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建立一种定量聚合酶链反应检测方法,用于检测橄榄石斑鱼(Paralichthys olivaceus)中的七棘孔绦虫(Kudoa septempunctata)。

Development of a quantitative polymerase chain reaction assay for detection of Kudoa septempunctata in olive flounder (Paralichthys olivaceus).

机构信息

Division of Bacteriology, Osaka Prefectural Institute of Public Health, 1-3-69 Nakamichi, Higashinari-ku, Osaka 537-0025, Japan.

出版信息

Int J Food Microbiol. 2012 May 15;156(2):161-7. doi: 10.1016/j.ijfoodmicro.2012.03.018. Epub 2012 Mar 26.

DOI:10.1016/j.ijfoodmicro.2012.03.018
PMID:22503550
Abstract

Kudoa septempunctata is a newly identified myxosporean parasite that infects the trunk muscles of olive flounder (Paralichthys olivaceus) and a causative agent of the increasing number of foodborne gastroenteritis outbreaks with unknown etiology which have occurred in Japan over the last few years. Here, we developed a quantitative polymerase chain reaction (QPCR) assay for the detection of K. septempunctata 18S rDNA in olive flounder muscle tissue samples. Additionally, we compared the relative efficacy of four DNA extraction methods, including two commercial kits, and assessed intrafish variability in the distribution of K. septempunctata spores in flounder using this QPCR method in order to establish a more accurate quantitative measurement. Our QPCR assay displayed high sensitivity, specificity, and reproducibility, and had good correlation with a microscopic detection method. Our data also indicated that the DNeasy® Blood & Tissue Kit was more efficient method for the extraction of K. septempunctata DNA than the three other methods (heating, alkaline lysis, and FastDNA® SPIN Kit method). We believe that our method would be useful for investigating foodborne outbreaks caused by K. septempunctata and for the monitoring and quantification of this parasite in retail or aquacultured olive flounders to prevent such outbreaks.

摘要

七斑孔肠孢子虫是一种新鉴定的粘孢子虫寄生虫,感染橄榄石斑鱼(Paralichthys olivaceus)的躯干肌肉,是近年来在日本发生的越来越多的不明病因食源性肠胃炎暴发的病原体。在这里,我们开发了一种定量聚合酶链反应(QPCR)检测方法,用于检测橄榄石斑鱼肌肉组织样本中的 K. septempunctata 18S rDNA。此外,我们比较了四种 DNA 提取方法的相对效果,包括两种商业试剂盒,并使用该 QPCR 方法评估了 K. septempunctata 孢子在石斑鱼中的分布的鱼内变异性,以建立更准确的定量测量。我们的 QPCR 检测方法显示出高灵敏度、特异性和重现性,并且与显微镜检测方法具有良好的相关性。我们的数据还表明,DNeasy® Blood & Tissue Kit 比其他三种方法(加热、碱性裂解和 FastDNA® SPIN 试剂盒法)更有效地提取 K. septempunctata DNA。我们相信,我们的方法将有助于调查由 K. septempunctata 引起的食源性暴发,并用于监测和量化零售或养殖的橄榄石斑鱼中的这种寄生虫,以防止此类暴发。

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