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Novodiag粪便寄生虫检测法用于检测肠道原生动物和微孢子虫的性能评估。

Evaluation of the Performance of the Novodiag Stool Parasites Assay for the Detection of Intestinal Protozoa and Microsporidia.

作者信息

Chauvin Pamela, Barba Florie, Guemas Emilie, Charpentier Eléna, Cottrel Claire, Fillaux Judith, Valentin Alexis, Baklouti Sarah, Cassaing Sophie, Ménard Sandie, Berry Antoine, Iriart Xavier

机构信息

Service de Parasitologie-Mycologie, Centre Hospitalier Universitaire de Toulouse, 31059 Toulouse, France.

Institut Toulousain des Maladies Infectieuses et Inflammatoires (Infinity), Université de Toulouse, CNRS UMR5051, INSERM UMR1291, Université Paul Sabatier, 31024 Toulouse, France.

出版信息

Pathogens. 2023 Jun 29;12(7):889. doi: 10.3390/pathogens12070889.

DOI:10.3390/pathogens12070889
PMID:37513736
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC10385646/
Abstract

OBJECTIVES

We aimed to assess the performance of the Novodiag Stool Parasites (NSP) assay in the diagnosis of the most common intestinal protozoan and microsporidia infections.

METHODS

A panel of 167 selected stool samples was retrospectively analysed with the NSP assay and compared to routine microscopy and qPCR methods for the detection of pathogenic protozoa and microsporidia.

RESULTS

Whereas specificity was high for all protozoa and microsporidia, NSP sensitivity was strongly dependent on the comparative method used as reference. When compared to microscopic methods, NSP sensitivity was high (96.7 to 100%) for , and but was lower for (85.2%) and ≤50% for and . In comparison to conventional qPCR, the NSP assay demonstrated lower sensitivity characteristics dependent on parasite loads, reaching 60 to 70% for , , spp. and Sensitivity was 100% for , but none of the five samples containing spp. were detected.

CONCLUSIONS

The overall performance of the NSP assay in the diagnosis of gastrointestinal protozoa and microsporidia seems to be better than or equivalent to that observed with microscopic methods but inferior to that obtainable with classical targeted qPCR.

摘要

目的

我们旨在评估Novodiag粪便寄生虫(NSP)检测法在诊断最常见肠道原生动物和微孢子虫感染方面的性能。

方法

对一组167份选定的粪便样本进行回顾性分析,采用NSP检测法,并与常规显微镜检查和qPCR方法进行比较,以检测致病性原生动物和微孢子虫。

结果

虽然所有原生动物和微孢子虫的特异性都很高,但NSP的敏感性强烈依赖于用作参考的比较方法。与显微镜检查方法相比,NSP对蓝氏贾第鞭毛虫、溶组织内阿米巴和结肠小袋纤毛虫的敏感性较高(96.7%至100%),但对隐孢子虫的敏感性较低(85.2%),对贝氏等孢球虫和微孢子虫的敏感性≤50%。与传统qPCR相比,NSP检测法的敏感性特征较低,取决于寄生虫载量,对微小隐孢子虫、人芽囊原虫、等孢球虫属和环孢子虫的敏感性达到60%至70%。对蓝氏贾第鞭毛虫的敏感性为100%,但未检测到五个含有肠微孢子虫属的样本中的任何一个。

结论

NSP检测法在诊断胃肠道原生动物和微孢子虫方面的总体性能似乎优于或等同于显微镜检查方法,但不如经典靶向qPCR方法。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/a34c/10385646/87797401dabc/pathogens-12-00889-g002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/a34c/10385646/313b4698135f/pathogens-12-00889-g001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/a34c/10385646/87797401dabc/pathogens-12-00889-g002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/a34c/10385646/313b4698135f/pathogens-12-00889-g001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/a34c/10385646/87797401dabc/pathogens-12-00889-g002.jpg

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Evaluation of the Allplex™ GI-Helminth(I) Assay, the first marketed multiplex PCR for helminth diagnosis.评估 Allplex™ GI-Helminth(I) 检测试剂盒,这是首个上市的用于寄生虫诊断的多重 PCR 检测方法。
Parasite. 2021;28:33. doi: 10.1051/parasite/2021034. Epub 2021 Apr 2.
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Evaluation of the Allplex Gastrointestinal Panel-Parasite Assay for Protozoa Detection in Stool Samples: A Retrospective and Prospective Study.
用于粪便样本中原生动物检测的Allplex胃肠检测组-寄生虫检测法的评估:一项回顾性和前瞻性研究
Microorganisms. 2020 Apr 15;8(4):569. doi: 10.3390/microorganisms8040569.
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Distribution and relevance of Dientamoeba fragilis and Blastocystis species in gastroenteritis: results from a case-control study.脆弱双核阿米巴和肠内芽囊原虫在肠胃炎中的分布和关联性:一项病例对照研究的结果。
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