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Using a Pan-Viral Microarray Assay (Virochip) to Screen Clinical Samples for Viral Pathogens

The diagnosis of viral causes of many infectious diseases is difficult due to the inherent sequence diversity of viruses as well as the ongoing emergence of novel viral pathogens, such as SARS coronavirus and 2009 pandemic H1N1 influenza virus, that are not detectable by traditional methods. To addr...

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Autores principales: Chen, Eunice C., Miller, Steve A., DeRisi, Joseph L., Chiu, Charles Y.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: MyJove Corporation 2011
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3169278/
https://www.ncbi.nlm.nih.gov/pubmed/21559002
http://dx.doi.org/10.3791/2536
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author Chen, Eunice C.
Miller, Steve A.
DeRisi, Joseph L.
Chiu, Charles Y.
author_facet Chen, Eunice C.
Miller, Steve A.
DeRisi, Joseph L.
Chiu, Charles Y.
author_sort Chen, Eunice C.
collection PubMed
description The diagnosis of viral causes of many infectious diseases is difficult due to the inherent sequence diversity of viruses as well as the ongoing emergence of novel viral pathogens, such as SARS coronavirus and 2009 pandemic H1N1 influenza virus, that are not detectable by traditional methods. To address these challenges, we have previously developed and validated a pan-viral microarray platform called the Virochip with the capacity to detect all known viruses as well as novel variants on the basis of conserved sequence homology(1). Using the Virochip, we have identified the full spectrum of viruses associated with respiratory infections, including cases of unexplained critical illness in hospitalized patients, with a sensitivity equivalent to or superior to conventional clinical testing(2-5). The Virochip has also been used to identify novel viruses, including the SARS coronavirus(6,7), a novel rhinovirus clade(5), XMRV (a retrovirus linked to prostate cancer)(8), avian bornavirus (the cause of a wasting disease in parrots)(9), and a novel cardiovirus in children with respiratory and diarrheal illness(10). The current version of the Virochip has been ported to an Agilent microarray platform and consists of ~36,000 probes derived from over ~1,500 viruses in GenBank as of December of 2009. Here we demonstrate the steps involved in processing a Virochip assay from start to finish (~24 hour turnaround time), including sample nucleic acid extraction, PCR amplification using random primers, fluorescent dye incorporation, and microarray hybridization, scanning, and analysis.
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spelling pubmed-31692782011-10-05 Using a Pan-Viral Microarray Assay (Virochip) to Screen Clinical Samples for Viral Pathogens Chen, Eunice C. Miller, Steve A. DeRisi, Joseph L. Chiu, Charles Y. J Vis Exp Immunology The diagnosis of viral causes of many infectious diseases is difficult due to the inherent sequence diversity of viruses as well as the ongoing emergence of novel viral pathogens, such as SARS coronavirus and 2009 pandemic H1N1 influenza virus, that are not detectable by traditional methods. To address these challenges, we have previously developed and validated a pan-viral microarray platform called the Virochip with the capacity to detect all known viruses as well as novel variants on the basis of conserved sequence homology(1). Using the Virochip, we have identified the full spectrum of viruses associated with respiratory infections, including cases of unexplained critical illness in hospitalized patients, with a sensitivity equivalent to or superior to conventional clinical testing(2-5). The Virochip has also been used to identify novel viruses, including the SARS coronavirus(6,7), a novel rhinovirus clade(5), XMRV (a retrovirus linked to prostate cancer)(8), avian bornavirus (the cause of a wasting disease in parrots)(9), and a novel cardiovirus in children with respiratory and diarrheal illness(10). The current version of the Virochip has been ported to an Agilent microarray platform and consists of ~36,000 probes derived from over ~1,500 viruses in GenBank as of December of 2009. Here we demonstrate the steps involved in processing a Virochip assay from start to finish (~24 hour turnaround time), including sample nucleic acid extraction, PCR amplification using random primers, fluorescent dye incorporation, and microarray hybridization, scanning, and analysis. MyJove Corporation 2011-04-27 /pmc/articles/PMC3169278/ /pubmed/21559002 http://dx.doi.org/10.3791/2536 Text en Copyright © 2011, Journal of Visualized Experiments http://creativecommons.org/licenses/by-nc-nd/3.0/ This is an open-access article distributed under the terms of the Creative Commons Attribution-NonCommercial-NoDerivs 3.0 Unported License. To view a copy of this license, visithttp://creativecommons.org/licenses/by-nc-nd/3.0/
spellingShingle Immunology
Chen, Eunice C.
Miller, Steve A.
DeRisi, Joseph L.
Chiu, Charles Y.
Using a Pan-Viral Microarray Assay (Virochip) to Screen Clinical Samples for Viral Pathogens
title Using a Pan-Viral Microarray Assay (Virochip) to Screen Clinical Samples for Viral Pathogens
title_full Using a Pan-Viral Microarray Assay (Virochip) to Screen Clinical Samples for Viral Pathogens
title_fullStr Using a Pan-Viral Microarray Assay (Virochip) to Screen Clinical Samples for Viral Pathogens
title_full_unstemmed Using a Pan-Viral Microarray Assay (Virochip) to Screen Clinical Samples for Viral Pathogens
title_short Using a Pan-Viral Microarray Assay (Virochip) to Screen Clinical Samples for Viral Pathogens
title_sort using a pan-viral microarray assay (virochip) to screen clinical samples for viral pathogens
topic Immunology
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3169278/
https://www.ncbi.nlm.nih.gov/pubmed/21559002
http://dx.doi.org/10.3791/2536
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