Evaluation of the Performance of the Novodiag<sup>®</sup> Stool Parasites Assay for the Detection of Intestinal Protozoa and Microsporidia
Pamela Chauvin,
Florie Barba,
Emilie Guemas,
Eléna Charpentier,
Claire Cottrel,
Judith Fillaux,
Alexis Valentin,
Sarah Baklouti,
Sophie Cassaing,
Sandie Ménard,
Antoine Berry,
Xavier Iriart
Affiliations
Pamela Chauvin
Service de Parasitologie—Mycologie, Centre Hospitalier Universitaire de Toulouse, 31059 Toulouse, France
Florie Barba
Service de Parasitologie—Mycologie, Centre Hospitalier Universitaire de Toulouse, 31059 Toulouse, France
Emilie Guemas
Service de Parasitologie—Mycologie, Centre Hospitalier Universitaire de Toulouse, 31059 Toulouse, France
Eléna Charpentier
Service de Parasitologie—Mycologie, Centre Hospitalier Universitaire de Toulouse, 31059 Toulouse, France
Claire Cottrel
Service de Parasitologie—Mycologie, Centre Hospitalier Universitaire de Toulouse, 31059 Toulouse, France
Judith Fillaux
Service de Parasitologie—Mycologie, Centre Hospitalier Universitaire de Toulouse, 31059 Toulouse, France
Alexis Valentin
Service de Parasitologie—Mycologie, Centre Hospitalier Universitaire de Toulouse, 31059 Toulouse, France
Sarah Baklouti
Laboratoire de Pharmacocinétique et Toxicologie, CHU de Toulouse, 31059 Toulouse, France
Sophie Cassaing
Service de Parasitologie—Mycologie, Centre Hospitalier Universitaire de Toulouse, 31059 Toulouse, France
Sandie Ménard
Institut Toulousain des Maladies Infectieuses et Inflammatoires (Infinity), Université de Toulouse, CNRS UMR5051, INSERM UMR1291, Université Paul Sabatier, 31024 Toulouse, France
Antoine Berry
Service de Parasitologie—Mycologie, Centre Hospitalier Universitaire de Toulouse, 31059 Toulouse, France
Xavier Iriart
Service de Parasitologie—Mycologie, Centre Hospitalier Universitaire de Toulouse, 31059 Toulouse, France
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.