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Performance of a commercial assay for detecting and quantifying HEV RNA in faeces

BACKGROUND: Detecting hepatitis E virus (HEV) RNA in faeces is useful for diagnosing and monitoring HEV infections, particularly in immunocompromised patients requiring ribavirin therapy. OBJECTIVES: This study evaluated the performance of the Altona RealStar HEV RNA kit for detecting and quantifyin...

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Autores principales: Abravanel, Florence, Lacipière, Audrey, Lhomme, Sébastien, Dubois, Martine, Minier, Luce, Peron, Jean-Marie, Alric, Laurent, Kamar, Nassim, Izopet, Jacques
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Elsevier B.V. 2018
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7106495/
https://www.ncbi.nlm.nih.gov/pubmed/30336371
http://dx.doi.org/10.1016/j.jcv.2018.10.003
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author Abravanel, Florence
Lacipière, Audrey
Lhomme, Sébastien
Dubois, Martine
Minier, Luce
Peron, Jean-Marie
Alric, Laurent
Kamar, Nassim
Izopet, Jacques
author_facet Abravanel, Florence
Lacipière, Audrey
Lhomme, Sébastien
Dubois, Martine
Minier, Luce
Peron, Jean-Marie
Alric, Laurent
Kamar, Nassim
Izopet, Jacques
author_sort Abravanel, Florence
collection PubMed
description BACKGROUND: Detecting hepatitis E virus (HEV) RNA in faeces is useful for diagnosing and monitoring HEV infections, particularly in immunocompromised patients requiring ribavirin therapy. OBJECTIVES: This study evaluated the performance of the Altona RealStar HEV RNA kit for detecting and quantifying HEV in faeces. STUDY DESIGN: RNA was extracted from 94 stool samples by two methods: QIAamp Viral RNA Mini kit and MagNA Pure 96 automate. The Altona results were compared to a reference laboratory-developed accredited ISO15189 RT-PCR assay. RESULTS: The Altona and reference assays detect HEV RNA in 77/93 (82.8%) and 83/93 (89.2%) of the QIAamp extracted samples, respectively, after exclusion of invalid result; they detected HEV RNA in 67/92 (72.8%) and 66/92 (71.7%) of the MagNA Pure extracted samples, respectively, which emphasizes the importance of the RNA extraction method. The HEV RNA concentrations obtained with Altona RT-PCR and the reference RT-PCR were well correlated whatever the extraction method, and Bland Altman analyses indicated that the Altona values were higher than the reference assay values. The Altona values for QIAamp-extracted and MagNA Pure-extracted HEV RNA were very similar. CONCLUSIONS: The Altona RealStar assay is suitable for quantifying HEV RNA in the faeces and monitoring HEV RNA shedding during ribavirin therapy. Extraction is critical for detecting faecal HEV with high performance RT-PCR assays.
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spelling pubmed-71064952020-03-31 Performance of a commercial assay for detecting and quantifying HEV RNA in faeces Abravanel, Florence Lacipière, Audrey Lhomme, Sébastien Dubois, Martine Minier, Luce Peron, Jean-Marie Alric, Laurent Kamar, Nassim Izopet, Jacques J Clin Virol Article BACKGROUND: Detecting hepatitis E virus (HEV) RNA in faeces is useful for diagnosing and monitoring HEV infections, particularly in immunocompromised patients requiring ribavirin therapy. OBJECTIVES: This study evaluated the performance of the Altona RealStar HEV RNA kit for detecting and quantifying HEV in faeces. STUDY DESIGN: RNA was extracted from 94 stool samples by two methods: QIAamp Viral RNA Mini kit and MagNA Pure 96 automate. The Altona results were compared to a reference laboratory-developed accredited ISO15189 RT-PCR assay. RESULTS: The Altona and reference assays detect HEV RNA in 77/93 (82.8%) and 83/93 (89.2%) of the QIAamp extracted samples, respectively, after exclusion of invalid result; they detected HEV RNA in 67/92 (72.8%) and 66/92 (71.7%) of the MagNA Pure extracted samples, respectively, which emphasizes the importance of the RNA extraction method. The HEV RNA concentrations obtained with Altona RT-PCR and the reference RT-PCR were well correlated whatever the extraction method, and Bland Altman analyses indicated that the Altona values were higher than the reference assay values. The Altona values for QIAamp-extracted and MagNA Pure-extracted HEV RNA were very similar. CONCLUSIONS: The Altona RealStar assay is suitable for quantifying HEV RNA in the faeces and monitoring HEV RNA shedding during ribavirin therapy. Extraction is critical for detecting faecal HEV with high performance RT-PCR assays. Elsevier B.V. 2018-12 2018-10-10 /pmc/articles/PMC7106495/ /pubmed/30336371 http://dx.doi.org/10.1016/j.jcv.2018.10.003 Text en © 2018 Elsevier B.V. All rights reserved. Since January 2020 Elsevier has created a COVID-19 resource centre with free information in English and Mandarin on the novel coronavirus COVID-19. The COVID-19 resource centre is hosted on Elsevier Connect, the company's public news and information website. Elsevier hereby grants permission to make all its COVID-19-related research that is available on the COVID-19 resource centre - including this research content - immediately available in PubMed Central and other publicly funded repositories, such as the WHO COVID database with rights for unrestricted research re-use and analyses in any form or by any means with acknowledgement of the original source. These permissions are granted for free by Elsevier for as long as the COVID-19 resource centre remains active.
spellingShingle Article
Abravanel, Florence
Lacipière, Audrey
Lhomme, Sébastien
Dubois, Martine
Minier, Luce
Peron, Jean-Marie
Alric, Laurent
Kamar, Nassim
Izopet, Jacques
Performance of a commercial assay for detecting and quantifying HEV RNA in faeces
title Performance of a commercial assay for detecting and quantifying HEV RNA in faeces
title_full Performance of a commercial assay for detecting and quantifying HEV RNA in faeces
title_fullStr Performance of a commercial assay for detecting and quantifying HEV RNA in faeces
title_full_unstemmed Performance of a commercial assay for detecting and quantifying HEV RNA in faeces
title_short Performance of a commercial assay for detecting and quantifying HEV RNA in faeces
title_sort performance of a commercial assay for detecting and quantifying hev rna in faeces
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7106495/
https://www.ncbi.nlm.nih.gov/pubmed/30336371
http://dx.doi.org/10.1016/j.jcv.2018.10.003
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