The Combined Effect of High Hydrostatic Pressure and Mild Heat on Inactivation of Pathogens in Milk and Poultry

1998 ◽  
Vol 61 (4) ◽  
pp. 432-436 ◽  
Author(s):  
MARGARET F. PATTERSON ◽  
DAVID J. KILPATRICK

The combined effects of high hydrostatic pressure and heat on the inactivation of Escherichia coli O157:H7 NCTC 12079 and Staphylococcus aureus NCTC 10652 in poultry meat and ultra-high-temperature-treated (UHT) milk were investigated. The simultaneous application of high pressure and mild heating was more lethal than either treatment alone. The substrate was found to have a significant effect on the survival of the pathogens during treatment. For E. coli O157:H7, a 15-min treatment of 400 MPa at 50°C resulted in approximately a 6.0-log10 reduction in CFU/g in poultry meat and a 5.0-log10 reduction in UHT milk; however, a < 1-log10 reduction was achieved with either treatment alone. In contrast, for S. aureus, a 15-min treatment of 500 MPa at 50°C was required to achieve a 5.0-log10 reduction in poultry meat and a 6.0-log10 reduction in UHT milk. As before, a <1-log10 reduction in numbers was achieved with either treatment alone. The pressure-temperature inactivation curves of each organism, in each substrate, were fitted using the Gompertz equation. Polynomial expressions derived from the Gompertz variables were used to devise simple models which predicted the inactivation of each pathogen at various pressure-temperature combinations. Thus, a number of different pressure-temperature conditions could be chosen to achieve a desired inactivation level. The use of such models will provide flexibility in selecting optimum pressure processing conditions without compromising microbiological safety.

1995 ◽  
Vol 58 (5) ◽  
pp. 524-529 ◽  
Author(s):  
MARGARET F. PATTERSON ◽  
MICHELE QUINN ◽  
RYAN SIMPSON ◽  
ARTHUR GILMOUR

The effect of high hydrostatic pressure (up to 700 MPa) at 20°C on the survival of vegetative pathogens was investigated in 10 mM phosphate buffer (pH 7.0), ultra high-temperature-treated (UHT) milk, and poultry meat. In buffer, Yersinia enterocolitica was most sensitive, with a pressure of 275 MPa for 15 min resulting in more than a 105 reduction in numbers of cells. Treatments of 350 MPa, 375 MPa, 450 MPa, 700 MPa, and 700 MPa for 15 min were needed to achieve a similar reduction in Salmonella typhimurium, Listeria monocytogenes, Salmonella enteritidis, Escherichia coli O157:H7, and Staphylococcus aureus respectively. A significant variation in pressure sensitivity was observed between different strains of both L monocytogenes and E. coli O157:H7. The most resistant strains (L. monocytogenes NCTC 11994 and E. coli O157:H7 NCTC 12079) were chosen for further studies on the effect of substrate on pressure sensitivity. In both cases the organisms were more resistant to pressure when treated in UHT milk than in poultry meat or buffer. There was evidence, assessed by differential plating using trypticase soy agar with and without additional NaCl, that sublethally injured cells were present at pressures lower than were required for death. This information may be of value if pressure is combined with preservation treatments such as mild heating. The variation in results obtained with different organisms and in different substrates should be recognized when recommendations for the pressure processing of foods are being considered.


PLoS ONE ◽  
2018 ◽  
Vol 13 (3) ◽  
pp. e0194477 ◽  
Author(s):  
Mahboobeh Kashiri ◽  
Cuauhtemoc Marin ◽  
Raquel Garzón ◽  
Cristina M. Rosell ◽  
Dolores Rodrigo ◽  
...  

2002 ◽  
Vol 269 (18) ◽  
pp. 4666-4674 ◽  
Author(s):  
Toshihiko Kinsho ◽  
Hiroshi Ueno ◽  
Rikimaru Hayashi ◽  
Chieko Hashizume ◽  
Kunio Kimura

2004 ◽  
Vol 70 (5) ◽  
pp. 2660-2666 ◽  
Author(s):  
Abram Aertsen ◽  
Kristof Vanoirbeek ◽  
Philipp De Spiegeleer ◽  
Jan Sermon ◽  
Kristel Hauben ◽  
...  

ABSTRACT A random library of Escherichia coli MG1655 genomic fragments fused to a promoterless green fluorescent protein (GFP) gene was constructed and screened by differential fluorescence induction for promoters that are induced after exposure to a sublethal high hydrostatic pressure stress. This screening yielded three promoters of genes belonging to the heat shock regulon (dnaK, lon, clpPX), suggesting a role for heat shock proteins in protection against, and/or repair of, damage caused by high pressure. Several further observations provide additional support for this hypothesis: (i) the expression of rpoH, encoding the heat shock-specific sigma factor σ32, was also induced by high pressure; (ii) heat shock rendered E. coli significantly more resistant to subsequent high-pressure inactivation, and this heat shock-induced pressure resistance followed the same time course as the induction of heat shock genes; (iii) basal expression levels of GFP from heat shock promoters, and expression of several heat shock proteins as determined by two-dimensional sodium dodecyl sulfate-polyacrylamide gel electrophoresis of proteins extracted from pulse-labeled cells, was increased in three previously isolated pressure-resistant mutants of E. coli compared to wild-type levels.


2010 ◽  
Vol 76 (1) ◽  
pp. M47-M53 ◽  
Author(s):  
Shigeaki Ueno ◽  
Toru Shigematsu ◽  
Toshimi Hasegawa ◽  
Jun Higashi ◽  
Mayumi Anzai ◽  
...  

Author(s):  
Wei-Min Qi ◽  
Ping Qian ◽  
Jian-Yong Yu ◽  
Chi-Yu Zhang ◽  
Xiao Chen ◽  
...  

Bacillus subtilis and Escherichia coli were chosen to investigate the combined effect of high hydrostatic pressure (HHP) and Nisin on loss of viability, membrane damage and release of intracellular contents of microorganisms. The results showed that the combination of 200 IU/mL Nisin and HHP exhibited a synergistic effect over 2 log on the inactivation of B. subtilis at pressure 300 MPa. The similar synergistic effect was observed on the membrane damage and release of intracellular contents of B. subtilis. The Nisin alone had no effect against E. coli, which belongs to gram negative bacteria. However, at pressure 300 MPa, Nisin caused the membrane damage from 55% to 80%. The synergistic effect of Nisin and HHP on loss of viability, membrane damage and release of intracellular contents of E. coli were also illustrated when the HHP pressure exceeded 300 MPa as the consequence of the serious changes produced by HHP at higher pressure in the cell envelope. It allows the entry of Nisin molecules to cell membrane.


2000 ◽  
Vol 63 (12) ◽  
pp. 1713-1718 ◽  
Author(s):  
ERROL V. RAGHUBEER ◽  
C. PATRICK DUNNE ◽  
DANIEL F. FARKAS ◽  
EDMUND Y. TING

The effects of high hydrostatic pressure (HPP; 545 MPa) on strains of Escherichia coli O157:H7, Listeria monocytogenes, enterotoxigenic Staphylococcus aureus, and nonpathogenic microorganisms were studied in tomato-based salsa. Products were evaluated for the survival of the inoculated pathogens following HPP treatment and after storage at 4°C and 21 to 23°C for up to 2 months. Inoculated samples without HPP treatment, stored under the same conditions, were also evaluated to determine the effects of the acid environment of salsa on the survival of inoculated strains. None of the inoculated pathogens were detected in the HPP-treated samples for all treatments throughout the storage period. Inoculated pathogens were detected in the non–HPP-treated samples stored at 4°C after 1 month, with L. monocytogenes showing the highest level of survivors. In the non–HPP-treated samples stored at 21 to 23°C, E. coli and S. aureus were not detected after 1 week, but L. monocytogenes was detected in low levels. Studies with nonpathogenic strains of the pathogens were conducted at Oregon State University using HPP treatments in a semicontinuous production system. The nonpathogenic microorganisms (E. coli, Listeria innocua, Listeria welshimeri, and nonenterotoxigenic S. aureus) were inoculated together into a feeder tank containing 100 liters of salsa. Microbiological results of samples collected before HPP treatment and from the aseptic filler were similar to those obtained for the pathogenic strains. No survivors were detected in any of the HPP-treated samples.


2015 ◽  
Vol 61 (5) ◽  
pp. 351-356 ◽  
Author(s):  
Gabriela María Olmedo ◽  
Mariana Grillo-Puertas ◽  
Luciana Cerioni ◽  
Viviana Andrea Rapisarda ◽  
Sabrina Inés Volentini

Bacterial biofilms are commonly formed on medical devices and food processing surfaces. The antimicrobials used have limited efficacy against the biofilms; therefore, new strategies to prevent and remove these structures are needed. Here, the effectiveness of brief oxidative treatments, based on the combination of sodium hypochlorite (NaClO) and hydrogen peroxide (H2O2) in the presence of copper sulfate (CuSO4),were evaluated against bacterial laboratory strains and clinical isolates, both in planktonic and biofilm states. Simultaneous application of oxidants synergistically inactivated planktonic cells and prevented biofilm formation of laboratory Escherichia coli, Salmonella enterica serovar Typhimurium, Klebsiella pneumoniae, and Staphylococcus aureus strains, as well as clinical isolates of Salmonella enterica subsp. enterica, Klebsiella oxytoca, and uropathogenic E. coli. In addition, preformed biofilms of E. coli C, Salmonella Typhimurium, K. pneumoniae, and Salmonella enterica exposed to treatments were removed by applying 12 mg/L NaClO, 0.1 mmol/L CuSO4, and 350 mmol/L H2O2for 5 min. Klebsiella oxytoca and Staphylococcus aureus required a 5-fold increase in NaClO concentration, and the E. coli clinical isolate remained unremovable unless treatments were applied on biofilms formed within 24 h instead of 48 h. The application of treatments that last a few minutes using oxidizing compounds at low concentrations represents an interesting disinfection strategy against pathogens associated with medical and industrial settings.


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