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

Author:

Chauvin Pamela1,Barba Florie1,Guemas Emilie12,Charpentier Eléna1,Cottrel Claire12,Fillaux Judith13ORCID,Valentin Alexis14,Baklouti Sarah56,Cassaing Sophie13ORCID,Ménard Sandie2ORCID,Berry Antoine12,Iriart Xavier12

Affiliation:

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

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

3. RESTORE Institute, UMR 1301-Inserm 5070-CNRS EFS Université Paul Sabatier, 31100 Toulouse, France

4. UMR 152 PHARMA-DEV, IRD, UPS, Université de Toulouse, 31062 Toulouse, France

5. Laboratoire de Pharmacocinétique et Toxicologie, CHU de Toulouse, 31059 Toulouse, France

6. INTHERES, Université de Toulouse, INRAE, ENVT, 31076 Toulouse, France

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 Blastocystis hominis, Entamoeba histolytica and Cyclospora cayetanensis but was lower for Giardia intestinalis (85.2%) and ≤50% for Cystoisospora belli and Dientamoeba fragilis. In comparison to conventional qPCR, the NSP assay demonstrated lower sensitivity characteristics dependent on parasite loads, reaching 60 to 70% for G. intestinalis, D. fragilis, Cryptosporidium spp. and E. histolytica. Sensitivity was 100% for Enterocytozoon bieneusi, but none of the five samples containing Encephalitozoon 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.

Funder

Hologic Inc.

Publisher

MDPI AG

Subject

Infectious Diseases,Microbiology (medical),General Immunology and Microbiology,Molecular Biology,Immunology and Allergy

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