Abuseir S, Epe C, Schnieder T, Klein G, Kühne M
Centre for Food Science, Institute for Food Quality and Safety, University of Veterinary Medicine Hannover, Bischofsholer Damm 15, 30173, Hannover, Germany.
Parasitol Res. 2006 Sep;99(4):405-9. doi: 10.1007/s00436-006-0158-3. Epub 2006 Apr 1.
A total of 267 cysts were collected from March to December 2004 from two main abattoirs in northern Germany. The cysts were classified by the usual organoleptic methods during meat inspection as Cysticercus bovis. The reported prevalence of cysticercosis in the abattoirs was 0.48 and 1.08%, respectively. The cysts were examined macroscopically for description of their morphology and constituents and classified as viable or degenerating (dead). The DNA was extracted from these cysts and subjected to polymerase chain reaction (PCR) for evaluation of the detection methods used and to make certain that the cysts did indeed belong to C. bovis, as indicated at the slaughterhouses. Two sets of primers were used with different sensitivity levels. The first, HDP1, was able to detect 200 fg of Taenia saginata DNA and 100 pg of C. bovis DNA. The other primer set, HDP2, was able to detect 1 pg of T. saginata DNA and 1 ng of C. bovis DNA. No more than 52.4% of the samples tested positive for C. bovis in the PCR using both primers, while 20% of the viable cysts and 49.2% of the degenerating cysts tested negative with both primers.
2004年3月至12月期间,从德国北部的两家主要屠宰场收集了总共267个囊肿。在肉类检查期间,通过常规感官方法将这些囊肿分类为牛囊尾蚴。据报道,屠宰场中囊尾蚴病的患病率分别为0.48%和1.08%。对囊肿进行宏观检查,描述其形态和成分,并分类为活的或退化的(死的)。从这些囊肿中提取DNA,并进行聚合酶链反应(PCR),以评估所使用的检测方法,并确定这些囊肿确实如屠宰场所示属于牛囊尾蚴。使用了两组具有不同灵敏度水平的引物。第一组引物HDP1能够检测到200 fg的牛带绦虫DNA和100 pg的牛囊尾蚴DNA。另一组引物HDP2能够检测到1 pg的牛带绦虫DNA和1 ng的牛囊尾蚴DNA。在使用这两种引物的PCR检测中,检测为牛囊尾蚴阳性的样本不超过52.4%,而20%的活囊肿和49.2%的退化囊肿在两种引物检测中均为阴性。