Survival of Campylobacter jejuni in Fresh and Heated Red Meat

1983 ◽  
Vol 46 (9) ◽  
pp. 771-774 ◽  
Author(s):  
PAUL KOIDIS ◽  
MICHAEL P. DOYLE

Studies were done to assess the ability of Campylobacter jejuni to survive in fresh ground beef during refrigerated storage and to identify time-temperature treatments needed to inactivate Campylobacter in ground and cubed red meat. The organism survived well in refrigerated ground beef containing large numbers of indigenous bacteria. Relatively little death (< 1.2-log10 reduction) occurred for 7 of 8 strains during 14 d at 4°C. C. jejuni inoculated into ground beef and cubed lamb meat was quite sensitive to heat treatment. D-values for inactivation of campylobacters in ground beef ranged from 5.9 to 6.3 min at 50°C and from 12 to 21 s at 58°C. D-values were generally greater when campylobacters were heated in lamb meat, ranging from 5.9 to 13.3 min and 12.5 to 15.8 s at 50 and 60°C, respectively. All strains of C. jejuni were more sensitive to heat than salmonellae, hence meat heated to a temperature sufficient to inactivate Salmonella spp. should be free of viable campylobacters.

1992 ◽  
Vol 55 (7) ◽  
pp. 492-496 ◽  
Author(s):  
I-PING D. HUANG ◽  
AHMED E. YOUSEF ◽  
ELMER H. MARTH ◽  
M. EILEEN MATTHEWS

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.


1982 ◽  
Vol 45 (6) ◽  
pp. 507-510 ◽  
Author(s):  
MICHAEL P. DOYLE ◽  
DEBRA J. ROMAN

Several factors were shown to influence the rate of inactivation of Campylobacter sp. when dried on a glass surface. These included strain, temperature and humidity, and medium used to suspend the organism. Of the strains evaluated, all of three isolates of Campylobacter jejuni exhibited greater tolerance to drying than did a strain of nalidixic acid resistant, thermophilic Campylobacter. Inconsistent results were obtained when organisms were dried and maintained at 25 C. Viable cells from two of four strains having an initial population of >107 were not recovered after 24 h in an anhydrous environment at 25 C. Under comparable conditions, drying C. jejuni FRI-CF8 in the presence of skim milk at 25 C resulted in a >107 log10 reduction of cells within 1 day in one instance; a 5 log10 decline after 7 days in another; and inactivation at an intermediate rate on a third occasion. Rates of death were greatly reduced when cells were dried and held at 4 C. At this temperature and in the presence of skim milk and an anhydrous environment, a 5 log10 reduction of CF8 occurred after 6 weeks. In all instances, greater survival occurred when organisms were dried in the presence of Brucella broth than in skim milk. When held in environments of different relative humidities (RH), survival was greatest in the presence of 14% or less RH. Results suggest that C. jejuni is generally quite sensitive to drying and storage at room temperature, but, at refrigeration temperature and the appropriate humidity, large numbers may survive drying and remain viable for several weeks.


Author(s):  
Linda Saucier ◽  
Éveline Plamondon

Mycobacterium avium subsp. paratuberculosis (Map) is the etiologic agent of Johne’s disease in bovine and other ruminants. Concern for public health was raised when the organism was also suggested to be responsible for Crohn’s disease in humans, although the evidence remains inconclusive. Nonetheless, limiting human exposure to Map is viewed as a proper precautionary measure. Hence, the efficacy of heat treatment to control the organism in milk has been studied but it has not been studied to the same extend in meat. In this study, aseptically prepared ground beef was obtained from beef semimembranosus muscle and inoculated with two stains of Map (ATCC 7080 and gN27) to determine the decimal reduction time (D-value) and temperature sensitivity (z-value) for each strain. A 25 g sample of meat was inoculated with 100 ul of culture to a final concentration of 107 cfu/g. The inoculum was evenly distributed in the meat, which was spread in a thin (2 mm) layer of to maximise heat transfer. Treatments were performed at 55, 60, 65 and 70 °C for times allowing a minimum 5-log reduction. D-values decreased significantly with temperature (P < 0.05) ranging from 80.5 ± 6.1 minutes to 12 ± 1 seconds for both Map strains. When compared to Escherichia coli ATCC 25922 and Enterococcus faecalis ATCC 7080, D-values were significantly lower for E. coli (P < 0.05) whereas E. faecalis was not consistently more resistant than the two Map strains and, therefore, cannot be used as a surrogate strain for Map control with heat treatment. The z-values were not significantly different (P > 0.05) amongst the four strains and ranged from 5.6 ± 0.1 °C to 6.2 ± 0.3 °C. The results suggest that a low concentration of Map could be controlled with conventional cooking methods.


1961 ◽  
Vol 16 (6) ◽  
pp. 955-959 ◽  
Author(s):  
W. Leonard Taylor ◽  
Albert R. Behnke

Body weight is frequently too gross as a reference base for physiologic parameters. Adequate techniques are available to measure such components as water and fat, but these procedures are time consuming and require special apparatus. The high correlation, however, between anthropometric circumferences, stature, and body weight makes possible a partition of weight into components, W( A) and W( B). In obese men it can be shown that the “trunk” W( A) component greatly exceeds the weight of W( B) referable chiefly to the extremities. In athletes, W( B) exceeds W( A). The average of W( A) and W( B) closely approximates body weight. From the anthropometric perimeters it is possible to calculate d values which can be used to construct a somatogram to provide quantitative representation of bodily configuration. The technique for procurement of the anthropometric data can be carried out on large numbers of individuals in minimal time and requires only a tape measure. Submitted on April 28, 1961


2018 ◽  
Vol 38 (9) ◽  
pp. 1838-1843
Author(s):  
Débora R. Silveira ◽  
Camile Milan ◽  
Marina M. Ferrasso ◽  
Priscila A. Dias ◽  
Thamíris P. Moraes ◽  
...  

RESUMO: Muitas espécies de animais silvestres de vida livre servem como reservatório de bactérias patogênicas que ameaçam a saúde humana e dos animais domésticos. Algumas bactérias, como Campylobacter jejuni, Campylobacter coli, Yersinia enterocolitica e Salmonella enterica, causam enfermidades em humanos e podem contaminar os animais domésticos e silvestres. O Núcleo de Reabilitação da Fauna Silvestre da Universidade Federal de Pelotas (NURFS-UFPel) soluciona uma demanda regional específica de atenção à fauna silvestre brasileira. O objetivo desse trabalho foi identificar a presença de Campylobacter jejuni, Campylobacter coli, Salmonella spp. e Yersinia enterocolitica em animais silvestres que se encontravam em processo de reabilitação. Foram coletadas amostras de fezes, com uso de zaragatoas estéreis, de 34 aves, 16 mamíferos e 23 répteis. Dos 73 animais amostrados, quatro (5,48%) albergavam Y. enterocolitica, sendo duas aves, um mamífero e um réptil. Salmonella e Campylobacter não foram isolados. Os perfis de bandas dos isolados de Y. enterocolitica analisados pela rep-PCR foram diferentes entre si. Esses resultados indicam que as cepas isoladas não estão relacionadas entre si, não possuindo uma origem comum recente. Vanellus chilensis, Turdus rufiventris, Didelphis albiventris e Pantherophis guttatus podem albergar Y. enterocolitica e eliminá-la nas fezes, oferecendo risco de disseminação desse micro-organismo no ambiente, além de constituírem possíveis fontes de contaminação para humanos e outros animais.


2003 ◽  
Vol 804 ◽  
Author(s):  
Randall S. Hay

ABSTRACTA combinatorial method to screen large numbers of dopants that affect the nucleation of yttrium-aluminum garnet was developed. The method involves heat-treatment of electron-transparent sol-derived thin films on TEM grids, and counting the number and size of nuclei by TEM. Advantages and limitations of the technique are discussed. Preliminary results are presented.


1999 ◽  
Vol 62 (7) ◽  
pp. 735-740 ◽  
Author(s):  
M. UYTTENDAELE ◽  
P. DE TROY ◽  
J. DEBEVERE

From January 1997 to May 1998, 772 samples of poultry carcasses and poultry products for sale on the retail market in Belgium were analyzed for the presence of Salmonella spp., Salmonella Enteritidis, Campylobacter jejuni, C. coli, and Listeria monocytogenes per 100 cm2 or 25 g. Poultry samples were contaminated with Salmonella (36.5%), C. jejuni and C. coli (28.5%), and L. monocytogenes (38.2%). In about 12.3% of the poultry samples, the L. monocytogenes contamination level exceeded 1 CFU per g or cm2. Significant differences in pathogen contamination rates of poultry products were noticed between the poultry products originating from Belgian, French, and U.K. abattoirs. Poultry products derived from broiler chickens running free in pine woods until slaughtering age (12 to 13 weeks) had a significantly (P &lt; 0.05) lower contamination rate of Salmonella than poultry products from enclosed broilers slaughtered at the age of 6 to 8 weeks. A significantly (P &lt; 0.05) lower pathogen contamination rate was noted for Salmonella, C. jejuni, and C. coli for poultry cuts without skin compared to poultry cuts with skin on. An increase in pathogen contamination rate was noticed during cutting and further processing. To diminish C. jejuni, C. coli, Salmonella, and L. monocytogenes contamination rates, hygienic rules of slaughter and meat processing must be rigorously observed. At the moment, zero tolerance for these pathogens is not feasible, and there is a need to establish criteria allowing these pathogens to be present at reasonable levels in the examined poultry samples.


1997 ◽  
Vol 60 (5) ◽  
pp. 471-475 ◽  
Author(s):  
ALICIA ORTA-RAMIREZ ◽  
JAMES F. PRICE ◽  
YIH-CHIH HSU ◽  
GIRIDARAN J. VEERAMUTHU ◽  
JAMIE S. CHERRY-MERRITT ◽  
...  

The USDA has established processing schedules for beef products based on the destruction of pathogens. Several enzymes have been suggested as potential indicators of heat processing. However, no relationship between the inactivation rates of these enzymes and those of pathogenic microorganisms has been determined. Our objective was to compare the thermal inactivation of Escherichia coli O157:H7 and Salmonella senftenberg to those of endogenous muscle proteins. Inoculated and noninoculated ground beef samples were heated at four temperatures for predetermined intervals of time in thermal-death-time studies. Bacterial counts were determined and enzymes were assayed for residual activity. The D values for E. coli O157:H7 were 46.10, 6.44, 0.43, and 0.12 min at 53, 58, 63, and 68°C, respectively, with a z value of 5.60°C. The D values for S. senftenberg were 53.00, 15.17, 2.08, and 0.22 min at 53, 58, 63, and 68°C, respectively, with a z value of 6.24°C. Apparent D values at 53, 58, 63, and 68°C were 352.93, 26.31, 5.56, and 3.33 min for acid phosphatase; 6968.64, 543.48, 19.61, and 1.40 min for lactate dehydrogenase; and 3870.97, 2678.59, 769.23, and 42.92 min for peroxidase; with z values of 7.41,3.99, and 7.80°C, respectively. Apparent D values at 53, 58, 63, and 66°C were 325.03, 60.07, 3.07, and 1.34 min for phosphoglycerate mutase; 606.72, 89.86, 4.40, and 1.28 min for glyceraldehyde-3-phosphate dehydrogenase; and 153.06, 20.13, 2.25, and 0.74 min for triose phosphate isomerase; with z values of 5.18, 4.71, and 5.56°C, respectively. The temperature dependence of triose phosphate isomerase was similar to those of both E. coli O157 :H7 and S. senftenberg, suggesting that this enzyme could be used as an endogenous time-temperature indicator in beef products.


2021 ◽  
Vol 9 (04) ◽  
pp. 304-313
Author(s):  
Jocelyn Constant Yapi ◽  
◽  
Jean Bedel Fagbohoun ◽  
Zranseu Ange Benedicte Deffan ◽  
Elvis Gbocho Serge Ekissi ◽  
...  

Peroxidase (POD) associated with the browning of fresh-cut fruits and vegetableswas extracted from purple skin eggplant(Solanum melongena L.) and characterised using reliable spectrophotometric methods. Maximal POD activity was found at 35 °C and pH 6.0 with guaiacol as the substrate. The enzyme was stable at his optimal temperature (35 °C) and hisat pH stability was in the range of 5.6 - 6.6.Peroxidase retained its full activity in the presence of ion K+, Cu2+, Na+, Pb2+ and Ba2+ but were inhibited strongly by the ion Fe2+ and Mg2+ and the reducing agents as sodium thiosulfateand ascorbic acid. Effect of heattreatment on eggplant peroxidase showed that D-values decreased with increasing temperature, indicating faster peroxidase inactivation at higher temperatures.At 60 °C, the D-values ranged from 20.42 to 54.24 min. Hence, heat treatment at 60 °C for 30 min reduced browning of eggplant fruit.These data can be used to predict prevention of browning in the purple skin eggplantby thermal inactivation and the use of chimical agents onthe enzyme.


1984 ◽  
Vol 47 (7) ◽  
pp. 530-531 ◽  
Author(s):  
MICHAEL H. BRODSKY

One hundred twenty-seven 60-d aged Cheddar cheese samples produced by 21 provincially inspected cheese plants were analyzed by 8 regional laboratories of the Ontario Ministry of Health. Coliforms were detected in 37 (31.2%) and fecal coliforms confirmed in 22 (18.3%) samples, with geometric mean counts per g of 92.5 and 79.3, respectively. Staphylococcus aureus was found in only two products at a level of &gt;1000 per g. Salmonella spp. and Campylobacter jejuni were not isolated from any of the samples tested. Yersinia enterocolitica was isolated from one product; however, the isolate was bile esculin-and salicin-positive, and considered a non-pathogenic biotype. The pH of these aged Cheddars ranged between 4.98 and 5.50, with a mean of 5.26. Alkaline phosphatase activity was detected in 94 (79.7%) of the 118 samples tested. These results suggest that 60-d aged raw milk Cheddar cheese produced in Ontario does not pose a significant bacteriological health risk.


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