Cavallero Serena, Bruno Alessandro, Arletti Enrico, Caffara Monica, Fioravanti Maria Letizia, Costa Antonella, Cammilleri Gaetano, Graci Stefania, Ferrantelli Vincenzo, D'Amelio Stefano
Department of Public Health and Infectious Diseases, Sapienza University of Rome, Italy.
Generon s.r.l., Modena, Italy.
Int J Food Microbiol. 2017 Sep 18;257:75-79. doi: 10.1016/j.ijfoodmicro.2017.06.011. Epub 2017 Jun 15.
Anisakids are parasitic nematodes responsible for a zoonosis that occurs following the ingestion of fish and fish products infected with larvae belonging to the genera Anisakis and Pseudoterranova. Rarely Contracaecum is found in association with gastric/intestinal illness, while Hysterothylacium is commonly considered not pathogenic. Although Real Time PCR assays have been recently used with the aim to detect and quantify these parasites in food products, methods applied did not undergo through extensive validation process, a feature highly desirable or mandatory in the case of testing laboratories accredited for the ISO EN 17025:2005. Here, a comprehensive study has been performed to validate a commercial kit based on multiplex real time PCR for the qualitative detection of Anisakis and Pseudoterranova. Inclusivity/exclusivity trials were carried out on DNA from species of the genera Anisakis, Pseudoterranova, Contracaecum, Hysterothylacium and Ascaris, on fish intentionally contaminated with Anisakis spp. and Pseudoterranova spp. and on marine organisms as fish, crustacean and squid to test the commercial kit on a large sample. The assay gave positive amplification for several Anisakis and Pseudoterranova species, while providing no signal for the members of the remaining genera. Each sample was correctly assigned either to Anisakis or Pseudoterranova, thus indicating that no cross-reaction occurred. The LOD was determined using two independent standard curves. Robustness was assayed by using two different thermocyclers in three distinct laboratories with different operators. The establishment of a validation dossier will permit the use of the commercial kit for the detection of Anisakis and Pseudoterranova DNA in fish and fish products intended for human consumption by public or private laboratories, following the requirements regarding the quality assurance processes described in the ISO EN 17025:2005.
异尖线虫是一种寄生性线虫,可引发人畜共患病,该病是在摄入感染了异尖线虫属和伪新地蛔线虫属幼虫的鱼类及鱼产品后发生的。很少发现对盲囊线虫与胃肠疾病有关,而宫脂线虫通常被认为无致病性。尽管最近已使用实时荧光定量聚合酶链反应(Real Time PCR)检测方法来检测和定量食品中的这些寄生虫,但所应用的方法并未经过广泛的验证过程,而这一特性在依据ISO EN 17025:2005认可的检测实验室中是非常必要或强制性的。在此,进行了一项全面研究,以验证一种基于多重实时荧光定量聚合酶链反应的商业试剂盒用于定性检测异尖线虫和伪新地蛔线虫。对异尖线虫属、伪新地蛔线虫属、对盲囊线虫属、宫脂线虫属和蛔虫属物种的DNA、故意感染异尖线虫属物种和伪新地蛔线虫属物种的鱼类以及鱼类、甲壳类动物和鱿鱼等海洋生物进行了包容性/排他性试验,以在大量样本上测试该商业试剂盒。该检测方法对几种异尖线虫和伪新地蛔线虫物种给出了阳性扩增结果,而对其余属的成员未给出信号。每个样本都被正确地归类为异尖线虫或伪新地蛔线虫,因此表明未发生交叉反应。使用两条独立的标准曲线确定了检测限。通过在三个不同实验室由不同操作人员使用两种不同的热循环仪来测定稳健性。建立验证档案将允许公共或私人实验室按照ISO EN 17025:2005中所述的质量保证程序要求,使用该商业试剂盒检测供人类食用的鱼类和鱼产品中的异尖线虫和伪新地蛔线虫DNA。