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Medycyna Weterynaryjna
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2010
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tom 66
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nr 07
s.495-498,tab.,bibliogr.
The aim of the research was to determine the variation in the fatty acid profile of rabbit fat as related to the fat location in the carcass and the breed of the animal. Research material consisted of samples of subcutaneous fat from the scapular area, perirenal fat and intramuscular fat from thigh and scapular muscles collected from carcasses of 30 meat breed rabbits and 30 crossbreeds. Both groups of rabbits (females) were bred in small farms during summer and fed mainly with green fodder and root crops supplemented with ground barley and a small quantity of hay. Fatty acid composition was determined with a Varian CP 3800 gas chromatograph. The comparison of fatty acid profiles of the intramuscular, perirenal and subcutaneous fat of the meat breed rabbits revealed that intramuscular fat was characterized by higher contents of stearic acid (C18:0) and polyunsaturated fatty acids (PUFA) with the exception of linoleic acid (C18:3). Perirenal fat was characterized by higher contents of tetradecanoic acid (C14:1) and linoleic acid (C18:2), whereas the content of palmitoleic acid (C16:1) was the highest in subcutaneous fat. Intramuscular fat of crossbreeds was characterized by the highest content of palmitic acid (C16:0), whereas the quantity of linoleic acid (C18:2) was significantly higher in perirenal fat. Despite differences in the content of the above-mentioned fatty acids, total amounts of saturated fatty acids (SFA), monounsaturated fatty acids (MUFA) and polyunsaturated fatty acids (PUFA) in all types of fat examined and in both groups of rabbits were comparable. Generally, lipids of crossbreeds were characterised by a lower percentage of SFA and a higher percentage of PUFA, including mainly linoleic acid (C18:3), in comparison with the meat breed. These lipids also demonstrated better SFA/UFA and PUFA/MUFA ratios. Moreover, the fat of crossbreeds was characterized by a highly favourable n-6/n-3 fatty acid ratio. The research findings suggest that rabbit fat, especially the fat of crossbreeds, is a rich source of polyunsaturated fatty acids, including NNKT, and their mutual proportions are close to dietary recommendations.
The caviar group of products includes a subgroup of caviar substitutes. The raw material used to manufacture a substitute called white caviar are eggs of garden snails of the Cornu aspersum species. The nutritional value of every foodstuff depends on its nutrient content and caloric value. The goal of this study was to determine the nutritional value and protein quality commercially available substitute caviar manufactured from the eggs of the Cornu genus snails. The basic composition and amino acid profile were determined according to a procedure based on international standards (ISO). The carbohydrate content and caloric value were calculated according to the literature. We established that the caviar substitute had a high water content (81.41%) and low contents of protein (4.23%), fat (0.09%), carbohydrates (6.62%), and ash (7.65%), so that its caloric value was also low (44.16 kcal/100 g). The total amount of essential amino acids was 51.13 grams per 100 grams of protein, and that of non-essential amino acids was 48.37 grams per 100 grams of protein. The biological value of proteins was determined by calculating the chemical score (CS) and the essential amino acid index (EAAI). To calculate these values, we used a standard protein established by a joint FAO/WHO/UNU expert group to quantify the daily requirement for essential amino acids for an adult person. The limiting amino acid for the product in question was the sum of methionine and cysteine. CS was 130.43, and EAAI was 190.45. The chemical composition of the caviar substitute was characterized by a low content of nutrients that determine the caloric value of a product. The protein content of the product was characterized by a favourable amino acid composition and a high nutritional value measured by the CS and EAAI indicators. However, due to the low protein content and the low quantity of the product consumed, it is not a foodstuff significant to meeting the daily requirement for essential amino acids for an adult person.
The research was aimed at evaluating the nutritional value of mechanically separated meat (MSM) of two different the poultry species and to compare it with the corresponding characteristics of hand-separated meat. The research was conducted on chicken and geese meat obtained by pressure separation (with a SIMO Meat Separator), in which muscle tissue is ground along with bones, cartilage, and sinews. The raw material for the production of MSM included backs, wings, necks, and trunks (except for breast muscles) of broiler chickens and slaughter geese, as well as whole goose carcasses that did not meet commercial standards. Samples were collected during 20 production cycles. The examination was conducted on chicken and goose MSM, as well as on hand-separated chicken and goose meat, which consisted of breast and thigh muscle samples. Hand-separated muscles were the control. The total protein content was determined by the Kjeldahl method, the fat content by the Soxhlet method, the water content by desiccation at 105°C, the calcium content by flame atomic absorption spectrometry with a Varian Spectra AA 2807S spectrometer, and the phosphorus content by spectrophotometry with a Shimadzu UV-1800 spectrophotometer. Fatty acid composition was determined by gas chromatography with a Varian CP 3800 chromatograph. The amino acid profile of mineralized proteins was determined with an AAA 400 amino acid analyser (Ingos Praha). The biological value of proteins was determined on the basis of their amino acid composition by calculating the chemical score (CS) and the essential amino acid index (EAAI). The significance of differences between the characteristics under analysis was evaluated by Tukey’s test at p ≤ 0.05. The chemical composition of MSM of chickens and geese showed significant differences. Chicken MSM contained significantly more proteins, water, and calcium, but less fat than goose MSM. Hand-separated meat had significantly higher contents of proteins and water, but lower contents of fat and calcium than both kinds of MSM. The two kinds of MSM did not differ significantly in their phosphorus content, which however was significantly lower (by 50%) than that in hand-separated meat. The content of most amino acids in proteins was significantly higher in chicken MSM than in goose MSM. The content of amino acids in both kinds of MSM was significantly lower than in hand-separated meat. This was also true about exogenous amino acids, which are particularly important for the biological value of proteins. Compared with the amino acid composition of model proteins, the proportion of exogenous amino acids in MSM was unfavourable from the point of view of human nutritional needs. Amino acids that limited (CS) the absorption of proteins were sulphur amino acids in the case of chicken meat (both mechanically and hand-separated) and aromatic amino acids in the case of goose meat. The content of saturated fatty acids (SFA) differed significantly between MSM and hand-separated meat, as well as between chicken and goose MSM. The same pattern was observed for polyunsaturated fatty acids (PUFA). Unlike mechanically separated and hand-separated goose meat, chicken and goose MSM differed significantly in their monounsaturated fatty acid (MUFA) content. Our own research revealed an unfavourable proportion of PUFA n-6 to PUFA n-3 in chicken MSM (18:1) and confirmed a high nutritional value of fat in goose MSM (8:1) and in hand-separated goose meat (8-9:1). Fat in chicken and goose MSM differed significantly in the proportions of SFA to MUFA and to PUFA The content of monounsaturated fatty acids was twice as high as that of saturated fatty acids both in goose meat and in MSM produced from it. Our own research demonstrated that the proportion of unsaturated fatty acids (UFA) to saturated fatty acids (SFA) in goose MSM is better than that in chicken MSM. The nutritional value of mechanically separated poultry meat is considerably lower than that of hand-separated poultry meat. An excessive use of mechanically separated poultry meat in the production of meat products may significantly reduce their biological value.
Intensive development of food industry and international food trade, combined with the increasing migration of people, led to the appearance of new food products in the market in the second half of the 20th century. This tendency has been driven by the search for new sources of animal protein and by increasingly sophisticated culinary tastes of consumers. An example of such food are edible mollusks (Mollusca), including snails (Gastropoda). This study provides basic information on the natural occurrence and commercial farming of snails from the families Helicidae and Achantinidae, as well as on the technology used in the production of frozen meat of the Burgundy snail (Helix pomatia) and snails of the genus Cornu. The most important qualities of snail meat related to its energy value, digestibility, organoleptic characteristics, and biological value (with special emphasis on the content of exogenous amino acids and the fatty acid profile) are also described. A section devoted to the safety of snail meat discusses the current microbiological food safety criteria and process hygiene criteria. In addition, this section reviews literature data on the occurrence of the most important pathogenic bacteria (Salmonella sp., L. monocytogenes, coagulase-positive staphylococci, Bacillus sp., Clostridium sp., as well as molds and yeast), microbial indicators (E. coli), and other potentially pathogenic microorganisms in snail meat. Other safety issues discussed in the study are related to the fact that snails are bioindicators of heavy metal pollution in the environment as well as vectors of the parasitic flatworms Fasciola hepatica and F. gigantica.
The aim of the research was to investigate the influence of herbal supplementation of feed mixtures for broiler chickens on the fatty acid profile of their intramuscular and abdominal fat. The research was carried out on 210 ROSS broiler chickens, which were divided into 6 experimental groups and fed with starter, grower, and finisher feeds with 2-percent additions of a specific herb (pansy, hop, linden leaf, lemon balm, mint, or nettle). A control group was fed with feeds supplemented with flavomycin. The feed mixtures and water were given ad libitum. On the 42nd day of rearing, out of each group of chickens 4 cocks and 4 hens closest to the average body weight in their group were selected. The selected animals were slaughtered and subjected to a simplified directional analysis. The content of fatty acids in intramuscular and abdominal fat was determined with a Varian CP 3800 gas chromatograph. The research findings suggest that the 2-percent addition of herbs had a significant effect on the fatty acid profile. In intramuscular fat the content of saturated fatty acids, including especially palmitic acid, rose significantly in all experimental groups. On the other hand, herbs were found to have no effect on the content of monounsaturated fatty acids. The influence of the herbs under examination on the content of poliunsaturated fatty acids (PUFA) was diverse. The content of these acids in intramuscular fat increased in the case of chickens fed with linden-supplemented mixture and decreased in chickens fed with feeds supplemented with mint and nettle. Abdominal fat was characterised by a lower content of saturated fatty acids, which is desirable from the dietary point of view. The amount of monounsaturated fatty acids increased in all experimental groups. The addition of hop had the greatest stimulating effect on the content of these acids. The content of poliunsaturated fatty acids, including linoleic and alpha-linoleic acids, was considerably smaller in the group fed with the hop supplement. In the other experimental groups the level of these acids was comparable or higher than in the control group.
Snails of the genus Cornu are farm-raised as edible molluscs. Dissection is one of the basic diagnostic tests available in the breeding of these animals, used to determine the cause of death or disease, and to collect material for further laboratory tests. The aim of this article was to present a method for the dissection of snails for veterinary use based on the experience gained from 200 mollusc dissections, and to present a short description of the anatomical structure of snails. The method described is characterized by its speed and simplicity. The observations made during the dissection, as presented in the article provide valuable diagnostic information for veterinarians responsible for care on snail farms.
The aim of the study was to establish the variation in microbial contamination of quail eggshell surfaces depending on the frequency of hygiene-sanitary practices carried out in cages (washing, disinfection and fecal waste removal). The studies involved eggs collected from three quail breeding farms situated in south-eastern Poland and characterized with different frequencies of hygiene practices. From October to April, 50 eggs were collected from each farm at five different collection times, at 3-week intervals. The freshly laid eggs were collected in a sterile way directly from the cages, cooled and transported to the laboratory to be subjected to a rinsing treatment with a sterile solution technique to obtain 10–1/cm2 dilution of the eggshell surface. The obtained study material was evaluated for a total count of aerobic bacteria, numbers of proteolytic bacteria and bacteria from the Staphylococcus genus, counts of aerobic bacteria and microorganisms from the Enterobacteriaceae family, as well as the number of yeasts and moulds. As per entire egg surface, the presence of pathogenic microorganisms from the Salmonella, Campylobacter and Listeria genus were detected. The determinations were performed in accordance to Polish Standards. Relatively slight contamination of eggshell surfaces was established (from 4.7 × 102 up to 4.7 × 103 cfu/cm2 ), and its contamination level varied between the farms. Out of the microbial groups under study, Staphylococcus spp. constituted the predominant part of microbial flora (32.7-51.5%), yet only a single sample was found to harbor coagulase-positive staphylococci (Staphylococcus aureus subsp. anaerobius). The presence of neither moulds nor yeasts was confirmed on the shell of eggs collected from farm 1, while their counts on the eggs obtained from two other farms did not differ significantly and ranged between 0.8 × 102 and 1.2 × 102 . In two samples, microorganisms from the Listeria genus were recovered; however, the PCR studies did not confirm their belonging to the L. monocytogenes species. The presence of Campylobacter and Salmonella genus bacteria on the eggshells under study was not detected. It was found that frequency of hygiene-sanitary practices carried out at a farm had a significant effect on the level of microbial contamination of quail eggshell surfaces. The cleaning of cages (washing and disinfection) together with daily removal of feces considerably reduced microbial contamination of eggshells. The absence of bacterial pathogens of Campylobacter and Salmonella genus and L. monocytogenes on the studied eggshell surfaces and a low level of total microbial contamination indicate that quail eggs are safe for consumers on condition that sanitary regulations are observed.
The aim of the study was to analyze the results of sanitary and veterinary examinations of rabbits carried out by the Veterinary Inspectorate in slaughterhouses in Poland in 2010-2018. In this period, 8,980,660 rabbits were examined. Lesions and quality deviations were found in 42,779 carcasses, i.e. 0.48% of all carcasses examined. The most frequent causes of the rejection of the carcasses and internal organs of the rabbits examined were sepsis and pyaemia (36,369 cases), followed by excessive emaciation (1,686 cases), upper respiratory tract disease (1,655 cases), other causes not specified by name (1,438 cases), and coccidiosis (1,318 cases). Abnormal exsanguination (303), parasitic diseases other than coccidiosis (67), infectious diseases (14), and leukemia (2) were much less often the cause of rejection. During the period analyzed, there was a decrease in the number of cases of coccidiosis (except in 2017) and other parasitic diseases, but there was a several-fold increase in the occurrence of sepsis and pyaemia (in the years 2015-2018). Compared with the results of veterinary and sanitary examinations of rabbits in 2000-2010, there was an increase in the number of rabbits slaughtered and a reduction in the percentage of carcasses with pathological changes and carcasses deemed unfit for consumption. In the years 2010-2018, there was also an increase in the number of cases of sepsis and pyaemia and a significant decrease in the percentage of parasitic diseases (mainly coccidiosis).
The objective of the research was to determine the occurrence of microorganisms from the Salmonella spp. and Listeria spp. in raw and frozen (cooked) snail meat obtained from both, free-living population and farmed edible snails. The research material comprised the meat samples (25g each) collected from three snail species, i.e. Roman snail (Helix pomatia – HP), small brown garden snail (Cornu aspersum aspersum – CAA) and large brown garden snail (Cornu aspersum maxima – CAM). Roman snails came from natural environment and were harvested in the Wielkopolskia and Lower Silesia province area (region A and B, respectively). The Cornu genus snails were obtained from two different heliciculture farms located in the above mentioned provinces (farm A and B, respectively). In both farms, the snails were maintained under the mixed rearing system. The raw meat specimens taken from the edible portion of snail, that is the foot with collar and a fragment of mantle, were obtained after the snails were sacrificed in the laboratory. Whereas the frozen meat specimens came from the snail meat processing facility. The presence of Salmonella was analysed in a total of 300 samples, while Listeria in 240 ones. The studies also included pooled soil samples of 0.5 kg each collected from the polytunnels (the pre-fattening stage) and outdoor farming park plots (fattening stage). The studies for the Salmonella presence were performed in accordance to PN-EN ISO 6579:2003, whereas for Listeria in compliance with PN-EN ISO 11290-1:1999. Species identification of Listeria monocytogenes was made by the PCR technique. The Salmonella presence was not confirmed in any of a total of 300 specimens of raw and cooked snail meat under study. These pathogens were not isolated from the soil samples, too. The absence of these bacteria in the raw meat specimens indicates that salmonella do not occur in both, the natural habitat of Roman snails or environment of two farms producing Cornu genus snails. Bacteria of Listeria genus was detected in 101(42,1%) snail meat samples under investigation. This particularly high microbiota load was reported in raw meat as these bacteria contaminated from 60% (HP from region A and CAM from farm B) up to 75% (CAA from farm A) samples under investigation. Notably, a markedly lower (35%) percentage of specimens with listerie was established only in the Roman snail raw meat samples from the region B. The Listeria spp. presence was also stated in all the soil specimens. The thermal treatment of meat achieved the substantial reduction in the Listeria spp. load, yet it did not eliminate its presence. Frequency of listeria occurrence in the frozen meat specimens was from 1,6 (CAM from farm A) up to 6,5-fold (CAA from farm B) lower compared to raw meat. The PCR technique was used for the species identification of 15 selected strains, in that 11 from the raw meat specimens and 4 from the cooked meat. A total of 5 isolates were recognized as Listeria monocytogenes (2,1% of total specimens examined and 4,95% specimens with listeria burden). They came solely from the raw meat samples collected from the farmed snails, in that one from farm A (from CAA) and four from farm B (3 from CAA and 1 from CAM). Bacteria from the Salmonella and Listeria genera occur in the natural habitat of edible snails and this, pose a potential hazard to human health. Efficient implementation of control programs at the primary production is the first step that could largely limit the presence of these pathogens in farmed snails and consequently, in snail meat.
For many years Poland has been a highly recognized producer and supplier of Cornu aspersum (Cornu aspersum aspersum, Cornu aspersum maxima) and Helix pomatia snails in European markets. Exports include both live snails and snail-derived food products such as snail meat and eggs. Slime, used in pharmaceutical and cosmetic industries, is another economically significant snail-derived product. This paper presents standardized terminology for farm snails and outlines regulations concerning snail farming, trade, processing plants and snail meat obtained. The current results of microbiological studies of snail meat obtained in Poland are shown as well. The analysis conducted in this paper indicates the need to clarify legislation, especially with regard to snail farming, and to elaborate regulations on snail meat processing.
The objective of the research was to determine the microbiological status of raw and frozen (cooked) snail meat obtained from both free-living and farmed edible snails. The research material comprised meat samples (10 g each) collected from three snail species, i.e. Roman snail (Helix pomatia – HP), small brown garden snail (Cornu aspersum aspersum – CAA) and large brown garden snail (Cornu aspersum maxima – CAM). Roman snails were collected in their natural environment in Greater Poland Voivodeship (region A: HPA) and Lower Silesian Voivodeship (region B: HPB). The Cornu genus snails were obtained from two different heliciculture farms in Greater Poland Voivodeship (farm A: CAAA and CAMA) and Lower Silesian Voivodeship (farm B: CAAB and CAMB). In both farms, snails were maintained under the mixed rearing system. Raw meat samples, taken from the edible portion of snails, that is, the foot with the collar and a fragment of the mantle, were obtained after the snails had been sacrificed in the laboratory. Frozen meat samples came from a snail meat processing facility. The samples were analyzed to determine the total aerobic bacterial count and the counts of Enterobacteriaceae, Escherichia coli, Enterococcus, Staphylococcus, Pseudomonas and Aeromonas, as well as psychotropic and proteolytic bacteria counts. Proteolytic bacteria were counted according to appropriate methodology, whereas the counts of other groups of microorganisms were obtained in accordance with the Polish Standards. Bacterial contamination levels (expressed as log cfu/g) were analyzed using the Statistica software (version 10.0). All values are presented as means and standard deviations. The total aerobic bacteria counts for HPA, HPB, CAAA, CAMA, CAAB and CAMB samples were, respectively, 5.78, 5.10, 6.00, 6.55, 5.12 and 5.21 log cfu/g in the case of raw meat, and 4.59, 4.75, 4.60, 5.13, 4.25 and 4.68 log cfu/g in the case of frozen meat. It was found that bacteria from the Enterobacteriaceae family were prevalent in both raw and frozen snail meat. The percentage of contaminated samples oscillated between 73.3% (HPB and CAMB) and 96.7% (CAAA and CAAB) for raw meat and between 20% (CAAA) and 100% (CAMA) for frozen meat. The quantitative contamination of raw meat with Enterobacteriaceae varied from 2.54 (HPB) to 4.75 log cfu/g (CAAA) and was higher by 1.0 to almost 2.0 log in farm snail meat as compared to Roman snail meat. The quantitative contamination of frozen meat was lower, ranging from 0.5 (HPA, CAAA and CAMA) to 1.65 log cfu/g (CAMB). All samples of raw and frozen snail meat were free from E. coli (contamination below 1 log cfu/g). In the raw snail meat, enterococci were recovered from 3 (10%) HPA, 6 (20%) HPB, 9 (30%) CAAA, 18 (60%) CAMA, 6 (20%) CAAB and 17 (56.6%) CAMB samples. The contamination levels for HPA, HPB, CAAA, CAMA, CAAB and CAMB raw meat samples were, respectively, 0.3, 0.63, 0.42, 2.0, 0.66 and 1.57 log cfu/g. In the frozen snail meat, enterococci were detected in 13 (43.3%) HPA, 13 (43.3%) HPB, 6 (20%) CAAA, 16 (53.3%) CAMA, 1 (3.3%) CAAB and 10 (30%) CAMB samples. The contamination level was similar for all kinds of samples, ranging between 0.48 (CAAA) and 2.11 log cfu/g (CAMA). The percentages of raw and frozen meat samples contaminated with staphylococci were similar, ranging from 50% (HPA) to 86.7% (CAAB) for raw meat and from 50% (HPA) to 100% (CAAA, CAMA and CAMB) for frozen meat. Quantitative contamination levels were also similar, oscillating between 1.48 (HPA) and 2.84 log cfu/g (CAMB) for raw meat and between 1.89 (HPA) and 3.28 log cfu/g (CAMA) for frozen meat. The percentage of samples contaminated with psychotrophic bacteria was also similar for raw and frozen snail meat, varying from 90% to 100%. Quantitative contamination with these bacteria oscillated between 3.17 (HPB) and 5.53 log cfu/g (CAMA) for raw meat and between 2.95 (HPA) and 4.12 log cfu/g (CAMA) for frozen meat. Bacteria from the Pseudomonas genus were confirmed in 63.3% of raw meat samples, in which the contamination level ranged from 2.22 (HPA) to 4.15 log cfu/g (CAAA), and in 96.7% of frozen meat samples, which contained from 1.12 (CAMA) to 2.21 log cfu/g (HPB) of these microorganisms. In raw meat, bacteria from Aeromonas genus were identified in all HPA samples as well as in 29 (96.7%) HPB, 26 (86.7%) CAAA, 21 (70%) CAMA, 29 (96.7%) CAAB and 17 (56.7%) CAMB samples. These bacteria were also present in a similar proportion of frozen meat samples (46.7-100%). The contamination level for raw meat samples oscillated between 2.74 (CAMB) and 4.73 log cfu/g (CAAA), whereas for frozen meat samples, it was substantially lower, ranging between 1.14 (CAMA) and 2.58 log cfu/g (CAAB). Proteolytic microbes were isolated more frequently from frozen snail meat. The percentage of contaminated samples varied from 80% (HPB and CAAA) to 100% (the rest) for frozen meat and from 36.7% (CAMA) to 93.3% (CAMB) for raw meat. The quantitative contamination level for frozen meat ranged from 3.17 (CAAA) to 4.44 log cfu/g (CAMA) and was generally lower than in the raw meat, where it varied between 2.07 (HPA) and 4.90 log cfu/g (CAMA). Snail meat is characterized by a high level of total microbiological contamination. The species of snails and the place where they live are often significant factors determining the level of contamination, which is higher in farm snail meat than in Roman snail meat. Heat treatment reduced the counts of bacteria found in raw meat. The increase in the number of staphylococci and enterococci in frozen meat (statistically significant only for staphylococci in snail meat from farm A) suggests the possibility of a secondary contamination of heat-treated meat. Therefore, a necessary condition for obtaining a safe and durable product is absolute compliance by the staff with appropriate procedures for hand hygiene and proper handling of food during production.
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