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HYGIENE AND SAFETY OF EDIBLE SNAILS

机译:卫生和食用蜗牛的安全

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The aim of the present work was to determine the microbial indicators and the presence of Salmonella spp. of live snails Helix aspersa and Helix lucorum intended for human consumption. Samples of live wild snails (Helix aspersa and Helix lucorum) from Greek markets and farmed snails (Helix aspersa) from experimental breeding of University of Thessaly were taken for microbiological analysis. The following microbiological parameters were counted: (a) Total Viable Counts on Tryptone Soy Agar, (b) Enterobacteriaceae using Violet Red Bile Glucose Agar (c) Escherichia coli / conliforms using chromogenic agar medium and (d) Enterococcus sp. on Kanamycin Aesculin Azide Agar. Detection of Salmonella spp was conducted as follows: pre-enrichment on Buffered Peptone Water, enrichment on Rappaport-Vasiliadis (RVS) and Mueller-Kaufmann Tetrathionate (MKTTn) broth. Xylose, Lysine Deoxycholate (XLD) and Brilliant Green Agar (BGA) were used to isolate the presumptive Salmonella spp. colonies. Confirmation of presumptive Salmonella spp. colonies was carried out using biochemical tests (API 20E, Biomerieux) and Salmonella 0, V kar Hi anti-sera. Salmonella spp. was detected in the intestines and body of wild snails Helix aspersa and Helix lucorum compare to farmed ones, where no Salmonella spp. was detected. The results showed population differences for all the categories of micro-organisms counted in intestines and body between wild Helix aspersa and Helix lucorum, as well as between wild and breeding Helix aspersa snails. Snails directed for human consumption contain high levels of bacterial populations in intestines and bodies and the presence of pathogens may be possible. The absent of Salmonella spp. in breeding snails shows that the controlled conditions decrease the possibility of pathogen presence and contribute to food safety and public human health.
机译:本工作的目的是确定微生物指标和沙门氏菌的存在。供人类食用的活蜗牛Helix aspersa和Helix lucorum系列。取自希腊市场的活野生蜗牛(Helix aspersa和Helix lucorum)样品以及色萨利大学实验品种的养殖蜗牛(Helix aspersa)样品进行微生物学分析。对以下微生物学参数进行了计数:(a)胰蛋白p大豆琼脂上的总存活计数,(b)使用紫红色胆汁葡萄糖琼脂的肠杆菌科细菌(c)使用生色琼脂培养基和(d)肠球菌sp。的大肠杆菌。卡那霉素七叶皂苷叠氮化物琼脂上。沙门氏菌属的检测方法如下:在缓冲蛋白Water水中进行预富集,在Rappaport-Vasiliadis(RVS)和Mueller-Kaufmann Tetrathionate(MKTTn)肉汤中富集。木糖,赖氨酸脱氧胆酸盐(XLD)和亮绿琼脂(BGA)用于分离推测的沙门氏菌属。群落。推定沙门氏菌的确认。使用生化测试(API 20E,Biomerieux)和沙门氏菌0,V kar Hi抗血清对菌落进行克隆。沙门氏菌在野蜗牛的肠和体内检测到的螺旋藻与未耕种沙门氏菌的养殖蜗牛相比。被检测到。结果表明,野生螺旋as和螺旋lu之间以及肠道和野生螺旋as螺之间在肠道和身体中计数的所有种类微生物的种群差异。供人类食用的蜗牛在肠道和身体中细菌含量高,可能存在病原体。沙门氏菌不存在。蜗牛的繁殖表明,受控条件降低了病原体存在的可能性,并有助于食品安全和公众健康。

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