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A reverse transcription loop-mediated isothermal amplification method for rapid detection of bovine viral diarrhea virus
A reverse transcription loop-mediated isothermal amplification (RT-LAMP) assay was developed and optimized to detect bovine viral diarrhea viral (BVDV) RNA. The RT-LAMP assay is highly sensitive and able to detect 4.67 × 10(0) copies of BVDV RNA. Additionally, the RT-LAMP method is capable of detect...
Autores principales: | , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Elsevier B.V. Published by Elsevier B.V.
2012
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7112856/ https://www.ncbi.nlm.nih.gov/pubmed/22947692 http://dx.doi.org/10.1016/j.jviromet.2012.08.007 |
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author | Fan, Qing Xie, Zhixun Xie, Liji Liu, Jiabo Pang, Yaoshan Deng, Xianwen Xie, Zhiqin Peng, Yi Wang, Xiuqing |
author_facet | Fan, Qing Xie, Zhixun Xie, Liji Liu, Jiabo Pang, Yaoshan Deng, Xianwen Xie, Zhiqin Peng, Yi Wang, Xiuqing |
author_sort | Fan, Qing |
collection | PubMed |
description | A reverse transcription loop-mediated isothermal amplification (RT-LAMP) assay was developed and optimized to detect bovine viral diarrhea viral (BVDV) RNA. The RT-LAMP assay is highly sensitive and able to detect 4.67 × 10(0) copies of BVDV RNA. Additionally, the RT-LAMP method is capable of detecting both genotypes of BVDV. No cross-reaction with other bovine viruses was observed. The ability of RT-LAMP to detect BVDV RNA from bovine fecal swabs was also evaluated. Of the 88 fecal swabs, 38 were found to be positive by RT-LAMP assay, whereas 39 were positive by real-time RT-PCR. Taken together, the BVDV specific RT-LAMP method is highly specific and sensitive and can be used as a rapid and direct diagnostic assay for testing clinical samples. |
format | Online Article Text |
id | pubmed-7112856 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2012 |
publisher | Elsevier B.V. Published by Elsevier B.V. |
record_format | MEDLINE/PubMed |
spelling | pubmed-71128562020-04-02 A reverse transcription loop-mediated isothermal amplification method for rapid detection of bovine viral diarrhea virus Fan, Qing Xie, Zhixun Xie, Liji Liu, Jiabo Pang, Yaoshan Deng, Xianwen Xie, Zhiqin Peng, Yi Wang, Xiuqing J Virol Methods Article A reverse transcription loop-mediated isothermal amplification (RT-LAMP) assay was developed and optimized to detect bovine viral diarrhea viral (BVDV) RNA. The RT-LAMP assay is highly sensitive and able to detect 4.67 × 10(0) copies of BVDV RNA. Additionally, the RT-LAMP method is capable of detecting both genotypes of BVDV. No cross-reaction with other bovine viruses was observed. The ability of RT-LAMP to detect BVDV RNA from bovine fecal swabs was also evaluated. Of the 88 fecal swabs, 38 were found to be positive by RT-LAMP assay, whereas 39 were positive by real-time RT-PCR. Taken together, the BVDV specific RT-LAMP method is highly specific and sensitive and can be used as a rapid and direct diagnostic assay for testing clinical samples. Elsevier B.V. Published by Elsevier B.V. 2012-12 2012-08-27 /pmc/articles/PMC7112856/ /pubmed/22947692 http://dx.doi.org/10.1016/j.jviromet.2012.08.007 Text en Copyright © 2012 Elsevier B.V. Published by 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 Fan, Qing Xie, Zhixun Xie, Liji Liu, Jiabo Pang, Yaoshan Deng, Xianwen Xie, Zhiqin Peng, Yi Wang, Xiuqing A reverse transcription loop-mediated isothermal amplification method for rapid detection of bovine viral diarrhea virus |
title | A reverse transcription loop-mediated isothermal amplification method for rapid detection of bovine viral diarrhea virus |
title_full | A reverse transcription loop-mediated isothermal amplification method for rapid detection of bovine viral diarrhea virus |
title_fullStr | A reverse transcription loop-mediated isothermal amplification method for rapid detection of bovine viral diarrhea virus |
title_full_unstemmed | A reverse transcription loop-mediated isothermal amplification method for rapid detection of bovine viral diarrhea virus |
title_short | A reverse transcription loop-mediated isothermal amplification method for rapid detection of bovine viral diarrhea virus |
title_sort | reverse transcription loop-mediated isothermal amplification method for rapid detection of bovine viral diarrhea virus |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7112856/ https://www.ncbi.nlm.nih.gov/pubmed/22947692 http://dx.doi.org/10.1016/j.jviromet.2012.08.007 |
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