (TSB) or egg yolk medium (EYM) before inoculation into liquid whole egg (LWE). D-values were obtained by regression analysis and the data showed that SE grown in EYM gave D-values 15 to 120% higher than those obtained for SE grown in TSB. Thermal inactivation studies performed with S. enteritidis grown in commercial broth media may therefore inaccurately represent thermal resistance of S. enteritidis grown in liquid or shell raw egg as may occur in egg-associated outbreaks. The continuous flow-injection system described herein may be adapted to study continuous flow pasteurization processes not easily examined by the traditional capillary tube method.


2003 ◽  
Vol 20 (5) ◽  
pp. 593-600 ◽  
Author(s):  
Pilar Mañas ◽  
Rafael Pagán ◽  
Ignacio Alvarez ◽  
Santiago Condón Usón

2012 ◽  
Vol 18 (3) ◽  
pp. 437-443 ◽  
Author(s):  
Young-Min BAE ◽  
Seung-Hee LEE ◽  
Jin-Hee YOO ◽  
Sun-Young LEE

1999 ◽  
Vol 62 (4) ◽  
pp. 414-417 ◽  
Author(s):  
J. J. FAN ◽  
J. H. CHEN

Welsh onion ethanol extracts were tested for their inhibitory activity against the growth and aflatoxin production of Aspergillus flavus and A. parasiticus. The survival of spores of A. flavus and A. parasiticus depended on both the extract concentration and the exposure time of the spores to the Welsh onion extracts. The mycelial growth of two tested fungi cultured on yeast extract–sucrose broth was completely inhibited in the presence of the Welsh onion ethanol extract at a concentration of 10 mg/ml during 30 days of incubation at 25°C. The extracts added to the cultures also inhibited aflatoxin production at a concentration of 10 mg/ml or permitted only a small amount of aflatoxin production with extract concentration of 5 mg/ml after 2 weeks of incubation. Welsh onion ethanol extracts showed more pronounced inhibitory effects against the two tested aflatoxin-producing fungi than did the same added levels of the preservatives sorbate and propionate at pH values near 6.5.


Author(s):  
M. M. Góngora-Nieto ◽  
L. Seignour ◽  
P. Riquet ◽  
P. M. Davidson ◽  
G. V. Barbosa-Cánovas ◽  
...  

2019 ◽  
Vol 11 (1) ◽  
Author(s):  
Hidas Karina Ilona ◽  
Ildikó Csilla Nyulas-Zeke ◽  
László Friedrich ◽  
Anna Visy ◽  
Judit Csonka ◽  
...  

Eggs are widely utilized because of their high nutrient value, coagulating, foaming, emulsifying and sometimes even colouring or flavouring facilities in food manufacturing. Production of processed egg products shows an increasing trend. Frozen products belong to first processing, their shelf life can increase up to 1 year. By freezing, a large reduction in microbial loss can be achieved. But different undesirable processes can occur. The effect of freezing on animal cells is highly dependent on freezing parameters. It has a different effect on egg subtituents. Egg yolk undergoes a gelation process while proteins can denaturate. In our study pasteurized liquid egg products (liquid egg white, liquid egg yolk and liquid whole egg) were frozen by dripping into liquid nitrogen. After that, a 14-day frozen storage experiment was carried out at -18°C. Before freezing and on the 1th, 7th and 14th days of storage experiment pH, dry matter content, colour and calorimetric properties (denaturation temperatures and enthalpy of denaturation) with differential scanning calorimetry were tested. For statistical analysis, one-way ANOVA (α = 0.05) was employed. In our experiment, we found no significant change in calorimetric properties of liquid egg white after freezing, but significant decreasing of enthalpy and denaturation temperatures of liquid egg yolk and liquid whole egg was identified. In contrast, frozen storage had a decreasing effect in all these products. Freezing caused a clearly visible colour change in LEW, a visible change in colour of LWE and a very clearly visible change in colour of LEY. In case of LEW and LEY changes increased to clearly visible 14 days. In conclusion, our results show that frozen storage had a greater effect on liquid egg products properties than freezing in liquid nitrogen.


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