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一种基于半自动磁捕获探针的DNA提取及实时PCR方法,应用于瑞典对赤狐(赤狐)粪便样本中多房棘球绦虫的监测。

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.

作者信息

Isaksson Mats, Hagström Åsa, Armua-Fernandez Maria Teresa, Wahlström Helene, Ågren Erik Olof, Miller Andrea, Holmberg Anders, Lukacs Morten, Casulli Adriano, Deplazes Peter, Juremalm Mikael

机构信息

Department of Virology Immunobiology and Parasitology, National Veterinary Institute, Uppsala, Sweden.

Institute of Parasitology, Vetsuisse and Medical Faculty, University of Zurich, Zurich, Switzerland.

出版信息

Parasit Vectors. 2014 Dec 19;7:583. doi: 10.1186/s13071-014-0583-6.

Abstract

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.

METHODS

We 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.

RESULTS

Of 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).

CONCLUSIONS

The 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.

摘要

背景

自2011年在瑞典首次发现多房棘球绦虫后,采用分段沉淀计数技术对2985只赤狐(赤狐属)进行了分析。这是一种劳动强度大的方法,需要处理狐狸的整个尸体,导致分析成本高昂。为了降低劳动力和样本处理成本,开发了一种替代方法。该方法对粪便样本中多房棘球绦虫的检测具有敏感性且部分自动化。该方法已在2012 - 2013年瑞典多房棘球绦虫监测项目中用于2000多个粪便样本。

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检测法(MC - PCR),用于检测赤狐粪便样本中的多房棘球绦虫DNA。通过在多房棘球绦虫高度流行的瑞士收集的狐狸样本中,将新方法与沉淀计数技术进行验证,来确定诊断敏感性。

结果

通过沉淀计数技术分析的177只狐狸中,93只检测到多房棘球绦虫。其中82只(88%,95%置信区间79.8 - 93.9)在MC - PCR中呈阳性。在蠕虫数量超过100条的狐狸中,46只中有44只(95.7%)的MC - PCR呈阳性。两个MC - PCR阴性样本来自仅有多房棘球绦虫未成熟蠕虫的狐狸。在蠕虫数量为100条或更少的狐狸中(n = 47),38只(80.9%)的MC - PCR呈阳性。使用瑞典筛查中收集的狐狸粪便评估MC - PCR的诊断特异性。在分析的2158个样本中,两个呈阳性。这意味着特异性至少为99.9%(置信区间 = 99.7 - 100)。

结论

MC - PCR被证明具有高敏感性和非常高的特异性。该检测部分自动化,但如果需要也可以手动进行。该检测非常适合全国性的多房棘球绦虫监测项目,在该项目中对狐狸粪便进行采样以降低采样成本,并且需要一种具有高敏感性和非常高特异性的检测方法。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/d39c/4282741/c072a936a326/13071_2014_583_Fig1_HTML.jpg

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