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Viral RNA extraction for in-the-field analysis

Retroviruses encode their genetic information with RNA molecules, and have a high genomic recombination rate which allows them to mutate more rapidly, thereby posting a higher risk to humans. One important way to help combat a pandemic of viral infectious diseases is early detection before large-sca...

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Detalles Bibliográficos
Autores principales: Zhong, Jiang F., Weiner, Leslie P., Burke, Kathy, Taylor, Clive R.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Elsevier B.V. 2007
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3635480/
https://www.ncbi.nlm.nih.gov/pubmed/17548117
http://dx.doi.org/10.1016/j.jviromet.2007.04.006
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author Zhong, Jiang F.
Weiner, Leslie P.
Burke, Kathy
Taylor, Clive R.
author_facet Zhong, Jiang F.
Weiner, Leslie P.
Burke, Kathy
Taylor, Clive R.
author_sort Zhong, Jiang F.
collection PubMed
description Retroviruses encode their genetic information with RNA molecules, and have a high genomic recombination rate which allows them to mutate more rapidly, thereby posting a higher risk to humans. One important way to help combat a pandemic of viral infectious diseases is early detection before large-scale outbreaks occur. The polymerase chain reaction (PCR) and reverse transcription-PCR (RT-PCR) have been used to identify precisely different strains of some very closely related pathogens. However, isolation and detection of viral RNA in the field are difficult due to the unstable nature of viral RNA molecules. Consequently, performing in-the-field nucleic acid analysis to monitor the spread of viruses is financially and technologically challenging in remote and underdeveloped regions that are high-risk areas for outbreaks. A simplified rapid viral RNA extraction method is reported to meet the requirements for in-the-field viral RNA extraction and detection. The ability of this device to perform viral RNA extraction with subsequent RT-PCR detection of retrovirus is demonstrated. This inexpensive device has the potential to be distributed on a large scale to underdeveloped regions for early detection of retrovirus, with the possibility of reducing viral pandemic events.
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spelling pubmed-36354802013-04-25 Viral RNA extraction for in-the-field analysis Zhong, Jiang F. Weiner, Leslie P. Burke, Kathy Taylor, Clive R. J Virol Methods Article Retroviruses encode their genetic information with RNA molecules, and have a high genomic recombination rate which allows them to mutate more rapidly, thereby posting a higher risk to humans. One important way to help combat a pandemic of viral infectious diseases is early detection before large-scale outbreaks occur. The polymerase chain reaction (PCR) and reverse transcription-PCR (RT-PCR) have been used to identify precisely different strains of some very closely related pathogens. However, isolation and detection of viral RNA in the field are difficult due to the unstable nature of viral RNA molecules. Consequently, performing in-the-field nucleic acid analysis to monitor the spread of viruses is financially and technologically challenging in remote and underdeveloped regions that are high-risk areas for outbreaks. A simplified rapid viral RNA extraction method is reported to meet the requirements for in-the-field viral RNA extraction and detection. The ability of this device to perform viral RNA extraction with subsequent RT-PCR detection of retrovirus is demonstrated. This inexpensive device has the potential to be distributed on a large scale to underdeveloped regions for early detection of retrovirus, with the possibility of reducing viral pandemic events. Elsevier B.V. 2007-09 2007-06-04 /pmc/articles/PMC3635480/ /pubmed/17548117 http://dx.doi.org/10.1016/j.jviromet.2007.04.006 Text en Copyright © 2007 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
Zhong, Jiang F.
Weiner, Leslie P.
Burke, Kathy
Taylor, Clive R.
Viral RNA extraction for in-the-field analysis
title Viral RNA extraction for in-the-field analysis
title_full Viral RNA extraction for in-the-field analysis
title_fullStr Viral RNA extraction for in-the-field analysis
title_full_unstemmed Viral RNA extraction for in-the-field analysis
title_short Viral RNA extraction for in-the-field analysis
title_sort viral rna extraction for in-the-field analysis
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3635480/
https://www.ncbi.nlm.nih.gov/pubmed/17548117
http://dx.doi.org/10.1016/j.jviromet.2007.04.006
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