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Y. enterocolitica is a Gram negative, straight, sometimes oval, short coccobacillus that belongs to the Enterobacteriaceae family. Y. enterocolitica is widely distributed and is found in the natural environment. The main reservoir for these bacteria is animals, but they are also found in water and soil that are contaminated with the fecal material of infected animals. Not all Y. enterocolitica strains are pathogenic for humans. Y. enterocolitica was divided into six bioserotypes: 1A, 1B, 2, 3, 4, 5 and human pathogenic strains usually belong to the bioserotypes 1B and 2-5, which are able to cause yersiniosis. The major animal reservoir for pathogenic strains are pigs. Infections are usually acquired by eating contaminated food, especially raw or undercooked pork products, but also unpasteurized milk, plant products, untreated water and other food stored at low temperatures, in which Y. enterocolitica is able to multiply. According to the EFSA report published in 2007, the percentage of food samples contaminated with Y. enterocolitica ranged from 0% in Spain and Italy to 26% in Austria. The infection of humans with Y. enterocolitica may result in a variety of symptoms. The most common are two forms: gastroenteritis and pseudoappendicitis. The first disease occurs most often in children, the second one mainly in adults. Culture methods which are commonly used in the identification of Y. enterocolitica are complicated, time-consuming, and the results are not always clear. Recently, several DNA-based methods have been developed to detect pathogenic Y. enterocolitica in different samples. The introduction of these methods into laboratory practice would facilitate the identification of these microorganisms.
A survey was conducted in order to determine the incidence of Campylobacter sp., Salmonella sp., L. monocytogenes, and VTEC in slaughtered cattle in Poland. Overall, 276 swab samples of cattle hides and 276 samples from the corresponding carcasses were analysed. Additionally, 238 beef meat samples, purchased at retail level, were tested. The hides were more frequently contaminated with Campylobacter sp. (24.6%) than with any other pathogens. On the other hand, the carcasses had the highest contamination with VTEC (10.9%). The occurrence of food-borne pathogens in minced beef was between 1.3% (VTEC) and 24.3% (L. monocytogenes). The findings reinforce the importance of controlling zoonotic pathogens in meat through a complete, continuous farm-to-fork test system.
The aim of the study was to investigate the prevalence of human pathogenic bacteria Salmonella, L. monocytogenes, Campylobacter and verotoxigenic E. coli (VTEC) in bovine carcasses and to assess the related health threat to consumer. The examined material consisted of 276 samples collected as swabs with sterile sponges from carcasses directly after evisceration in slaughterhouses, from 400 cm² of the brisket area. The samples were analyzed at a laboratory for the identification of the four above-mentioned pathogens by slightly modified ISO methods and molecular techniques. The bovine carcasses were mostly contaminated with VTEC (30 positive samples, 10.9%) as found by the amplification of the Shiga toxin stx gene by the PCR technique. The other microorganisms were identified in smaller proportions of the carcasses. Eight samples (2.9%) proved positive for Campylobacter spp., 7 (2.5%) for L. monocytogenes, and 5 (1.8%) were contaminated with Salmonella spp. The influence of the animals’ age on the carcass contamination was also analyzed: it was noted that the majority of isolates were present in samples recovered from cattle over 6 years old. Moreover, the influence of seasonality on the occurrence of the pathogens in the carcasses was tested, and it was demonstrated that the majority of L. monocytogenes were isolated in October and November. In the case of VTEC, most of the bacteria were isolated from the carcasses in October, November and December (83.3% of the isolates) whereas no VTEC was found in winter (January-March) and spring (April-June). Most of the Salmonella spp. positive samples (4 out of 5 carcasses) were found in the period of May-July. No seasonality was found in the case of Campylobacter spp. present in the bovine carcasses tested. The results of the study show that bovine carcasses are quite frequently contaminated with pathogenic microorganisms which may be a source of food-borne diseases. Taking this into account, proper hygiene throughout the entire food chain, especially at the stage of carcass processing in slaughterhouses, is necessary to protect the health of consumers.
Aim of the study: The study was conducted to assess the molecular relationship of verotoxigenic E. coli (VTEC) isolated from cattle slaughtered in abattoirs in the eastern part of Poland. Materials and Methods: A total of 50 non-O157 VTEC strains isolated from bovine hides and the corresponding carcasses were tested with the pulsed field gel electrophoresis (PFGE) method. Results and discussion: The XbaI restriction analysis enabled the clustering of the isolates into 19 PFGE profiles. Seven of them contained more than two strains with two groups of 8 isolates each. Furthermore, three profiles grouped two isolates and the remaining nine PFGE types were represented by only one strain. The PFGE results were analyzed in relation to identified VTEC serotypes (O186:H16, O185:H7, O181:H49, O177:H25, O175:H21, O174:H2, O153:H25, O153:H2, O148:H8, O139:H19, O117:H4, O91:HNT, O84:H28, O36:H19, O21:H25, O2:H6, O2:H32, ONT:H34) and presence of their virulence genes. It was found that strains of the same PFGE type were usually of the same serotype and possessed the same pathogenic markers. The most numerous profile was represented by eight isolates: all of these strains were identified as O2:H32 serotype and had the same virulence genes – vtx2 and vtx2e. Furthermore, the majority of the PFGE profiles grouped the strains isolated during the same day. PFGE analysis revealed that among the isolates obtained from hides and the corresponding carcasses five pairs of strains had an identical molecular profile. The present study provided valuable information concerning the molecular characterization of VTEC isolated from cattle at the slaughter level. The results reflected a low genetic diversity among VTEC isolates tested and may suggest a common source of contamination within the abattoir.
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