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The research objective was to determine the degree of microbial contamination of the soil from a silver fox farm and animal feces in accordance to the season of the year and sampling location. The air temperature and relative humidity as well as sample moisture at the sampling sites were also evaluated. The studies were performed from October until September. Soil samples were collected from under the cages (GI), between the rows of the cages (GII) and at a distance of 30 m from the cages (GIII), whereas fox feces were taken from under the cages (KI), between the rows of the cages (KII) and 45 m from the cages (KIII). The soil and feces samples underwent qualitative and qualitative microbial assessment. The total count of mesophilic, psychrophilic, proteolytic bacteria, actinomycetes, from the group of coli and E.coli was established, according to the Polish Norms. The qualitative evaluation included genus identification of bacteria from the family Enterobacteriaceae in compliance with commonly applied procedures. The highest bacterial count under study was found in October in the soil samples from under the cages (GI). Bacteria E. coli and Salmonella rods were recovered from the soil (GI) and (GII) throughout the year, while Enterobacter spp. and Citrobacter spp. were isolated only from some GI samples. The highest average number of bacteria in fox feces was also established in the samples collected from under the cages at the turn of December and January. It was found that increasing relative humidity significantly decreased the count of all the bacteria studied in fox feces, whereas elevated air temperature contributed to declining numbers of psychrophilic bacteria and from the coli group. In the feces samples taken throughout the research period E. coli, Salmonella spp. and Shigella spp. bacteria occurred, while Klebsiella spp., Enterobacter spp. were isolated in single samples. The growth of all the studied bacteria was affected by relative humidity and sample moisture, whereas psychrophilic bacteria and from the coli group by air temperature. Microbial contamination of the environment is substantially influenced by the season of the year and the pertaining atmospheric conditions, as the largest bacterial load in soil and feces was determined in autumn and winter. The highest bacterial numbers occur in soil and feces collected from under the cages, which is associated with increased organic matter (feces and feed leftover) content and medium moisture optimal for bacteria. Therefore, it is recommended to undertake preventive measures within the sanitary-veterinary supervision aiming at improvement of the state of health of fur bearing animals.
The purpose of the research was to evaluate the chilling environment - the waters from the spin-chillers and the air from the chilling rooms - on the bacterial contamination of broiler chicken carcasses after slaughter. The research was conducted on two chilling systems for poultry used in Polish slaughterhouses: immersion and evaporative chilling. Forty samples of water from the spin-chillers underwent microbiological analysis as well as 20 samples of air from chilling rooms of both chilling systems. The following were determined from the above-mentioned materials: the total count of aerobic bacteria and coliforms, as well as the psychrotrophic and proteolytic groups. The presence of Salmonella was only evaluated in the water samples from the refrigerators (20 samples from each of the systems). A significant influence of the type of chilling system on the contamination of the water from the spin-chillers has been demonstrated on all the evaluated groups of bacteria. Water derived from the evaporative chilling system contained significantly more microflora (8.9 × 10³ cfu/ml) in comparison to the immersion system (7.0 × 10³ cfu/ml), which might have been caused by the manual eviscerating of the carcasses. The chilling system varied the percentage of particular groups of evaluated bacteria in the total microflora contamination in the water from the spin-chillers. Depending on the chilling system the percentage of the coliforms was 5-9% of the total count of bacteria, the percentage of psychrotrophic bacteria from 43-52%, proteolytic bacteria from 27-40%. The presence of Salmonella was confirmed in the water from the spin- -chillers of both of the systems. They were isolated more frequently in the immersion system (90% of the samples were positive) than in the evaporative chilling (50%). The most frequently isolated serotype was S. Enteritidis, the presence of which was confirmed in half of all water samples under examination. The remaining serotypes (S. Agona, S. Infantis, S. Hadar and S. Cremieu) were isolated less frequently. The analysis of the microbiological contamination of the air from the chilling rooms only demonstrated significant differences between both systems in the Coli and proteolytic groups. The count of the above-mentioned bacteria in l m³ of air was lower in a chilling room of the immersion system than in an evaporative chilling. There were no differences in the total count of bacteria and in the psychrotrophic bacteria. The total contamination in l m3 of air in the immersion system amounted to 2.9 × 10³ cfu. The count of coliforms in this system was 6.8 × 10 cfu/m³, which constituted 2.34% of the total count of bacteria, while in the evaporative chilling it was 2.7 × 10² cfu (10%). The psychrotrophic bacteria contamination constituted l.4 × 10³ (48.27%) in the immersion and l.6 × 10³ (59.25%) in the evaporative chilling. Proteolytic bacteria constituted from 10% in the immersion to 33% in the evaporative chilling of the total count of bacteria. The chilling room environment has a significant impact on the bacterial contamination of broiler chicken carcasses in the final phase of their production - primarily through the water from the spin-chillers, but also as a result the air movement.
The objective of the research was to determine bacterial contamination on the surface of chicken carcasses as influenced by the order in which chickens were slaughtered during the day. The research was conducted on 75 carcasses of chickens aged 6-8 weeks, originating from a plant licensed to trade on the markets of the EU and to export to third countries. The plant complied with the HACCP system and had obtained ISO certificates related to production hygiene. The daily production of the plant amounted to 60 thousand chickens. The plant used an evaporative chilling system. Samples were collected on consecutive days of a production week. Each day, samples were collected three times: at the beginning of production (from the first 1,000 carcasses), in the middle (3,000-31,000 carcasses) and at the end (59,000-60,000 carcasses). A sample for examination consisted of skin removed from the breast and the thigh areas. Directly after chilling, 20 cm² of skin was collected by a destructive method from each carcass. The number of the following bacteria was determined per 1 cm² of skin: aerobic bacteria, psychrotrophic bacteria, Enterobacteriaceae and Enterococcus. The presence of Salmonella was determined in 25 g samples consisting of neck skin tissue from three carcasses. All microbiological examinations were conducted in accordance with Polish Standards. The results obtained were expressed as logarithms. The significance of differences was evaluated by Tukey’s multiple range test. The total count of aerobic bacteria amounted to 4.78 log CFU/cm² at the beginning of a slaughter cycle, 5.11 log CFU/cm² in the middle, and 5.19 log CFU/cm² at the end. The bacterial contamination of carcasses at the beginning of a slaughter day was significantly lower than contamination in the middle or at the end of the day, between which there was no significant difference. A similar pattern was observed for psychrotrophic bacteria, which numbered 4.56 CFU/cm² at the beginning of a slaughter cycle, 5.02 CFU/cm² in the middle, and 5.10 CFU/cm² at the end. The number of Enterobacteriaceae amounted to 2.97 CFU/cm² at the beginning of a slaughter cycle, 3.01 CFU/cm² in the middle, and 3.16 CFU/cm² at the end. No significant differences in contamination with this group of micro-organisms were observed between the three batches of samples. The number of Enterococcus amounted to 3.28 CFU/cm² at the beginning of a slaughter cycle, 3.33 CFU/cm² in the middle, and 3.38 CFU/cm² at the end. Salmonella were found on the skin of chickens from all three batches of samples collected during a slaughter day. They were detected in 7 samples (28%) collected at the beginning and at the end of a production day, and in 6 samples (24%) collected in the middle of the day. The predominant serotype was S. Enteritidis, but S. Virchow was also found in two samples collected at the beginning of a production day. The order in which chickens were slaughtered during a slaughter day had a significant influence on the general level of bacterial contamination and on the level of contamination with psychrotrophic bacteria. Carcasses of chickens slaughtered at the beginning of a production day were characterized by a lower general level of contamination, including contamination with psychrotrophic bacteria, compared with carcasses produced later during the day. No such pattern was observed for contamination with Enterobacteriaceae and Enterococcus. Salmonella were detected in 27% of carcasses examined. The time of slaughter did not appear to have any significant effect on contamination with these bacteria.
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