Robertson L J, Gjerde B
Parasitology Laboratory, Department of Food Safety and Infection Biology, Norwegian School of Veterinary Science, 0033 Oslo, Norway.
J Food Prot. 2008 May;71(5):959-66. doi: 10.4315/0362-028x-71.5.959.
Investigation of shellfish for Cryptosporidium oocysts and Giardia cysts is of public health interest because shellfish may concentrate these pathogens in their bodies, and because shellfish are frequently eaten raw or lightly cooked. To date, the methods used for the analysis of shellfish for these parasites are based on those originally designed for water concentrates or fecal samples; the reported recovery efficiencies are frequently relatively low and the amount of sample examined is small. Here, we describe the development and use of a pepsin digestion method for analyzing shellfish samples for these parasites. The conditions of the isolation method did not affect subsequent parasite detection by immunofluorescent antibody test, and allowed examination of 3-g samples of shellfish homogenate, with recovery efficiencies from blue mussel homogenates of between 70 and 80%, and similar recoveries from horse mussel and oyster homogenates. Although exposure of the parasites to the conditions used in the technique affected their viability, as assessed by vital dyes, the maximum reduction in viability after 1-h incubation in digestion solution was 20%. In a preliminary survey of shellfish collected from the Norwegian coast, Cryptosporidium oocysts were detected in blue mussel homogenates in 6 (43%) of 14 batches and Giardia cysts in 7 (50%) of these batches. However, this relatively high occurrence, compared with other surveys, may be due to the higher recovery efficiency of the new method, and the relatively large sample size analyzed. A more comprehensive study of the occurrence of these parasites in shellfish would be of pertinence to the Norwegian shellfish industry.
对贝类进行隐孢子虫卵囊和贾第虫包囊的调查具有公共卫生意义,因为贝类可能在其体内富集这些病原体,而且贝类经常被生食或轻度烹饪。迄今为止,用于分析贝类中这些寄生虫的方法是基于最初为水浓缩物或粪便样本设计的方法;报道的回收率通常相对较低,且检测的样本量较小。在此,我们描述了一种胃蛋白酶消化法的开发及应用,用于分析贝类样本中的这些寄生虫。该分离方法的条件不会影响随后通过免疫荧光抗体试验进行的寄生虫检测,并且能够检测3克贝类匀浆样本,蓝贻贝匀浆的回收率在70%至80%之间,马贻贝和牡蛎匀浆的回收率与之相似。尽管通过活体染料评估,寄生虫暴露于该技术所用条件下会影响其活力,但在消化液中孵育1小时后活力的最大降低幅度为20%。在对从挪威海岸采集的贝类进行的初步调查中,14批蓝贻贝匀浆中有6批(43%)检测到隐孢子虫卵囊,其中7批(50%)检测到贾第虫包囊。然而,与其他调查相比,这种相对较高的检出率可能是由于新方法回收率较高以及分析的样本量相对较大。对贝类中这些寄生虫的发生情况进行更全面的研究将对挪威贝类产业具有重要意义。