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Development of a TaqMan-based real-time RT-PCR assay for the detection of SADS-CoV associated with severe diarrhea disease in pigs
Swine acute diarrhea syndrome coronavirus (SADS-CoV) is a novel coronavirus which was first reported in southern China in 2017. It can cause severe diarrhea disease in pigs. In order to detect this new emerging virus rapidly and reliably, a TaqMan-based real-time RT-PCR assay was established in this...
Autores principales: | , , , , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Elsevier B.V.
2018
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7113665/ https://www.ncbi.nlm.nih.gov/pubmed/29427670 http://dx.doi.org/10.1016/j.jviromet.2018.02.002 |
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author | Zhou, Ling Sun, Yuan Wu, Jiao-ling Mai, Kai-jie Chen, Gui-hua Wu, Zi-xian Bai, Yang Li, Di Zhou, Zhi-hai Cheng, Jian Wu, Rui-ting Zhang, Xiang-bin Ma, Jing-yun |
author_facet | Zhou, Ling Sun, Yuan Wu, Jiao-ling Mai, Kai-jie Chen, Gui-hua Wu, Zi-xian Bai, Yang Li, Di Zhou, Zhi-hai Cheng, Jian Wu, Rui-ting Zhang, Xiang-bin Ma, Jing-yun |
author_sort | Zhou, Ling |
collection | PubMed |
description | Swine acute diarrhea syndrome coronavirus (SADS-CoV) is a novel coronavirus which was first reported in southern China in 2017. It can cause severe diarrhea disease in pigs. In order to detect this new emerging virus rapidly and reliably, a TaqMan-based real-time RT-PCR assay was established in this study. Specific primers and probe were designed and synthesized based on the conserved region within the N gene of the viral genome. Results showed that the lowest limit of detection was 3.0 × 10(1) copies/μL. This approach was specific for SADS-CoV, and there were no cross-reaction observed against other 15 swine viruses. It was 10 times more sensitive than the conventional PCR and gave higher SADS-CoV positive detection rate (70.69%, 123/174) than the conventional PCR (51.15%, 89/174) from clinical samples. These data indicated that the TaqMan-based real-time RT-PCR assay established here was an effective method with high sensitivity, specificity and reproducibility for faster and more accurate detection and quantification of SADS-CoV. |
format | Online Article Text |
id | pubmed-7113665 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2018 |
publisher | Elsevier B.V. |
record_format | MEDLINE/PubMed |
spelling | pubmed-71136652020-04-02 Development of a TaqMan-based real-time RT-PCR assay for the detection of SADS-CoV associated with severe diarrhea disease in pigs Zhou, Ling Sun, Yuan Wu, Jiao-ling Mai, Kai-jie Chen, Gui-hua Wu, Zi-xian Bai, Yang Li, Di Zhou, Zhi-hai Cheng, Jian Wu, Rui-ting Zhang, Xiang-bin Ma, Jing-yun J Virol Methods Article Swine acute diarrhea syndrome coronavirus (SADS-CoV) is a novel coronavirus which was first reported in southern China in 2017. It can cause severe diarrhea disease in pigs. In order to detect this new emerging virus rapidly and reliably, a TaqMan-based real-time RT-PCR assay was established in this study. Specific primers and probe were designed and synthesized based on the conserved region within the N gene of the viral genome. Results showed that the lowest limit of detection was 3.0 × 10(1) copies/μL. This approach was specific for SADS-CoV, and there were no cross-reaction observed against other 15 swine viruses. It was 10 times more sensitive than the conventional PCR and gave higher SADS-CoV positive detection rate (70.69%, 123/174) than the conventional PCR (51.15%, 89/174) from clinical samples. These data indicated that the TaqMan-based real-time RT-PCR assay established here was an effective method with high sensitivity, specificity and reproducibility for faster and more accurate detection and quantification of SADS-CoV. Elsevier B.V. 2018-05 2018-02-07 /pmc/articles/PMC7113665/ /pubmed/29427670 http://dx.doi.org/10.1016/j.jviromet.2018.02.002 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 Zhou, Ling Sun, Yuan Wu, Jiao-ling Mai, Kai-jie Chen, Gui-hua Wu, Zi-xian Bai, Yang Li, Di Zhou, Zhi-hai Cheng, Jian Wu, Rui-ting Zhang, Xiang-bin Ma, Jing-yun Development of a TaqMan-based real-time RT-PCR assay for the detection of SADS-CoV associated with severe diarrhea disease in pigs |
title | Development of a TaqMan-based real-time RT-PCR assay for the detection of SADS-CoV associated with severe diarrhea disease in pigs |
title_full | Development of a TaqMan-based real-time RT-PCR assay for the detection of SADS-CoV associated with severe diarrhea disease in pigs |
title_fullStr | Development of a TaqMan-based real-time RT-PCR assay for the detection of SADS-CoV associated with severe diarrhea disease in pigs |
title_full_unstemmed | Development of a TaqMan-based real-time RT-PCR assay for the detection of SADS-CoV associated with severe diarrhea disease in pigs |
title_short | Development of a TaqMan-based real-time RT-PCR assay for the detection of SADS-CoV associated with severe diarrhea disease in pigs |
title_sort | development of a taqman-based real-time rt-pcr assay for the detection of sads-cov associated with severe diarrhea disease in pigs |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7113665/ https://www.ncbi.nlm.nih.gov/pubmed/29427670 http://dx.doi.org/10.1016/j.jviromet.2018.02.002 |
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