Fate of Small Populations of Listeria monocytogenes on Poultry Processed Using Moist Heat

1989 ◽  
Vol 52 (11) ◽  
pp. 768-770 ◽  
Author(s):  
SANDRA L. CARPENTER ◽  
MARK A. HARRISON
Keyword(s):  
Listeria Monocytogenes ◽  
Sampling Period ◽  
Small Populations ◽  
Inoculum Concentration ◽  
Heating Method ◽  
Initial Inoculum ◽  
Moist Heat ◽  
Cooking Process ◽  
Storage Temperatures

The survival of small populations of Listeria monocytogenes on poultry processed using a moist heating method was determined. Various inoculum concentrations (3.2 × 102, 4.8 × 103, and 4.7 × 104) were applied to chicken breasts which were cooked to an internal endpoint temperature of 73.9°C (165°F). After cooking, portions were either vacuum-packaged or wrapped in an oxygen permeable film and stored for up to 4 wk at 4°C or up to 10 d at 10°C. Some Listeria survived the cooking process regardless of the inoculum levels. Significant increases (p<0.05) in the L. monocytogenes population occurred for each inoculum concentration at both storage temperatures within the first sampling period (week 1 for 4°C and day 3 for 10°C). Samples stored at both temperatures were able to re-establish themselves to population levels at or above the initial inoculum. No differences were noted due to packaging.

Survival of Large Populations of Listeria monocytogenes on Chicken Breasts Processed Using Moist Heat

1989 ◽  
Vol 52 (6) ◽  
pp. 376-378 ◽  
Author(s):  
MARK A. HARRISON ◽  
SANDRA L. CARPENTER
Keyword(s):  
Growth Rate ◽  
Listeria Monocytogenes ◽  
Heat Treatments ◽  
Microbial Populations ◽  
Heating Method ◽  
Moist Heat ◽  
Three Samples ◽  
Large Populations ◽  
Storage Temperatures

The ability of Listeria monocytogenes to survive and proliferate on chicken processed using a moist heating method was investigated. Chicken breasts were inoculated with 106–107 microorganisms/g, cooked to one of five different cooking temperatures, then either vacuum packaged or wrapped in an oxygen permeable film and stored at 4°C for up to 4 weeks or at 10°C for up to 10 d. Lethality was directly related to the cooking temperatures employed in this study, however survivors were encountered at each of the heat treatments employed. By the fourth week of storage at 4°C, the L. monocytogenes population in all of the samples, except those cooked to 82.2°C increased significantly. In contrast, within the first week of storage at 4°C the population increased in only three samples (73.9°C film overwrap, 65.6°C and 71.1°C vacuum packaged). Storage at 10°C allowed microbial populations in 6 of the 10 treatments to significantly increase within 3 d, with the remaining 4 significantly increasing within 10 d. Differences in packaging influenced the growth rate of L. monocytogenes at both storage temperatures.

Inhibitory Activity of Colicin E1 against Listeria monocytogenes

2007 ◽  
Vol 70 (5) ◽  
pp. 1256-1262 ◽  
Author(s):  
BRENDA S. PATTON ◽  
JAMES S. DICKSON ◽  
STEVEN M. LONERGAN ◽  
SARA A. CUTLER ◽  
CHAD H. STAHL
Keyword(s):  
Escherichia Coli ◽  
Listeria Monocytogenes ◽  
Inhibitory Activity ◽  
Storage Temperature ◽  
Strain Differences ◽  
Inoculum Concentration ◽  
Gram Negative ◽  
Initial Inoculum ◽  
Colicin E1 ◽  
And Storage

Colicins are gram-negative bacteriocins produced by and effective against Escherichia coli and related species. Colicin E1 (ColE1) is composed of three functional domains, which collectively have a pore-forming effect on targeted bacteria. ColE1 binding and translocation domains are highly specific in contrast to the pore-forming domain, implying that ColE1 could be broadly effective. In this study, the activity of ColE1 against Listeria monocytogenes was evaluated in broth and on surfaces of ready-to-eat products. Individual strains of L. monocytogenes were examined in broth containing ColE1 at 0, 0.1, 1, or 10 μg/ml. Although strain differences in sensitivity to ColE1 existed, growth was significantly reduced in all strains at doses as low as 0.1 μg/ml. Sterilized ham slices were submerged in a five-strain L. monocytogenes cocktail (either 7 or 4 log CFU/ml) and placed in vacuum packages containing 0, 1, 5, 10, 25, or 50 μg of ColE1. Ham slices were then stored at 4 or 10°C, and samples were removed and examined for L. monocytogenes after 1, 3, 7, and 14 days. Reduction of L. monocytogenes by ColE1 was dependent on initial inoculum concentration and storage temperature. For slices stored at 4°C, treatment with 25 μg reduced Listeria growth below detection limits for the slices inoculated with 4 log CFU/ml for the entire 14 days, whereas for the 7-log CFU/ml slices, growth was detected at 7 days postinoculation. For slices stored at 10°C, 10 μg/ml ColE1 significantly inhibited growth of L. monocytogenes for up to 3 days for both inoculation groups. These data indicate that ColE1 is highly effective against Listeria.

scholarly journals Optimization of cultivation conditions for Microcystis aeruginosa for biodiesel production using response surface methodology

2020 ◽  
Vol 44 (1) ◽  
Author(s):  
Samar A. El-Mekkawi ◽  
N. N. El-Ibiari ◽  
Ola A. El-Ardy ◽  
Nabil M. Abdelmonem ◽  
Ahmed H. Elahwany ◽  
...  
Keyword(s):  
Response Surface ◽  
Microcystis Aeruginosa ◽  
Biomass Yield ◽  
Bubble Column ◽  
Biodiesel Production ◽  
Cultivation Conditions ◽  
Inoculum Concentration ◽  
Initial Inoculum ◽  
High Lipid ◽  
Oil Concentration

Abstract Background Biodiesel is expected to play a key role in the development of a sustainable, economical, and environmentally safe source of energy. The third generation of biodiesel is derived from microalgae and cyanobacteria that have sufficient amount of oil. The optimization of biomass and oil content in biodiesel production based on algal cultivation relies upon several factors. The present experimental work aims at optimizing some of the cultivation conditions to obtain maximum oil and biomass yield and create a prediction model that describe the effect of the initial inoculum concentration, and irradiance on the biomass yield and oil concentration were designed using Design Expert 6.0.8. Results The results revealed that the optimum surface-to-volume ratio for the airlift bubble column photobioreactor was 0.9, and the most applicable model for describing Microcystis aeruginosa growth was the hyperbolic tangent model with a model constant value of 1.294 mg·L− 1·d− 1/μmol·m− 2·s− 1. The optimum cultivation conditions were 81 μmol·m− 2·s− 1 irradiance and 67 mg·L− 1 initial inoculum concentration, and these conditions achieved a biomass yield of 163 mg·L− 1·d− 1 and an oil concentration of 143 mg·L− 1. Conclusions This work focused on the cultivation of microalgae in closed systems. Cyanobacteria as M. aeruginosa has high lipid content, and high lipid productivity makes it suitable as a lipid feed stock for biodiesel production. The response surface method was the most suitable route to study the simultaneous influence of irradiance and initial inoculum concentration through statistical methods as well as to establish a model for predicting the biomass yield and oil concentration of M. aeruginosa.

Listeria monocytogenes in Raw Milk: Detection, Incidence, and Pathogenicity

1987 ◽  
Vol 50 (3) ◽  
pp. 188-192 ◽  
Author(s):  
J. LOVETT ◽  
D. W. FRANCIS ◽  
J. M. HUNT
Keyword(s):  
United States ◽  
Listeria Monocytogenes ◽  
Sampling Period ◽  
Raw Milk ◽  
The United States ◽  
Isolation Method ◽  
Listeria Species ◽  
Adult Mice ◽  
Listeria Ivanovii

To determine the incidence of Listeria monocytogenes in raw milk, an isolation method was evaluated and used to analyze milk from three areas of the United States. The incidence varied by area from 0% in California to 7% in Massachusetts, with an overall incidence of 4.2%. The highest incidence found in any area during a single sampling period was 12% in Massachusetts in March 1985. During that same sampling, the incidence for all Listeria species was 26%. Of the 27 L. monocytogenes strains isolated during the survey, 25 were pathogenic in adult mice. One of three Listeria ivanovii isolated was pathogenic. No other isolates demonstrated pathogenicity.

Transfer of Salmonella and Campylobacter from Stainless Steel to Romaine Lettuce†

2003 ◽  
Vol 66 (12) ◽  
pp. 2231-2236 ◽  
Author(s):  
CHRISTINA M. MOORE ◽  
BRIAN W. SHELDON ◽  
LEE-ANN JAYKUS
Keyword(s):  
Stainless Steel ◽  
Salmonella Typhimurium ◽  
Sampling Period ◽  
Stainless Steel Surface ◽  
Inoculum Level ◽  
Drying Time ◽  
Initial Inoculum ◽  
Significant Difference ◽  
Serovar Typhimurium ◽  
Handling Practices

The degree of transfer of Campylobacter jejuni and Salmonella enterica serovar Typhimurium was evaluated from a stainless steel contact surface to a ready-to-eat food (lettuce). Stainless steel coupons (25 cm2) were inoculated with a 20-μl drop of either C. jejuni or Salmonella Typhimurium to provide an inoculum level of ~106 CFU/28 mm2. Wet and dry lettuce (Lactuca sativa var. longifolia) pieces (9 cm2) were placed onto the inoculated stainless steel surface for 10 s after the designated inoculum drying time (0 to 80 min for C. jejuni; 0 to 120 min for Salmonella Typhimurium), which was followed by the recovery and enumeration of transferred pathogens (lettuce) and residual surface pathogens (stainless steel coupons). For transfers of Salmonella Typhimurium to dry lettuce, there was an increase from 36 to 66% in the percent transfer of the initial inoculum load during the first 60 min of sampling and then a precipitous drop from 66 to 6% in percent transfer. The transfer of Salmonella Typhimurium to wet lettuce ranged from 23 to 31%, with no statistically significant difference between recoveries over the entire 120-min sampling period. For C. jejuni, the mean percent transfer ranged from 16 to 38% for dry lettuce and from 15 to 27% for wet lettuce during the 80-min sampling period. The results of this study indicate that relatively high numbers of bacteria may be transferred to a food even 1 to 2 h after surface contamination. These findings can be used to support future projects aimed at estimating the degree of risk associated with poor handling practices of ready-to-eat foods.

Effect of Oxygen Stress on Growth and Survival of Clostridium perfringens, Campylobacter jejuni, and Listeria monocytogenes under Different Storage Conditions

2015 ◽  
Vol 78 (4) ◽  
pp. 691-697 ◽  
Author(s):  
HAMZAH AL-QADIRI ◽  
SHYAM S. SABLANI ◽  
MAHMOUDREZA OVISSIPOUR ◽  
NIVIN AL-ALAMI ◽  
BYJU GOVINDAN ◽  
...  
Keyword(s):  
Listeria Monocytogenes ◽  
Campylobacter Jejuni ◽  
Clostridium Perfringens ◽  
Foodborne Pathogens ◽  
Storage Conditions ◽  
Growth And Survival ◽  
Anoxic Conditions ◽  
Initial Inoculum ◽  
Log Reduction ◽  
Packaged Food

This study investigated the growth and survival of three foodborne pathogens (Clostridium perfringens, Campylobacter jejuni, and Listeria monocytogenes) in beef (7% fat) and nutrient broth under different oxygen levels. Samples were tested under anoxic (<0.5%), microoxic (6 to 8%), and oxic (20%) conditions during storage at 7°C for 14 days and at 22°C for 5 days. Two initial inoculum concentrations were used (1 and 2 log CFU per g of beef or per ml of broth). The results show that C. perfringens could grow in beef at 22°C, with an increase of approximately 5 log under anoxic conditions and a 1-log increase under microoxic conditions. However, C. perfringens could not survive in beef held at 7°C under microoxic and oxic storage conditions after 14 days. In an anoxic environment, C. perfringens survived in beef samples held at 7°C, with a 1-log reduction. A cell decline was observed at 2 log under these conditions, with no surviving cells at the 1-log level. However, the results show that C. jejuni under microoxic conditions survived with declining cell numbers. Significant increases in L. monocytogenes (5 to 7 log) were observed in beef held at 22°C for 5 days, with the lowest levels recovered under anoxic conditions. L. monocytogenes in refrigerated storage increased by a factor of 2 to 4 log. It showed the greatest growth under oxic conditions, with significant growth under anoxic conditions. These findings can be used to enhance food safety in vacuum-packed and modified atmosphere–packaged food products.

Growth Modeling of Listeria monocytogenes in Pasteurized Liquid Egg

2013 ◽  
Vol 76 (9) ◽  
pp. 1549-1556 ◽  
Author(s):  
MIHO OHKOCHI ◽  
SHIGENOBU KOSEKI ◽  
MASAAKI KUNOU ◽  
KATSUAKI SUGIURA ◽  
HIROKAZU TSUBONE
Keyword(s):  
Listeria Monocytogenes ◽  
Specific Growth ◽  
Storage Temperature ◽  
Growth Parameters ◽  
Root Model ◽  
Natural Flora ◽  
Mean Square Errors ◽  
Kinetics Of ◽  
Storage Temperatures ◽  
Maximum Population Density

The growth kinetics of Listeria monocytogenes and natural flora in commercially produced pasteurized liquid egg was examined at 4.1 to 19.4°C, and a growth simulation model that can estimate the range of the number of L. monocytogenes bacteria was developed. The experimental kinetic data were fitted to the Baranyi model, and growth parameters, such as maximum specific growth rate (μmax), maximum population density (Nmax), and lag time (λ), were estimated. As a result of estimating these parameters, we found that L. monocytogenes can grow without spoilage below 12.2°C, and we then focused on storage temperatures below 12.2°C in developing our secondary models. The temperature dependency of the μmax was described by Ratkowsky's square root model. The Nmax of L. monocytogenes was modeled as a function of temperature, because the Nmax of L. monocytogenes decreased as storage temperature increased. A tertiary model of L. monocytogenes was developed using the Baranyi model and μmax and Nmax secondary models. The ranges of the numbers of L. monocytogenes bacteria were simulated using Monte Carlo simulations with an assumption that these parameters have variations that follow a normal distribution. Predictive simulations under both constant and fluctuating temperature conditions demonstrated a high accuracy, represented by root mean square errors of 0.44 and 0.34, respectively. The predicted ranges also seemed to show a reasonably good estimation, with 55.8 and 51.5% of observed values falling into the prediction range of the 25th to 75th percentile, respectively. These results suggest that the model developed here can be used to estimate the kinetics and range of L. monocytogenes growth in pasteurized liquid egg under refrigerated temperature.

scholarly journals Verification of prediction of growth of Listeria monocytogenes micro-organism in chicken meat

2000 ◽  
Vol 18 (No. 5) ◽  
pp. 183-186
Author(s):  
A. Landfeld ◽  
M. Karpíšková R Houška ◽  
K. Kýhos ◽  
P. Novotná
Keyword(s):  
Listeria Monocytogenes ◽  
Incubation Temperature ◽  
Chicken Meat ◽  
Raw Material ◽  
Plate Count ◽  
Raw Meat ◽  
Total Plate Count ◽  
Measured Water ◽  
Number Of Bacteria ◽  
Storage Temperatures

Raw chicken meat was comminuted and homogenised. There were measured water activity and pH (aw = 1 for temperature 25°C, pH = 5.8 for temperature 8°C). Input raw material was investigated for the presence of Listeria monocytogenes (negative) and the raw meat was inoculated by Listeria monocytogenes CCM 4699. Number of Listeria monocytogenes, total plate count and number of coliforms were determined in the range 0–7 days by bacteriological survey for the storage temperatures 4.9, 7 and 8.3°C. The increase of Listeria monocytogenes counts has been registered for temperature 4.9°C about log 1.5 CFU/g after 6 days, for temperatures 7 and 8.3°C about 2 log CFU/g (regarding to the starting counts). The prediction for listeria growth with the aid of Food MicroModel was also made. The best agreement between the experimentally analysed number of bacteria and prediction was received for the lowest incubation temperature 4.9°C.

Inhibition of Listeria monocytogenes and Escherichia coli O157:H7 on Beef by Application of Organic Acids†

1996 ◽  
Vol 59 (4) ◽  
pp. 370-373 ◽  
Author(s):  
R. K. PODOLAK ◽  
J. F. ZAYAS ◽  
C. L. KASTNER ◽  
D. Y. C. FUNG
Keyword(s):  
Escherichia Coli ◽  
Listeria Monocytogenes ◽  
Fumaric Acid ◽  
Rank Order ◽  
Escherichia Coli O157 ◽  
Inoculum Level ◽  
Initial Inoculum ◽  
E Coli ◽  
Lean Beef ◽  
Lactic Acids

Lean beef surfaces were inoculated with Escherichia coli O157:H7 and Listeria monocytogenes and then sanitized with fumaric, acetic, or lactic acid alone and in combined solutions of those acids at 55°C for 5 s. The initial inoculum level was 8.62 log CFU/cm2 and 5.13 log CFU/cm2 for L. monocytogenes and E. coli O157:H7, respectively. Fumaric acid at a concentration of 1% was the most effective acid in reducing the populations of L. monocytogenes by up to 1 log unit and E. coli O157:H7 by up to 1.3 log units when compared with acetic or lactic acids. The rank order of acids tested against the growth of L. monocytogenes and E. coli O157:H7 was fumaric acid followed by lactic and acetic acids. Fumaric acid at concentrations of 1.0% and 1.5% was more effective than any of the combined solutions of acids.

Effect of Single or Sequential Hot Water and Lactic Acid Decontamination Treatments on the Survival and Growth of Listeria monocytogenes and Spoilage Microflora during Aerobic Storage of Fresh Beef at 4, 10, and 25°C

2004 ◽  
Vol 67 (12) ◽  
pp. 2703-2711 ◽  
Author(s):  
KONSTANTINOS P. KOUTSOUMANIS ◽  
LAURA V. ASHTON ◽  
IFIGENIA GEORNARAS ◽  
KEITH E. BELK ◽  
JOHN A. SCANGA ◽  
...  
Keyword(s):  
Lactic Acid ◽  
Listeria Monocytogenes ◽  
Lactic Acid Bacteria ◽  
Hot Water ◽  
Microbial Profile ◽  
Spoilage Bacteria ◽  
Brochothrix Thermosphacta ◽  
Survival And Growth ◽  
Spoilage Microflora ◽  
Storage Temperatures

The survival and growth of Listeria monocytogenes and spoilage microflora during storage of fresh beef subjected to different decontamination treatments was studied. Fresh beef inoculated with a five-strain mixture of L. monocytogenes (5.18 log CFU/cm2) was left untreated (control) or was immersed (30 s) in hot water (HW; 75°C), 2% lactic acid (LA; 55°C), hot water followed by lactic acid (HW-LA), or lactic acid followed by hot water (LA-HW) and then stored aerobically at 4, 10, and 25°C for 25, 17, and 5 days, respectively. Initial populations of L. monocytogenes were reduced by 0.82 (HW), 1.43 (LA), 2.73 (HW-LA), and 2.68 (LA-HW) log CFU/cm2. During storage, the pathogen grew at higher rates in HW than in control samples at all storage temperatures. Acid decontamination treatments (LA, HW-LA, and LA-HW) resulted in a weaker inhibition of L. monocytogenes (P < 0.05) at 25°C than at 4 and 10°C. In general, the order of effectiveness of treatments was HW-LA > LA > LA-HW > HW > control at all storage temperatures tested. In untreated samples, the spoilage microflora was dominated by pseudomonads, while lactic acid bacteria, Enterobacteriaceae, and yeasts remained at lower concentrations during storage. Brochothrix thermosphacta was detected periodically in only a limited number of samples. Although decontamination with HW did not affect the above spoilage microbial profile, acid treatments shifted the predominant microflora in the direction of yeasts and gram-positive bacteria (lactic acid bacteria). Overall, the results of the present study indicate that decontamination with LA and combinations of LA and HW could limit growth of L. monocytogenes and inhibit pseudomonads, which are the main spoilage bacteria of fresh beef stored under aerobic conditions. However, to optimize the efficacy of such treatments, they must be applied in the appropriate sequence and followed by effective temperature control.

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