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Species-specific identification of variola, monkeypox, cowpox, and vaccinia viruses by multiplex real-time PCR assay

A method of one-stage rapid identification of variola (VARV), monkeypox (MPXV), cowpox (CPXV), and vaccinia (VACV) viruses, pathogenic for humans, utilizing multiplex real-time TaqMan PCR (MuRT-PCR) assay was developed. Four pairs of oligonucleotide primers and four hybridization probes with various...

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Autores principales: Shchelkunov, Sergei N., Shcherbakov, Dmitrii N., Maksyutov, Rinat A., Gavrilova, Elena V.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Elsevier B.V. 2011
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9628778/
https://www.ncbi.nlm.nih.gov/pubmed/21635922
http://dx.doi.org/10.1016/j.jviromet.2011.05.002
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author Shchelkunov, Sergei N.
Shcherbakov, Dmitrii N.
Maksyutov, Rinat A.
Gavrilova, Elena V.
author_facet Shchelkunov, Sergei N.
Shcherbakov, Dmitrii N.
Maksyutov, Rinat A.
Gavrilova, Elena V.
author_sort Shchelkunov, Sergei N.
collection PubMed
description A method of one-stage rapid identification of variola (VARV), monkeypox (MPXV), cowpox (CPXV), and vaccinia (VACV) viruses, pathogenic for humans, utilizing multiplex real-time TaqMan PCR (MuRT-PCR) assay was developed. Four pairs of oligonucleotide primers and four hybridization probes with various fluorescent dyes and the corresponding fluorescence quenchers were concurrently used for MuRT-PCR assay. The hybridization probe specific for the VARV sequence contained FAM/BHQ1 as a dye/quencher pair; MPXV-specific, TAMRA/BHQ2; CPXV-specific, JOE/BHQ1; VACV-specific, Cy5/BHQ3. The specificity and sensitivity of the developed method were assessed by analyzing DNA of 29 strains belonging to six orthopoxvirus species as well as the DNA samples isolated from archive clinical specimens of human smallpox cases and experimental specimens isolated from CPXV-infected mice and MPXV-infected marmot.
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spelling pubmed-96287782022-11-03 Species-specific identification of variola, monkeypox, cowpox, and vaccinia viruses by multiplex real-time PCR assay Shchelkunov, Sergei N. Shcherbakov, Dmitrii N. Maksyutov, Rinat A. Gavrilova, Elena V. J Virol Methods Article A method of one-stage rapid identification of variola (VARV), monkeypox (MPXV), cowpox (CPXV), and vaccinia (VACV) viruses, pathogenic for humans, utilizing multiplex real-time TaqMan PCR (MuRT-PCR) assay was developed. Four pairs of oligonucleotide primers and four hybridization probes with various fluorescent dyes and the corresponding fluorescence quenchers were concurrently used for MuRT-PCR assay. The hybridization probe specific for the VARV sequence contained FAM/BHQ1 as a dye/quencher pair; MPXV-specific, TAMRA/BHQ2; CPXV-specific, JOE/BHQ1; VACV-specific, Cy5/BHQ3. The specificity and sensitivity of the developed method were assessed by analyzing DNA of 29 strains belonging to six orthopoxvirus species as well as the DNA samples isolated from archive clinical specimens of human smallpox cases and experimental specimens isolated from CPXV-infected mice and MPXV-infected marmot. Elsevier B.V. 2011-08 2011-05-26 /pmc/articles/PMC9628778/ /pubmed/21635922 http://dx.doi.org/10.1016/j.jviromet.2011.05.002 Text en Copyright © 2011 Elsevier B.V. All rights reserved. Elsevier has created a Monkeypox Information Center (https://www.elsevier.com/connect/monkeypox-information-center) in response to the declared public health emergency of international concern, with free information in English on the monkeypox virus. The Monkeypox Information Center is hosted on Elsevier Connect, the company's public news and information website. Elsevier hereby grants permission to make all its monkeypox related research that is available on the Monkeypox Information Center - including this research content - immediately available in publicly funded repositories, 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 Monkeypox Information Center remains active.
spellingShingle Article
Shchelkunov, Sergei N.
Shcherbakov, Dmitrii N.
Maksyutov, Rinat A.
Gavrilova, Elena V.
Species-specific identification of variola, monkeypox, cowpox, and vaccinia viruses by multiplex real-time PCR assay
title Species-specific identification of variola, monkeypox, cowpox, and vaccinia viruses by multiplex real-time PCR assay
title_full Species-specific identification of variola, monkeypox, cowpox, and vaccinia viruses by multiplex real-time PCR assay
title_fullStr Species-specific identification of variola, monkeypox, cowpox, and vaccinia viruses by multiplex real-time PCR assay
title_full_unstemmed Species-specific identification of variola, monkeypox, cowpox, and vaccinia viruses by multiplex real-time PCR assay
title_short Species-specific identification of variola, monkeypox, cowpox, and vaccinia viruses by multiplex real-time PCR assay
title_sort species-specific identification of variola, monkeypox, cowpox, and vaccinia viruses by multiplex real-time pcr assay
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9628778/
https://www.ncbi.nlm.nih.gov/pubmed/21635922
http://dx.doi.org/10.1016/j.jviromet.2011.05.002
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