The aim of the study was to assess the ability of pathogens metabolic repair from injury within 10 days of refrigerated storage of milk after high pressure treatment. Two pathogenic strains – Listeria monocytogenes ATCC 7644 (LM) and Escherichia coli ATCC 25922 (EC) were inoculated in ultrahigh-temperature treated (UHT) milk at concentration of about 107 CFU mLE-1 and treated at 400, 500, 550, and 600 MPa for 15 min with inlet temperatures 20 °C, and then stored at 4 ± 2 °C to evaluate survival and growth of pathogens. By increasing the applied pressure, an increased rate of the pathogens’ inactivation was achieved. After 10 days of storage, milk treated at 400 MPa showed growth over 3.5 log CFU mLE-1 of L. monocytogenes and 1.7 log CFU mLE-1 of E. coli. In 550 MPa and 600 MPa treated milk samples after 8 and 10 days of storage colony formation occurred (3 CFU mLE-1 (550 LM) and 2 CFU mLE-1 (550 EC, 600 LM and 600 EC)). Although high pressure treatment is effective method for reducing of pathogenic bacteria, the metabolic repair from injury of bacterial cells in milk during storage should be considered.

A total of 120 food samples from 6 traditional and 3 non-traditional (Oriental) public catering establishments in Latvia were taken. Preliminary all food samples were divided in three food groups (categories) depending on the components of the products and processing methods. Ready-to-eat foods (RTE) with high level of total amount of microorganisms (aerobic colony count-ACC) and total coliforms (TC), as well as appropriate infringements of hygienic requirements in public catering establishments which had an impact on microbial contamination were clarified. The reasons for microbiological contamination of RTE and the growth of the microorganisms were analyzed in dependence on food category group, the activity of hydrogen ions (pH) in food, food temperature at the sampling point, their processing mode and composition. Different indicator microorganisms including Staphylococcus, Enterobacter, Escherichia, Bacillus, yeasts, moulds and etc. were identified. The comparison between the temperature and pH and the level of microbiological contamination of the samples of food and hygienic practice in the catering establishments were clarified.