Division of Bacteriology, Osaka Prefectural Institute of Public Health, Osaka, Japan.
J Clin Microbiol. 2012 Sep;50(9):2964-8. doi: 10.1128/JCM.01218-12. Epub 2012 Jul 3.
Kudoa septempunctata is a newly identified myxosporean parasite of olive flounder (Paralichthys olivaceus) and a suspected causative agent of several food-borne gastroenteritis outbreaks in Japan. Here, we report the detection of K. septempunctata 18S ribosomal DNA in fecal samples of outbreak patients using an efficient method based on real-time PCR. We first performed a spiking experiment to assess whether our previously developed real-time PCR assay was applicable to detect K. septempunctata in feces. Simultaneously, we compared the relative extraction efficacy of K. septempunctata DNA using three commercial kits. Finally, our detection method was validated by testing 45 clinical samples obtained from 13 food-borne outbreaks associated with the consumption of raw flounder and 41 fecal samples from diarrhea patients epidemiologically unrelated to the ingestion of raw fish. We found that the FastDNA Spin Kit for Soil (MP Biomedicals) was the most efficient method for extracting K. septempunctata DNA from fecal samples. Using this kit, the detection limit of our real-time PCR assay was 1.6 × 10(1) spores per g of feces, and positive results were obtained for 21 fecal and 2 vomitus samples obtained from the food-borne outbreaks. To our knowledge, this is the first report to describe the detection of K. septempunctata DNA in patient fecal samples. We anticipate that our detection method will be useful for confirming food-borne diseases caused by K. septempunctata in laboratory investigations.
多态尾孢虫是一种新发现的寄生在橄榄石斑鱼(Paralichthys olivaceus)体内的粘孢子虫,被怀疑是日本几起食源性肠胃炎暴发的病原体。在这里,我们报告了使用基于实时 PCR 的有效方法,从暴发患者的粪便样本中检测到多态尾孢虫 18S 核糖体 DNA。我们首先进行了加标实验,以评估我们之前开发的实时 PCR 检测方法是否适用于检测粪便中的多态尾孢虫。同时,我们比较了三种商业试剂盒提取多态尾孢虫 DNA 的相对提取效率。最后,我们通过检测与食用生石斑鱼有关的 13 起食源性暴发中获得的 45 份临床样本和与食用生鱼无关的 41 份腹泻患者粪便样本,验证了我们的检测方法。我们发现 FastDNA Spin Kit for Soil(MP Biomedicals)是从粪便样本中提取多态尾孢虫 DNA 最有效的方法。使用该试剂盒,我们的实时 PCR 检测方法的检测限为每克粪便 1.6×10(1)个孢子,从食源性暴发中获得的 21 份粪便和 2 份呕吐物样本的检测结果为阳性。据我们所知,这是首次描述在患者粪便样本中检测到多态尾孢虫 DNA。我们预计,我们的检测方法将有助于在实验室调查中确认由多态尾孢虫引起的食源性疾病。