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Validation Study of a Direct Real-Time PCR Protocol for Detection of Monkeypox Virus

Monkeypox has recently been described as a public health emergency of international concern by the World Health Organization and a public health emergency by the United States. If the outbreak continues to grow, rapid scalability of laboratory testing will be imperative. During the early days of the...

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Autores principales: Chelsky, Zachary L., Dittmann, David, Blanke, Timothy, Chang, Michael, Vormittag-Nocito, Erica, Jennings, Lawrence J.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Association for Molecular Pathology and American Society for Investigative Pathology. Published by Elsevier Inc. 2022
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9534136/
https://www.ncbi.nlm.nih.gov/pubmed/36113759
http://dx.doi.org/10.1016/j.jmoldx.2022.09.001
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author Chelsky, Zachary L.
Dittmann, David
Blanke, Timothy
Chang, Michael
Vormittag-Nocito, Erica
Jennings, Lawrence J.
author_facet Chelsky, Zachary L.
Dittmann, David
Blanke, Timothy
Chang, Michael
Vormittag-Nocito, Erica
Jennings, Lawrence J.
author_sort Chelsky, Zachary L.
collection PubMed
description Monkeypox has recently been described as a public health emergency of international concern by the World Health Organization and a public health emergency by the United States. If the outbreak continues to grow, rapid scalability of laboratory testing will be imperative. During the early days of the coronavirus disease 2019 (COVID-19) pandemic, laboratories improved the scalability of testing by using a direct-to-PCR approach. To improve the scalability of monkeypox testing, a direct real-time PCR protocol for the detection of monkeypox virus was validated. The assay retains the sensitivity and accuracy of the indirect assay while eliminating the need for nucleic acid extraction kits, reducing laboratory technologist time per sample and decreasing exposure to an infectious agent. The direct method will make it easier for laboratories across the world to rapidly develop, validate, and scale testing for monkeypox virus.
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spelling pubmed-95341362022-10-07 Validation Study of a Direct Real-Time PCR Protocol for Detection of Monkeypox Virus Chelsky, Zachary L. Dittmann, David Blanke, Timothy Chang, Michael Vormittag-Nocito, Erica Jennings, Lawrence J. J Mol Diagn Regular Article Monkeypox has recently been described as a public health emergency of international concern by the World Health Organization and a public health emergency by the United States. If the outbreak continues to grow, rapid scalability of laboratory testing will be imperative. During the early days of the coronavirus disease 2019 (COVID-19) pandemic, laboratories improved the scalability of testing by using a direct-to-PCR approach. To improve the scalability of monkeypox testing, a direct real-time PCR protocol for the detection of monkeypox virus was validated. The assay retains the sensitivity and accuracy of the indirect assay while eliminating the need for nucleic acid extraction kits, reducing laboratory technologist time per sample and decreasing exposure to an infectious agent. The direct method will make it easier for laboratories across the world to rapidly develop, validate, and scale testing for monkeypox virus. Association for Molecular Pathology and American Society for Investigative Pathology. Published by Elsevier Inc. 2022-11 2022-09-13 /pmc/articles/PMC9534136/ /pubmed/36113759 http://dx.doi.org/10.1016/j.jmoldx.2022.09.001 Text en © 2022 Association for Molecular Pathology and American Society for Investigative Pathology. Published by Elsevier Inc. 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 Regular Article
Chelsky, Zachary L.
Dittmann, David
Blanke, Timothy
Chang, Michael
Vormittag-Nocito, Erica
Jennings, Lawrence J.
Validation Study of a Direct Real-Time PCR Protocol for Detection of Monkeypox Virus
title Validation Study of a Direct Real-Time PCR Protocol for Detection of Monkeypox Virus
title_full Validation Study of a Direct Real-Time PCR Protocol for Detection of Monkeypox Virus
title_fullStr Validation Study of a Direct Real-Time PCR Protocol for Detection of Monkeypox Virus
title_full_unstemmed Validation Study of a Direct Real-Time PCR Protocol for Detection of Monkeypox Virus
title_short Validation Study of a Direct Real-Time PCR Protocol for Detection of Monkeypox Virus
title_sort validation study of a direct real-time pcr protocol for detection of monkeypox virus
topic Regular Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9534136/
https://www.ncbi.nlm.nih.gov/pubmed/36113759
http://dx.doi.org/10.1016/j.jmoldx.2022.09.001
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