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Comparative Assessment of In-House Real-Time PCRs Targeting Enteric Disease-Associated Microsporidia in Human Stool Samples

Microsporidiosis is an infection predominantly occurring in immunosuppressed patients and infrequently also in travelers. This study was performed to comparatively evaluate the diagnostic accuracy of real-time PCR assays targeting microsporidia with etiological relevance in the stool of human patien...

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Autores principales: Tanida, Konstantin, Hahn, Andreas, Eberhardt, Kirsten Alexandra, Tannich, Egbert, Landt, Olfert, Kann, Simone, Feldt, Torsten, Sarfo, Fred Stephen, Di Cristanziano, Veronica, Frickmann, Hagen, Loderstädt, Ulrike
Formato: Online Artículo Texto
Lenguaje:English
Publicado: MDPI 2021
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8229491/
https://www.ncbi.nlm.nih.gov/pubmed/34073403
http://dx.doi.org/10.3390/pathogens10060656
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author Tanida, Konstantin
Hahn, Andreas
Eberhardt, Kirsten Alexandra
Tannich, Egbert
Landt, Olfert
Kann, Simone
Feldt, Torsten
Sarfo, Fred Stephen
Di Cristanziano, Veronica
Frickmann, Hagen
Loderstädt, Ulrike
author_facet Tanida, Konstantin
Hahn, Andreas
Eberhardt, Kirsten Alexandra
Tannich, Egbert
Landt, Olfert
Kann, Simone
Feldt, Torsten
Sarfo, Fred Stephen
Di Cristanziano, Veronica
Frickmann, Hagen
Loderstädt, Ulrike
author_sort Tanida, Konstantin
collection PubMed
description Microsporidiosis is an infection predominantly occurring in immunosuppressed patients and infrequently also in travelers. This study was performed to comparatively evaluate the diagnostic accuracy of real-time PCR assays targeting microsporidia with etiological relevance in the stool of human patients in a latent class analysis-based test comparison without a reference standard with perfect accuracy. Thereby, two one-tube real-time PCR assays and two two-tube real-time PCR assays targeting Enterocytozoon bieneusi and Encephalocytozoon spp. were included in the assessment with reference stool material (20), stool samples from Ghanaian HIV-positive patients (903), and from travelers, migrants and Colombian indigenous people (416). Sensitivity of the assays ranged from 60.4% to 97.4% and specificity from 99.1% to 100% with substantial agreement according to Cohen’s kappa of 79.6%. Microsporidia DNA was detected in the reference material and the stool of the HIV patients but not in the stool of the travelers, migrants, and the Colombian indigenous people. Accuracy-adjusted prevalence was 5.8% (n = 78) for the study population as a whole. In conclusion, reliable detection of enteric disease-associated microsporidia in stool samples by real-time PCR could be demonstrated, but sensitivity between the compared microsporidia-specific real-time PCR assays varied.
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spelling pubmed-82294912021-06-26 Comparative Assessment of In-House Real-Time PCRs Targeting Enteric Disease-Associated Microsporidia in Human Stool Samples Tanida, Konstantin Hahn, Andreas Eberhardt, Kirsten Alexandra Tannich, Egbert Landt, Olfert Kann, Simone Feldt, Torsten Sarfo, Fred Stephen Di Cristanziano, Veronica Frickmann, Hagen Loderstädt, Ulrike Pathogens Article Microsporidiosis is an infection predominantly occurring in immunosuppressed patients and infrequently also in travelers. This study was performed to comparatively evaluate the diagnostic accuracy of real-time PCR assays targeting microsporidia with etiological relevance in the stool of human patients in a latent class analysis-based test comparison without a reference standard with perfect accuracy. Thereby, two one-tube real-time PCR assays and two two-tube real-time PCR assays targeting Enterocytozoon bieneusi and Encephalocytozoon spp. were included in the assessment with reference stool material (20), stool samples from Ghanaian HIV-positive patients (903), and from travelers, migrants and Colombian indigenous people (416). Sensitivity of the assays ranged from 60.4% to 97.4% and specificity from 99.1% to 100% with substantial agreement according to Cohen’s kappa of 79.6%. Microsporidia DNA was detected in the reference material and the stool of the HIV patients but not in the stool of the travelers, migrants, and the Colombian indigenous people. Accuracy-adjusted prevalence was 5.8% (n = 78) for the study population as a whole. In conclusion, reliable detection of enteric disease-associated microsporidia in stool samples by real-time PCR could be demonstrated, but sensitivity between the compared microsporidia-specific real-time PCR assays varied. MDPI 2021-05-26 /pmc/articles/PMC8229491/ /pubmed/34073403 http://dx.doi.org/10.3390/pathogens10060656 Text en © 2021 by the authors. https://creativecommons.org/licenses/by/4.0/Licensee MDPI, Basel, Switzerland. This article is an open access article distributed under the terms and conditions of the Creative Commons Attribution (CC BY) license (https://creativecommons.org/licenses/by/4.0/).
spellingShingle Article
Tanida, Konstantin
Hahn, Andreas
Eberhardt, Kirsten Alexandra
Tannich, Egbert
Landt, Olfert
Kann, Simone
Feldt, Torsten
Sarfo, Fred Stephen
Di Cristanziano, Veronica
Frickmann, Hagen
Loderstädt, Ulrike
Comparative Assessment of In-House Real-Time PCRs Targeting Enteric Disease-Associated Microsporidia in Human Stool Samples
title Comparative Assessment of In-House Real-Time PCRs Targeting Enteric Disease-Associated Microsporidia in Human Stool Samples
title_full Comparative Assessment of In-House Real-Time PCRs Targeting Enteric Disease-Associated Microsporidia in Human Stool Samples
title_fullStr Comparative Assessment of In-House Real-Time PCRs Targeting Enteric Disease-Associated Microsporidia in Human Stool Samples
title_full_unstemmed Comparative Assessment of In-House Real-Time PCRs Targeting Enteric Disease-Associated Microsporidia in Human Stool Samples
title_short Comparative Assessment of In-House Real-Time PCRs Targeting Enteric Disease-Associated Microsporidia in Human Stool Samples
title_sort comparative assessment of in-house real-time pcrs targeting enteric disease-associated microsporidia in human stool samples
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8229491/
https://www.ncbi.nlm.nih.gov/pubmed/34073403
http://dx.doi.org/10.3390/pathogens10060656
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