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A novel 5-Plex qPCR-HRM assay detecting human diarrheal parasites

BACKGROUND: Intestinal parasitic diseases occur worldwide, and their diagnosis poses considerable challenges. Cryptosporidium spp., Entamoeba histolytica, Giardia intestinalis, (and, arguably, Dientamoeba fragilis and Blastocystis spp.) are among the most important and common parasitic protozoans ca...

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Autores principales: Lamien-Meda, Aline, Schneider, Renate, Walochnik, Julia, Auer, Herbert, Wiedermann, Ursula, Leitsch, David
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2020
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7257150/
https://www.ncbi.nlm.nih.gov/pubmed/32514315
http://dx.doi.org/10.1186/s13099-020-00365-6
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author Lamien-Meda, Aline
Schneider, Renate
Walochnik, Julia
Auer, Herbert
Wiedermann, Ursula
Leitsch, David
author_facet Lamien-Meda, Aline
Schneider, Renate
Walochnik, Julia
Auer, Herbert
Wiedermann, Ursula
Leitsch, David
author_sort Lamien-Meda, Aline
collection PubMed
description BACKGROUND: Intestinal parasitic diseases occur worldwide, and their diagnosis poses considerable challenges. Cryptosporidium spp., Entamoeba histolytica, Giardia intestinalis, (and, arguably, Dientamoeba fragilis and Blastocystis spp.) are among the most important and common parasitic protozoans causing diarrhea. Several multiplex real-time PCR assays have been developed for the synchronous detection of these parasites. However, most assays include the use of hydrolysis probes, increasing the cost of stool examination. In this study, we designed and evaluated a real-time PCR protocol, based on high-resolution melting (HRM) curve analysis, to simultaneously detect and differentiate five gastrointestinal parasites. RESULTS: Using a blinded panel of 143 clinical samples with laboratory diagnostic data to evaluate the method, we obtained a 95.8% concordance with conventional methods. Moreover, 4.2% of the samples were positive for D. fragilis and 2.8% additional Cryptosporidium infections were found with our multiplex assay. Our method is sensitive and specific for the selected parasites with the additional possibility of being run in single-plex as a backup control for mixed infections. CONCLUSIONS: The assay is a convenient and cost-effective method that could contribute to a quicker and accurate diagnosis as well as to more targeted therapies of parasite-derived diarrhea. Finally, this new multiplex PCR assay could also be instrumental in epidemiology studies on these parasites.
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spelling pubmed-72571502020-06-07 A novel 5-Plex qPCR-HRM assay detecting human diarrheal parasites Lamien-Meda, Aline Schneider, Renate Walochnik, Julia Auer, Herbert Wiedermann, Ursula Leitsch, David Gut Pathog Research BACKGROUND: Intestinal parasitic diseases occur worldwide, and their diagnosis poses considerable challenges. Cryptosporidium spp., Entamoeba histolytica, Giardia intestinalis, (and, arguably, Dientamoeba fragilis and Blastocystis spp.) are among the most important and common parasitic protozoans causing diarrhea. Several multiplex real-time PCR assays have been developed for the synchronous detection of these parasites. However, most assays include the use of hydrolysis probes, increasing the cost of stool examination. In this study, we designed and evaluated a real-time PCR protocol, based on high-resolution melting (HRM) curve analysis, to simultaneously detect and differentiate five gastrointestinal parasites. RESULTS: Using a blinded panel of 143 clinical samples with laboratory diagnostic data to evaluate the method, we obtained a 95.8% concordance with conventional methods. Moreover, 4.2% of the samples were positive for D. fragilis and 2.8% additional Cryptosporidium infections were found with our multiplex assay. Our method is sensitive and specific for the selected parasites with the additional possibility of being run in single-plex as a backup control for mixed infections. CONCLUSIONS: The assay is a convenient and cost-effective method that could contribute to a quicker and accurate diagnosis as well as to more targeted therapies of parasite-derived diarrhea. Finally, this new multiplex PCR assay could also be instrumental in epidemiology studies on these parasites. BioMed Central 2020-05-29 /pmc/articles/PMC7257150/ /pubmed/32514315 http://dx.doi.org/10.1186/s13099-020-00365-6 Text en © The Author(s) 2020 Open AccessThis article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons licence, and indicate if changes were made. The images or other third party material in this article are included in the article's Creative Commons licence, unless indicated otherwise in a credit line to the material. If material is not included in the article's Creative Commons licence and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this licence, visit http://creativecommons.org/licenses/by/4.0/. The Creative Commons Public Domain Dedication waiver (http://creativecommons.org/publicdomain/zero/1.0/) applies to the data made available in this article, unless otherwise stated in a credit line to the data.
spellingShingle Research
Lamien-Meda, Aline
Schneider, Renate
Walochnik, Julia
Auer, Herbert
Wiedermann, Ursula
Leitsch, David
A novel 5-Plex qPCR-HRM assay detecting human diarrheal parasites
title A novel 5-Plex qPCR-HRM assay detecting human diarrheal parasites
title_full A novel 5-Plex qPCR-HRM assay detecting human diarrheal parasites
title_fullStr A novel 5-Plex qPCR-HRM assay detecting human diarrheal parasites
title_full_unstemmed A novel 5-Plex qPCR-HRM assay detecting human diarrheal parasites
title_short A novel 5-Plex qPCR-HRM assay detecting human diarrheal parasites
title_sort novel 5-plex qpcr-hrm assay detecting human diarrheal parasites
topic Research
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7257150/
https://www.ncbi.nlm.nih.gov/pubmed/32514315
http://dx.doi.org/10.1186/s13099-020-00365-6
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