Department of Food and Environmental Hygiene, Faculty of Veterinary Medicine, University of Helsinki, Helsinki, Finland.
Microbiology Unit, Department of Animal Diseases and Food Safety Research, Finnish Food Safety Authority Evira, Mustialankatu, Helsinki, Finland.
J Appl Microbiol. 2010 Mar;108(3):956-964. doi: 10.1111/j.1365-2672.2009.04494.x. Epub 2009 Jul 23.
The aim of this study was to evaluate the efficiency of four isolation methods for the detection of pathogenic Yersinia enterocolitica from pig intestinal content.
The four methods comprised of 15 isolation steps using selective enrichments (irgasan-ticarcillin-potassium chlorate and modified Rappaport broth) and mildly selective enrichments at 4 or 25 degrees C. Salmonella-Shigella-desoxycholate-calcium chloride agar, cefsulodin-irgasan-novobiocin agar were used as plating media. The most sensitive method detected 78% (53/68) of the positive samples. Individual isolation steps using cold enrichment as the only enrichment or as a pre-enrichment step with further selective enrichment showed the highest sensitivities (55-66%). All isolation methods resulted in high numbers of suspected colonies not confirmed as pathogenic Y. enterocolitica.
Cold enrichment should be used in the detection of pathogenic Y. enterocolitica from pig intestinal contents. In addition, more than one parallel isolation step is needed.
The study shows that depending on the isolation method used for Y. enterocolitica, the detected prevalence of Y. enterocolitica in pig intestinal contents varies greatly. More selective and sensitive isolation methods need to be developed for pathogenic Y. enterocolitica.
本研究旨在评估四种从猪肠内容物中检测致病性肠炎耶尔森菌的分离方法的效率。
这四种方法包括使用选择性增菌(irgasanit-ticarcillin-potassium chlorate 和改良 Rappaport 肉汤)和 4 或 25°C 温和选择性增菌的 15 个分离步骤。使用沙门氏菌-志贺氏菌-去氧胆酸钠-氯化钙琼脂、头孢磺啶-irgasanit-新生霉素琼脂作为平板培养基。最敏感的方法检测到 78%(53/68)的阳性样本。单独使用冷增菌作为唯一增菌或作为进一步选择性增菌的预增菌步骤的增菌步骤显示出最高的敏感性(55-66%)。所有分离方法都导致大量疑似但未被确认为致病性肠炎耶尔森菌的菌落。
在从猪肠内容物中检测致病性肠炎耶尔森菌时,应使用冷增菌。此外,需要进行多个平行的分离步骤。
本研究表明,由于使用的分离方法不同,猪肠内容物中肠炎耶尔森菌的检出率差异很大。需要开发更具选择性和敏感性的分离方法来检测致病性肠炎耶尔森菌。