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A semi-automated magnetic capture probe based DNA extraction and real-time PCR method applied in the Swedish surveillance of Echinococcus multilocularis in red fox (Vulpes vulpes) faecal samples

机译:一种基于半自动磁捕获探针的DNA提取和实时PCR方法,用于瑞典狐狸粪样中多叶棘球Swedish的瑞典监测

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摘要

Background: Following the first finding of Echinococcus multilocularis in Sweden in 2011, 2985 red foxes (Vulpes vulpes) were analysed by the segmental sedimentation and counting technique. This is a labour intensive method and requires handling of the whole carcass of the fox, resulting in a costly analysis. In an effort to reduce the cost of labour and sample handling, an alternative method has been developed. The method is sensitive and partially automated for detection of E. multilocularis in faecal samples. The method has been used in the Swedish E. multilocularis monitoring program for 2012¿2013 on more than 2000 faecal samples.MethodsWe describe a new semi-automated magnetic capture probe DNA extraction method and real time hydrolysis probe polymerase chain reaction assay (MC-PCR) for the detection of E. multilocularis DNA in faecal samples from red fox. The diagnostic sensitivity was determined by validating the new method against the sedimentation and counting technique in fox samples collected in Switzerland where E. multilocularis is highly endemic.ResultsOf 177 foxes analysed by the sedimentation and counting technique, E. multilocularis was detected in 93 animals. Eighty-two (88%, 95% C.I 79.8-93.9) of these were positive in the MC-PCR. In foxes with more than 100 worms, the MC-PCR was positive in 44 out of 46 (95.7%) cases. The two MC-PCR negative samples originated from foxes with only immature E. multilocularis worms. In foxes with 100 worms or less, (n¿=¿47), 38 (80.9%) were positive in the MC-PCR.The diagnostic specificity of the MC-PCR was evaluated using fox scats collected within the Swedish screening. Of 2158 samples analysed, two were positive. This implies that the specificity is at least 99.9% (C.I. =99.7 -100).ConclusionsThe MC-PCR proved to have a high sensitivity and a very high specificity. The test is partially automated but also possible to perform manually if desired. The test is well suited for nationwide E. multilocularis surveillance programs where sampling of fox scats is done to reduce the costs for sampling and where a test with a high sensitivity and a very high specificity is needed.
机译:背景:继2011年在瑞典首次发现多叶棘球oc虫后,通过分段沉积和计数技术分析了2985只赤狐(Vulpes vulpes)。这是一种劳动密集型方法,需要处理整个狐狸的尸体,导致分析成本很高。为了减少人工和样品处理的成本,已经开发了一种替代方法。该方法灵敏且部分自动化,可检测粪便样品中的多眼大肠杆菌。该方法已在瑞典2012年至2013年的多眼大肠杆菌监测程序中使用,对2000多个粪便样品进行了分析。方法我们描述了一种新的半自动磁捕获探针DNA提取方法和实时水解探针聚合酶链反应测定(MC-PCR) ),用于检测赤狐粪便中的多叶大肠杆菌(E. multilocularis)DNA。通过验证针对沉积多计数的瑞士狐狸样本的新方法,该方法对多狐猴高度流行的瑞士样本的诊断敏感性得到了确定。结果通过沉积计数技术分析的177只狐狸中,在93只动物中检测到多狐狸。其中八十二(88%,95%C.I 79.8-93.9)在MC-PCR中呈阳性。在蠕虫超过100的狐狸中,MC-PCR在46例病例中有44例(95.7%)呈阳性。这两个MC-PCR阴性样品来自仅具有未成熟多叶大肠杆菌的蠕虫。在蠕虫少于或等于100的狐狸中(n = 47),MC-PCR阳性38(80.9%)。MC-PCR的诊断特异性使用瑞典筛查中收集的狐狸粪便进行评估。在分析的2158个样本中,有两个是阳性的。这意味着特异性至少为99.9%(C.I. = 99.7 -100)。结论MC-PCR被证明具有很高的灵敏度和很高的特异性。该测试是部分自动化的,但如果需要,也可以手动执行。该测试非常适合全国范围内的多眼大肠杆菌监测计划,在该计划中,对狐狸粪便进行采样以降低采样成本,并且需要进行高灵敏度和高特异性检测。

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    Isaksson, Mats; et al;

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  • 年度 2014
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  • 正文语种 eng
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