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Reliable resolution of ambiguous hepatitis C virus genotype 1 results with the Abbott HCV Genotype Plus RUO assay

Accurate subtyping of hepatitis C virus genotype 1 (HCV-1) remains clinically and epidemiologically relevant. The Abbott HCV Genotype Plus RUO (GT Plus) assay, targeting the core region, was evaluated as a reflex test to resolve ambiguous HCV-1 results in a challenging sample collection. 198 HCV-1 s...

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Autores principales: Saludes, V., Antuori, A., Reinhardt, B., Viciana, I., Clavijo, E., Schreiber, L., Tenenbaum, M., Rodriguez-Frias, F., Quer, J., Matas, L., Martró, E.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Nature Publishing Group UK 2019
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6403303/
https://www.ncbi.nlm.nih.gov/pubmed/30842623
http://dx.doi.org/10.1038/s41598-019-40099-3
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author Saludes, V.
Antuori, A.
Reinhardt, B.
Viciana, I.
Clavijo, E.
Schreiber, L.
Tenenbaum, M.
Rodriguez-Frias, F.
Quer, J.
Matas, L.
Martró, E.
author_facet Saludes, V.
Antuori, A.
Reinhardt, B.
Viciana, I.
Clavijo, E.
Schreiber, L.
Tenenbaum, M.
Rodriguez-Frias, F.
Quer, J.
Matas, L.
Martró, E.
author_sort Saludes, V.
collection PubMed
description Accurate subtyping of hepatitis C virus genotype 1 (HCV-1) remains clinically and epidemiologically relevant. The Abbott HCV Genotype Plus RUO (GT Plus) assay, targeting the core region, was evaluated as a reflex test to resolve ambiguous HCV-1 results in a challenging sample collection. 198 HCV-1 specimens were analysed with GT Plus (38 specimens with and 160 without subtype assigned by the Abbott RealTime Genotype II (GT II) assay targeting the 5’NC and NS5B regions). Sanger sequencing of the core and/or NS5B regions were performed in 127 specimens without subtype assignment by GT II, with “not detected” results by GT Plus, or with mixed genotypes/subtypes. The remaining GT Plus results were compared to LiPA 2.0 (n = 45) or just to GT II results if concordant (n = 26). GT Plus successfully assigned the subtype in 142/160 (88.8%) samples. “Not detected” results indicated other HCV-1 subtypes/genotypes or mismatches in the core region in subtype 1b. The subtyping concordance between GT Plus and either sequencing or LiPA was 98.6% (140/142). Therefore, combined use of GT II and GT Plus assays represents a reliable and simple approach which considerably reduced the number of ambiguous HCV-1 results and enabled a successful subtyping of 98.9% of all HCV-1 samples.
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spelling pubmed-64033032019-03-08 Reliable resolution of ambiguous hepatitis C virus genotype 1 results with the Abbott HCV Genotype Plus RUO assay Saludes, V. Antuori, A. Reinhardt, B. Viciana, I. Clavijo, E. Schreiber, L. Tenenbaum, M. Rodriguez-Frias, F. Quer, J. Matas, L. Martró, E. Sci Rep Article Accurate subtyping of hepatitis C virus genotype 1 (HCV-1) remains clinically and epidemiologically relevant. The Abbott HCV Genotype Plus RUO (GT Plus) assay, targeting the core region, was evaluated as a reflex test to resolve ambiguous HCV-1 results in a challenging sample collection. 198 HCV-1 specimens were analysed with GT Plus (38 specimens with and 160 without subtype assigned by the Abbott RealTime Genotype II (GT II) assay targeting the 5’NC and NS5B regions). Sanger sequencing of the core and/or NS5B regions were performed in 127 specimens without subtype assignment by GT II, with “not detected” results by GT Plus, or with mixed genotypes/subtypes. The remaining GT Plus results were compared to LiPA 2.0 (n = 45) or just to GT II results if concordant (n = 26). GT Plus successfully assigned the subtype in 142/160 (88.8%) samples. “Not detected” results indicated other HCV-1 subtypes/genotypes or mismatches in the core region in subtype 1b. The subtyping concordance between GT Plus and either sequencing or LiPA was 98.6% (140/142). Therefore, combined use of GT II and GT Plus assays represents a reliable and simple approach which considerably reduced the number of ambiguous HCV-1 results and enabled a successful subtyping of 98.9% of all HCV-1 samples. Nature Publishing Group UK 2019-03-06 /pmc/articles/PMC6403303/ /pubmed/30842623 http://dx.doi.org/10.1038/s41598-019-40099-3 Text en © The Author(s) 2019 Open Access This 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 license, and indicate if changes were made. The images or other third party material in this article are included in the article’s Creative Commons license, unless indicated otherwise in a credit line to the material. If material is not included in the article’s Creative Commons license 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 license, visit http://creativecommons.org/licenses/by/4.0/.
spellingShingle Article
Saludes, V.
Antuori, A.
Reinhardt, B.
Viciana, I.
Clavijo, E.
Schreiber, L.
Tenenbaum, M.
Rodriguez-Frias, F.
Quer, J.
Matas, L.
Martró, E.
Reliable resolution of ambiguous hepatitis C virus genotype 1 results with the Abbott HCV Genotype Plus RUO assay
title Reliable resolution of ambiguous hepatitis C virus genotype 1 results with the Abbott HCV Genotype Plus RUO assay
title_full Reliable resolution of ambiguous hepatitis C virus genotype 1 results with the Abbott HCV Genotype Plus RUO assay
title_fullStr Reliable resolution of ambiguous hepatitis C virus genotype 1 results with the Abbott HCV Genotype Plus RUO assay
title_full_unstemmed Reliable resolution of ambiguous hepatitis C virus genotype 1 results with the Abbott HCV Genotype Plus RUO assay
title_short Reliable resolution of ambiguous hepatitis C virus genotype 1 results with the Abbott HCV Genotype Plus RUO assay
title_sort reliable resolution of ambiguous hepatitis c virus genotype 1 results with the abbott hcv genotype plus ruo assay
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6403303/
https://www.ncbi.nlm.nih.gov/pubmed/30842623
http://dx.doi.org/10.1038/s41598-019-40099-3
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