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Accurate and precise real-time RT-PCR assays for the identification of astrovirus associated encephalitis in cattle

A novel bovine astrovirus genotype species (BoAstV-CH13/NeuroS1) was recently identified in brain tissues of cattle as a plausible cause of encephalitis. The purpose of the present study was to develop and validate real time RT-PCR assays for the detection of BoAstV-CH13/NeuroS1 in brain tissues of...

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Autores principales: Lüthi, Ramona, Boujon, Céline L., Kauer, Ronja, Koch, Michel C., Bouzalas, Ilias G., Seuberlich, Torsten
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Nature Publishing Group UK 2018
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6003944/
https://www.ncbi.nlm.nih.gov/pubmed/29907784
http://dx.doi.org/10.1038/s41598-018-27533-8
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author Lüthi, Ramona
Boujon, Céline L.
Kauer, Ronja
Koch, Michel C.
Bouzalas, Ilias G.
Seuberlich, Torsten
author_facet Lüthi, Ramona
Boujon, Céline L.
Kauer, Ronja
Koch, Michel C.
Bouzalas, Ilias G.
Seuberlich, Torsten
author_sort Lüthi, Ramona
collection PubMed
description A novel bovine astrovirus genotype species (BoAstV-CH13/NeuroS1) was recently identified in brain tissues of cattle as a plausible cause of encephalitis. The purpose of the present study was to develop and validate real time RT-PCR assays for the detection of BoAstV-CH13/NeuroS1 in brain tissues of cattle. Three different primer-probe combinations were designed based on BoAstV-CH13/NeuroS1 full-genome sequences of 11 different strains identified in cattle, and established in three distinct one-step real time RT-PCR protocols. These protocols were compared regarding their diagnostic performance using brain tissues of cattle with and without astrovirus associated encephalitis. The limit of detection (LOD) of all three assays was between 1.34 × 10(1) and 1.34 × 10(2) RNA copies, leading to an analytical sensitivity two orders of magnitude superior compared to a conventional pan-astrovirus RT-PCR protocol (LOD 1.31 × 10(4) RNA copies). Amplification efficiency was in the range of 97.3% to 107.5% with linearity (R(2)) > 0.99. The diagnostic sensitivity and specificity of the assays was determined as 100%, and all three revealed good intra- and inter-test repeatability. In conclusion, the newly developed RT-qPCRs are sensitive, specific, and reliable test formats that will facilitate BoAstV-CH13/NeuroS1 detection in routine diagnostics as well as in research settings.
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spelling pubmed-60039442018-06-26 Accurate and precise real-time RT-PCR assays for the identification of astrovirus associated encephalitis in cattle Lüthi, Ramona Boujon, Céline L. Kauer, Ronja Koch, Michel C. Bouzalas, Ilias G. Seuberlich, Torsten Sci Rep Article A novel bovine astrovirus genotype species (BoAstV-CH13/NeuroS1) was recently identified in brain tissues of cattle as a plausible cause of encephalitis. The purpose of the present study was to develop and validate real time RT-PCR assays for the detection of BoAstV-CH13/NeuroS1 in brain tissues of cattle. Three different primer-probe combinations were designed based on BoAstV-CH13/NeuroS1 full-genome sequences of 11 different strains identified in cattle, and established in three distinct one-step real time RT-PCR protocols. These protocols were compared regarding their diagnostic performance using brain tissues of cattle with and without astrovirus associated encephalitis. The limit of detection (LOD) of all three assays was between 1.34 × 10(1) and 1.34 × 10(2) RNA copies, leading to an analytical sensitivity two orders of magnitude superior compared to a conventional pan-astrovirus RT-PCR protocol (LOD 1.31 × 10(4) RNA copies). Amplification efficiency was in the range of 97.3% to 107.5% with linearity (R(2)) > 0.99. The diagnostic sensitivity and specificity of the assays was determined as 100%, and all three revealed good intra- and inter-test repeatability. In conclusion, the newly developed RT-qPCRs are sensitive, specific, and reliable test formats that will facilitate BoAstV-CH13/NeuroS1 detection in routine diagnostics as well as in research settings. Nature Publishing Group UK 2018-06-15 /pmc/articles/PMC6003944/ /pubmed/29907784 http://dx.doi.org/10.1038/s41598-018-27533-8 Text en © The Author(s) 2018 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
Lüthi, Ramona
Boujon, Céline L.
Kauer, Ronja
Koch, Michel C.
Bouzalas, Ilias G.
Seuberlich, Torsten
Accurate and precise real-time RT-PCR assays for the identification of astrovirus associated encephalitis in cattle
title Accurate and precise real-time RT-PCR assays for the identification of astrovirus associated encephalitis in cattle
title_full Accurate and precise real-time RT-PCR assays for the identification of astrovirus associated encephalitis in cattle
title_fullStr Accurate and precise real-time RT-PCR assays for the identification of astrovirus associated encephalitis in cattle
title_full_unstemmed Accurate and precise real-time RT-PCR assays for the identification of astrovirus associated encephalitis in cattle
title_short Accurate and precise real-time RT-PCR assays for the identification of astrovirus associated encephalitis in cattle
title_sort accurate and precise real-time rt-pcr assays for the identification of astrovirus associated encephalitis in cattle
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6003944/
https://www.ncbi.nlm.nih.gov/pubmed/29907784
http://dx.doi.org/10.1038/s41598-018-27533-8
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